|Year : 2017 | Volume
| Issue : 1 | Page : 147-150
Differentiation of mesenchymal stem cells into vascular endothelial cells: the future revascularization therapy in ischemic tissue
Rawhia H El-Edela1, Hala G Metwally2, Seham A Khodeer1, Rasha I Nor El-Din1, Thoria A Abd El-Hameed Omar MBBCh 1
1 Department of Clinical Pathology, Faculty of Medicine, Menoufia University, Menoufia, Egypt
2 Department of Clinical Pathology, Faculty of Medicine, Cairo University, Giza, Egypt
|Date of Submission||10-Apr-2016|
|Date of Acceptance||26-Jun-2016|
|Date of Web Publication||25-Jul-2017|
Thoria A Abd El-Hameed Omar
Department of Clinical Pathology, Faculty of Medicine, Menoufia University, Shebin El-Kom, Menoufia, 32511
Source of Support: None, Conflict of Interest: None
The objective of this study was to investigate the in-vitro differentiation of mesenchymal stem cells (MSCs) into cells of the endothelial lineage.
All tissues depend on the blood supply, and blood supply depends on endothelial cells (ECs). Vascular ECs derived from stem cells could be used in therapeutic strategies for the repair and revascularization of ischemic tissue in patients exhibiting vascular defects. MSCs that can be separated from different tissues have the ability for self-renewal, they can be differentiated into different tissues, and they help in the regeneration of damaged tissue in tissue engineering.
Materials and methods
This study was carried out on 20 bone marrow samples. A volume of 5 ml of bone marrow was aspirated. Mononuclear cells were separated using Ficoll–Hypaque solution. MSCs were separated from the mononuclear cell fraction using plastic adherence. MSCs were subcultured in 35-mm Petri dishes and then treated with vascular endothelial growth factors.
MSCs were generated out of mononuclear bone marrow cells. Isolated MSCs were positive for the marker CD44 and negative for CD34. They were able to differentiate into ECs. ECs can be identified by morphology, flow cytometric analysis to detect CD34+, and hematoxylin and eosin staining.
The present study shows that bone-marrow-derived MSCs can be differentiated in vitro to ECs as future revascularization therapy in ischemic tissue.
Keywords: bone marrow, endothelial cells, flow cytometry, mesenchymal stem cells, vascular endothelial growth factor
|How to cite this article:|
El-Edela RH, Metwally HG, Khodeer SA, Nor El-Din RI, Abd El-Hameed Omar TA. Differentiation of mesenchymal stem cells into vascular endothelial cells: the future revascularization therapy in ischemic tissue. Menoufia Med J 2017;30:147-50
|How to cite this URL:|
El-Edela RH, Metwally HG, Khodeer SA, Nor El-Din RI, Abd El-Hameed Omar TA. Differentiation of mesenchymal stem cells into vascular endothelial cells: the future revascularization therapy in ischemic tissue. Menoufia Med J [serial online] 2017 [cited 2019 Sep 21];30:147-50. Available from: http://www.mmj.eg.net/text.asp?2017/30/1/147/211487
| Introduction|| |
Mesenchymal stem cells (MSCs) are a heterogeneous population of stem/progenitor cells with pluripotent capacity to differentiate into mesodermal and nonmesodermal cell lineages . Stem cells have the potential to develop into mature cells that have characteristic shapes and specialized functions, such as heart cells, skin cells, or nerve cells. Stem cells can be isolated from bone marrow, adipose tissue, and umbilical cord, and they can be stored long term without major loss of potency and no adverse reactions to allogeneic MSC transplant .
Vascular endothelial cells (ECs) line the entire circulatory system, from the heart to the smallest capillaries. These cells have many functions including fluid filtration, blood vessel tone, hemostasis, neutrophil recruitment, and hormone trafficking .
Endothelial dysfunction is a broad pathological disorder of the endothelium, which is assigned by vasoconstriction, thrombosis, and ischemic diseases, alone or with other disorders such as coronary artery disease, hypertension, and atherosclerosis .
