Neural Stem/Progenitor Cells Promote Endothelial Cell Morphogenesis and Protect Endothelial Cells against Ischemia via HIF-1α-Regulated VEGF Signaling

Cell Culture

Neural stem/progenitor cells: Neural stem/progenitor cells were established from the telencephalon of gestational day 14 mouse embryos of the C57BL/6-TgN (ACTβEGFP) strain (The Jackson Laboratory, Bar Harbor, ME, USA), which express enhanced green fluorescent protein (EGFP) under a β-actin transcriptional promoter (Okabe et al, 1997). After the removal of meninges, telencephalons were mechanically dissociated by trituration with a P-1000 pipetman in Hank's balanced salt solution (HBSS). After brief centrifugation (3 mins, 1,300 r.p.m.), the cells were resuspended in culture medium and plated into six-well poly-l-lysine-coated tissue culture dishes (Becton-Dickinson, Franklin Lakes, NJ, USA) at the density of approximately one embryonic telencephalon per well of a six-well culture dish. The cells were expanded in a defined serum-free DMEM (Dulbecco's modified Eagle's medium)/F12 medium containing 15 mmol/L HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid), 2.5 mmol/L l-glutamine (Gibco, Grand Island, NY, USA), 3 mmol/L sodium bicarbonate, 25 μg/mL insulin, 16 μg/mL putrescine, 30 nmol/L sodium selenite, 100 μg/mL apo-transferrin, and 20 μmol/L progesterone (as previously described in Reynolds and Weiss, 1992), with additional modifications by K Nakashima and X Zhao (personal communication), plus 10 ng/mL epidermal growth factor (EGF) and 10 ng/mL basic fibroblast growth factor (bFGF) (Invitrogen, Carlsbad, CA, USA). Fresh growth factors were added every 2 days and media were changed every 4 days. At passaging, NSPCs were replated in a fresh growth medium at a concentration of 1.5 times 10⁵ cells/cm². Neural stem/progenitor cell cultures fulfilled criteria of multipotentiality and self-renewal. As shown in Supplementary Figure 1, NSPCs spontaneously differentiated into both neurons and glia after growth factor withdrawal. Neural stem/progenitor cells could also be propagated as neurospheres when plated at clonal density for up to six passages (Supplementary Figure 1). For the current studies, NSPCs were used in coculture experiments after second passage.

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Figure 1

Neural stem/progenitor cells support ECs morphogenesis and survival in serum-free conditions. Micrographs show ECs and NSPC/EC cocultures plated on Matrigel matrix. GFP-positive NSPCs are shown using the green channel. (A) Confocal DIC images, bar = 50 μm. (B) Confocal images showing immunofluorescence for the endothelial cell marker CD31/PECAM-1 (red), bar = 20 μm. Endothelial cells were plated in the presence of serum (A and B, left panels), in the absence of serum (A and B, middle panels), or in the presence of NSPCs in serum-free, growth factor-free cell medium (A and B, right panels). (C) Quantification of endothelial cell morphogenesis, n = 3 coverslips per group.

Brain endothelial cells: The bEnd.3 mouse brain endothelial cell line was obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) and expanded in DMEM culture medium (Gibco) containing 10% fetal bovine serum, 4 mmol/L l-glutamine, 4.5 g/L glucose, and 1.5 g/L sodium bicarbonate, according to the supplier recommendations.

Direct neural stem/progenitor cell—endothelial cell coculture: Confluent brain ECs were trypsinized and plated at the density 2 times 10⁴ cells per 12 mm diameter coverslip precoated with Matrigel matrix (growth factor reduced matrigel matrix without phenol red, BD Biosciences, San Jose, CA, USA). The ECs were cultured for 6 h in the EC culture medium. The medium was then removed and ECs were rinsed before coculturing with NSPCs. A total of 2 times 10⁴ NSPCs were plated directly onto the EC cultures. Neural stem/progenitor cell and EC cocultures were grown in growth factor- and serum-free NSPC media to prevent the astrocytic differentiation of NSPCs. The NSPC/EC cocultures were analyzed after 3, 5, or 10 days using live cell microscopy and immunofluorescence staining.

