Succination of Protein Disulfide Isomerase Links Mitochondrial Stress and Endoplasmic Reticulum Stress in the Adipocyte During Diabetes

Mitochondrial stress drives ER stress in adipocytes matured in high glucose

The development of mitochondrial stress as a direct result of increased glucose oxidation (Fig. 1) is expected to increase the basal oxygen consumption rate (OCR) of the adipocyte under diabetic conditions. We matured 3T3-L1 adipocytes in glucose and insulin concentrations that we had previously shown as physiologically representative of normal versus hyperglycemic/hyperinsulinemic conditions (5 mM glucose/0.3 nM insulin vs. 30 mM glucose/3 nM insulin) (53). We observed a ∼90% increase in the basal OCR of adipocytes matured in 30 mM glucose compared with in 5 mM glucose after 2 days of maturation (Supplementary Figs. S1B and S12B; Supplementary Data are available online at www.liebertpub.com/ars). Our previous analyses of uncoupled respiration in adipocytes cultured in high glucose demonstrated that the cells are operating close to their maximal respiratory capacity, a manifestation of mitochondrial stress (53). Metabolomic analyses confirmed that Krebs cycle intermediates, including fumarate, were increased in concert in high-glucose conditions as a consequence of respiratory control and the inhibition of NAD⁺-dependent dehydrogenases (Fig. 2A and Supplementary Fig. S1B, E). The increase in malate as well as fumarate confirms that the adipocyte is overwhelmed due to excessive ATP production (12), and immunoblotting using the anti-2SC antibody verifies that protein succination is significantly increased in adipocytes matured in high- versus normal glucose concentrations (Supplementary Fig. S1C) (38). Adipocytes were matured in 5 mM glucose and treated with 0, 2, or 4 mM dimethyl succinate (DMS), an esterified form of the Krebs cycle intermediate succinate, to confirm that the anaplerotic supply of an alternative intermediate could augment endogenous fumarate production and protein succination. An anti-2SC immunoblot (IB) confirms increased succination of target proteins in the succinate-supplemented adipocytes (Supplementary Figs. S1A and S12A). These results emphasize that adipocytes matured in high glucose exhibit features of mitochondrial stress early in maturation, with a subsequent increase in protein succination after 8 days of maturation (Fig. 1). In contrast, adipocytes that mature and accumulate lipid normally in 5 mM glucose show no evidence of mitochondrial stress and have limited protein succination.

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FIG. 2.

Mitochondrial stress drives ER stress in adipocytes matured in high glucose. (A) Krebs cycle metabolites were extracted from adipocytes matured in 5 or 30 mM glucose or 30 mM glucose and 2 μM niclosamide for 3 days before quantification by GC-MS. High-glucose concentrations result in significantly increased levels of both fumarate and malate relative to the levels quantified in 5 mM glucose (n = 3/group, mean ± SEM, *p < 0.05). (B) Adipocytes were matured in 5 or 30 mM glucose for 8 days. A Western blot was performed with 30 μg of protein from duplicate representative samples by using anti-2SC antibody to detect succinated proteins. Molecular-weight markers are shown on the far left. (C) Adipocytes were matured in 5 or 30 mM glucose with 2 μM nicolsamide for 8 days. Western blots were performed with 30 μg of protein to detect ER stress markers with anti-CHOP, -GRP78, -Ero1, and -PDI antibodies. Coomassie blue stain of the blot confirms equal loading of all samples. (D) An immunoblot probed with anti-adiponectin antibody shows the levels of secreted adiponectin assessed in the conditioned medium collected after 4 h from adipocytes matured in 5 or 30 mM glucose treated with 2 μM niclosamide. This is a merged image (merged between lanes 3 and 4). Immunoblots are representative of n = 3 experiments. CHOP, C/EBP homologous protein; Ero1, ER oxidoreductin 1; GRP78, 78 kDa glucose-related protein; SEM, standard error of the mean. To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

Protein succination occurs as a direct result of mitochondrial respiratory control in the metabolically challenged adipocyte (Fig. 1) (12); therefore, we hypothesized that uncoupling the inner mitochondrial membrane by using niclosamide would lower fumarate and 2SC levels. 3T3-L1 adipocytes were matured in 5 or 30 mM glucose or 30 mM glucose and treated with 2 μM niclosamide for 8 days. Metabolomic analyses substantiated the data that uncoupling the inner mitochondrial membrane, demonstrated by the acute increase in the basal OCR (Supplementary Fig. S1D) (54), prevents the accumulation of Krebs cycle intermediates in adipocytes matured in high glucose concentrations (Fig. 2A and Supplementary Fig. S1E). Immunoblotting with the anti-2SC antibody demonstrates that niclosamide treatment reduces the degree of protein succination in adipocytes matured in 30 mM glucose concentrations (Fig. 2B and Supplementary Fig. S6A). The lower panels depict shorter exposure times of the same anti-2SC IB and highlight the decreased succination of several higher-molecular-weight proteins (50–150 kDa) (Fig. 2B and Supplementary Fig. S6A). Examining the relationship between protein folding, ER stress, and glucose concentration, we assessed the levels of CHOP, Ero1, and PDI in adipocytes matured in 5 or 30 mM glucose. The levels of CHOP were pronouncedly increased in adipocytes matured in high glucose compared with normal glucose (Supplementary Figs. S1C and S12C), confirming that persistent ER stress is selectively present in adipocytes matured under hyperglycemic conditions (53). It is important to note that we did not detect differences in the protein levels of GRP78 or any components of the PERK, IRE1, or ATF6 branches of the UPR in adipocytes in normal/high glucose as the UPR is induced as a normal function of adipocyte maturation in the presence of insulin (16, 36, 53). To establish a novel link between mitochondrial stress and the sustained ER stress, we examined CHOP protein expression levels in adipocytes matured in 5, 30, or 30 mM glucose treated with 2 μM niclosamide for 8 days (Fig. 2C and Supplementary Fig. S6B). The data confirm that alleviating mitochondrial stress prevents the presence of prolonged ER stress generated by high-glucose conditions. Although the transcription of ER chaperones may be upregulated in parallel with ER stress, we did not detect any changes in the total protein levels of Ero1 or PDI between groups (Fig. 2C, Supplementary Figs. S1C, S6B, and S12C). Importantly, the alleviation of both mitochondrial and ER stress with niclosamide corresponds to improved adiponectin secretion (Fig. 2D and Supplementary Fig. S6C), confirming that mitochondrial stress and succination impair adiponectin oligomer processing in the ER (11). These data confirm that mitochondrial stress and protein succination influence the development of ER stress and reduce adiponectin secretion from the adipocyte.

