Transplantation of Mesenchymal Stem Cells Exerts a Greater Long-Term Effect than Bone Marrow Mononuclear Cells in a Chronic Myocardial Infarction Model in Rat

Isolation and Characterization of Cells

All eGFP cells (bone marrow) were isolated from 4–6-week-old Sprague-Dawley eGFP rats. Bone marrow cells were harvested from rat femurs and isolated by means of a Ficoll-Paque density gradient centrifugation. For BM-MNC transplantation, cells were washed and resuspended in culture media (DMEM, Invitrogen, Leiden, The Netherlands) without supplements at a concentration of 10⁶ cells in 70 μl. Viability by trypan blue dye exclusion was shown to be above 98%.

MSC were obtained from mononuclear cells. Briefly, cells were seeded at 50,000 cells/cm² in aMEM (Invitrogen) with 10% fetal calf serum (FCS, Cambrex, Milano, Italy), 1% penicillin/streptomycin, and 10 ng/ml bFGF (Sigma, Madrid, Spain) and maintained in a humidified atmosphere in 5% CO₂. Subconfluent MSC were obtained within a week and passed at 5000 cells/cm². Cells were used for transplant after five passages. Characterization of MSC was performed by FACS and differentiation capacity. Cells were stained with antibodies against RT1A, RT1B, CD31, CD44, CD45, CD73, and CD90 (all purchased from BD, Madrid, Spain). For osteogenic differentiation, cells were plated at 6000 cells/cm² in osteogenic media [αMEM with 10% FCS, 1% antibiotics, 10 mM β-glicerolphosphate (Sigma), 0.2 mM ascorbate-2-phosphate (Sigma), and 0.01 μM dexamethasone (Sigma)]. Condrogenic differentiation was performed with 200,000 pelleted cells suspended in condrogenic media [DMEM-high glucose (Invitrogen) with 1% antibiotics, 10 ng/ml TGF-β3 (R&D Systems, Minneapolis, MN, USA), 50 mg/ml ITS+Premix (BD), 40 μg/ml proline (Sigma), 500 ng/ml BMP6 (R&D Systems), 50 μg/ml ascorbate-2-P, and 0.1 μM dexamethasone]. For adipogenic differentiation, when cells reached 95–100% confluence, expansion media was replaced with adipogenic media [αMEM with 10% FCS, 1% antobiotics, 50 μM indomethacin (Sigma), 0.5 mM IBMX (Sigma), and 1 μM dexamethasone]. All differentiation protocols were maintained for 21 days. Analysis of cell differentiation was performed by histochemical staining by Oil red O (adipogenic), Alizarin red (osteogenic), and toluidine blue (condrogenic) following previously described protocols (62).

Experimental Model

A total of 115 female Sprague-Dawley rats (Harlan IBERICA S.L. Barcelona, Spain) underwent coronary artery ligation of the left coronary artery as previously described (3). Only those animals that survived (n = 97) and with a LVEF below 40% at 1 month post-MI were included in the study (n = 75). Five weeks after myocardial infarction induction, rats were reoperated by sternotomy and allocated to receive 10⁶ cells per animal (total volume: 70 μl) of BM-MNC (n = 24), MSC (n = 25), or control medium (n = 26) in two points of the infarct border region. Due to the allogeneic origin of the cells, animals were daily immune-suppressed with cyclosporin A (20 mg/kg/day, IP, Sandimmun, Novartis) from 2 days pretransplantation until sacrifice. Rate of survival over the course of the experiment was over 98%. All experiments, including bone marrow cell isolation, were performed in accordance with the principles of laboratory animal care formulated by the National Society for Medical Research and the guide for the care and use of laboratory animals by the Institute of Laboratory Animal Resources (Commission on Life Science, National Research Council). All animal procedures were approved by the University of Navarra Institutional Committee on Care and Use of Laboratory Animals.

