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Endothelial stem cell

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301:(EPC) is more specialized than an ESC, and an EC is more specialized than an EPC. The further specialized a cell is, the more differentiated it is and as a result it is considered to be more committed to a certain cellular lineage. Stem cell self-renewal is an extremely important process that is a way for organisms to replace the cells that are no longer working properly. Self-renewal is essential to keep the organism functioning properly and efficiently. The process of self-renewal occurs because of the signals the cells receive from the environment and the things the cell expresses to the environment (Fuchs & Chen 2013) . The signals and receptors must function properly at all times so the cells will know what they are supposed to do (Fuchs & Chen 2013). As stated before, proper functioning of the self-renewal system is essential for the organism to live a long healthy life. 549:. When there is any dysfunction in the endothelium, the body aims to repair the damage. Resident ESCs can generate mature ECs that replace the damaged ones. However, the intermediate progenitor cell cannot always generate functional ECs. This is because some of the differentiated cells may just have angiogenic properties. The employs many different protective mechanisms when there is endothelium dysfunction that occurs. The reason so many mechanisms are employed is so that the body is protected the best it can, and will be able to respond to any type of pathogen that should happen to invade the body during this dysfunction. 610:, which regulates cell growth and cell mobility. With uncontrolled beta-catenin, the cell loses its adhesive properties. As ECs get packed together to create the lining of a new blood vessel, a single cancer cell is able to travel through the vessel to a distant site. If that cancer cell implants itself and begins forming a new tumor, the cancer has metastasized. The cancer cells also do not have to travel to a distant site, they can also stay in one location and this is known as the tumor being benign. 1957: 38: 627:. Scientists are still trying to find a way to definitely distinguish the stem cell from the progenitor. In the case of endothelial cells, it is even difficult to distinguish a mature EC from an EPC. However, because of the multipotency of the ESC, the discoveries made about EPCs will parallel or understate the powers of the ESC. 1491:
Deanfield J, Donald A, Ferri C, Giannattasio C, Halcox J, Halligan S, Lerman A, Mancia G, Oliver JJ, Pessina AC, Rizzoni D, Rossi GP, Salvetti A, Schiffrin EL, Taddei S, Webb DJ (2005). "Endothelial function and dysfunction. Part I: Methodological issues for assessment in the different vascular beds:
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gene is deleted then both HPC and EC differentiation comes to a halt in embryos. VEGF promotes angioblast differentiation; whereas, VEGFR-1 stops the hemangioblast from becoming an EC. In addition, basic fibroblast growth factor FGF-2 is also involved in promoting angioblasts from the mesoderm. After
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by both lineages. The fact that this expression was seen in both EC and HPC lineages led researchers to propose a common origin. However, endothelial markers like Flk1/VEGFR-2 are exclusive to ECs but stop HPCs from progressing into an EC. It is accepted that VEGFR-2+ cells are a common precursor for
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ECs were first thought to arise from extraembryonic tissues because blood vessels were observed in the avian and mammalian embryos. However, after histological analysis, it was seen that ECs were found just in the embryo. This meant that blood vessels come from an intraembryonic source, the mesoderm.
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Stem cells have always been a huge interest for scientists due to their unique properties that make them unlike any other cell in the body. Generally, the idea boils down to harnessing the power of plasticity and the ability to go from an unspecialized cell to a highly specialized differentiated
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There are a number of models used to study vasculogenesis. Avian embryos, Xenopus laevis embryos, are both fair models. However, zebrafish and mouse embryos have widespread use for easily observed development of vascular systems, and the recognition of key parts of molecular regulation when ECs
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each and every day. If the cells were not able to do this, humans would not be able to survive. There was an experiment that was done involving quail embryos on chicken yolk sacs that found complete opposite results of the experiment done by Sabin. In this experiment, it was found that yolk-sac
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compared to the embryo. This experiment also showed that blood cells that were made by the yolk sac were not present when the bird hatched. Over time there have been experiments done that add to the confusion if the blood cells and red blood cells are related in the yolk sac and embryo.
