Human Insulin Secreted from Insulinogenic Xenograft Restores Normoglycemia in Type 1 Diabetic Mice without Immunosuppression

hAMs Isolation and Culture

Placentae were harvested within 4 h of delivery after cesarean section from the volunteers who had given informed consent. Isolation and culture of hAMs were prepared as described previously (22). In brief, human fresh amnion was mechanically separated from the chorion, and the epithelial cell layer was removed by 0.25% trypsin (Gibco BRL, Gaithersburg, MD, USA) three times each for 30 min. The remaining amnion tissue pieces were treated with 2 mg/ml collagenase A (Roche, Rotkreuz, Switzerland) and 0.05 mg/ml DNase (Roche) to liberate dissociated cells. The cells were cultured in Dulbecco's modified Eagle's medium low glucose (DMEM-LG, Gibco BRL) supplemented with 1% (vol./vol.) penicillin/ streptomycin solution (Gibco BRL), 3.7 mg/ml sodium bicarbonate (Sigma, St. Louis, MO, USA), and 10% (vol./vol.) fetal bovine serum (FBS) (Hyclone, Logan, UT, USA) at 37°C in 5% CO₂-humidified atmosphere. After 2 weeks, culture dishes were filled with plastic-adherent, fibroblast-like cells. These cells were subcultured using trypsin/EDTA (Gibco BRL). Adherent cells at passage 3 (p3) uniformly showed fibroblastic morphology. The culture medium was changed twice a week.

Reverse-Transcription Polymerase Chain Reaction (RT-PCR)

RNA was isolated using Tri-reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer's instructions. The purity of RNA was assessed by determining the ratio of absorbance at 260 nm to that at 280 nm (>1.8). RT-PCR was performed using a Primus 96 Universal (PeqlabBiotechnologie, Erlangen, Germany). Subsequent PCR reactions were performed using cDNA, primer pairs (Table 1) and PCR mixture (Fermentas, St. Leon-Rot, Germany) according to the manufacturer's instructions. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. Negative control was prepared by an identical manner but without cDNA. RNAs from human embryonic stem cells were kindly donated from Prof. Kim (Korea University, South Korea). Human total RNAs from pancreas (hPAN) and liver were purchased from Ambion (Austin, TX, USA).

OPEN IN VIEWER

Table 1.