Protein succination induces ER stress independent of glucose concentration

Lentiviral delivery of fumarase short hairpin ribonucleic acid (shRNA) to adipocytes matured in normal glucose was used to increase fumarate levels in the adipocyte independent of glucotoxicity, since this prevents the hydration to malate and permits fumarate accumulation. The successful transduction of both the scrambled control and fumarase knockdown lentivirus was evaluated by monitoring green fluorescent protein (GFP)-positive adipocytes 6 days post-transduction (Supplementary Fig. S2A). Adipogenesis proceeded normally in fumarase knockdown cells and was confirmed by the elevated expression of adiponectin and peroxisome proliferator-activated receptor gamma (PPARγ) isoforms (Fig. 3A and Supplementary Fig. S7A). Reduced serum adiponectin species are a hallmark of type 2 diabetes. We observed a decrease in secreted adiponectin profiles from the fumarase knockdown adipocytes versus the scrambled controls (Supplementary Figs. S2D and S13), again confirming that elevated fumarate and succination lead to reduced serum adiponectin levels (11). The quantification of the triglyceride content in control and fumarase knockdown adipocytes matured in 5 or 30 mM glucose (Fig. 3B), as well as the documented lipid accumulation by Oil Red O staining (Supplementary Fig. S2B) verified that knocking down the expression of fumarase does not interfere with adipogenesis. The ∼50% knockdown of fumarase levels observed was sufficient to increase protein succination in the adipocytes (Fig. 3A and Supplementary Fig. S7A). The pronounced escalation in protein succination in the fumarase knockdown adipocytes is directly proportional to the dramatic increase in the intracellular fumarate production. Analysis of mitochondrial metabolites from control and fumarase knockdown adipocytes matured in 5 mM glucose reveals a ∼30-fold increase in fumarate compared with controls (Fig. 3C and Supplementary Fig. S2C). Fumarase knockdown adipocytes displayed significant increases in the secretion of the pro-inflammatory cytokines tumor necrosis factor alpha (TNFα), interleukin 1 alpha (IL-1α), and interleukin 1 beta (IL-1β), as well as vascular endothelial growth factor (VEGF), versus control adipocytes (Fig. 3D and Supplementary Fig. S2E). This was similar to the significant increases in TNFα, MCP-1, and VEGF that we previously observed in adipocytes matured in 30 mM versus 5 mM glucose (53). These data suggest that elevated fumarate and protein succination may play a role in the chronic low-grade inflammatory state of adipose tissue observed during diabetes. Elevated CHOP levels were observed in both 30 mM glucose and fumarase knockdown adipocytes matured in 5 mM glucose (Fig. 3E and Supplementary Fig. S7B), confirming that protein succination alone functionally contributes to both the development of ER stress and the pro-inflammatory state of adipocytes, independent of other glucose-derived metabolic stressors. To mechanistically understand how succination might contribute to ER stress, we examined the succination of PDI in adipocytes during glucotoxicity. PDI was immunoprecipitated from adipocytes matured in 5 or 30 mM glucose and examined by two-dimensional immunoblotting to detect succination (Fig. 3F, top panels) followed by reprobing with anti-PDI (Fig. 3F, lower panels). Compared with the total levels of immunoprecipitated PDI, there was significantly more succinated PDI in adipocytes matured in high glucose. We also confirmed increased PDI succination in fumarase knockout (Fh ^−/−) mouse embryonic fibroblasts (MEFs), whose endogenous fumarate concentrations are ∼5 mM (55) (Supplementary Figs. S3 and S14). Overall, the results confirm that PDI is succinated in the presence of excess fumarate, potentially interfering with protein folding.

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FIG. 3.