Tissue Processing and Staining

For histological analysis, three animals per group were sacrificed at 1, 2, and 4 weeks, respectively and eight animals per group at 3 months. After sacrifice, rat hearts were excised, fixed in 4% paraformaldehyde for 4 h at 4°C, and cut in three equal size blocks (apical, midventricular, and basal). Hearts were either dehydrated in ethanol 70% (4°C o/n) and embedded in paraffin or saturated in 25% sucrose (4°C o/n), embedded in O.C.T. compound, and snap frozen in nitrogen-cooled isopentane. For histological analysis 5-μm sections were cut. Cell detection was based upon the presence of GFP-positive signals by inmunohistochemical [anti-GFP polyclonal Ab (pAb, Invitrogen) or anti-GFP raised in chicken pAb (Abcam, Cambridge, UK) diluted 1:500 in TBS] or immunofluorescence methods. For immunofluorescence, a tyramide amplifying kit (Invitrogen) or a secondary antibody anti-chicken IgY coupled to 655 nm emitting quantum dots were used following manufacturer's instructions. Immunolabeling was performed with antibodies against α-smooth muscle actin (α-SMA) [mouse monoclonal antibody (mAb) diluted 1:1000 in TBS; Sigma, Madrid, Spain] coupled to Cy3, cardiac troponin T (cTT) (mAb, diluted 1:100 in TBS; Labvision), ventricular myosin (mAb diluted 1:2 in TBS; Bio-Cytex), Ki-67 (mAb, diluted 1:25 in TBS; DAKO, Barcelona, Spain), PCNA (mAb, diluted 1:100 in PBS; Santa Cruz), CD68 (mAb, diluted 1:200 in TBS; Serotec, Oxford, UK), caveolin-1 (mAb, diluted 1:100 in TBS, BD), connexin 43 (pAb, diluted 1:200 in TBS, Sigma). Secondary antibodies labeled with AlexaFluor-594 or AlexaFluor-488 were purchased from Molecular Probes (Invitrogen) if needed and used following the manufacturer's instructions. EnVision^™-HRP conjugated system (Dako) was used as secondary reagent for immunohistochemistry. For nuclear staining, TOPRO-3 (diluted 1:50 in PBS-glycerol) for confocal microscopy or DAPI (diluted 1:4 in PBS-glycerol) for conventional IF microscopy were utilized. For confocal microscopy, a LSM 510 META (Carl Zeiss, Minneapolis, USA) microscope was used.

For Sirius Red staining, sections were deparaffinized and immersed in Sirius Red (Sigma) for 90 min, differentiated 2 min in HCl (Sigma) 0.01 N, dehydrated, and mounted in DPX. Hematoxylin-eosin staining was performed as detailed elsewhere (16). Briefly, sections where stained in Ehrlich's hematoxylin (Sigma) for 7 min, differentiated through water-HCl and Li₂CO₃ solutions, immersed in eosin (Sigma) for 10 s, dehydrated, and mounted in DPX.

Electron Microscopy

For electron microscopy studies, six to eight animals per group were sacrificed and hearts were fixed with 4% paraformaldehyde 0.5% glutaraldehyde. Sections were postfixed with 1% osmium (30 min), rinsed, dehydrated, and embedded in araldite (Durcupan, Fluka). Semithin sections (1.5 μm) were cut with a diamond knife and stained lightly with 1% toluidine blue. Later ultrathin (0.05 μm) sections were cut with a diamond knife, stained with lead citrate, and examined under a Fei Tecnai spirit electron microscopy. Over 15 samples per animal were analyzed.