Indirect neural stem/progenitor cell/endothelial cell coculture using transwells: Neural stem/progenitor cells were harvested by trypsinization, and plated on poly-l-lysine-coated wells at a density of 1 times 10⁵ cells per well (9.5 cm² area per well of six-well plate). Neural stem/progenitor cells were expanded in serum-free media containing FGF and EGF for 2 days. Endothelial cells were trypsinized and plated into the upper compartment of transwell inserts (0.4 μm pore size, BD Falcon, Franklin Lakes, NJ, USA), at a density of 1 times 10⁴ cells per 4.2 cm² area and expanded in a serum containing EC medium for 2 days. Neural stem/progenitor cells and ECs were both rinsed with serum-free, growth factor-free NSPCs culture media, and the upper transwell compartments containing ECs were placed into the culture well. Indirect NSPC/EC cocultures were maintained in serum-free, growth factor-free, and insulin-free media for 3 days, harvested, and processed separately for western blot and immunoassay analysis.

This coculture system allowed NSPCs and ECs to share the same growth medium, and allowed substances to freely diffuse through cell culture insert or cell strainer pores without physical contact between the two cell types.

Oxygen and Glucose Deprivation

Cell cultures were subjected to OGD injury as described previously (Wetzel et al, 2008). Cultures were placed in an anaerobic chamber (Coy Laboratories, Grass lake, MI, USA) containing a gas mixture of 5% H₂, 5% CO₂, and 85% N₂ to obtain < 0.2% O₂. Normal culture medium was replaced with deoxygenated, glucose-free Earle's Balanced Salt Solution (EBSS), and cells were exposed to glucose-free anaerobic conditions for 3 or 5 h at 37°C. Control cell cultures were placed in EBSS containing 25 mmol/L glucose and incubated under normal tissue culture conditions for the same period.

Endothelial Cell Morphogenesis Assay

Endothelial cells were trypsinized, and after centrifugation, resuspended in EC medium, containing 10% fetal bovine serum and plated at the density of 2 times 10⁴ cells per 12 mm diameter glass coverslips precoated with Matrigel matrix. Six hours after plating, the ECs were either cocultured with NSPCs (see direct NSPC/EC cocultures above) or incubated with a growth factor-free NSPC-conditioned medium (NSPC-CM) (medium collected from NSPCs cultured for 3 days). When plated on Matrigel or collagen, ECs form cellular networks (mesh-like structures) and capillary tubes. In addition, for better EC visualization, immunofluorescence staining for endothelial marker CD31 was performed before analyses.

Endothelial cell morphogenesis was assessed under an inverted confocal microscope, and images were taken using LSM-META confocal imaging system. A total of 10 to 15 images per coverslip were taken systematically across the coverslips. The number and diameter of capillary-like structures were counted using LSM Image Browser. Statistical analysis was performed using GraphPad Prism software.

Immunocytochemistry

Cells were fixed with 4% paraformaldehyde solution and quenched with 50 mmol/L ammonium chloride. After permeabilization with 0.1% (v/v) Triton X-100 and blocking with 1% horse serum, cells were incubated with primary antibodies for 1 h followed by fluorophore-conjugated secondary antibodies for 40 to 60 mins at room temperature. The following antibodies were used: mouse monoclonal anti-nestin (1:1,000; BD Pharmingen, San Diego, CA, USA), mouse monoclonal (1:1,000) and rabbit polyclonal (1:500) anti-GFAP (Accurate Chemical & Scientific Corp., Westbury, NY, USA), goat polyclonal anti-doublecortin (1:300; Santa Cruz Biotechnology, Santa Cruz, CA, USA), mouse monoclonal anti-βIII tubulin/Tuj1 (1:300; Promega, Madison, WI, USA), Alexa Fluor-conjugated rat monoclonal anti-mouse CD106/VE-cadherin (1:300; BioLegend, San Diego, CA, USA), rat monoclonal anti-mouse CD31/PECAM-1 (platelet—endothelial cell adhesion molecule-1) (1:300; BD Biosciences), mouse monoclonal anti-VEGF (1:200; Abcam, Cambridge, MA, USA), and rabbit polyclonal anti-HIF-1α (1:300; Chemicon, Temecula, CA, USA). Secondary antibodies were used at a common dilution of 1:200, and included Cy3-conjugated goat anti-rabbit, FITC-conjugated goat anti-mouse, Cy3-conjugated donkey anti-goat, and Cy3-conjugated donkey anti-mouse (Jackson ImmunoResearch Laboratories, West Grove, PA, USA). 4',6-Diamidino-2-phenylindole (DAPI) staining was used for detection of nuclei.