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The use of stem cells for treatment has become a growing interest in the scientific community. Distinguishing between an ESC and its intermediate progenitor is nearly impossible, so research is now being done broadly on EPCs. One study showed that brief exposure to
471:. Even though there is evidence that corroborates a hemangioblast, the isolation and exact location in the embryo has been difficult to pinpoint. Some researchers have found that cells with hemangioblast properties have been located in the posterior end of the 517:
angioblasts commit to becoming an EC, the angioblasts gather and rearrange to assemble in a tube similar to a capillary. Angioblasts can travel during the formation of the circulatory system to configure the branches to allow for directional blood flow.
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In 1917, Florence Sabin first observed that blood vessels and red blood cells in the yolk sac of chick embryos occur in close proximity and time. Then, in 1932, Murray detected the same event and created the term "hemangioblast" for what Sabin had seen.
459:. A study found that in the beginning stages of mouse embryogenesis, commencing at embryonic day 7.5, HPCs are produced close to the emerging vascular system. In the yolk sac's blood islands, HPCs and EC lineages emerge from the extraembryonic 991:
Gehling U, Ergun S, Schumacher U, Wagener C, Pantel K, Otte M, Schuch G, Schafhausen P, Mende T, Kilic N, Kluge K, Schafer B, Hossfeld D, Fiedler W (2000). "In vitro differentiation of endothelial cells from AC133-positive progenitor cells".
571:. Further, there is an inverse relationship between age and levels of EPCs. Inverse of endothelial dysfunction also occurs when other risk factors are treated. With a decline in EPCs the body loses its ability to repair the endothelium. 588:, the EPCs were able to adhere to endothelial cells better. When combining the results from both of the studies, results show that sevoflurane was able to improve the function of EPCs significantly in three different areas of interest. 605:
induce angiogenesis, which is the formation of new blood vessels. These cancerous cells do this by secreting factors such as VEGF and by reducing the amount of PGK, an anti-VEGF enzyme. The result is an uncontrolled production of
346:. The former requires differentiation of endothelial cells from hemangioblasts and then the further organization into a primary capillary network. The latter occurs when new vessels are built from preexisting blood vessels. 329:
occurs the cells transform into different versions throughout the process to eventually become the earliest blood vessels. The cells going through stages from one form to another form is one of the major differences between
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Both parts consist of ECs that show differential expression of various genes. A study showed that ectopic expression of Prox-1 in blood vascular ECs (BECs) induced one-third of LEC specific gene expression. Prox-1is a
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promoted growth and proliferation of EPCs. Sevoflurane is used in general anesthesia, but this finding shows the potential to induce endothelial progenitors. Using stem cells for cell replacement therapies is known as
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is the process by which a cell becomes more specialized. For stem cells, this usually occurs through several stages, when a cell proliferates giving rise to daughter cells that are further specialized. For example, an
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of VEGF. Not only is VEGF critical for mesoderm cells to become an EC, but also for EPCs to differentiate into mature endothelium. Understanding this process can lead to further research in vascular regeneration.
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cell. ESCs play an incredibly important role in establishing the vascular network that is vital for a functional circulatory system. Consequently, EPCs are under study to determine the potential for treatment of
556:. CEPs are derived from EPCs within the bone marrow, and the bone marrow is a reservoir of stem and progenitor cells. These cell types accelerate the healing process and prevent further complications such as 143:
cells, which are intermediate stem cells that lose potency. Progenitor stem cells are committed to differentiating along a particular cell developmental pathway. ESCs will eventually produce
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Kovina MV, Krasheninnikov ME, Dyuzheva TG, Danilevsky MI, Klabukov ID, Balyasin MV, et al. (March 2018). "Human endometrial stem cells: High-yield isolation and characterization".