cDNA Pairs Used in the Present Study

Gene	Primer Sequence	Accession Number	Size (bp)	Annealing Temperature
OCT4	5′-cga cca tct gcc gct ttg ag-3′ 5′-ccc cct gtc ccc cat tcc ta-3′	NM_001173531.1	573	60
REX1	5′-atg gct atg tgt gct atg agc-3′ 5′-gga tgc act agg aag ttg agg-3′	NM_174900	449	57
SCF	5′-cca ttg atg cct tca agg ac-3′ 5′-ctt cca gta taa ggc tcc aa-3′	NM_000899.4	275	55
Nanog	5′-act ggc cga aga ata gca-3′ 5′-aaa gca gcc tcc aag tca-3′	XM_002344635.1	283	55
TERT	5′-aga gtg tct gga gca agt tgc-3′ 5′-cgt agt cca tgt tca caa tcg-3′	NM_198253.2	183	57
NEUROG3	5′-cgt gaa ctc ctt gaa ctg agc ag-3′ 5′-tgg cac tcc tgg gac aga ttt c-3′	AF234829	211	61
PDX1	5′-ccc atg gat gaa gtc tac c-3′ 5′-gtc ctc ctc ctt ttt cca c-3′	NM_000209.3	262	54
ISL1	5′-agcatcaatgtcctctcaacttcc-3′ 5′-tgtttggcaaggcaatgacc-3′	NM_002202.2	496	57
Nkx6-1	5′-acacgagacccactttttccg-3′ 5′-tgctggacttgtgcttcttcaac-3′	NM_006168.2	336	59
NEUROD1	5′-cag aac cag gac atg ccc-3′ 5′-atc aaa gga agg gct ggt g-3′	NM_002500.2	218	59
PC1/3	5′-ttg gct gaa aga gaa cgg gat aca tct-3′ 5′-act tct ttg gtg att gct ttg gcg gtg-3′	NM_000439.4	457	60
GLUT1	5′-ctc act gct caa gaa gac atg g-3′ 5′-ctg ggt aac agg gat caa aca g-3′	NM 006516.2	366	60
INS	5′-ac caa cac ctg tgc ggc tc-3′ 5′-aag ggc ttt att cca tct ctc tcg-3′	NM_000207.2	322	59
GCG	5′-atg aac gag gac aag cgc-3′ 5′-gta acg aac cga cca ctt-3′	NM_002054.3	236	57
SST	5′-ggc tgc gct gtc cat cgt cct g-3′ 5′-ttg cgt tct cgg ggt gcc ata gc-3′	NM_001048.3	276	63
PPY	5′-ctc tgt tac tac agc cac tg-3′ 5′-agt cgt agg aga cag aag gt-3′	NM_002722.3	261	55
GCK	5′-ccc cca gag acc ttt tc-3′ 5′-ggt ttc ttc ctg agc cag cg-3′	NM_033508.1	176	61
GLP1R	5′-gtt ccc ctg ctg ttt gtt gt-3′ 5′-ctt ggc aag tct gca ttt ga-3′	NM_002062.3	228	55
PC2	5′-gca tca agc aca gac cta cac tcg-3′ 5′-gag aca caa cca ccc ttc atc ctt c-3′	NM_002594.2	315	63
GLUT2	5′-agc ttt gca gtt ggt gga at-3′ 5′-aat aag aat gcc cgt gac ga-3′	NM_000340.1	301	57
HLAABC	5′-gta ttt ctt cac atc cgt gtc ccg-3′ 5′-gtc cgc cgc ggt cca aga gcg cag-3′	XM_003119986	394	70
HLADR	5′-ctg atg agc gct cag gaa tca ttg-3′ 5′-tgc att ggc caa cat agc tg-3′	NM_019111.4	220	60
HLADM	5′-cca gcc caa tgg aga ctg-3′ 5′-cag ccc agg tgt cca gtc-3′	NM002118.4	136	57
beta2M	5′-gtg gag cat tca gac ttg tc-3′ 5′-aac aag ctt tga gtg caa gag-3′	NM_004048.2	479	57
CD80	5′-aac tcg cat cta ctg gca aaa gga gaa-3′ 5′-ggg aaa ctg ttg tgt tga tgg cat tta-3′	NM_005191.3	389	60
CD86	5′-gta ttt tgg cag gac cag ga-3′ 5′-gcc gct tct tct tct tcc-3′	NM006889.3	664	57
Gene	Primer Sequence	Accession Number	Size (bp)	Annealing Temperature
CD40	5′-aga agg ctg gca ctg tac ga-3′ 5′-cag tgttggagc cag gaa ga-3′	NM_001250.4	425	60
CD59	5′-atg gga atccaa gga ggg t-3′ 5′-atg aag gct cca ggc tgc t-3′	NM_203331.2	381	59
TAP1	5′-tct cct ctc ttg ggg aga tg-3′ 5′-gag aca tga tgt tac ctg tct g-3′	NM_000593.5	273	58
TAP2	5′-ctc ctc gtt gcc ggc ttc ttt c-3′ 5′-ttc agc tcc cct gtc tta gtc-3′	NM_018833.2	299	58
hAlu	5′-cga ggc ggg tgg atc atg agg t-3′ 5′-tct gtc gcc cag gcc gga ct-3′	NT_007592.15	230	66
hGAPDH	5′-aca act ttg gta tcg tgg aa-3′ 5′-aaa ttc gtt gtc ata cca gg-3′	NM_002046.3	458	55
mGAPDH	5′-gag tgg gag ttg ctg ttg aag tcg c-3′ 5′-tgt gat ggg tgt gaa cca cga g-3′	NM_008084.2	483	55

OCT4, octamer binding transcription factor 4; REX1, reduced expression protein 1; SCF, stem cell factor; TERT, telomerase reverse transcriptase; NEUROG3, Neurogenin 3; PDX1, pancreatic and duodenal homeobox 1; ISL1, insulin gene enhancer protein 1; Nkx6-1, NK6 homeobox 1; NEUROD1, neuronal differentiation 1; PC1/3, proprotein convertase 1/3; GLUT1, glucose transporter type 1; INS, Insulin; GCG, Glucagon; SST, Somatostatin; PPY, pancreatic polypeptide; GCK, glucokinase; GLP1R, glucagon-like peptide 1 receptor; HLA, human leukocyte antigen; beta2M, beta 2 microglobulin; CD80, cluster of differentiation 80; TAP1, ATP-binding cassette transporter 1; hAlu, transposable elements of the human (h) genome; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; m, mouse.