Protein succination induces ER stress independent of glucose concentrations. (A) 3T3-L1 fibroblasts were transduced with fumarase knockdown shRNA and grown to confluence. Fumarase knockdown or control adipocytes were matured in 5 or 30 mM glucose for 8 days. A merged image of the same 1D immunoblot probed with anti-2SC and -fumarase antibodies displays increased protein succination in both fibroblasts and adipocytes when fumarase expression is knocked down. The blot was stripped and reprobed with anti-PPARγ antibody to confirm that fumarase knockdown 3T3-L1 fibroblasts differentiate normally to adipocytes. The blot was reprobed with anti-α tubulin antibody that served as a protein loading control. (B) Control or fumarase knockdown adipocytes were matured in 5 or 30 mM glucose for 8 days. The triglyceride content was measured as described in the Materials and Methods section (n = 3/group, mean ± SEM, *p < 0.05). (C) Krebs cycle metabolites were extracted from adipocytes transduced with scrambled control or fumarase knockdown lentivirus, matured in 5 mM glucose for 3 days, and derivatized before quantification by GC-MS. Limited fumarase expression results in a significant increase in the levels of all metabolites. The increases are expressed relative to the levels quantified in control adipocytes that have normal levels of fumarase present (n = 3/group, mean ± SEM, *p < 0.05). (D) Secreted levels of pro-inflammatory cytokines were measured by a mouse obesity ELISA as described in the Materials and Methods section (n = 4/group, mean ± SEM, *p < 0.05). (E) Adipocytes transduced with fumarase knockdown or scrambled control lentivirus were matured in 5 or 30 mM glucose for 8 days. One-dimensional immunoblots of duplicate samples probed with anti-2SC and -fumarase antibodies show that knocking down fumarase levels increases protein succination in adipocytes to the greatest degree versus both 5 and 30 mM glucose treatments when fumarase is present. Western blotting with anti-CHOP antibody confirms that ER stress is present in both adipocytes matured in 30 mM glucose and fumarase knockdown adipocytes matured in 5 mM glucose. (F) Protein (500 μg) from adipocytes matured in 5 or 30 mM glucose was immunoprecipitated with anti-PDI antibody. The antibody-antigen complex was captured with Protein G beads. The eluted complex was isoelectrically focused on strips with a pI range of 3.9–5.1. After 2D electrophoresis and protein transfer, a Western blot was performed to detect succination by using anti-2SC (upper panel), followed by reprobing with anti-PDI to verify PDI immunoprecipitation (lower panel). 1D, one dimensional; 2D, two dimensional; ELISA, enzyme-linked immunosorbent assay; IL-1α, interleukin 1α; IL-1β, interleukin 1β; PPARγ, peroxisome proliferator-activated receptor gamma; shRNA, short hairpin ribonucleic acid; TNFα, tumor necrosis factor alpha; VEGF, vascular endothelial growth factor. To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

We were also interested in determining whether Ero1, the thiol-dependent protein responsible for re-oxidizing PDI active-site cysteines, is also susceptible to succination by fumarate. Since mammalian Ero1 also contains redox-sensitive cysteine thiols (20), we hypothesized that Ero1 might be a novel target of succination in the adipocyte. We incubated recombinant Ero1α (4) with increasing concentrations of fumarate in vitro to investigate whether Ero1 is susceptible to succination. One-dimensional (1D) immunoblotting with anti-2SC and anti-Ero1 antibodies confirmed that Ero1 is succinated when incubated with 5 or 25 mM fumarate (Supplementary Figs. S4A and S15A). We next immunoprecipitated Ero1 from adipocytes matured in 5 or 30 mM glucose and immunoblotted with the anti-2SC antibody. However, Ero1 succination was not detected in the adipocytes (Supplementary Figs. S4B and S15B). The blot was reprobed with an anti-Ero1 antibody to confirm the presence of Ero1 in the immunoprecipitates (Supplementary Figs. S4B and S15B). Therefore, although recombinant Ero1 could be succinated in vitro, there were no detectable increases in the endogenous succination of Ero1 in adipocytes.

Succination inhibits PDI reductase activity in vitro

The succination of catalytically important thiols in the metabolic enzymes GAPDH and aconitase has been shown to reduce their enzymatic activity (7, 55). We hypothesized that succination at the active-site cysteines of PDI might also reduce enzymatic activity. Incubation of recombinant wild-type PDI (PDI-WT) with either 5 or 25 mM fumarate increased the PDI succination compared with the unmodified control (Fig. 4A and Supplementary Fig. S8A). Succination of PDI in vitro functionally decreased PDI reductase activity by 15% and 21% for 5 and 25 mM fumarate, respectively (n = 5, **p < 0.01) (Fig. 4A, B). In addition, we used a mutant form of PDI (PDI^FLFL) to determine whether succination of PDI active-site cysteines is essential for inhibition of PDI reductase activity. The residues His and Lys, adjacent to either side of the C-terminal active-site cysteines, are mutated to Phe and Leu (H55ΔF:K57ΔL and H399ΔF:K401ΔL), respectively, in both the a and a′ domains of the mutant form of PDI (62). While remaining enzymatically functional, these simultaneous mutations are predicted to alter the active-site thiol pK_a, and to prevent S-gluthionylation of PDI (62). In contrast to the data obtained with PDI-WT, the mutant PDI could not be succinated in the presence of increasing fumarate concentrations in vitro, and its reductase activity was unaffected (Fig. 4C, D and Supplementary Fig. S8B), indicating that active-site cysteine modification by fumarate is necessary for inhibition of PDI reductase activity.

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FIG. 4.