Morphometric Analysis

Quantification of vascular density was performed in animals sacrificed 3 months posttransplantation. For capillary density (capillaries/mm²), a total of 15 serial sections including the infarct area, 30 μm apart, were stained with caveolin-1 and a total of 30 infarct border images were analyzed. Arteriolar density (arterioles/mm²) and arteriolar area (μm²) were quantified in a similar way after staining with anti-α-SMA-Cy3 in the following sections. Pictures were taken on a Nikon Eclipse E800 microscope equipped with epifluorescence optics and digital images were analyzed using imaging software (Jay Image), or on a Zeiss LSM 510 META laser confocal microscope. The degree of fibrosis was determined by quantification of collagen deposition stained by Sirius red as previously described (16). Briefly, a mean of 15 serial sections were stained, each 30 μm apart. Infarct size was assessed as the mean percent of infarcted area versus total LV area, whereas fibrosis was measured in high-power photographs within the infarct as percent of collagen area (red) versus total tissue area using AnalySIS^R software. Cell engraftment was quantified after GFP immunostaining. Positive cells were only counted if their nucleus was identifiable. Tissue sections were screened and GFP cells quantified from the first to the last section with engrafted cells. This was made relative to the quantity of injected cells (10^6M) as the percentage of surviving cells.

Macrophage density was measured as number of CD68-positive cells per area unit in a mean of 15 sections, each 30 μm apart. Finally, cell proliferation was quantified in animals sacrificed 1 and 2 weeks after cell injection by counting PCNA-positive cells in sections stained for GFP, PCNA, and a lineage-specific marker, either caveolin-1 for endothelium or α-SMA for myofibroblast or smooth muscle. Number of sections was the same as for macrophage density. All photographs were taken on a Zeiss LSM 510 META laser confocal microscope.

Echocardiographic Studies

Animals were slightly anesthetized prior to study with 2% isoflurane (Forane®, Lab. ABBOTT S.A, Madrid, Spain) in 100% O₂ gas and placed in the supine or lateral position on a warming pad for transthoracic two-dimensional echocardiography, M-mode recordings, and Doppler ultrasound measurements as previously described (3). Echocardiography was performed using a Sonos 4500 ultrasound system (Philips) with a 12 MHz linear array transducer and Doppler measurement. Left ventricular remodeling was assessed by measuring end systolic and diastolic volumes and diameters according to the American Society of Echocardiology. The left ventricular ejection fraction was determined in parasternal short axes (41) and diastolic function was assessed by measuring E and A waves of the mitral filling pattern by pulsed echo-Doppler technique in four-chamber apical views. Echocardiographic studies were performed at baseline (before infarct), before cell transplantation, and at day 90 posttransplant by the same blinded investigator. Measurements were done in three cycles and the mean value was obtained.

¹⁸F-FDG PET Imaging Protocols, Image Reconstruction, and Semiquantitative Evaluation

Immediately before injection of cells and 90 days later, animals were subjected to PET analysis using the technique previously described by our group demonstrating that ¹⁸F-FDG-micro-PET provides valuable semiquantitative information and allow noninvasive follow-up of heart glucose metabolism, representing a useful strategy for assessment of novel therapies in cardiac regeneration (49). Rats were anesthetized with 2% isoflurane in 100% O₂ gas and after tail vein injection of ¹⁸F-FDG (75 MBq in 100–200 μl), immediately awakened, and placed back in the cage. Two hours after tracer injection, animals were anesthetized with isoflurane, placed prone on the PET scanner cradle, and kept during the overall study under continuous influx of the anesthetic. A static 60-min study (sinogram) was acquired in a Mosaic (Philips) small-animal dedicated imaging tomograph. Scanner efficiency normalization, dead time, and decay corrections were applied during reconstruction. Images were reoriented for further processing and polar maps obtained using the specific cardiac imaging software package of the PET scanner. After reorientation of transaxial images into short- and long-axis slices polar maps were generated and divided into 17 different ROIs. Individual quantification of the ¹⁸F-FDG uptake in each of them was calculated. The total number of counts obtained for each of the ROIs was divided by its corresponding area to obtain counts per area unit. For each PET study, the maximal value of the 17 ROIs was considered as 100% and the remaining data transformed into percentage values. All further calculations and statistical analysis were performed on these sets of rescaled numerical data.