ECs are of great interest because of their potential in cell therapy for vascular diseases and ischemic tissue, tissue engineering for vascular grafts and vascularized tissue beds, and modeling for pharmaceutical transport across endothelial barriers .
MSCs can transdifferentiate into lineage with functional and phenotypic features of ECs and participate in angiogenesis directly .
| Materials and Methods|| |
The present study was conducted at Department of Clinical Pathology, Faculty of Medicine, Menoufia University during the period from January 2015 to February 2016.
This study was carried out on 20 bone marrow samples. Samples were aseptically collected from patients who already have indication for bone marrow examination, after obtaining written consent from them.
Our scientific ethical committee approved this work.
A volume of 5 ml of bone marrow was aspirated under complete sterile conditions from posterior superior iliac spin from patients undergoing bone marrow aspiration for nonmalignant reasons collected in a 15-ml sterile heparinized Falcon tube (Sharma Scientific Traders, New Delhi, Delhi). Under laminar flow, the bone marrow aspirate was diluted with sterile PBS in the ratio of 1: 1 and then layered on top of Ficoll–Hypaque solution (density 1.077 g/l). The tube was centrifuged for 20 min at 1800 rpm.
The mononuclear cell fraction was collected carefully and then transferred into a sterile 15-ml conical centrifuge tube. The cells were washed twice in 5 ml of sterile PBS and spun at 1500 rpm for 10 min.
The cell pellet was resuspended in 1 ml of Dulbecco's Modified Eagle Medium (DMEM), counted using a hemocytometer, and cell viability was assessed by trypan blue staining. The mononuclear cell suspension was seeded at a concentration of million cells/ml and allowed to adhere to 25-cm 2 tissue culture plastic flasks incubated in 5 ml of the fresh complete nutrient medium, which was constituted of the following:
- Low-glucose DMEM with l-glutamine (2 mmol/l)
- Fetal bovine serum (100 μg/ml)
- Penicillin–streptomycin (100 U/ml penicillin and 100 μg/ml streptomycin) (10 μg/ml)
- Fungizone (0.25 μg/ml)
The flasks were incubated in a horizontal position in a humidified incubator at 37°C and 5% CO2. The medium was changed every 4 days for removal of nonadherent cells.
At day 9, when fibroblast-like cells reach 80–90% confluency, these cells were harvested by trypsinization.
The medium was aseptically removed. A volume of 1–2 ml of trypsin–EDTA detachment solution was added. The cells were examined microscopically for detachment every 2–3 min. The time required for complete detachment was about 3–5 min.
After complete detachment, DMEM containing 1% serum fetal bovine serum was added. The cells were transferred to a 15-ml Falcon tube and centrifuged at 1800 rpm for 10 min. The cells were resuspended in complete medium.
Cells were examined under the microscope, counted and the viability was assessed by trypan blue staining. The cells were used for MSC identification and endothelial differentiation.
Identification of mesenchymal stem cells
MSCs were identified by morphology and flow cytometric analysis of surface markers CD44 and CD34.
Flow cytometric analysis
Cells were washed with PBS and centrifuged at 3200 rpm for 5 min and resuspended in 1 ml of PBS. A volume of 100 μl of cell suspension was added to 10 μl of fluorochrome-conjugated reagent phycoerythrin-conjugated anti-CD34+ 10-μl fluorescein isothiocyanate anti-CD44. Cells were then incubated in the dark for 30 min after light vortexing. Finally, cells were analyzed using a Flow Cytometer (Becton Dickinson FACSCalibur, San Jose, CA, USA) .
The endothelial differentiation was induced by adding 50 ng/ml vascular endothelial growth factor (VEGF) to complete nutrient medium for 7 days. The medium was changed every 3 days and examined daily with assessment of the cell morphological changes.
Evaluation of endothelial differentiation
- Postinduction morphological changes: assessment by microscopic examination
- Identification of ECs: by flow cytometry with positive CD34 characterization
- Hematoxylin and eosin staining: staining was performed according to Lynch et al. .