Succination inhibits PDI reductase activity in vitro . (A, B) Both the WT and mutant recombinant PDI were incubated with indicated fumarate concentrations for 24 h. A Western blot with 2.77 μg of protein was probed with anti-2SC and anti-PDI antibodies. Immunoblots are representative of n = 5. (C, D) 2.77 μg of wild-type or mutant recombinant PDI was incubated in the presence or absence of the indicated fumarate concentrations for 24 h. PDI reductase activity of control and succinated PDI was assayed as described in the Materials and Methods section by using a fluorescent insulin turbidity assay. Fluorescence was measured at λ_ex = 500 nm and λ_em = 603 nm (n = 5/group, mean ± SEM, **p < 0.01). RFU, relative fluorescent units; WT, wild type. To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

We confirmed that direct succination of active-site cysteines was mechanistically responsible for the inhibition of PDI reductase activity by LC-MS/MS mass spectrometry. Recombinant PDI that had been incubated in the presence or absence of fumarate (Supplementary Figs. S5A and S15C) was alkylated with 4-vinylpyridine to produce a control pyridylethyl (PE) modification (C^PE, +105.058 Da) on the remaining free thiols. The tryptic precursor ion masses for control (C^PE, C^PE) and succinated (C^PE, C^2SC, +116.011 Da) peptides were analyzed by LC-MS/MS to determine the specific site of succination. We identified the MS/MS spectrum corresponding to the succinated peptide ⁴⁵YLLVEFYAPWC^PEGHC^2SCK⁵⁹ ([M + 3H]³⁺: 683.9882 mass/charge ratio [m/z]) and ³⁸⁸KNVFVEFYAPWC^PEGHC^2SCK⁴⁰³ ([M + 3H]³⁺: 717.0033 m/z) in the recombinant PDI sample modified by fumarate (Supplementary Fig. S5B, D), as well as each analogous control peptide (Cys55^PE, Cys58^PE) (Cys399^PE, Cys402^PE) in the unmodified recombinant PDI sample (Supplementary Fig. S5C, E). In the case of both active-site peptides, the succination site was confirmed to be the second (C-terminal) cysteine, and it was only detected in the PDI samples incubated with fumarate in vitro.

Succination inhibits PDI reductase activity in 3T3-L1 adipocytes

Succination of PDI active-site cysteines inhibits reduction of insulin disulfide bonds in vitro (Fig. 4), whereas the assay is not specific for PDI activity in cell lysates due to the presence of other oxidoreductases. Di-Eosin-GSSG is a fluorescent, self-quenching, synthetic PDI-specific substrate (28, 43) that is frequently utilized to evaluate PDI reductase activity in protein lysates (37, 61). PDI reductase activity was decreased by ∼36% (Fig. 5A, D, n = 3, *p < 0.05) in adipocytes matured in high glucose versus normal glucose, and increased succination was detected at the molecular weight of PDI (∼57 kDa, arrow, Fig. 5B and Supplementary Fig. S9A) where the total levels of PDI remained similar between all samples (Fig. 5B and Supplementary Fig. S9A). One-dimensional immunoblotting of PDI immunoprecipitates with anti-2SC verified that succination of PDI increased in fumarase knockdown versus control adipocytes (Fig. 5C and Supplementary Fig. S9B). The evaluation of PDI reductase activity in fumarase knockdown adipocytes demonstrated specifically that succination of PDI accounted for a 15% decrease in PDI reductase activity versus controls (Fig. 5D, n = 3, *p < 0.05).

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FIG. 5.

Succination of PDI active-site Cys inhibits PDI reductase activity in 3T3-L1 adipocytes. (A) Adipocytes were matured in 5 or 30 mM glucose for 7 days. Six micrograms of adipocyte cell lysate protein was incubated with 1.08 μM Di-Eosin-GSSG for 1 h. Fluorescence was measured at λ_ex = 510 nm and λ_em = 550 nm, and the initial rate of reaction was calculated (n = 4/group, mean ± SEM, *p < 0.05). (B) Western blots with anti-2SC and -PDI antibodies show succination of PDI in the adipocytes matured in 30 mM glucose (black arrow) and representative equal amounts of PDI in each sample. An immunoblot with anti-actin antibody displays equal protein loading. (C) Protein (400 μg) from control or fumarase knockdown adipocytes matured in 5 mM glucose was immunoprecipitated with anti-PDI antibody, and the antibody-antigen complex was captured with Protein G beads. The eluted complex was subjected to 1D immunoblotting and probed with anti-2SC (upper panel) and anti-PDI (lower panel) antibodies. (D) Six micrograms of adipocyte cell lysate protein was incubated with 1.08 μM Di-Eosin-GSSG for 1 h. Fluorescence was measured at λ_ex = 510 nm and λ_em = 550 nm (n = 3/group, mean ± SEM, *p < 0.05). (E) The active-site peptides of PDI from adipocytes matured in 5 or 30 mM glucose for 8 days were analyzed by LC-ESI-MS/MS. The detection of the y13 fragment ion at retention time ∼36.4 min represents the presence of the control (C55^PE, C58^PE) PDI active-site peptide from adipocytes matured in both 5 mM (panel 1) and 30 mM (panel 3) glucose. The detection of the y13 fragment ion at the retention time ∼36.6 min represents the presence of the succinated (C55^PE, C58^2SC) active-site peptide in adipocytes matured in 30 mM glucose (panel 4) and the absence of the succinated peptide in adipocytes matured in 5 mM glucose (panel 2). (F) The detection of the y13 fragment ion at retention time ∼33.4 min shows the presence of the control (C399^PE, C402^PE) active-site peptide in PDI from adipocytes matured in both 5 mM (panel 1) and 30 mM (panel 3) glucose. The detection of the y13 fragment ion at the retention time ∼35.5 min indicates the presence of the succinated (C399^PE, C402^2SC) active-site peptide in adipocytes matured in 30 mM glucose (panel 4) and the absence of the succinated peptide in adipocytes matured in 5 mM glucose (panel 2). m/z, Mass/charge ratio; PE, pyridylethyl. To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