Flow Cytometry

To examine cell surface antigens, undifferentiated hAMs at p4 were incubated with primary antibodies for 20 min at 4°C. After washing, cells were analyzed by fluorescence-activated cell sorter (FACS) Calibur apparatus (Beckman Coulter, Brea, CA, USA). Monoclonal antibodies for flow cytometry were purchased from the following companies: cluster of differentiation 14 (CD14), CD31, CD73, CD90, human leukocyte antigen (HLA)-ABC, and HLA-DR from BD Bioscience (Franklin Lakes, NJ, USA), TRA-1-60, stage-specific embryonic antigen (SSEA)-3, SSEA-4 from Millipore (Temecula, CA, USA), and CD105 from Invitrogen.

To evaluate the differentiation efficiency of hAMs into hAM-ISCs, hAM-ISCs were fixed with 10% formaldehyde for 10 min. After washing with phosphate-buffered saline (PBS, Invitrogen) containing 0.1% Triton X-100 (Sigma), cells were permeabilized with PBS containing 0.5% Triton X-100 for 15 min. Following washing with PBS three times, cells were incubated with polyclonal anti-human insulin antibody (Cell Signaling Technology, Boston, MA, USA) for 20 min at 4°C. After washing, cells were labeled with fluorescein isothiocyanate (FITC)-conjugated goat polyclonal secondary antibody (Abcam, Cambridge, MA, USA).

Differentiation of hAMs Into Insulin-Secreting Cells In Vitro

Cells were induced to differentiate into insulin-secreting cells according to the previous method (20). Briefly, hAMs at p3–p4 were plated on 48-well dishes (Nunc, Rochester, MN, USA) at 5 × 10³ cells/well and then cultured in control or insulinogenic differentiation medium consisting of 10 mmol nicotinamide (Sigma) and 4 nmol activin A (Peprotech, Rocky Hill, NJ, USA), and 10 nmol glucagonlike peptide-1 (GLP-1, Sigma). For the first week of culture, they were grown in DMEM-HG containing 10% FBS, and during the subsequent 2 weeks, they were cultured in DMEM-LG containing 10% FBS.

Measurement of Insulin and c-Peptide

To measure the amount of human insulin and c-peptide secreted in vitro, cells were treated with DMEM-LG containing 0.5% bovine serum albumin (BSA, Sigma) for 12 h, washed with PBS, and then stimulated by DMEM-HG for 2 h at 37°C. The amount of insulin and c-peptide, a peptide fragment released from the proinsulin molecule during processing into mature insulin, in media was measured using the human insulin and c-peptide ELISA kit (Mercodia, Uppsala, Sweden) according to the manufacturer's instructions. For the measurement of human insulin and c-peptide levels in serum, blood were taken by cardiac puncture from mice, which were fasted overnight and then intraperitoneally injected with glucose (1.5 g/kg body weight), and serum levels were measured. A mouse pancreatic cell line, MIN6N8, and human dermal fibroblasts (hDFs, Lonza) were similarly cultured as in the above except that 1 × 10⁵ cells were seeded per well of 48-well dishes. Mouse insulin and c-peptide in mouse serum were determined using mouse-specific insulin ELISA kit (Mercodia) and c-peptide ELISA kit (Yanaihara, Shizuoka, Japan).

Transplantation of hAM-ISCs Into STZ-Induced Type 1 Diabetic Mice

Female C57BL/6 mice (16–18 g, 8 weeks) were purchased from the Samtako Bio Korea (Osan, South Korea). They were maintained in accordance with the policies of the Institutional Animal Care and Use Committee of Seoul Women's University. Mice that need to be sacrificed before spontaneous death were killed by cervical dislocation as recommended by the University Committee. Type 1 diabetes was induced by a single intraperitoneal injection of STZ (180 mg/kg body weight, Sigma) in 100 mM citrate buffer (pH 4.5). After 7 days, blood glucose level was measured using an ACCUCHEK Active (Roche Diagnostics, Basel, Switzerland) following a 12-h fast. Diabetic mice with glucose level >350 mg/dl were randomly allocated to a saline-injected sham group of 12 mice, a hAMs transplant group of 12 mice, and a hAM-ISCs transplant group of 16 mice. Untreated 12 normal mice were used as a control group. A total of 1.5 × 10⁶ cells were loaded using a PE50 polyethylene tubing (Becton Dickinson, Sparks, MD, USA) and were transplanted underneath the kidney capsule using a Hamilton syringe (Fisher, Pittsburg, PA, USA) at 14 days after STZ injection. No immunosuppressive agent was given to mice throughout the experiment. Undifferentiated hAMs and differentiated hAM-ISCs were obtained by culture of hAMs at p3 for 3 weeks in the control or differentiation medium, respectively. Blood glucose level was measured after a 12-h fast. Nephrectomy of the graft-bearing kidney was performed 6 weeks later, and blood glucose was monitored until death (n = 2). Survival curves were prepared using the Kaplan–Meier method and analyzed for a significant difference by the log-rank Mantel–Cox test using SPSS 12.0 statistical software (SPSS, Chicago, IL, USA).

