Endothelial Progenitor Cells and Endothelial Cells

Vertebrates have a highly evolved, closed circulatory system consisting of a distinct and dynamic network of blood vessels

  • Document # DX20360
  • Version 1.0.0
  • Jun 2015


Vertebrates have a highly evolved, closed circulatory system consisting of a distinct and dynamic network of blood vessels. The lumen of each blood vessel is surrounded by a thin layer of endothelial cells (ECs) supported by a basement membrane and mural cells (pericytes and smooth muscle cells). ECs form the physical interface between the blood and surrounding solid tissues, and as such, regulate physiological events including vasodilatation and vasoconstriction, blood coagulation, nutrient delivery, gas exchange, and the homing of regulatory cells.1,2 In the adult, the formation of new blood vessels occurs via angiogenesis, arteriogenesis, and vasculogenesis.3,4 These processes are driven by the proliferation, migration, and remodeling of ECs from pre-existing vessels (angiogenesis and arteriogenesis) or the differentiation of progenitor cells derived from mesodermal precursors (vasculogenesis).5-8

Angiogenesis is essential for wound healing and as a response to tissue ischemia, and plays a role in the formation of tumor vasculature. Post-natal vasculogenesis is also necessary for revascularization of ischemic tissues and wound healing, and plays a role in pathologies such as cancer, diabetic retinopathy, and retinopathy of prematurity.9

Endothelial Progenitor Cells

The progenitor cells that are able to differentiate into functional endothelial cells and sustain vasculogenesis are broadly called endothelial progenitor cells (EPCs). Asahara et al10 initially identified and isolated a putative EPC in adult human peripheral blood. Since then, distinctly different cell populations have been isolated and called EPCs.9,11 These cell populations have subsequently been shown to improve vascular function through two principal mechanisms (i) actual incorporation into injured endothelium with formation of a functional blood vessel (inosculation)12 and/or (ii) local secretion of proangiogenic factors with a paracrine effect on the cells actually forming the vessel.13

Given the potential of such a progenitor cell to treat a variety of diseases, many studies in the last fifteen years have aimed to isolate and characterize them. EPCs have also been studied as biomarkers for cardiovascular diseases and proposed as a potent cell-based therapy for their capacity to stimulate vascular repair in physiological and pathological conditions.5,14-15 A summary of different cell populations often referred to as EPCs is given in Table 1.

Table 1. Subtypes of Putative EPCs, Angiogenic and Vasculogenic Cells

Endothelial progenitor cell
This term is used to refer to multiple cell types in the literature
Asahara, 199710
Colony-forming unit-endothelial cell
Multiple papers reference CFUECs, with different definitions
Gehling, 200044
Colony-forming unit-Hill
Often referred to as a type of CFU-EC
Hill, 200314
Prater, 200747
Circulating angiogenic cell
No colonies formed
Rehman, 200345
Circulating endothelial precursors
Type of putative EPC
Gill, 200046
Endothelial colony-forming cell
Cells defined by an in vitro and in vivo assay to establish proliferative and functional potential
Ingram, 200418
Low proliferative potential-ECFC
Cell capable of 20-30 populations doubling in vitro
Ingram, 200418
High proliferative potential-ECFC
Cell capable of > 100 populations doubling in vitro
Ingram, 200418
Early Outgrowth EPC
Arises after 5 to 7 days in culture. Term used for multiple populations.
Prater, 200747
Late Outgrowth EPC
Arises after 10 to 14 days in culture
Prater, 200747

Types of Endothelial Progenitor Cell Populations are Defined by Different Culture Methods

Three different populations of putative human EPCs, with a variety of names in the literature, have been defined using four cell culture and cell sorting protocols:

1. Circulating Angiogenic Cells (CACs)

CACs are obtained from the low density mononuclear cell (MNC) fraction of human peripheral blood or cord blood. Cells are plated on fibronectin-coated plates and incubated with a cocktail of cytokines.16 After 4-7 days in culture, the non-adherent cells are removed and the remaining cells are examined for their ability to take up acetylated low-density lipoprotein (AcLDL) and to bind to Ulex europaeus agglutinin1 (lectin), both considered to be hallmarks of EC function. CACs are further characterized by their morphology, adhesion to fibronectin, and cell surface protein expression. The isolated cells display pro-angiogenic activity both in vitro (by secretion of angiogenic cytokines) and in vivo, but lack the capacity to inosculate into a new blood vessel.