PDI was enriched from adipocytes matured in 5 or 30 mM glucose and analyzed by LC-MS/MS to confirm the endogenous sites of succination. A fragment ion (y13) representative of both control precursor ions containing active-site cysteines was detected in adipocytes matured in both 5 mM ([M + 3H]³⁺: 680.3434 m/z) ([M + 3H]³⁺: 670.6406 m/z) and 30 mM ([M + 3H]³⁺: 680.3387 m/z) ([M + 3H]³⁺: 670.6228 m/z) glucose (Fig. 5E, F; panels 1 and 3). In contrast, the mass of the representative y13 fragment ion from each succinated precursor ion containing active-site cysteines ([M + 3H]³⁺: 683.3942 m/z) ([M + 3H]³⁺: 674.3534 m/z) was only detected in adipocytes matured in 30 mM glucose (Fig. 5E, F; panel 2 vs. 4). The fragment ion profile was unique to these succinated peptides, whereas the N-terminal or C-terminal location of the succinated cysteine could not be assigned; however, modification of either cysteine is sufficient to impair PDI function as both thiols participate in the oxidoreductase mechanism of PDI. Importantly, these measurements confirm that the endogenous succination of active-site cysteines in PDI selectively occurs in adipocytes matured in high glucose.

Succination inhibits PDI reductase activity in adipose tissue of db/db mice

Control and db/db mice at 15 weeks of age were used for the analysis of protein succination. The total epididymal fat pad weight, fasting blood glucose, and plasma triglyceride levels of the db/db mice were all elevated compared with age-matched control mice (Fig. 6A). To establish whether succination impacts PDI functionality in vivo, we examined PDI enzymatic activity in the epididymal adipose tissue of db/db diabetic mice. Succinated PDI is found only in the epididymal adipose tissue of db/db mice and is absent in the epididymal adipose tissue of the control mice (Fig. 6B, upper panels and Supplementary Fig. S10A). Total PDI is detectable in both the control and db/db adipose tissue samples ∼57 kDa (Fig. 6B, lower panels and Supplementary Fig. S10A). Assessment of PDI reductase activity by using Di-Eosin-GSSG in control and db/db adipose tissue demonstrated that activity was reduced by 52.6% in the diabetic mice (n = 4, *p < 0.05, Fig. 6C), whereas immunoblotting demonstrated equal amounts of PDI (Fig. 6C and Supplementary Fig. S10B). Immunoblotting with anti-GRP78 antibody verified our in vitro results that emphasize no alteration in the protein levels of GRP78 in the adipose tissue during diabetes; however, probing with anti-CHOP confirmed the existence of ER stress in the epididymal adipose tissue from db/db mice versus controls, (Fig. 6C and Supplementary Fig. S10B) (64). The succination of PDI occurs in parallel with reduced PDI reductase activity and the development of ER stress in the epididymal adipose tissue of db/db mice.

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FIG. 6.

Succination inhibits PDI reductase activity in adipose tissue of db/db mice. (A) Epididymal fat pads were removed and weighed at the time of sacrifice. Fasting blood glucose was measured from the tail vein, and serum triglyceride levels were measured (n = 5–6 mice/group, mean ± SEM, **p < 0.01, ***p < 0.001). All in vivo analyses were performed at 15 weeks of age. (B) Two hundred micrograms of protein from control (top) and db/db (lower) mouse epididymal adipose tissue was isoelectrically focused on a pI range 4–7. After 2D electrophoresis and protein transfer, a Western blot was performed to detect succination by using anti-2SC antibody, followed by reprobing to verify PDI. Enlarged 2D immunoblot images in the pI 4.7–4.9 region of the control and db/db adipose tissue depict the presence of PDI at 57 kDa (pI ∼4.85) in each sample. Molecular-weight markers are shown on the far left and right. (C) Six micrograms of protein from control and db/db mouse epididymal adipose tissue was incubated with 1.08 μM Di-Eosin-GSSG for 1 h. Fluorescence was measured at λ_ex = 510 nm and λ_em = 550 nm (n = 3/group, mean ± SEM, *p < 0.05). A Western blot with anti-PDI antibody shows representative equal amounts of PDI in each sample. Immunoblotting 30 μg of total protein lysate from control and db/db mouse epididymal adipose tissue with anti-CHOP and -GRP78 antibodies of demonstrates increased levels of CHOP and no change in the levels of GRP78 in the adipose tissue from db/db versus control mice (representative of n = 6 mice). To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

Glucose levels regulate succination of PDI in adipocytes

We have reported that decreasing glucotoxicity prevents the accumulation of succinated proteins in adipocytes (12), alleviating mitochondrial stress and permitting the turnover of succinated proteins. In the current study, we examined whether limiting chronic glucose exposure would be beneficial for recovery from ER stress in adipocytes. The accumulation of succinated proteins after 4 days of maturation (53) was prevented when the high-glucose medium was removed and replaced with normal glucose concentrations (30 → 5, Fig. 7A and Supplementary Fig. S11A). Notably, CHOP levels were also restored to those observed in normal glucose concentrations (Fig. 7A and Supplementary Fig. S11A), suggesting that limiting chronic high-glucose exposure is sufficient to ameliorate ER stress in the adipocyte. To determine the mechanism of ER stress reduction, PDI was immunoprecipitated from adipocytes matured in 5, 30, or 30 → 5 mM glucose. Immunoblotting verified that succination of PDI was the greatest in adipocytes matured in 30 mM glucose for all 8 days of maturation, whereas 4 days of recovery under normal glucose concentrations rescued the amount of succinated PDI (Fig. 7B and Supplementary Fig. S11B). PDI reductase activity was 60% lower in adipocytes matured in 30 mM glucose versus 5 mM glucose, whereas the adipocytes matured in 30 → 5 mM glucose displayed a 46% decrease in PDI reductase activity (Fig. 7C), indicating that a significant fraction of PDI functionality had been restored. The rescue of PDI reductase activity due to reduced succination of PDI contributes to an improved protein folding capacity, and to diminished levels of ER stress in the adipocyte.