Immunocytochemistry

hAMs cultivated in Lab-Tekchamber slides (Nunc) were washed with PBS and then permeabilized in 0.5% Triton X-100 for 10 min. Endogenous peroxidase activity was inactivated with 3% hydrogen peroxide (DakoCytomation, Carpinteria, CA, USA) for 15 min at room temperature (RT). Then the slides were incubated in a blocking solution, PBS containing 2% BSA, for 1 h at RT. After washing with PBS containing 0.1% BSA, cells on slides were treated with mouse anti-human insulin monoclonal antibody (1:500, Abcam) or mouse anti-human c-peptide monoclonal antibody (1:500, Monosan, AM Uden, the Netherlands) for 1 h at RT. Cells were then incubated with biotinylated goat anti-mouse or anti-rabbit IgG (Vectastatin ABC kit, Vector Laboratories, Burlingame, CA, USA) followed by horseradish peroxidase-conjugated streptavidin (Vector Laboratories) for 20 min, respectively, at RT. Immunoreactivity was visualized using 3,3′-diaminobenzidine tetrahydrochloride (DakoCytomation) and counterstained with Mayer's hematoxylin (Sigma). Negative control was prepared by an identical manner but without primary antibody. Cells were photographed under a microscope using a bright-field illumination (Axioskop2+, Carl Zeiss, Oberkochen, Germany).

Immunohistochemistry

Graft-bearing kidneys and pancreata were removed from normal and hAM-ISCs-transplanted mice at 8 weeks or 6 months posttransplantation. Tissues were fixed with 4% paraformaldehyde, embedded in paraffin, and cut into 4-μm sections followed by permeabilization with 1% Triton X-100 in PBS (PBST) for 10 min. For antigen retrieval, tissue sections immersed in 10 mM citrate buffer solution (pH 6.0) were placed in microwave for 20 min. For graft-bearing kidney tissue sections, the sections were incubated in 1% BSA in PBS at RT for 20 min. Then the sections were incubated overnight at 4°C with a mixture of two primary antibodies, mouse anti-human nuclei monoclonal (1:100, Chemicon, Temecula, CA, USA), and rabbit anti-human insulin polyclonal antibodies (1:100; Abcam) in PBST containing 1% BSA. After washing, they were incubated with another mixture of two secondary antibodies, Texas red-conjugated anti-rabbit sheep IgG (1:200, Abcam) and FITC-conjugated anti-mouse goat IgG (1:200, Abcam) for 1 h at RT. Cell nuclei were visualized by incubating for 1 min with 1 μg/ml 4′-6′ diamidino-2-phenylindole (DAPI) in PBS. Fluorescence imaging was visualized by confocal microscope (Nikon, Tokyo, Japan). For pancreatic tissue, the sections were incubated in 0.1% horse serum at RT for 20 min. Then the sections were incubated with anti-mouse insulin monoclonal antibody (1:100, Abcam) for 1 h at RT, biotin-labeled anti-mouse/rabbit house antibody and then horseradish peroxidase-conjugated streptavidin (Vectastatin ABC Kit). Counterstaining was done with Mayer's hematoxylin. Some of the sections were stained with Mayer's hematoxylin/eosin for histochemistry. Imaging was visualized by microscope (Axioskop2+).

Dithizone (DTZ) Staining

After differentiation of hAMs into insulin-secreting cells for 3 weeks in vitro, cells were stained by 100 μg/ml DTZ (Sigma) solution at 37°C for 15 min.

Intraperitoneal Glucose Tolerance Test (IPGTT)

IPGTT was performed in fasting unanesthetized mice at 6 weeks after transplantation. After baseline blood glucose measurements, mice were received an intraperitoneal injection of 1.5 g of glucose per kilogram body weight. Tail vein blood glucose concentrations were measured again 30, 60, 90, 120, and 150 min using an ACCUCHEK Active.

Statistical Analysis

Data were expressed as mean ± SEM. Statistical significance was analyzed by one-way ANOVA followed by Scheffe's test using SPSS 12.0. A value of p < 0.05 was considered to be statistically significant.