Flow cytometric analysis was used in 1997 by Asahara and colleagues to identify CD34+KDR+ circulating cells as putative endothelial progenitor cells. CD34+ KDR+ cells cultured on fibronectin for seven days express high levels of endothelial antigens such as CD31, Tie-2, and E selectin, and when injected into a mouse in a model of hindlimb ischemia are able to migrate to sites of vascular injury and to target vessels. Despite the fact these two antigens have continued to be used as markers for circulating cells with vascular reparative properties, it was not demonstrated that the infused cells directly formed new blood vessels.10

The loss of CD133 expression was proposed as a marker to distinguish EPCs from mature endothelial cells.5 However, it was later demonstrated that triple positive CD34+ KDR+CD133+ cells do not form endothelial colonies in vitro but do form hematopoietic colonies.18 Nor do these triple positive cells form capillary-like structures on Matrigel™. Interestingly, CD34+CD45- cells do form endothelial colonies and capillary-like structures in the respective assays, suggesting that the true EPC may express CD34 and lack expression of CD45.17

2. Colony-Forming Unit-Hill (CFU-Hill) & CFU-Endothelial Cells (CFU-EC)

CFU-Hill are also obtained from the MNC fraction of peripheral blood. MNCs are plated on fibronectin-coated dishes for two days, after which the non-adherent cell population, containing the cells of interest, is removed and replated once more on fibronectin-coated plates. After three days, positive colonies are identified as having a central core of “round” cells, with more elongated “sprouting” cells at the periphery (See page 206, Figure 1). The unique colonies that are formed in this five day assay are referred to as Colony-Forming Unit-Hill colonies (CFU-Hill) or sometimes CFU-EC. Immunohistochemical staining has confirmed that cells generated in this assay express the endothelial cell markers von Willebrand factor, VEGFR2 and CD31, but they lack the capability to form new vessels in vivo. In healthy individuals, the number of colonies generated in this assay correlates inversely with the Framingham cardiovascular risk score and positively with vascular function, as measured by flowmediated brachial artery reactivity.14

3. Late outgrowth endothelial cells (OECs) or endothelial colony forming cells (ECFCs)

OECs or ECFCs are obtained by plating human peripheral blood or cord blood-derived MNC on rat collagen I-coated dishes in medium containing endothelial growth factors. Non-adherent cells are discarded daily and fresh medium is added; within one to three weeks cells possessing clonal ability appear with endothelial cobblestone morphology and different proliferative potentials. Among the ECFC population it is possible to identify a unique population of high proliferative potential endothelial colony forming cells (HPP-ECFCs), which give rise to low proliferative potential endothelial colony-forming cells (LPP-ECFCs), generating endothelial clusters and finally mature non-dividing endothelial cells.18 HPP-ECFC can be replated in secondary and tertiary colonies and retain high telomerase activity. HPP-ECFCs, with the ability to form colonies after 100 population doublings, are found in cord blood. The colonies contain cells that can differentiate into endothelial capillary-like tubes in vitro.18,19 Adult peripheral blood contains LPP-ECFCs with the ability to proliferate for 20 - 30 population doublings.

ECFC-derived cells express many EC antigens, including CD31, CD105, CD144, CD146, VWF, KDR, and UEA-1.18 Importantly, cells derived from ECFCs do not express the hematopoietic marker CD45 or the monocyte markers CD14 and CD115 (Table 2).

Table 2. A Comparision of CFU-Hill, CACs and ECFCs

Clonal proliferative status
Replating ability
In vitro tube formation
In vivo de novo vessel formation
Homing to ischemic sites in vivo
Paracrine augmentation of angiogenesis
acLDL uptake
UEA-1 lectin binding
von Willebrand

(Modified from Hirshci KK, et al. Arterioscler Thromb Vasc Biol. 28: 1584-1595, 2008)

When ECFCs are plated in collagen/ fibronectin gels and implanted in NOD/SCID mice, they form neovessels comprised of human endothelial cells. Importantly, ECFCs have a demonstrated capacity to enhance revascularization when injected in animal models of ischemia.19 They appear to synergize with CFU-Hill-derived cells and CAC to enhance revascularization of ischemic limbs in immunodeficient mouse models and to enhance wound healing in vivo.20 CACs, including CFU-Hill-derived cells, and ECFCs have all been considered EPCs, and it is not completely understood which cell type contributes to what extent in different stages of vascular repair. Both CACs, able to secrete growth factors locally, and ECFCs, able to inosculate into host tissue and become part of a new vessel, may have therapeutic potential.

EC-Cult™-XF Culture Kit

Derive and Expand Endothelial Colony-Forming Cells

Use the xeno-free EC-Cult™-XF Culture Kit to derive, expand, and maintain human ECFCs and mature endothelial cells.