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FIG. 7.

Reducing glucose concentrations rescues PDI reductase activity and ameliorates ER stress in adipocytes. (A) Adipocytes were matured in 5 or 30 mM glucose for 8 days or 30 mM glucose for 4 days, followed by a switch to 5 mM glucose for the remaining 4 days of maturation (30 → 5 mM). Western blotting was performed with 30 μg of protein by using anti-2SC antibody to detect succinated proteins. A merged image of the same blot displays duplicate representative samples. Molecular-weight markers are shown on the far left. An immunoblot with the identical samples was probed with anti-CHOP, PDI, and actin antibodies to detect changes in protein expression. (B) Protein (300 μg) from adipocytes matured in 5, 30, or 30 → 5 mM glucose was immunoprecipitated with anti-PDI antibody. After 1D electrophoresis and protein transfer, a Western blot was performed to detect succination using anti-2SC (upper panel), followed by reprobing with anti-PDI to verify PDI (lower panel). (C) Adipocytes were matured in 5, 30, or 30 → 5 mM glucose. Six micrograms of adipocyte cell lysate protein was incubated with 1.08 μM Di-Eosin-GSSG for 1 h, after which fluorescence was measured at λ_ex = 510 nm and λ_em = 550 nm (n = 3/group, mean ± SEM, *p < 0.05). To see this illustration in color, the reader is referred to the web version of this article at www.liebertpub.com/ars

Animals

Homozygous male db/db mice (C57BLKS-Leprdb) and their heterozygous littermates (Leprdb/+) were purchased at 6 weeks of age from Jackson Laboratories (Bar Harbour, ME). All mice were housed until 15 weeks of age, according to the guidelines of the University of South Carolina Institutional Animal Care and Use Committee. Fasting blood glucose measurements were performed after an overnight fast by collecting tail vein blood by using a Bayer (Whippany, NJ) Contour^® blood glucose meter for control animals and the glucose oxidase assay for db/db mice. The mice were sacrificed after CO₂ asphyxiation, and adipose tissues were collected and immediately frozen.

Cell culture and lentiviral transduction

3T3-L1 mouse fibroblasts were differentiated and matured as previously described (38). After differentiation (∼3 days), the adipocytes were matured in 5 mM glucose and 0.3 nM insulin or 30 mM glucose and 3.0 nM insulin for an additional 8 days. These conditions were selected as it had been observed that adipocytes cultured in normal glucose/insulin are a more appropriate control for the high-glucose/-insulin (diabetic) conditions (53). The adipocytes were treated with 2 μM niclosamide on standard medium change every 48 h. 3T3-L1 fibroblasts were incubated overnight with 150 μL of filtered conditioned medium containing Fh1 shRNA or control lentivirus. Successfully transduced fibroblasts were selected by using 1 μg/ml puromycin. The selected fibroblasts were propagated until confluent; then, they were differentiated to adipocytes and matured for 8 days in 5 or 30 mM glucose as described earlier. The accumulation of triglycerides was observed by light microscopy as the cells matured in both glucose concentrations (38, 53). Adipocytes were incubated in 1 ml of serum-free and phenol red-free medium with 5 or 30 mM glucose for 4 h. The medium was collected and frozen at −80°C for analysis of secreted adiponectin. Total cellular protein was collected after lysis in radioimmunoprecipitation assay (RIPA) buffer as previously described (38) and was quantified by the Lowry assay.

Lentiviral vector production

The lentiviral vectors were prepared by the University of South Carolina Viral Vector Facility. Lentiviral vectors were generated by using a transient transfection protocol, as previously described (22). Briefly, TRC2 Fh1 shRNA, clone-TRCN0000246831, or SHC202 MISSION TRC2 pLKO.5-puro non-mammalian shRNA control plasmids (Sigma-Aldrich, St. Louis, MO) were used to generate the lentiviral vectors. The vectors also contained a puromycin resistance gene. Fifteen micrograms of vector plasmid, 10 μg of psPAX2 packaging plasmid (No. 12260; Addgene, Cambridge, MA), 5 μg of pMD2.G envelope plasmid (No. 12259; Addgene), and 2.5 μg of pRSV-Rev plasmid (No. 12253; Addgene) were transfected into 293T cells. The filtered conditioned medium was collected and stored at −80°C until use.