Stem Cell Properties of hAMs

After the first subculture, plastic-adherent hAMs exhibited uniform, fibroblastic morphology. Flow cytometric analyses of hAMs at p4 showed that they were strongly positive for CD73, CD166, CD105, and CD90, weakly positive for SSEA-4, and negative for CD14, CD31, TRA-1–60, and SSEA-3 antigens (Fig. 1A). The hAMs also showed distinct expression of genes including octamerbinding transcription factor 4 (OCT4), Nanog, stem cell factor (SCF), reduced expression protein 1 (REX1), and telomerase reverse transcriptase (TERT) that are specific to embryonic stem cells and many somatic stem cells (Fig. 1B).

OPEN IN VIEWER

Figure 1.

Stem cell-related properties of hAMs. (A) Flow cytometry results showing that hAMs at p4 were strongly positive for CD73, CD166, CD105, CD90, and HLA-ABC, weakly positive for SSEA-4, and negative for CD14, CD31, TRA-1–60, SSEA-3, and HLA-DR. (B) Expression of stem cell-related genes by hAMs. CD73, cluster of differentiation 73; HLA, human leukocyte antigen; SSEA-4, stage-specific embryonic antigen-4; FITC, fluorescein isothiocyanate; PE, phycoerythrin; APC, allophycocyanin; hAMs, human amniotic mesenchymal stem cells; hESCs, human embryonic stem cells; NC, negative control. See Table 1 for gene definitions.

Immunophenotypes of hAMs

RT-PCR analysis of the expression of selected immune-related genes in hAMs showed three different expression patterns during ex vivo expansion (Fig. 2A). Genes of β-2-microglobulin (β2M), CD59, ATP-binding cassette transporter 1 (TAP1), and TAP2 were consistently expressed from the primary until p13, but HLA-DM, CD80, and CD86 were not expressed in any passage. The other group of genes showed gradually decreasing expression during ex vivo expansion. HLA-ABC gene was expressed from primary culture until p12, but not expressed later; CD40 gene was expressed until p11, but not expressed since then. HLA-DR gene was expressed only in earlier passages until p3 and not expressed thereafter. Immunocytochemical analyses also showed that hAMs at p4, p8, and p13 did not exhibit expression of HLA-DR protein (Fig. 2B). In contrast, hAMs showed gradual reduction of expression of HLA-ABC protein from p4 until p13 unlike the consistent mRNA expression during the same period.

OPEN IN VIEWER

Figure 2.

Immunogenic properties of hAMs. (A) Immune-related gene expression profile by hAMs cultured from primary culture until p13 in vitro. See Table 1 for gene definitions. (B) Immunocytochemistry of hAMs against HLA-ABC and HLA-DR. Scale bar: 100 μm. P, primary culture; hLiver, human liver total RNA; NC, negative control.

In Vitro Differentiation of hAMs Into Insulin-Secreting Cells

After differentiation culture for 3 weeks, some of hAMs formed clusters of which cells were strongly stained with DTZ, a zinc-chelating agent known to selectively stain pancreatic β cells (Fig. 3A). RT-PCR analyses revealed that both expression of β-cell-related genes, including insulin (INS), pancreatic and duodenal homeobox 1 (PDX1), NK6 homeobox 1 (Nkx6-1), neurogenin 3 (NEUROG3), insulin gene enhancer protein 1 (ISL1), neuronal differentiation 1 (NEUROD1), glucose transporter type 1 (GLUT1), GLUT2, proprotein convertase 1/3 (PC1/3), PC2, and glucokinase (GCK), and expression of pancreas-related genes, including pancreatic polypeptide (PPY), somatostatin (SST), and glucagon (GCG), were prominent in the hAM-ISCs, while undifferentiated hAMs showed little expression of these genes, except NEUROD1, GLUT1, PC2, and GCK genes (Fig. 3B). To determine whether these hAM-ISCs could secrete insulin in a high-glucose-dependent manner, we performed human insulin ELISA. Undifferentiated hAMs secreted 15.3 ± 1.4 and 16.5 ± 4.3 pg/ml, respectively, in response to 5.5 or 25 mmol glucose stimulation (Fig. 3C). In contrast, hAM-ISCs secreted 20.8 ± 3.8 and 102.4 ± 6.5 pg/ml, respectively. Under the same condition, human dermal fibroblast cells as a negative control secreted 5.0 ± 0.2 and 4.5 ± 0.2 pg/ml of insulin, respectively. Human c-peptide ELISA showed similar results as that undifferentiated hAMs secreted 18.9 ± 6.0 pg/ml to 5.5 mmol glucose and 29.0 ± 3.0 pg/ml to 25 mmol glucose stimulation, whereas hAM-ISCs released 29.3 ± 3.0 and 239.3 ± 47.7 pg/ml, respectively (Fig. 3D). Human fibroblasts secreted 29.5 ± 2.3 and 27.6 ± 4.8 pg/ml of c-peptide responding to a 5.5- or 25-mmol glucose challenge, respectively. When an insulinoma cell line MIN6N8 was similarly examined using mouse-specific ELISA kit, they secreted 3.8 ± 1.1 and 12.5 ± 1.9 ng/ml of mouse insulin and 0.8 ± 0.1 and 4.2 ± 0.1 ng/ml of mouse c-peptide upon 5.5 or 25 mmol glucose challenging, respectively (Fig. 3E). Immunocytochemical studies showed that undifferentiated hAMs were almost negative against both anti-human insulin and c-peptide antibodies, whereas hAM-ISCs, particularly cells in cluster-like structure, were strongly positive to both antibodies (Fig. 3F). However, flow cytometry analysis revealed the insulinogenic differentiation efficiency of 8.7 ± 0.2% (Fig. 4A), as shown in double immunofluorescence imaging against DAPI and anti-human insulin antibody (Fig. 4B). These results indicate that hAMs could successfully differentiate into insulin-secreting cells, hAM-ISCs, in vitro.