Statistical Analysis

All data are expressed as mean ± SEM or median (Q25; Q75). Comparisons for repeated measurements were performed by ANOVA accompanied by Tukey's HDS for intergroup comparisons or Kruskal-Wallis and Mann-Whitney test with Finner's correction of significance. Shapiro-Wilk test was used to verify that the data had a Gaussian distribution, which justifies the use of a parametric test. Statistical analysis was performed with the SPSS 11.0 software and differences were considered statistically significant when p < 0.05.

Cell Culture and Characterization

MSC presented a typical spindle-shape in culture conditions. GFP expression was monitored during culture and before transplantation, ensuring that over 90% of the cells were positive (not shown). At passage 4, this population had a FACS expression profile as follows: RT1A, CD44, CD73, and CD90 positive and RT1B, CD31, and CD45 negative (Fig. 1A, representative histograms are shown). Moreover, MSC differentiated towards condrogenic, adipogenic, and osteogenic lineages (Fig. 1B), thus proving their multipotency. BM-MNC were obtained following previously reported protocols (48).

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Figure 1.

MSC characterization. (A) MSC were stained with antibodies against RT1B, CD31, CD45, RT1A, CD44, CD73, and CD90 (red line) or isotype controls (dashed line). (B) MSC were differentiated in vitro towards chondrocites (as shown by toluidine blue staining), adipocytes (Oil red O staining), and osteocytes (Alizarin red staining). Scale bars: 25 μm.

Mesenchymal Cell Injection Induces a Long-Lasting Improvement of Cardiac Function and Tissue Metabolism

In order to assess if cell therapy was capable of inducing a long-lasting improvement in a model of rat chronic MI, cardiac function and tissue metabolism were monitored by echocardiography and microPET, 3 months after injection of BM-MNC, MSC, or control media. Artery ligation provoked a marked reduction of the left ventricular ejection fraction (LVEF) from baseline (72.23 ± 8.47%, mean ± SD) to preinjection (5 weeks later) (27.82 ± 6.69%), which did not differ between all three groups. Compared to their preimplant values, both BM-MNC and MSC treatment induced a statistically significant improvement of left ventricular (LV) function (BM-MNC: 26.61 ± 2.01% to 42.61 ± 3.7%; MSC: 27.5 ± 1.28% to 38.8 ± 3.2% pretransplant and 3 months, respectively; p < 0.05), whereas animals injected with medium did not show any improvement in the cardiac function (29.87 ± 2.84% to 28.1 ± 1.59%) (Fig. 2). No significant differences were detected between both cell-treated groups (BM-MNC vs. MSC; p = 0.97), indicating no superior benefit from one or the other cell population. Analysis of polar maps including the whole left ventricle (the 17 cardiac segments) showed that MSC-treated animals had a significant improvement in cardiac metabolism compared with their preinjection parameters (72.15±1.17% to 76.31 ± 1.1%; p < 0.01) (Fig. 3A). MSC treatment proved to have a positive effect not only in global tissue metabolism, but more importantly when the analysis was restricted to the infarcted segments (7, 13, 16, and 17) as depicted by the significant increase in their metabolism (46.8 ± 3.35% to 53.02 ± 3.55%, p < 0.05) (Fig. 3B, C). On the contrary, BM-MNC injection did not have a significant effect in tissue metabolism (all segments: 70.87 ± 1.88% to 73.55 ± 1.88%; infarcted segments: 44.8 ± 4.3% to 50.4 ± 4.63%).

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Figure 2.

BM-MNC and MSC improve cardiac function. LVEF was assessed by echocardiography before and 3 months after transplantation of BM-MNC or MSC. Cell culture medium was injected in the control group. Results are shown as mean ± SD and statistical significance was calculated by comparing the LVEF values 3 months after transplantation versus preimplantation, in each group (*p < 0.05).