Rodent Endothelial Progenitor Cell Markers and Isolation

Rodent EPCs are believed to be derived from the bone marrow compartment21 and can be isolated using a combination of cell surface markers including stem cell antigen 1 (Sca1), cKit, Flk1, CD31, Tie2 and CXCR4, CD133, or CD144 expression.22-24 The general protocol for isolating and defining CACs in the mouse system follows that of the human system. Cells are selected through adhesion to fibronectin plates and identified after four to seven days in culture by the ability to take up acetylated LDL and bind to lectin. Mouse CACs are recognized to be myeloid and pro-angiogenic. ECFC have not been isolated from mouse peripheral blood at the single animal level; whole blood pooled from four to six mice produces only one ECFC, and this in less than 30% of attempts.25

Recently, resident microvascular endothelial progenitor cells (RMPEC) have been successfully isolated from rat lung.26 These cells are equivalent to human ECFCs in that they display neovasculogenic capacity and a hierarchy of cells which could be distributed along the tissue structure.27

Bioengineered Tissue: ECFC Co-Culture with Progenitor and Stem Cells

To improve the in vivo functionality of ECFCs, mesenchymal stem cells (MSCs), adipose stromal cells (ASCs), and smooth muscle progenitor cells (SMPCs) have been tested in in vitro co-culture systems and in in vivo experiments. These cells have been reported to stabilize and enhance human endothelial-derived vessels.19,28 For example, Melero Martin et al29 showed that co-implantation of ECFCs with either bone marrow-derived or cord blood-derived MSCs into immunodeficient mice resulted in the formation of vascular networks after one week, compared to no microvessel formation when ECFC were implanted alone. The extent of the engineered vascular networks was highly influenced by the ratio of ECFCs to MSCs, with a progressive increase in vessel density and consistency of vascularized implants as the contribution of MSCs rose to 60%. Tracktuev and colleagues30 demonstrated that ASC synergize with human ECFCs in de novo formation of vascular networks in collagen matrices implanted into mice. More recently, the co-transplantation of ECFCs and SMPCs was shown in a mouse ischemic hind limb model to induce robust in vivo neovascularization, as well as improved blood perfusion and tissue repair.31 These studies support a therapeutic neovascularization strategy incorporating more than one type of autologous progenitor derived from adult peripheral and cord blood.

ECFCs co-cultured with biologically compatible material have been used as tissue engineered structures for replacement of vascular structures. Development of functional vascular networks is not only important for treatment of ischemia such as that arising from diabetic complications and cardiovascular disease, but also for tissue engineering to repair and regenerate damaged or diseased tissue.32,33

Scientists continue to search for the best biomaterial to mimic the extracellular matrix and serve as a scaffold for tissue regeneration. The ideal matrix will improve cell survival and guide appropriate vessel formation. For example, collagen fibril density and stiffness has a significant effect on the formation of functional blood vessels by ECFCs in vivo.34,39 Some materials have been functionalized, since their properties are not always ideal for tissue engineering applications. For example, Melero-Martin and colleagues demonstrated that photo-crosslinkable methacrylated gelatin (GelMA) hydrogels are compatible with ECFC-based vascular morphogenesis.35 GelMA hydrogels, when injected with liquid, polymerize rapidly, which limits dissemination at the implantation site and eliminates the need for pre-polymerizing the constructs and for surgical incisions. This results in a better integration with the surrounding host tissue and better vascularity (~3 fold) in injected constructs than in constructs that are polymerized ex vivo prior to implantation.36

Biological Role and Potential Use of ECFCs in Human Diseases

The concentrations and functionality of various circulating EPCs have been enumerated and correlated to disease states as biomarkers for disease detection or disease stage.37-39 The notion that EPC dysfunction exists in certain patient categories may have implications for currently explored cell-based clinical strategies to enhance tissue perfusion in patients with ischemic coronary and peripheral artery disease. For example, defects in CD34+KDR+ function have been shown in some diabetic patients, and thus therapies based on restoring EPC function have been proposed.40 To date, clinical trials using putative EPCs have been conducted in patients with heart disease, diabetes, peripheral arterial disease, pulmonary disease, and cancer. The therapeutic use of these cells appears to be safe but also of limited efficacy and rarely provides a durable response, thus limiting the clinical application of autologous stem cells to treat vascular diseases. ECFC cell-based therapy has been primarily limited by the extremely low frequency of less than one ECFC per million nucleated cells in peripheral blood. Culture expansion of ECFCs will therefore be required for their use in cellular therapies.

Endothelial Colony-Forming Cells

Therapeutic Application of ECFCs for Retinal Diseases

Dr. Sakimoto and Dr. Marchetti discuss the potential application of human ECFCs to treat vascular abnormalities in the eye.

Watch the Webinar >

Serum-Free Media for ECFC Derivation and Expansion

The original protocols for the ex vivo derivation and expansion of ECFCs depend on the presence of fetal bovine serum (FBS) or fetal calf serum (FCS) in the culture medium. Animal products can contain potentially harmful xenogeneic compounds associated with the risk of transmitting infectious agents when used in human transplantation, and also the risk of the host developing antibodies against FBS components.