584:", which is a booming field that is now working on transplanting cells as opposed to bigger tissues or organs. There was another study done that also showed that after exposure to 1581:"Stem cell-like human endothelial progenitors show enhanced colony-forming capacity after brief sevofluorane exposure: preconditioning of angiogenic cells by volatile anesthetics" 525:
cells encircle ECs when they are differentiating into arterial or venous arrangements. Surrounding the ECs creates a brace to help stabilize the vessels known as the pericellular
651: 223:, all of which promote pluripotent stem cells to differentiate into mesoderm, endothelial progenitor cells, and then into mature endothelium. It is important to talk more about 1210:"Preliminary note on the differentiation of angioblasts and the method by which they produce blood-vessels, blood-plasma and red blood-cells as seen in the living chick" 1937: 552:
Studies have shown that when vascular trauma occurs, EPCs and circulating endothelial progenitors (CEPs) are attracted to the site due to the release of specific
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Fan CL, Li Y, Gao PJ, Liu JJ, Zhang XJ, Zhu DL (2003). "Differentiation of endothelial progenitor cells from human umbilical cord blood CD 34+ cells in vitro".
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for the vascular endothelial growth factor receptor 3 (VEGFR-3). The ligand-receptor interaction is essential for normal development of lymphatic tissues.
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Stem cells have the unique ability make identical copies of themselves. This property maintains unspecialized and undifferentiated cells within the body.
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are much harsher form of cancer because the tumors must be treated at many different locations, compared to just one location when the tumor is benign.
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found in lymphatic ECs (LECs). For example, specific mRNAs such as VEGFR-3 and p57Kip2 were expressed by the BEC that was induced to express Prox-1.
467:, and together they give rise to mature ECs. This observation gave rise to the hypothesis that the two lineages come from the same precursor, termed 1942: 1030:
Stratman, Amber N.; Yu, Jianxin A.; Mulligan, Timothy S.; Butler, Matthew G.; Sause, Eric T.; Weinstein, Brant M. (2015), "Blood Vessel Formation",
1288: 491: 313:, blood vessels play a critical role in transporting blood throughout the body. Consequently, ECs have unique functions such as fluid filtration, 1047: 916: 1628:
Munteanu Vlad, Adelina; Isvoranu, Gheorghita; Gilca, Marilena; Ceafalan, Laura; Surcel, Mihaela; Stoian, Irina; Manda, Gina (1 April 2015).
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and hormone trafficking. ECs are the most differentiated form of an ESC. Formation of new blood vessels occurs by two different processes:
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Since these cells come from the mesoderm, it can become a wide variety of different things found in many different parts of the body.
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Petrova TV, Makinen T, Makela TP, Saarela J, Virtanen I, Ferrell RE, Finegold DN, Kerjaschki D, Y, a-Herttuala S, Alitalo K (2002).
95: 1630:"Sevoflurane Increases Proliferation, Adhesion on HUVEC and Incorporation in Tubular Structures of Endothelial Progenitor Cells" 858: 958: 861:(2008). "Endothelial Progenitor Cells, Angioblasts, and Angiogenesis- Old terms Reconsidered from a new current perspective". 251:. There is also differences that occur in the signaling pathways of these two pathways that makes them noticeably different. 1448:
Rafil S, Lyden D (2003). "Therapeutic stem and progenitor cell transplantation for organ vascularization and regeneration".
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which is essentially the extension of this. Another difference major difference between the two formation processes is that
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is actually required for vascular remodeling of the capillary network, rather than early endothelial development itself.
167:. Endothelial cells can be found throughout the whole vascular system and they also play a vital role in the movement of 568: 298: 20: 393:
Fetal liver kinase-1 (Flk-1) is a cell surface receptor protein that is commonly used as a marker for ESCs and EPCs.
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a statement by the Working Group on Endothelin and Endothelial Factors of the European Society of Hypertension".
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Endothelium dysfunction is a prototypical characteristic of vascular disease, which is common in patients with
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Further evidence to corroborate hemangioblasts come from the expression of various genes such as CD34 and
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Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter (2002).
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ESCs and EPCs eventually differentiate into ECs. The endothelium secretes soluble factors to regulate
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because this is what makes ECs different from other types of cells that are found in the body. During
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gene is specifically found in the vascular endothelium and developing brain. This gene encodes the
673:"Generation of functional blood vessels from a single c-kit+ adult vascular endothelial stem cell" 1610: 1579:
Lucchinetti E, Zeisberger SM, Baruscotti I, Wacker J, Feng J, Dubey R, Zisch AH, Zaugg M (2009).