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Figure 3.

MSC positively affect tissue metabolism. ¹⁸F-FDG uptake was evaluated by microPET before and 3 months after transplantation. A significant increase in the tissue metabolism was detected in the MSC-treated but not in the BM-MNC-treated hearts when all 17 segments were analyzed (mean ± SD, **p < 0.01) (A) and also when only the infarcted ones were analyzed (*p < 0.05) (B). Representative images (cross and longitudinal views) of the hearts, 3 months after cell or medium injection, are shown (C).

MSC Engraft in the Ischemic Tissue and Induce a Reduced Inflammatory Reaction Than BM-MNC

Cell fate was analyzed by immunohistochemical and immunofluorescence detection of GFP-positive cells at 1 and 2 weeks and 1 and 3 months after their transplantation in the border zone of the infarct. We found large patches of GFP-positive cells at the injection site in rats treated with MSC 1 and 2 weeks after transplantation, but not from 1 month onwards (Fig. 4A–D). Cell engraftment was quantified in MSC-treated animals as described in Materials and Methods. One week after transplant, 1.85% (0.53; 3.02) [median (Q25; Q75)] of the total number of injected cells were still present in the myocardium of infarcted animals, and this number decreased to 1.33% (0.52; 2.14) at 2 weeks, were almost not detectable at 1 month, and disappeared at 3 months. On the other hand, presence of GFP-BM-MNC could not be detected even at 1 week posttransplant (Fig. 4E–H). No positive signal was found on medium-injected animals (Fig. 4I–L).

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Figure 4.

Cell engraftment. Presence of transplanted cells was assessed by immunohistochemistry against GFP at 1 and 2 weeks and 1 and 3 months after their injection. Engraftment was only detected for MSC at 1 and 2 weeks. (A–D) DMEM; (E–H) BM-MNC; (I–L) MSC. Scale bars: 100 μm.

It is possible that, despite immunosuppression, the GFP antigen could be recognized by the macrophages, which in turn could react against the transplanted cells (33). In order to study this, CD68 immunostaining was performed in animals sacrificed 1 week after transplant. Intra- and peri-infarct sections were analyzed and, as depicted in Figure 5, a strong macrophage infiltration was found in BM-MNC-treated animals, both in the infarct (327.6 ± 49.67 positive cells/mm², p < 0.01 vs. medium) (Fig. 5A–D) and peri-infarct (1945.78 ± 372.08 positive cells/mm², p < 0.01 vs. medium) (Fig. 5E–H) regions in comparison with media-injected animals (Medium, intra-infarct: 94.5 ± 6.05 positive cells/mm²; peri-infarct: 167.48 ± 39.91 positive cells/mm²). MSC-transplanted animals did also show an increase in CD68-positive cells, albeit significantly lower than BM-MNC (intra-infarct: 230.86 ± 59.27 positive cells/mm², p < 0.01 vs. medium; peri-infarct: 427.21 ± 71.7 positive cells/mm²; p < 0.01 vs. control; p < 0.01 vs. BM-MNC). The increase in macrophage infiltration in the BM-MNC-transplanted animals was not due to the direct contribution of the transplanted cells as demonstrated by the lack of CD68⁺/GFP⁺ cells. Furthermore, double staining for GFP and CD68 revealed a strong infiltration of macrophages in close contact with injected MSC (Fig. 5I-M). Presence of GFP vesicles could be detected in the inflammatory cells by immunofluorescence (Fig. 5M) and confirmed by electronic microscopy (Fig. 6), suggesting host cell-mediated immune rejection of the transplanted cells.

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Figure 5.