OPEN IN VIEWER

Figure 3.

Differentiation of hAMs into insulin-secreting cells in vitro. Cells at p3–4 were cultivated in differentiation medium for 3 weeks and then analyzed for the β-cell characters. (A) Cells cultured in control medium (control) exhibited little staining with DTZ, whereas those in a differentiation medium (hAM-ISCs) showed intense staining. (B) Expression profile of β-cell-related genes by hAM-ISCs. hPan, human pancreatic mRNA; NC, negative control. See Table 1 for gene definitions. (C, D) ELISA analyses of insulin (C) and c-peptide (D) in response to 5.5 or 25 mmol glucose challenge. Results were obtained from three independent experiments. b indicates a significant difference (p < 0.05). (E) Mouse insulin and c-peptide level of MIN6N8 cell line in response to 5.5 or 25 mmol glucose stimulation. (F) Immunocytochemistry of hAMs (control) and hAM-ISCs against anti-human insulin or anti-human c-peptide antibody. Scale bar: 200 μm. hAM-ISCs, human amniotic mesenchymal stem cell-derived insulin-secreting cells.

OPEN IN VIEWER

Figure 4.

Differentiation efficiency of hAMs into hAM-ISCs. (A) hAMs and hAM-ISCs were labeled with DAPI and FITC-conjugated anti-human insulin antibody followed by flow cytometric analysis. (B) Some of both types of cells were visualized under a fluorescence microscope. Arrows indicate hAM-ISCs stained with both antibodies. Scale bar: 100 μm.

Blood Glucose Level of Type 1 Diabetic Mice Could Be Normalized by Transplantation of hAM-ISCs

To examine whether hAM-ISCs could act as therapeutic cells for the type 1 diabetes, we transplanted hAM-ISCs into the kidneys of hyperglycemic mice induced by STZ pretreatment and analyzed their effects. Mice treated with saline (sham, n = 12) began to die at 18 days after transplantation, and all 12 mice died within 45 days (Fig. 5A). Mice transplanted with undifferentiated cells (hAMs, n = 12) similarly began to die at 22 days after transplantation, and all 12 mice died within 55 days. In contrast, 9 of the 16 mice that have been transplanted with differentiated cells (hAM-ISCs, n = 16) survived even for 210 days after transplantation. The rest of the mice began to die as early as 12 days, and all seven mice were dead within 65 days after transplantation. During 70 days of experimental period, mice of both sham group and hAMs group consistently showed high blood glucose level until death (Fig. 5B). In contrast, mice of the hAM-ISCs group exhibited lowered glucose level, and from 35 to 70 days of transplantation, their glucose level was not statistically different from those of normal mice (Fig. 5B). Individual recording of blood glucose level of all 16 mice exhibited by the hAM-ISCs group is shown in Figure 5C. Nine mice (Nos. 1–9) exhibited lowering of blood glucose level reaching to normal level after 7–14 days of hAM-ISCs transplantation, and all of them maintained normoglycemia until 55 days. One mouse (No. 10) exhibited similarly lowered level until 28 days but then showed hyperglycemia and eventually died after 65 days. Other six mice (Nos. 11–16) remained hyperglycemia until death. At 56 days of hAM-ISCs transplantation, graft-bearing kidneys were removed from two mice whose blood glucose level was in a range between 99 and 101 mg/dl. Following nephrectomy, their blood glucose level markedly increased reaching to 424 or 467 mg/dl during the next 7 days and eventually died after 14 and 20 days, respectively. During the experimental period, average body weight of both sham and hAMs group mice gradually decreased until death, that of hAM-ISCs group mice progressively increased similar to that of normal mice (Fig. 5D). However, individual recording of body weight of all 16 hAM-ISCs mice showed that seven mice (Nos. 10–16), which remained hyperglycemic until death, as seen in Figure. 5C, gradually lost body weight throughout the period. The rest of the mice of which blood glucose level was lowered (Nos. 1–9) progressively gained weight (Fig. 5E).