Measurement of metabolites

The quantification of metabolites was performed by GC-MS at the David H. Murdock Research Institute (DHMRI, Kannapolis, NC). Metabolite extraction was performed in an adaptation of previous methods (42). Briefly, adipocyte lysates harvested in methanol from confluent 100 × 20 mm plates were washed three times with ice-cold phosphate-buffered saline (PBS) followed by the immediate addition of 20 volumes of ice-cold chloroform:methanol (2:1). The samples were vortexed and allowed to stand on ice for 10 min with intermittent vortexing before the addition of 0.2 volumes of H₂O. The samples were sonicated and allowed to stand on ice for an additional 2 min, followed by centrifugation at 3220 × g for 20 min. The aqueous supernatant was transferred into a clean tube and dried under air. The extraction was repeated an additional time by adding equal parts of methanol and deionized water, centrifuging, and transferring the aqueous layer into the respective tube to dry. The protein interface for each sample was removed for quantification of protein by the Lowry assay. Before derivatization, the extracts were resuspended in ethyl acetate and transferred to GC-MS vials. The samples were dried with N₂, and an internal standard (100 μM succinate-13C4; Cambridge Isotope Laboratories, Inc.) was added to each of the samples and fumarate standards. The samples and standards were derivatized with 200 μl of methylamine (20 mg/ml in pyridine; M.P. Biomedicals, Solon, OH) at 30°C for 90 min, followed by drying under N₂. This was followed by the addition of 120 μl of N-methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA; Sigma, St. Louis, MO) with 1% trimethylchlorosilane (TMCS, Sigma); the mixture was incubated at 70°C for 60 min. The derivatized product was stored in a −20°C freezer for 1h. A 100 μl aliquot of the prepared product was transferred to a deactivated glass insert in a 2 ml glass vial (Agilent Technologies, Santa Clara, CA) for GC/MS analysis. An Agilent 7890A GC system, coupled to an Agilent 5975C electron ionization (EI) mass selective detector (MSD), was used to analyze the TMS-derivatized samples. A column with dimensions 30 m × 0.25 mm I.D., 0.25 μm film thickness (Restek, Bellefonte, PA) was used, and the column operation conditions were as follows: helium carrier gas at 1.0 ml/min, GC oven temperature program of 70°C (2 min), 70–100°C (30°C/min, 1 min), 100–140°C (10°C/min, 4 min), 140–188°C (4°C/min, 12 min), and 188–280°C (5 min), with a transfer line temperature of 270°C. The GC-MS was operated under a splitless mode (inlet at 250°C). The mass spectrometry was performed at an electron energy of −70 eV, and the ion source temperature was 230°C. Selected ion monitoring (SIM) was performed for fumarate, and the peak areas obtained were normalized to the added internal standard. Absolute quantitation was performed based on standard curves obtained from the normalized reference standards, and the final metabolite concentrations were normalized to the protein content of the cells.

Measurement of triglycerides and inflammatory markers

Control and fumarase knockdown adipocytes were matured for 8 days in 5 or 30 mM glucose concentrations and harvested in PBS solution for triglyceride quantification. Control and db/db serum triglyceride levels were analyzed in 15-week-old mice. The triglyceride concentration was determined by using Infinity^™ Triglycerides assay kit (Thermo Fisher Scientific, Waltham, MA), according to the manufacturer's instructions. The media on scrambled control or fumarase knockdown 3T3-L1 adipocytes matured for 6 days were replaced with serum-free Dulbecco's modified Eagle's medium (DMEM) for 6 h before collection of the media. Pro-inflammatory cytokines in serum-free conditioned media were analyzed by enzyme-linked immunosorbent assay (ELISA) according to the manufacturer's instructions (Mouse Obesity ELISA; Signosis, Santa Clara, CA).

Measurement of basal respiration

3T3-L1 fibroblasts were plated in V7-microassay plates on 0.2% gelatin at 10,000 cells per well and differentiated as described earlier. XF Assay Medium (Seahorse Biosciences, North Billerica, MA), supplemented with glucose, insulin, and 1 mM sodium pyruvate, was added to replace the culture media 1 h before the analysis (53). The basal OCR (pmol/min) of adipocytes matured in 5 or 30 mM glucose for 2 days was assessed on an XF Flux Analyzer (Seahorse Biosciences). The OCR data were normalized to the total DNA content of the wells by using the CyQuant^® Assay (Invitrogen, Grand Island, NY), and the data were expressed in pmoles/min/ng DNA as previously described (53).

Immunoblotting and immunoprecipitation

Protein electrophoresis and Western blotting were performed on a BioRad Criterion system as previously described (38). Polyclonal antibodies to actin (sc-1616), Ero1α (sc-365526), and PDI (sc-30932) were from Santa Cruz Biotechnology, Inc. (Dallas, TX); adiponectin (AF1119) was from R&D Systems (Minneapolis, MN). Monoclonal antibodies to PDI (MA3-019) and CHOP (MA1-250) were from Pierce (Rockford, IL). The polyclonal anti-2SC antibody was prepared as previously described (36). Ero1α and PDI were immunoprecipitated from 300 to 500 μg adipocyte cell lysates by using 5 μg of anti-PDI or anti-Ero1α, as previously described (11). The beads were re-suspended in 2 × loading buffer and boiled at 95°C for 8 min to remove the bound antibody-antigen complex before immunoblotting. To quantify secreted adiponectin before immunoblotting, the adipocytes were incubated with 1 ml of serum-free medium after 8 days of maturation for 4 h, and total adiponectin levels were quantified by using the mouse adiponectin ELISA according to the manufacturer's instructions (MRP300; R&D Systems). An equal amount of adiponectin from each sample was subjected to non-reducing sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by Western blotting with anti-adiponectin antibody.

Two-dimensional gel electrophoresis

Two-dimensional polyacrylamide gel electrophoresis was performed as previously described (11, 38). Briefly, 200 μg of protein from WT or Fh1^−/− MEFs, control and db/db adipose tissue, or the total PDI immunoprecipitate sample were re-suspended in rehydration buffer (7 M urea, 2 M thiourea, 2% CHAPS, 1% IPG buffer, and 50 mM dithiothreitol [DTT], 3.0% DeStreak, 0.5% ampholytes) and focused on IPG strips with a pI range of 3.9–5.1 (No. 163–2024; BioRad, Richmond, CA) before SDS-PAGE in the second dimension. Western blotting was performed with anti-2SC antibody, followed by IB stripping (62.5 mM Tris, pH 6.8, 2% SDS, and 0.7% [v/v] beta mercaptoethanol) and reprobing with anti-PDI antibody.