Cell transplantation in chronic MI is associated with macrophage infiltration. Sections of hearts obtained 1 and 2 weeks and 1 and 3 months after cell or media transplant were stained with antibodies against CD68 (red) and GFP (green) and macrophage infiltration was quantified as described in Materials and Methods. A significant (**p < 0.01) increase in macrophage density within the infarcted area of BM-MNC-implanted but not of MSC-implanted animals was found (A–D). Also in the peri-infarct area, there was a significant increase (**p < 0.01) in CD68-positive cell density in the peri-infarct region of BM-MNC- and MSC-treated rats, although this was less pronounced in the MSC than in the BM-MNC group (**p < 0.01) (E–H). Detailed CD68-positive macrophages infiltrating MSC injection areas are shown (I–M) with detectable GFP-positive vesicles in some of the phagocytes (arrowheads) (M). Images correspond to animals sacrificed 1 week after cell or medium injection. CD68 marker (Alexa-594): red; GFP (Alexa-488): green; nuclear staining (TOPRO3): blue. Scale bars: (B–D, F–H) 35 μm; (I–L) 20 μm; (M) 5 μm.

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Figure 6.

Electron microscopy of macrophages within cell-engrafted areas. One week after MSC transplantation, presence of macrophages (arrowheads) was confirmed by electronic microscopy, in the areas of cell injection (collagen deposits are indicated with asterisks) (A). A higher magnification field shows a GFP vesicle-containing macrophage. GFP deposits could be detected after previous immunogold GFP staining (arrowheads) (B). Scale bars: (A) 6 μm; (B) 2 μm.

MSC Do Not Differentiate Towards Vascular or Cardiac Phenotypes In Vivo

In vivo differentiation of MSC was analyzed by double immunofluorescence with antibodies against GFP and lineage-specific markers in tissue obtained at 1 and 2 weeks posttransplant. Transplanted MSC did not colocalize with endothelial markers such as caveolin-1, indicating lack of differentiation to endothelium (data not shown). On the other hand, although α-SMA-GFP cells were detected [percentage of double positive cells: 1 week: 12.80 (7.5; 20.6); 2 weeks 9.48 (10; 20.74), median (Q25; Q75)], these cells did not form vessel-like structures remaining with a fibroblastic morphology consistent with myofibroblast (Fig. 7A). Furthermore, expression of this marker was not surprising, as MSC do express α-SMA in in vitro culture (data not shown). Cardiac contribution could not be detected by double staining for GFP and the cardiac markers MLC2v or cTT (data not shown).

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Figure 7.

Analysis of cell fate and in vivo proliferation. One and 2 weeks after transplant, heart sections were stained with antibodies against α-SM-actin-Cy3 and PCNA (Alexa-594: red) and GFP (Alexa-488: green). Nuclear staining was performed with TOPRO3 (blue). Expression of lineage-specific markers was tested by double immunofluorescence. Engrafted GFP-MSC were positive for α-SM-actin (higher magnification field: arrowheads) although remained as myofibroblasts and did not contribute to the vascular net (A). Proliferating GFP-positive MSC (arrowheads) were also observed surrounded by proliferating non-GFP cells (asterisks) (B). GFP-positive cells were identified after GFP immunogold staining as fibroblast-like cells, which were surrounded by areas of collagen deposition (asterisks). Top right: higher magnification showing a GFP-positive cell; bottom right: caveoli in the membrane of GFP-MSC (arrowheads) (C). Images were taken from animals sacrificed 1 week after treatment. Scale bars: (A, B) 25 μm; higher magnification (B): 10 μm; (C) 2 μm; top right: 400 nm; bottom right: 100 nm.

In order to confirm these data and identify the phenotypic identity of the mesenchymal cells once transplanted, electron microscopy after preembedding immunohistochemistry for GFP was performed. Four rats sacrificed 1 or 2 weeks after injection were studied and a mean of 30 cells/rat were analyzed. Confirming the results obtained in the immunofluorescence analysis, no vascular or cardiac GFP-positive cells were found and GFP-positive cells showed a typical fibroblastic phenotype with an elongated nucleus with a central nucleolus, small clumps chromatin organization, and a high density of RER cisterns (Fig. 7B). Implanted cells also presented big dictosomes and large mitochondrias and caveoli (Fig. 7B, arrowheads) along their surface. Interestingly, a consistent collagen network was found around them (Fig. 7B, asterisks).