Western Blot Analyses

The cells were scraped from the cell culture dishes and filter inserts either directly with 2 × SDS sample buffer, or in lysis buffer (250 μL per filter) containing 1% (vol/vol) Triton X-100, 150 mmol/L NaCl, 10 mmol/L Tris-HCl, pH 7.4, and a protease inhibitor cocktail. To ensure equal protein loading, the relative protein concentration in the samples (lysed with 1% Triton X-100 lysis buffer) was quantified according to absorbance at 280 nm. Protein loading was additionally confirmed by comparing actin immunoreactivity across lanes. The proteins were separated on 4 to 20% gradient Criterion precast gels (Bio-Rad, Hercules, CA, USA). A broad-range molecular weight calibration marker from 10,000 to 250,000 MW (Bio-Rad) was used as a standard. The proteins were transferred onto nitrocellulose membrane and identified using mouse monoclonal anti-VEGF (1:100; Abcam) and rabbit polyclonal anti-actin (1:1,000, Sigma, St Louis, MO, USA). Horseradish peroxidase-labeled secondary antibodies were obtained from Amersham Biosciences (Piscataway, NJ, USA) and used in dilution of 1:3,000. For HIF-1α detection, we used a biotinylated anti-HIF-1α antibody (200 ng/mL) provided in the Surveyor™ IC Intracellular HIF-1α immunoassay kit (R&D Systems, Minneapolis, MN, USA), followed by horseradish peroxidase-conjugated streptavidin (1:200). Incubation with both primary and secondary antibodies was performed for 1 h at room temperature.

MTT Colorimetric Cell Viability Assay

Cells were incubated with 0.5 mg/mL methyltetrazolium (MTT, Sigma) for 4 h at 37°C, and treated with 1:1 ethanol/DMSO (dimethyl sulfoxide) for 20 mins at room temperature. The ability of cells to convert MTT into purple formazan provides an indication of the mitochondrial integrity and activity, interpreted as a degree of cell viability. The optical density was measured at 570 nm (with background subtraction at 630 nm) using a microplate reader (Dynex Technologies, Chantilly, VA, USA). Absorbance at 570 nm is directly proportional to the number of viable cells. SU1498 was purchased from Calbiochem (San Diego, CA, USA) and used at concentrations of 5 to 20 μmol/L; Flt-1-Fc (Sigma) was used at a concentration of 30 ng/mL.

Vascular Endothelial Growth Factor and Hypoxia-Inducible Factor-1α Immunoassay

For VEGF immunoassay, conditioned medium was collected, filtered to remove cells and debris, and concentrated eightfold using iCON™ concentrator with 9K molecular weight cut-off (Pierce, Rockford, IL, USA) and centrifugation at 3,000g for 30 mins at 4°C. Quantikine™ VEGF Immunoassay (R&D Systems) was performed according to the manufacturer's recommendations. For HIF-1α intracellular immunoassay, cells were harvested and analyzed using the Surveyor IC Intracellular HIF-1α immunoassay (R&D Systems). Each HIF-1α assay sample was prepared from ∼2 times 10⁶ NSPCs, and the assay was performed according to the manufacturer's recommendations. For both VEGF and HIF-1α immunoassay, the optical density of each well was determined using SpectraMax M5 microplate reader and SoftMaxPro Software (Molecular Devices, Sunnyvale, CA, USA). Readings were performed at 450 nm wavelength, with correction at 540 nm. A standard curve was generated, and total VEGF or HIF-1α concentration in the samples was calculated using the GraphPad Prism software. Values were corrected for relative protein content within the media (VEGF) or cell lysates (HIF-1α), which was detected with Bradford protein assay. Additional normalization was performed by electrophoresis of sample aliquots followed by coomassie staining (VEGF) and by western blotting for actin immunoreactivity (HIF-1α) for each sample. The density of the major protein bands was determined using the GS-800 Calibrated Densitometer and Quantity One software (BioRad). Data were subjected to one-way analysis of variance and Tukey's multiple comparison post hoc analysis using GraphPad Prism software.