Descriptive study was used.
| Results|| |
Morphological examination of mesenchymal stem cells
At day 7, cells showed multipolar fibroblastoid cells and a 60% confluence, which gradually increased to 80–90% confluence at about 9 days [Figure 1].
|Figure 1: Inverted microscope image ×100 of adherent mesenchymal stem cells after removal of floating nonadherent cells showed 80–90% fibroblast confluence.|
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Identification of mesenchymal stem cells by flow cytometry
MSCs showed positive expression of CD44 (X ± SD: 81.2 ± 12.4) and negative expression of CD34 (X ± SD: 1.97 ± 1.5) [Table 1].
|Table 1 Descriptive analysis of flow cytometric results of CD34 and CD44 (percentage) on mesenchymal stem cells|
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Characterization of endothelial cells
Postinduction morphological changes
MSCs induced with VEGF show spindle shape with no much morphology difference form MSCs [Figure 2].
|Figure 2: Inverted microscope image ×200 of bone-marrow-derived mesenchymal stem cells cultured with vascular endothelial growth factor medium.|
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Results of flow cytometric analysis of postinduction bone marrow mesenchymal stem cells
Induced MSCs showed positive expression of CD34 (X ± SD: 83.4 ± 10.4).
Hematoxylin and eosin staining
The harvested ECs were identified by using hematoxylin and eosin stain. The ECs appear typically spindle shaped with pink cytoplasm and blue nucleus [Figure 3].
|Figure 3: Inverted microscope image ×200 of endothelial cells stained with hematoxylin and eosin.|
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| Discussion|| |
MSCs are a population of multipotent cells found primarily in the bone marrow. They have long been known to be capable of osteogenic, adipogenic, and chondrogenic differentiation. It has been proven that MSCs aid the stimulation of angiogenesis, neurogenesis, and regeneration of damaged tissue .
ECs have a major role in new vessel formation. ECs are needed to line artificial vessels and to restore vascularization of ischemic tissues. This is a crucial point in therapy of peripheral vascular diseases .
ECs derived from stem cells could potentially lead to a variety of clinically relevant applications. These cells could be used in therapeutic strategies for the repair and revascularization of ischemic tissue in patients exhibiting vascular defects .
In the present study, change of MSC morphology was observed; after 7 days of incubation, MSCs exhibit fibroblast-like morphology. This is in agreement with the study by Oswald et al. , who demonstrated a fibroblast-like, spindle-shaped morphology that appears at day 7 after incubation. With regard to MSC identification in this study, flow cytometric analysis showed that these cells were positive for human MSC marker CD44 (81.2 ± 12.4) and negative for CD34 (1.97 ± 1.5); this is in agreement with the study by Chen et al. , who defined MSCs as being able to express CD29, CD73, CD44, CD90, CD105 antigens, and not expressing neither the hematopoietic cell markers CD34, CD45, and major histocompatibility complex class II antigen nor endothelial lineage cell marker.
As regards morphological changes, cells were spindle shaped with no much morphology difference form MSCs, and this result is in agreement with the study by Siddiqui , who reported that differentiation into endothelial-like cells can be induced by cultivating confluent MSCs in the presence of 50 ng/ml VEGF for 7 days. Cell morphology showed no difference compared with undifferentiated MSCs. With flow cytometric analysis, ECs showed positive expression of CD34 (83.4 ± 10.4). This result was in agreement with the study by Liu et al. , who reported that differentiated ECs expressed endothelial markers such as CD34, CD144, KDR, CD105, CD31, and UEA-1 lectin binding.
As regards hematoxylin and eosin staining, the harvested ECs appear typically spindle shaped with pink cytoplasm and blue nucleus. This morphology is the same as that found by Portalska et al. .
| Conclusion|| |
This study showed that bone-marrow-derived MSCs can be differentiated in vitro into ECs. This opens the future for the use of MSCs for revascularization therapy of ischemic tissue.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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[Figure 1], [Figure 2], [Figure 3]