On the other hand, although vascular or cardiac direct contribution could not be detected, a small percentage of engrafted MSC (approximately 10% of engrafted cells at 1 week) did costained with PCNA (Fig. 7C, arrowheads), indicating their ability to proliferate within the damaged tissue. GFP cycling cells were not detected after 2 weeks posttransplant, suggesting either that proliferation occurred during a short time or that immune rejection was involved in the lack of proliferating cells. Interestingly, non-GFP cells located in the area of injection also expressed PCNA (Fig. 7C, asterisks), suggesting an (auto)paracrine effect of the MSC that promotes cell proliferation. Although most proliferating cells were of hematopoietic lineage (not shown), cell-implanted animals also showed a marked increase in the density of endothelial-proliferating cells both in the peri-infarct and infarct regions in the groups of animals treated with MSC (peri-infarct: 1 week: 69.44 ±13 cells/mm²; 2 weeks: 56.88 ± 5.29 cells/mm²; p < 0.01 vs. medium; infarct: 1 week: 100 ± 16.61 cells/mm, sup > 2; 2 weeks: 48.73 ± 14.13 cells/mm²; p < 0.01 vs. medium) and BM-MNC (peri-infarct: 78.19± 11.26 cells/mm²; 2 weeks: 54.13 ± 10.99 cells/mm²; p < 0.01 vs. medium; infarct: 1 week: 42.89 ± 8.5 cells/mm²; 2 weeks: 38.27 ± 7.97 cells/mm²; p < 0.01 vs. medium) (Fig. 8A). MSC-treated hearts also presented an augmented density of cycling myofibroblasts (peri-infarct: 1 week: 113.17 ± 26.57 cells/mm²; 2 weeks: 43.57 ± 10.03 cells/mm²; p < 0.01 vs. medium; p < 0.01 vs. BM-MNC) that were rarely found in BM-MNC-treated animals and even less in control animals. Finally, although some dividing smooth muscle cells were identified, their numbers were only significantly increased in MSC-treated animals 1 week after injection (17.49 ± 6.08 cells/mm²; p < 0.05 vs. medium). Representative images are shown in Figure 8B. No proliferating endothelial cells, myofibroblasts, or smooth muscle cells were detected 1 or 2 weeks after media injection (6 and 7 weeks after myocardial infarction) in animals treated with media alone.

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Figure 8.

Host cell proliferation. Percentage of proliferating endothelial cells (caveolin-1 positive), myofibroblasts (α-SMA positive, spindle shape), or smooth muscle cells (α-SMA positive, forming vessels) was determined by quantification of PCNA-positive cells, within the peri-infarct and infarct areas 1 and 2 weeks after treatment (*p < 0.05 vs. medium-injected animals; **p < 0.01 vs. medium-treated rats; #p < 0.05 BM-MNC vs. MSC: ##p < 0.01 BM-MNC vs. MSC) (A). Representative pictures of proliferating endothelial cells (PCNA⁺Cav1⁺), myofibroblasts (PCNA⁺a-SMA⁺, spindle shape), and smooth muscle cells (PCNA⁺a-SMA⁺, vessels) within the peri-infarct and the infarct areas at 1 and 2 weeks performed by confocal microscopy, are shown (arrowheads: PCNA-positive cells) (B). GFP (Quantum Dot-655): white; caveolin-1 (Alexa-594) and α-SMA-Cy3 markers: red; PCNA (Alexa-488): green; nuclear staining (TOPRO-3): blue. Scale bars: 15 μm.