Cell Transplantation and Middle Cerebral Artery Occlusion

All surgical procedures were approved by the University of New Mexico Animal Care Committee and conformed to the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals. Eight-week-old male C57BL/6 mice 20 to 25 g (The Jackson Laboratory) were used. Mice received buprenorphine (0.05 mg/kg, s.c.) at the onset of all surgery as analgesic. Anesthesia was induced with 1.5% isoflurane and maintained with 1.0% isoflurane in 1 L O₂, using a vaporizer (Summit Medical Equipment, Bend, OR, USA). Enhanced green fluorescent protein NSPCs were implanted into the corpus striatum of 8-week-old C57BL/6 mouse recipients. Mice received stereotaxic injections using a Hamilton microsyringe with a 26-gauge blunt needle. Each animal received an injection of 2.5 μL of cell suspension (5 times 10⁴ cells per μL in phosphate-buffered saline; PBS) at the rate of 1 μL per min at the following stereotactic coordinates (from bregma: A + 1.0 mm, L + 2.0 mm, V −2.6 mm). Sham-transplanted mice were injected with the same volume of PBS at the same stereotactic coordinates. At 3 days after transplantation, mice were either killed or subjected to MCAO as described below (n = 5 mice per group).

Mild transient focal ischemia was induced by right MCAO using the intraluminal thread method as previously described (Kokovay et al, 2006). After the induction of anesthesia as described above, the right common carotid artery was exposed and ligated with 6-0 silk suture. A 6-0 round tip nylon suture was introduced into the common carotid artery to occlude the middle cerebral artery. Successful MCAO resulted in 80% decrease of blood flow to the right cerebral hemisphere as assessed by laser Doppler analysis. After 30 mins, the intraluminal thread was withdrawn and the common carotid artery was ligated with a silk suture above the point of thread insertion. Reperfusion occurred via the Circle of Willis for 3 days before mice were killed for histologic analysis.

Histologic Procedures and Image Analysis

Mice were overdosed with sodium pentobarbital administered intraperitoneally (150 mg/kg) and transcardially perfused with PBS containing 0.1% procaine and 2 U/mL heparin, followed by 4% paraformaldehyde containing 0.075 M lysine and 0.01 M sodium periodate. Brains were postfixed overnight, cryoprotected in 30% sucrose, and sectioned at 30 μm thickness in the coronal plane using a sliding knife freezing microtome. Floating sections were subjected to immunofluorescence staining as previously described (Kokovay et al, 2006). Sections were permeabilized with 0.1% (v/v) Triton X-100, blocked with 5% donkey serum, and incubated with primary antibodies overnight at 4°C. Primary antibodies and dilutions were as follows: rabbit anti-HIF-1α (1:150; Chemicon), biotinylated anti-HIF-1α from the Surveyor IC Intracellular HIF-1α immunoassay kit (200 ng/mL; R&D Systems), mouse anti-VEGF (1:200; Abcam), and rabbit anti-GLUT-1 (1:200; Chemicon). Cy3- and FITC-conjugated secondary antibodies, and Cy3-conjugated streptavidin were used at a 1:250 dilution (Jackson ImmunoResearch Laboratories). All samples were imaged on a Zeiss LSM510 or Zeiss LSM510-META confocal imaging system.

Microvascular Density: NIH Image J image analysis software was used to compare GLUT-1 (glucose transporter 1; Chemicon) immunofluorescence microvascular density in histologic brain sections. Images were digitally captured at × 10 magnification using a BX51 Olympus microscope equipped with epifluorescence and an Olympus Microfire digital camera. Eight images of striatum were digitally photographed per histologic section, across three histologic sections per mouse. The images were converted to 8-bit gray and an area selection tool was used to outline the striatal perimeter on each histologic section. The percentage of striatal area covered by GLUT-1 immunostaining was determined using pixel thresholding.

Ki67/Glucose Transporter 1 Colocalization: Five microscopic fields within the perimeter of each striatum were digitally captured using a × 20 objective and a Zeiss LSM510-META confocal imaging system. The percentage of blood vessels that contained Ki67 + nuclei was estimated by visualizing blood vessels within each digital image using the LSM Image Browser software, and scoring each blood vessel as positive or negative depending whether it contained a Ki67+ nucleus. Five microscopic fields were analyzed in each of five histologic sections per mouse (n = 3 mice per group).