OPEN IN VIEWER

Figure 5.

Physiological analyses of normal and type 1 diabetic mice after cell transplantation. Mice were given saline (sham), hAMs, or hAM-ISCs under their left kidney capsules. (A) Survival rate. (B) Blood glucose level. Blood glucose levels of hAM-ISC-transplanted mice for 35–70 days of experimental period were not statistically different from those of normal mice during the same period by one-way ANOVA. Nephrectomy (arrow) was done in two mice, which exhibited normalized glucose level following hAM-ISC transplantation. (C) Individual recording of blood glucose level of 16 hAM-ISC transplanted mice as shown in (B). Nos. 1 and 2 represent hAM-ISC transplanted mice that have been nephrectomized as in (B). (D) Changes of average body weight of mice. (E) Individual recording of body weight of 16 hAM-ISC transplanted mice as shown in (D). Nos. 1 and 2 represent hAM-ISC-transplanted mice that have been nephrectomized as in (B). There was no significant difference between the normal group and hAM-ISCs group based on one-way ANOVA test from 35 to 70 days after transplantation. (F) Glucose tolerance test. Normal mice and mice showing normoglycemia at 42 days following hAM-ISC transplantation were given glucose solution intraperitoneally, and their blood glucose level was monitored. N.S., no significant difference between the normal group and hAM-ISCs group based on one-way ANOVA test. Data are shown as mean ± SEM except (A).

To evaluate a physiological function of transplanted hAM-ISCs, IPGTT was performed on normal mice (n = 5), sham-operated mice (n = 2), and hAM-ISCs transplanted mice (n = 5), which exhibited normoglycemia at 42 days following transplantation (Fig. 5F). Blood glucose levels in normal mice and hAM-ISC-transplanted mice rose with peak level at 30 min, followed by a drop to initial range within 150 min. Glucose level of the hAM-ISCs transplanted mice appeared a little higher than that of the normal but was not significant. In contrast, sham mice showed absence of tolerance against glucose challenging. These results demonstrate that hAM-ISC transplantation could normalize the blood glucose level of hyperglycemia in type 1 diabetic mice.