MSC Promotes Revascularization and Cardiac Remodeling

Despite the low engraftment rate and the lack of differentiation, a functional benefit was detected in the rats transplanted with bone marrow-derived cells, with a stronger benefit in the animals treated with MSC. In order to elucidate the mechanisms involved in such functional improvement, we analyzed the effect of treatment on angiogenesis and vasculogenesis. Capillary density was determined 3 months after injection, by quantifying the small-caliber caveolin-1-positive vessels/mm² present in the peri-infarct region. As depicted in Figure 9A, only transplantation of MSC was able to induce a significant increase in vessel count (medium: 683.9 ± 37.8 capillaries/mm²; BM-MNC: 705.8 ± 38.8 capillaries/mm²; MSC: 897.1 ± 61.6 capillaries/mm²; p < 0.05) (Fig. 9B-D). On the other hand, both cell treatments induced an increase in big caliber vessels, quantified as α-SMA-positive vessels/mm² (medium: 64.1 ± 5.4; BM-MNC: 130.1 ± 11; MSC: 145.7 ± 7.8; p < 0.01 in both cell-treated groups vs. medium) and α-SMA-positive area (medium: 1.2 ± 0.1%; BM-MNC: 2.09 ± 0.14%; MSC: 2.53 ± 0.15%; p < 0.01 in both cell-treated groups vs. medium). Importantly, such increase in arterioles/arteries density in the peri-infarct region was significantly higher in the animals treated with MSC than in the BM-MNC-treated animals (p < 0.01 MSC vs. BM-MNC) (Fig. 9E–H).

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Figure 9.

Cell transplant is associated with an increase in vasculogenesis/angiogenesis and decreased in fibrosis and infarct size. Capillary and arterioles/arteries densities were respectively determined by quantification of the small-caliber (5–10 μm) caveolin-1-positive capillaries/mm² (mean ± SD) (A-D) and α-SMA-positive area (%) (mean ± SD) (E-H) in the peri-infarcted zones, 3 months after media or cell (BM-MNC or MSC) transplant. A significant increase in capillary (*p < 0.05) (A) and in arterioles/arteries area (**p < 0.01) (E) was determined in the MSC-treated hearts (D, H) in comparison with the media-treated ones (B, F). On the contrary, BM-MNC did not exert any effect in the capillary density (C) and, albeit, it positively affected the big vessel revascularization (*p < 0.05) (G); this increase was significantly lower than in the MSC group (H) (**p<0.01). Representative images of immunofluorescence for caveolin-1 (B-D) or α-SMA (F-H) staining are shown. Vessel markers (Alexa-594): red; nuclear staining (DAPI): blue. Morphometric analysis in serial sirius red-stained sections (I-P) showed also a significant smaller scar size (*p < 0.05) in the left ventricles of the MSC-treated hearts in comparison with the media-treated hearts, 3 months posttransplantation (I-L). Furthermore, fibrosis degree in the infarcted zone was also significantly smaller in the MSC group (*p < 0.05). BM-MNC did not have a positive effect either in the scar size or in the fibrosis degree (M-P). Scale bars: (B-D, F-H, N-P) 100 μm; (J-L) 2.5 mm.

As together with the revascularization processes, tissue remodeling may have an important role in the functional benefits. We analyzed infarct size and collagen content in the treated versus control animals and, as shown in Figure 9I-L, MSC- but not BM-MNC-treated hearts induced a significant decrease in infarct size compared to medium-injected controls (medium: 19.66 ± 1.21%; BM-MNC: 17.47 ± 4.62%; MSC: 12.78 ± 1.66%; p < 0.05, percentages referred to the total LV area). Furthermore, a smaller infarct was associated with a decrease in collagen vascular fraction (CVF) (Fig. 9M-P) in MSC-injected animals (control group: 66.26 ± 0.93%; BM-MN: 63.77 ± 8.53%; MSC: 58.54 ± 1.36%, p<0 05), showing a positive correlation between both parameters (R² = 0.73, p < 0.01), thereby demonstrating the superior effect of the MSC versus the BM-MNC.