Neural Stem/Progenitor Cells Promote Endothelial Cell Morphogenesis and Prevent Endothelial Cell Death after Serum Starvation and Oxygen and Glucose Deprivation

The vasculotrophic effects of NSPCs were initially tested in vitro using direct contact NSPC/EC cocultures, where both cell types were plated together in direct contact on Matrigel matrix. When grown in the presence of serum, EC monocultures appeared healthy and underwent normal morphogenesis within 3 days of plating, characterized by the formation of capillary tube-like structures (Figures 1A and 1B, left panels). In striking contrast, EC monocultures grown in the absence of serum survived poorly and underwent minimal morphogenesis by 3 days (Figures 1A and 1B, middle panel). Importantly, the detrimental effects of serum deprivation on EC survival and morphogenesis were largely eliminated when ECs were grown in the presence of NSPCs in direct coculture (Figures 1A and 1B, right panel). The vasculotrophic effects of NSPCs were confirmed by quantifying the number and size of CD31/PECAM-1⁺ capillary-like structures in NSPC/EC cocultures (Figure 1C). At 3 days in coculture, the majority of NSPCs remained undifferentiated and expressed the neural stem cell marker nestin, with only sparse cells expressing the marker for neuroblasts, doublecortin (Figures 3A and 3B). This suggests that as early as at 3 days in coculture, the undifferentiated NSPCs were able to provide support for survival and morphogenesis of ECs under conditions of serum deprivation.

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Figure 3

Phenotypic analysis of EGFP/NSPCs in coculture with ECs. Neural (doublecortin for neuroblasts; Tuj-1 for neurons, and GFAP for astrocytes), stem cell (nestin), and endothelial cell (VE-cadherin, CD31) markers were used to characterize the phenotype of NSPCs cocultured with ECs. Enhanced green fluorescent protein-neural stem/progenitor cells (green) were cocultured with ECs for 3 days (A and B) or 10 days (C to F) and immunostained for doublecortin (A, red), nestin (B, red), Tuj1 (C and D, red), and GFAP (C and D, blue); VE-cadherin (E, red) and CD31/PECAM-1 (F, red). The VE-cadherin and CD31-positive endothelial cells were not captured, because the NSPCs were imaged in a different focal plane. However, ECs were clearly visible at Z-stack composite confocal images (data not shown in the figure). Cells were imaged on a Zeiss LSM510-META confocal imaging system. Bars = 20 μm (A to C), 50 μm (D), and 5 μm (E and F).

To determine whether NSPCs provide trophic support to ECs under conditions of in vitro ischemia, EC monocultures or NSPC/EC cocultures were exposed to 3 h OGD, followed by growth under normoxic conditions for 7 days in the absence of serum. As shown in Figure 2, EC monocultures grown alone in the absence of serum underwent further cell damage and cell loss in response to 3 h OGD exposure (Figure 2, left panels). The OGD-induced EC degeneration was not observed in the presence of NSPCs (right panels). Both EC cell shape and number appeared robustly preserved in NSPC/EC cocultures exposed to OGD (Figure 2, right panels). Moreover, ECs formed and maintained capillary-like structures in the presence of NSPCs even under OGD conditions (Figure 2, inset). After 10 days of coculture, NSPCs underwent differentiation, expressing both neural and EC markers, formed large capillary-like structures (Figures 3C and 3D), and began to express the EC markers, VE-cadherin, and PECAM-1 (Figures 3E and 3F). These experiments show that NSPCs provide support for both EC cell survival and morphogenesis under conditions of in vitro ischemia, and also indicate potent reciprocal signaling between NSPCs and ECs (i.e., NSPCs promote EC survival and morphogenesis, and ECs promote reciprocal expression of an endothelial-like phenotype by NSPCs in vitro).

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Figure 2

Neural stem/progenitor cells support morphology and survival of ECs after oxygen-glucose deprivation (OGD). Direct NSPC/EC cocultures and EC cultures (both grown in serum-free and growth factor-free medium) were subjected to 3-hour OGD and analyzed at 7 days after OGD (middle and bottom panels). Control cultures (top panel), grown in the same experimental conditions, were not subjected to OGD. Endothelial cell morphology was assessed using DIC confocal microscopy imaging and immunostaining with the antibody against CD31/PECAM-1 (bottom panels). Enhanced green fluorescent protein-neural stem/progenitor cells are shown on the green channel. Bars = 50 μm.