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Proceedings of the Royal Society of London. Series B, Containing Papers of a Biological Character
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is another marker that can be found on the surface of ESCs and EPCs. It is characteristic of
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increase the production of ECs in EB. A method that IGF employs to increase vasculogenesis is
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stem cell can give rise to all types. ESCs have the characteristic properties of a stem cell:
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The vascular system is made up of two parts: 1) Blood vasculature 2) Lymphatic vessels
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in near unison. This creates a formation in which early erythrocytes are enveloped by
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Lymphatic-specific vascular endothelial growth factors VEGF-C and VEGF-D function as
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process forms new blood vessels form blood vessels that have already been through
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are able to undergo self-renewal because the human body needs billions of new
452: 428: 140: 120: 1655: 1544: 926: 648:, also known as endometrial stem cells, derived from mammalian uterus lining. 1772: 1529:"Endothelial Dysfunction: Cardiovascular Risk Factors, Therapy, and Outcome" 797:"Insulin-like growth factors promote vasculogenesis in embryonic stem cells" 518: 424: 1731: 1696: 1606: 1562: 1513: 1469: 1431: 1348: 1323:"From hemangioblast to hematopoietic stem cell: An endothelial connection?" 1273: 1248: 1194: 1145: 1097: 1079: 1013: 934: 882: 840: 776: 708: 1412: 1362:
Cheek D, Graulty R, Bryant S (2002). "Meet the multitasking endothelium".
1225: 207:(EB) derived from embryonic stem cells; this process in EB is similar to " 460: 448: 359: 248: 212: 200: 160: 131:, which describes the ability to give rise to many cell types, whereas a 1136: 1119: 101: 45:+ endothelial cell among a population of bovine aortic endothelial cells 1461: 795:
Piecewicz SM, Pandey A, Roy B, Xiang SH, Zetter BR, Sengupta S (2012).
751:"Mechanisms of endothelial differentiation in embryonic vasculogenesis" 602: 369: 208: 1527:
Hadi, Hadi AR; Carr, Cornelia S; Al Suwaidi, Jassim (September 2005).
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fail to develop past embryonic day 9.5. However, the study found that
211:" vasculogenesis. Important signaling factors for vasculogenesis are 1834: 1824: 232: 1669:
Enzyme eliminated by cancer cells holds promise for cancer treatment
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by gathering the cellular materials to reconstruct the endothelium.
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structure and functions as a transcription factor. Embryos lacking
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Role of insulin-like growth factors in endothelium differentiation
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and differentiation. These parent stem cells, ESCs, give rise to
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Understanding more about ESCs is important in cancer research.
1396:"Endothelial progenitor cells: what use for the cardiologist?" 1161:"Hematopoietic stem cell: self-renewal versus differentiation" 309:
Blood vessels are made of a thin layer of ECs. As part of the
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Stem cell in bone marrow that gives rise to endothelial cells
1289:"Bone Marrow (Hematopoietic) Stem Cells | stemcells.nih.gov" 899:
Patan, Sybill (2004). "Vasculogenesis and Angiogenesis".