Protein identification by mass spectrometry

For the identification of succination sites in PDI, we first incubated 2.0 μg of recombinant PDI with 100 mM fumarate for 24 h at 37°C. We then investigated the sites of endogenous succination of PDI via immunoprecipitation of PDI from adipocytes matured in 5 or 30 mM glucose for 8 days. In all cases, samples were resolved by SDS-PAGE, and the gels were stained with Coomassie Brilliant blue. After destaining, PDI was excised from the gel and incubated in the presence of 10 mM DDT, followed by alkylation by 170 mM 4-vinylpyridine and proteolytic digestion in 50 mM ammonium bicarbonate buffer with 2 pmol of Promega sequencing grade modified trypsin (Promega, Madison, WI). SIM was performed to identify select pyridylethylated and succinated cysteine-containing tryptic peptides. The digested samples were analyzed on a Dionex Ultimate 3000-LC system (Thermo Scientific, Rockford, IL) that was coupled to a Velos Pro Orbitrap mass spectrometer (Thermo Scientific). A 75-μm C18 stationary-phase LC column was used with a 60-min gradient from 2% acetonitrile in 0.1% formic acid solution (solvent A) to 70% solvent A and 30% solvent B (40% water in acetonitrile containing 0.1% formic acid). The Orbitrap was operated in the data-dependent MS/MS analysis mode and excluded all ions below 200 counts. An inclusion list of a maximum of six abundant isotopic masses ±3 amu was used to select the specific peptides for selected resonance monitoring and for determination of the site of modification. To further identify specific succinated sites, multiple reaction monitoring was used to monitor select pyridylethylated and succinated tryptic peptide masses of interest (generated using Protein Calculator software) for CID (collision-induced dissociation)-MS/MS analysis. The data-dependent and CID-MS/MS data were analyzed by using Proteome Discover 1.4 software with SEQUEST search engine against the uniprot_database October 2014 (Mus musculus 52,474 proteins). The CID-MS/MS data were sequenced manually by using Thermo Xcalibur 2.2 software to confirm the modified peptides. The variable modifications of methionine oxidation, proline hydroxylation, cysteine pyridylethylation (C^PE, +105.058 Da), or cysteine succination by fumarate (C^2SC, +116.011 Da) were considered in each data search.

PDI reductase activity assays

Recombinant PDI-WT and a mutant form of PDI (PDI^FLFL) were generously provided by Dr. Danyelle Townsend (Medical University of South Carolina, Charleston, SC). 13.85 μg of recombinant PDI-WT or PDI^FLFL was incubated in 0.1 M potassium phosphate buffer (pH 7) with 2 mM ethylenediaminetetra acetic acid (EDTA) and 0, 1, 5, or 25 mM fumarate. PDI reductase activity was monitored according to the PROTEOSTAT^® PDI assay kit instructions (Enzo Life Sciences, Inc., Farmingdale, NY). Di-Eosin-GSSG was generously provided by Dr. Bulent Mutus, University of Windsor (Ontario, Canada) (43). Six micrograms of protein lysate from 3T3-L1 adipocytes or control and db/db adipose tissue was incubated with 1.06 μM Di-Eosin-GSSG, 5 μM DTT, and 100 μM diethylenetriaminepenta acetic acid (DTPA) in 0.1 M potassium phosphate buffer, pH 7. Fluorescence was measured kinetically (30 s intervals) on a TECAN Safire² microplate reader at λ_ex = 510 nm and λ_em = 550 nm.

Oil Red O staining

0.5 g of Oil Red O was thoroughly mixed in 100 ml isopropanol and diluted 6:4 in distilled water. The dye was allowed to stand for 10 min and filtered through Whatman No. 1 filter paper. One hundred percent of confluent 3T3-L1 fibroblasts and differentiated fumarase knockdown adipocytes were fixed for 1 h in 4% formaldehyde. The cells were washed with PBS, stained with the Oil Red O dye for 1 h, and washed with water. The lipid droplets were visualized by brightfield microscopy, and the images were obtained with the Invitrogen^™ EVOS^™ FL Auto Cell Imaging System (Thermo Fisher Scientific).

Detection of Ero1 succination

The Ero1α immunoprecipitate samples from 3T3-L1 adipocytes were immunoblotted with anti-2SC and anti-Ero1α antibodies as described earlier. Recombinant Ero1α isolated from Escherichia coli strain BL21(DE3) was generously provided by Dr. Kazutaka Araki (Kyoto Sangyo University) (4); 2.77 μg of protein was incubated in 0.1 M potassium phosphate buffer with 2 mM EDTA, 100 μM DTPA, and 0, 1, 5, or 25 mM fumarate at 37°C for 24 h before SDS-PAGE and immunoblotting with anti-2SC and anti-Ero1 antibodies.

Statistical analysis

The comparison of metabolite and inflammatory marker differences and the initial rate of reaction corresponding to PDI reductase activity was analyzed in Sigmaplot 11, by using the student t-test (n = 3, *p < 0.05, **p < 0.01, ***p < 0.001). PDI reductase activity in vitro was analyzed by using a one-way analysis of variance (ANOVA; n = 5, **p < 0.01).