Hypoxia-Inducible Factor-1α and Vascular Endothelial Growth Factor are Constitutively Expressed by Cultured Neural Stem/Progenitor Cells and Become Upregulated after Oxygen and Glucose Deprivation

To determine whether NSPCs respond to OGD via increased expression of the transcription factor, HIF-1α, and its downstream target, VEGF, we used western blot analysis, enzyme-linked immunoassay, and immunofluorescence (Figure 4). Neural stem/progenitor cells constitutively expressed of both HIF-1α and VEGF under normoxic conditions, as shown by western blot and immunoassay (Figures 4A and 4B). Furthermore, both HIF-1α expression and VEGF release were increased approximately twofold in response to 3 h exposure to OGD (Figure 4B). Immunostaining of NSPC cultures under normoxic conditions also showed prominent expression of VEGF and HIF-1α (Figures 4C and 4D). The pattern of VEGF immunofluorescence appeared vesicular within the cytoplasm, whereas HIF-1α immunofluorescence was present in both the cytoplasm and nucleus of many cells. The nuclear localization of HIF-1α, confirmed by colocalization with DAPI nuclear staining (Figure 4D, arrow), suggests transcriptional activity. Western blotting showed no detectable HIF-1α or VEGF in EC monocultures (Figure 4A). These results indicate that cultured NSPCs constitutively express both HIF-1α and VEGF, and respond to ischemic conditions in vitro via upregulation of these hypoxia-responsive factors.

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Figure 4

Neural stem/progenitor cells constitutively express both HIF-1α and VEGF in culture, and upregulate expression after exposure to OGD. (A) Western blot analysis of intracellular VEGF (top) and HIF-1α (bottom) in NSPC and EC lysates. (B) Neural stem/progenitor cell-conditioned media and cell lysates were assayed for VEGF and HIF-1α, respectively, under conditions of normoxia (open bars) or 3 days after exposure to 3 h OGD (filled bars). One-way ANOVA and Tukey's multiple comparison post hoc analysis were performed for statistical analysis. **P < 0.01; ***P < 0.001, n = 3 samples per group assayed in triplicate. (C, D) Cultured NSPCs maintained under normoxic conditions were immunostained with the antibodies against VEGF (C, red channel) and HIF-1α (D, red channel). Nuclear localization of HIF-1α was verified bycolocalization with DAPI staining (blue, arrow). Cells were imaged on a Zeiss LSM510-META confocal imaging system. Bars = 10 μm.

These results also indicate that NSPCs show increased resistance to OGD, compared with ECs, as evidenced by their robust morphologic appearance and upregulated expression of HIF1-α and VEGF at 3 days after the 3 h OGD exposure. Unlike ECs, NSPCs grown in monoculture survive 7 days after a 3-h OGD exposure, and maintain their ability to differentiate (Supplementary Figure 1D).

Inhibition of Vascular Endothelial Growth Factor Signaling Impairs Neural Stem/Progenitor Cell-Mediated Survival and Morphogenesis of Endothelial Cells after Serum Deprivation

To determine whether diffusible VEGF mediates the protective effects of NSPCs against serum withdrawal, ECs were incubated for 3 days in serum-free medium conditioned by NSPCs in the presence or absence of the VEGFR2 tyrosine kinase inhibitor SU1498 (5 to 20 μmol/L) or Flt-1-Fc (30 ng/mL). Flt-1-Fc is a fusion protein comprising human IgG-Fc fragment fused to the high-affinity ligand-binding ectodomain of VEGFR1, and acts as a decoy receptor to inhibit VEGF signaling. As shown in Figure 5 (open bars), NSPC conditioned media (NSPC-CM) protected ECs against serum withdrawal, and SU1498 potently inhibited this protection in a dose-dependent manner with 55% inhibition beginning at the lowest dose of 5 μmol/L. Exposure of ECs to 20 μmol/L SU1498 for the same duration had no effect on EC survival, indicating that SU1498 is not directly toxic at the concentrations used in this experiment (data not shown). Similarly, incubation with Flt-1-Fc significantly reduced the protective effect of NSPC-CM by approximately 50%.