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form while the organism is still an embryo, compared to
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List of human cell types derived from the germ layers
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They are 125:bone marrow 66:Identifiers 60:Bone marrow 1984:Stem cells 1820:Totipotent 1773:Stem cells 855:Kovacic JC 658:References 554:chemokines 531:mesenchyme 453:macrophage 429:mast cells 141:progenitor 121:stem cells 1890:Unipotent 1656:0892-6638 1545:1176-6344 1234:221400744 927:0927-3042 859:Graham RM 519:Pericytes 425:platelets 123:found in 1978:Category 1962:Category 1732:29397307 1697:12617768 1615:23763818 1607:19762739 1563:17319104 1514:15643116 1478:10294635 1470:12778169 1432:20298532 1406:(6): 6. 1349:16140151 1303:14 April 1195:20890962 1146:12569121 1098:12198161 1014:10807776 935:15015550 883:18308194 841:22363814 801:PLOS ONE 777:16123328 709:23091420 640:See also 618:Research 567:such as 461:mesoderm 449:monocyte 360:homeobox 283:Function 249:mesoderm 201:in vitro 161:arteries 56:Location 1554:1993955 1423:2834645 1261:Bibcode 1186:2950323 973:6 March 832:3283730 809:Bibcode 700:3473016 603:Tumours 558:hypoxia 475:during 370:ligands 350:Markers 325:. 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The 233:plexus 219:, and 1830:Spore 1611:S2CID 1474:S2CID 1230:S2CID 994:Blood 213:TGF-β 203:" in 165:veins 100:[ 72:Latin 1728:PMID 1693:PMID 1652:ISSN 1603:PMID 1559:PMID 1541:ISSN 1510:PMID 1466:PMID 1428:PMID 1345:PMID 1305:2020 1191:PMID 1142:PMID 1094:PMID 1044:ISBN 1010:PMID 975:2012 931:PMID 923:ISSN 913:ISBN 879:PMID 837:PMID 773:PMID 705:PMID 521:and 509:Tie2 397:CD34 388:Tal1 384:Tal1 376:Tal1 334:and 321:and 272:IGF2 270:and 268:IGF1 221:VEGF 217:BMP4 163:and 155:and 117:ESCs 43:CD34 1720:doi 1642:doi 1593:doi 1589:109 1549:PMC 1502:doi 1458:doi 1418:PMC 1408:doi 1372:doi 1335:doi 1269:doi 1257:111 1222:doi 1181:PMC 1173:doi 1132:doi 1084:PMC 1076:doi 1036:doi 1002:doi 905:doi 871:doi 827:PMC 817:doi 763:doi 695:PMC 685:doi 1980:: 1866:: 1726:. 1716:20 1714:. 1689:24 1687:. 1675:^ 1650:. 1638:29 1636:. 1632:. 1609:. 1601:. 1587:. 1583:. 1571:^ 1557:. 1547:. 1535:. 1531:. 1508:. 1498:23 1496:. 1472:. 1464:. 1452:. 1440:^ 1426:. 1416:. 1402:. 1398:. 1384:^ 1366:. 1343:. 1331:33 1329:. 1325:. 1313:^ 1291:. 1267:. 1255:. 1251:. 1228:. 1218:13 1216:. 1212:. 1189:. 1179:. 1167:. 1163:. 1140:. 1128:17 1126:. 1122:. 1106:^ 1092:. 1082:. 1072:21 1070:. 1066:. 1042:, 1022:^ 1008:. 998:95 996:. 983:^ 961:. 943:^ 929:. 921:. 911:. 891:^ 877:. 867:18 865:. 835:. 825:. 815:. 803:. 799:. 785:^ 771:. 759:25 757:. 753:. 739:^ 729:. 717:^ 703:. 693:. 681:10 679:. 675:. 533:. 479:. 447:, 443:, 439:, 435:, 431:, 427:, 262:, 215:, 84:TH 1765:e 1758:t 1751:v 1734:. 1722:: 1699:. 1658:. 1644:: 1617:. 1595:: 1565:. 1537:1 1516:. 1504:: 1480:. 1460:: 1454:9 1434:. 1410:: 1404:2 1378:. 1374:: 1368:6 1351:. 1337:: 1307:. 1277:. 1271:: 1263:: 1236:. 1224:: 1197:. 1175:: 1169:2 1148:. 1134:: 1100:. 1078:: 1038:: 1016:. 1004:: 977:. 937:. 907:: 885:. 873:: 843:. 819:: 811:: 805:7 779:. 765:: 733:. 711:. 687:: 580:" 451:/ 423:/ 115:( 104:] 23:.

Index

Endothelial progenitor cell

CD34
Bone marrow
Latin
TH
H2.00.01.0.00003
Anatomical terms of microanatomy
edit on Wikidata
stem cells
bone marrow
multipotent
pluripotent
self-renewal
progenitor
endothelial cells
endothelium
blood vessels
lymphatic vessels
arteries
veins
white blood cells
vasculogenesis
mesodermal progenitor cells
angiogenesis
in vitro
embryoid bodies
in vivo
TGF-β
BMP4

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