hAM-ISCs Directly Regulate the Blood Glucose Level of Type 1 Diabetic Mice

We further investigated whether transplanted hAM-ISCs could directly regulate the blood glucose level of recipient mice via the insulin they produced, overcoming immune rejection. RT-PCR analyses showed that kidney tissues of the mice that normalized blood glucose level following transplantation with hAM-ISCs 8 weeks or 6 months earlier expressed human genes of INS, PDX1, GLUT1, glucagon-like peptide 1 receptor (GLP1R), NKX6-1, NEUROD1, NEUROG3, and hAlu (transposable elements of the human genome) (Fig. 6A). Normal mouse kidney tissue did not express any of these human genes. Immunohistochemical analyses showed the presence of a number of transplanted human cells residing within a mouse kidney capsule where they were injected (Fig. 6B). Coimmunofluorescence images of the tissue section demonstrate that most of these cells colocalized human insulin protein and human nuclei proteins (Fig. 6C). To clarify the presence and origin of insulin in the blood of the normalized mice, three randomly chosen mice whose blood glucose level ranges between 128 and 138 mg/dl following hAM-ISCs transplantation were sacrificed after 56 days. Immunohistochemical studies showed that both size and number of pancreatic islets were markedly decreased in the pancreas of these mice compared to those of the normal mice (Fig. 7A). Mouse insulin and c-peptide levels in the blood of hAM-ISCs transplant mice were negligible compared to 1.9 ± 0.1 ng/ml of mouse insulin and 3.1 ± 0.4 ng/ml of mouse c-peptide in normal mice (Fig. 7B). In contrast, human insulin and c-peptide levels in hAM-ISCs transplant mice were 0.4 ± 0.1 and 0.6 ± 0.0 ng/ml, respectively. Both proteins were hardly detected in the blood of normal mice (Fig. 7C). These results demonstrate that human insulin was solely responsible for the regulation of the blood glucose level of hAM-ISC-transplanted mice. The results also suggest that transplanted hAM-ISCs could survive and actively synthesize human insulin in the kidneys of immunocompetent mice without the aid of any immunosuppressive drugs. To investigate how hAM-ISCs could overcome immune rejection of xenogeneic grafts, we examined the expression profile of immunity-related genes (Table 2) in hAMs, hAM-ISCs, and kidney tissues of two mice that were allowed to live for 56 days or 6 months, maintaining normal blood glucose level. Immune-related genes of HLA-ABC, β2M, CD40, CD59, TAP1, and TAP2 were consistently expressed in hAMs and hAM-ISCs regardless of differentiation in vitro (Fig. 7D). However, genes of HLA-DR, CD80, and CD86 were not expressed in both types of cells. Similarly, kidney tissues of hAM-ISCs transplant mice also showed expression of β2M, TAP1, and TAP2 at 2 and 6 months after transplantation. Interestingly, CD40 transcript was not detected in both mice kidneys, whereas HLA-ABC and CD59 transcripts were seen at 2 months but disappeared after 6 months of transplantation.

OPEN IN VIEWER

Figure 6.

Human gene and protein expression in graft-bearing kidneys. (A) Human β-cell-related gene expression in graft-bearing kidney tissues removed from mice described in Figure. 5B. GMK1, GMK2, mouse kidneys transplanted with hAM-ISCs 8 weeks or 6 months earlier, respectively; NMK, normal mouse kidney; NC, negative control. See Table 1 for gene definitions. (B) Hematoxylin/eosin-stained, graft-bearing kidney section. Arrowheads indicate boundary between transplanted hAM-ISCs residing in mouse kidney capsule and the region of mouse kidney tissue. Scale bar: 100 μm. (C) Immunofluorescence staining of the upper region of transplanted hAM-ISCs in graft-bearing kidney shown in (B). Immunostaining was done against anti-human insulin (hINS) and anti-human nuclei antibodies (hNUCLEI). Arrows indicate colocalization of both proteins. Scale bar: 50 μm. Boxes a and b are enlarged view. Scale bar: 10 μm.

OPEN IN VIEWER

Figure 7.

Regulation of mouse blood glucose level by human insulin from transplanted hAM-ISCs. (A) Pancreata section of normal mice and mice whose blood glucose level was normalized by human insulin secreted from transplanted hAM-ISCs. (B) Mouse insulin and c-peptide in sera of normal mice and mice transplanted with hAM-ISCs. (C) Human insulin and c-peptide in sera of normal mice and mice transplanted with hAM-ISCs (n = 3). a, b are significantly different from each other, p < 0.05. (D) Expression of human immune-related genes by hAMs and hAM-ISCs in vitro and by kidneys of GMK1 and GMK2 as in Figure 6A. Pancreata section was stained by anti-mouse insulin antibodies. Scale bar: 100 μm. See Table 1 for gene definitions.

OPEN IN VIEWER

Table 2.

Function of Immune-Related Molecules

Gene	Function
CD40	A receptor molecule on the cell surface of all mature B cells, monocytes, dendritic cells, endothelial cells, and epithelial cells.
	CD40 is a member of the tumor necrosis factor superfamily and an important contributor to the inflammatory processes that lead to atherosclerosis and thrombosis.
CD59	A cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction.
	This protein is a potent inhibitor of the complement membrane attack complex and also plays a role in signal transduction pathways in the activation of T cells.
CD80(B7-1)/	The B-lymphocyte activation antigen.
CD86(B7-2)	This provides regulatory signals for T lymphocytes as a consequence of binding to the CD28 and CTLA4 ligands of T cells.
β2M	A component of MHC class I molecules, which are present on all nucleated cells.
	Involved in the transport of antigens from the cytoplasm to the endoplasmic reticulum for association with MHC class I molecules. Also acts as a molecular scaffold for the final stage of MHC class I folding, namely, the binding of peptide.
TAP1/TAP2	The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters.
	ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White).
	This protein is a member of the MDR/TAP subfamily.