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Figure 5

Inhibition of VEGF signaling impairs NSPC-mediated survival and morphogenesis of ECs after serum deprivation and OGD. (open bars, left) Viability of ECs after 3 days of culture in the presence or in the absence of serum, NSPC-conditioned medium (NSPC-CM), or the VEGF inhibitors, SU1498 or FIt-1-Fc. (filled bars, right) Viability of ECs exposed to 3 h of OGD, followed by 3 days of incubation with or without serum, NSPC-CM, or VEGF inhibitors. Percent viability in each culture condition was compared with the viability of EC cultures grown under normoxic conditions in the presence of serum, which was set to 100% (far left open bar = control). Neural stem/progenitor cell-CM represents media conditioned for 3 days by monocultures of NSPCs grown in serum-free and growth factor-free media. Data were acquired using the MTT colorimetric viability assay as described under Materials and methods section, **P < 0.01; ***P < 0.0001, One-way ANOVA with Tukey's multiple comparison post hoc analysis, n = 3 cultures per group, assayed in triplicate.

To determine whether VEGF signaling is obligatory for NSPC-mediated protection against OGD, ECs were exposed to 3 h of OGD followed by growth in NSPC-CM with or without SU1498 or Flt-1-Fc for 3 days. Both SU1498 (10 μmol/L) and Flt-1-Fc (30 ng/mL) potently inhibited the protective effects of NSPC-CM under conditions of OGD (Figure 5, filled bars). The vasculotrophic effect of NSPC-CM against OGD was not influenced by incubation with control IgG-Fc. Taken together, these data suggest that VEGF signaling mediates the protective effects of NSPC-CM against both serum starvation and OGD conditions in vitro.

Neural Stem/Progenitor Cells Provide Vasculotrophic Support against Mild Focal Ischemia after Intracerebral Transplantation

To determine whether NSPCs are vasculotrophic in vivo, EGFP-NSPCs were transplanted directly into the dorsal striatum (Supplementary Figure 2) 3 days before the induction of transient focal ischemia induced by 30 mins ipsilateral MCAO. Our goal was to mimic our in vitro results with NSPC/EC cocultures, such that NSPCs were present within the brain during the ischemic event. Mice were killed 3 days after ischemic injury. EGFP⁺ NSPCs were observed at the site of transplantation at 3 days (Figure 6 and Supplementary Figure 2). Microvascular density within the perimeter of ipsilateral striatum was compared with that of contralateral striatum measuring the density of vessels immunofluorescent for Glut-1, the blood—brain barrier glucose transporter expressed by brain ECs (Pardridge et al, 1990) (Figures 6A and 6B). Neural stem/progenitor cell transplants stimulated a 1.6-fold increase in microvascular density within the ipsilateral versus contralateral striatum, whereas sham injections of PBS had no effect on microvascular density at 3 days after MCAO (Figure 6, graph). Endothelial cells were anatomically juxtaposed to transplanted EGFP-NSPCs (Figure 6C). A survey of blood vessels throughout the entire striatal area of NSPC-MCAO recipients using high-resolution confocal microscopy revealed that approximately 21.31% ± 0.82% of the Glut-1 + structures were also Ki67+ (n = 3 mice, Figures 6D and 6E), whereas Ki67+ nuclei were not observed within the contralateral unlesioned striatum. Both HIF-1α and VEGF continued to be expressed by the EGFP-NSPC grafts at 3 days after transplantation (Supplementary Figure 3).

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Figure 6

Neural stem/progenitor cells support brain revascularization after ischemia. (A and B) Coronal sections through the lesioned striatum of EGFP-NSPC recipients (B) or recipients of control PBS injections (A) immunostained for the endothelial cell marker Glut-1 (red). Transplanted EGFP-NSPCs are visible as green cells. (C to E) Double labeling of endothelial cells (Glut-1 +, red) and proliferating cells (Ki67 +, blue). Enhanced green fluorescent protein-NSPC grafts are shown on green channel. The presence of Ki67 + nuclei within Glut-1 + blood vessels was assessed using confocal microscopy viewed in three-dimensional (D) and orthogonal (E) image projections. The images were acquired using Zeiss LSM510-META confocal imaging system. Bars = 20 μm (A to C), 10 μm (D), and 2 μm (E). (Graph) The percentage of striatal area covered by Glut-1-immunoreactive vessels in PBS control mice (open bars) versus EGFP-NSPC recipients (filled bars). Image analysis was performed over entire striatal area within three histologic sections containing grafted cells or PBS injection sites on both lesioned (ipsilateral) and nonlesioned (contralateral) sides.