Moreover, FBS and FCS contain undefined components that make standardized cell preparation very complex. Finally, in the rare instance in which a few ECFCs could be grown without serum, transcriptomic analysis reveals a broad down-regulation of genes involved in cell cycle progression and up-regulation of genes involved in stress response and apoptosis in ECFC grown without serum compared to those grown with serum.41 Therefore, researchers have looked for a way to derive and expand ECFCs in the absence of serum.

In 2009, a protocol for obtaining a humanized large-scale expansion of ECFCs in serum-free medium was established.42 Using human platelet lysate and unmanipulated blood cells, Strunk et al. efficiently derived, expanded, and cryopreserved human ECFCs with intact proliferation potential and function. These cells participated in new blood vessel formation in two different models of neo-vasculogenesis.

Subsequently, Yoder and colleagues showed that human umbilical cord blood plasma could replace FBS for the in vitro expansion of functional human ECFCs.43 ECFCs cultured in serum-free conditions retain their endothelial and progenitor phenotype both in vitro and in vivo. Importantly, serum-free derived ECFCs exhibit a complete hierarchy of proliferative potential, demonstrating that it is possible to expand ECFCs in serum-free conditions while maintaining their functionality.

Explore our products for endothelial research, including the EC-Cult™-XF Culture Kit for ECFC derivation and expansion.


  1. Cines DB, et al. Blood 91: 3527-3561,1998
  2. Edgington TS. FASEB 9: 841-842, 1995
  3. Flamme I, et al. J Cell Physiol 173: 206-210, 1997
  4. Conway DM, et al. Cardiovasc Res 49: 507-521, 2001
  5. Rafii S, et al. Nat Med 9: 702-712, 2003
  6. Masuda H, et al. Cardiovasc Res 58: 390-398, 2003
  7. Choi K, et al. Development 125: 725-732, 1998
  8. Bailey AS, et al. Exp Hematol 31: 987-993, 2003
  9. Yoder MC, et al. Cold Spring Harb Perspect Med 2: a006692, 2012
  10. Asahara T, et al. Science 275: 964-967, 1997
  11. Fadini GP, et al. Circ Res 110: 624-637, 2012
  12. Grunewald M, et al. Cell 124: 175-189, 2006
  13. Hill JM, et al. N Engl J Med 348: 593-600, 2003
  14. Werner N, et al. N Engl J Med 353: 999-1007, 2005
  15. Ito H, et al. Cancer Res 59: 5875-5877, 1999
  16. Case J, et al. Exp Hematol 35: 1109-1118, 2007
  17. Ingram DA, et al. Blood 104: 2752-2760, 2004
  18. Bouvard C, et al. Arterioscler Thromb Vasc Biol 30: 1569-1575, 2010
  19. Schwarz TM, et al. Arterioscler Thromb Vasc Biol 32: e13-21, 2012
  20. Yoon YS, et al. Circulation 111: 2073-2085, 2005
  21. Yang J, et al. PLoS One 6: e20219, 2011
  22. Asahara T, et al. FASEB 18: 3964-3972, 1999
  23. Gallagher KA, et al. J Clin Invest 117: 1249-1259, 2007
  24. Gao D, et al. Science 319: 195-198 Doi, 2008
  25. Somani A, et al. Transl Res 150: 30-39, 2007
  26. Alvarez DF, et al. Am J Physiol Lung Cell Mol Physiol 294: L419-430, 2008
  27. Alphonse RS, et al. Circulation 129: 2144-2157, 2014
  28. Allen P, et al. J Tissue Eng Regen Med doi: 10.1002/term.1803, 2013
  29. Melero-Martin JM, et al. Circ Res 103: 194-202, 2008
  30. Traktuev DO, et al. Circ Res 104: 1410-1420, 2009
  31. Joo HJ, et al. Biochem Biophys Res Commun 449: 405-411, 2014
  32. Jain RK, et al. Nat Biotechnol 23: 821-823, 2005
  33. Kawamoto A, et al. Catheter Cardiovasc Interv 70: 477-484, 2007
  34. Bailey JL, et al. Biopolymers 95: 77-93, 2011
  35. Lin RZ, et al. Biomaterials 34: 6785-6796, 2013
  36. Reinisch A, et al. Blood 113: 6716-6725, 2009
  37. Alaiti MA, et al. Transl Res 3: 112-129, 2010
  38. Fadini P, et al. Diabetologia 10: 2156-2163, 2007
  39. Crister PJ, et al. Microvasc Res 80: 23-30, 2010
  40. Loomans CJ, et al. Diabetes 53: 195-199, 2004
  41. Huang L, et al. Cytotherapy 13: 712-721, 2011
  42. Zeisberger SM, et al. Genes Cells 15: 671-687, 2010
  43. Hirschi KK, et al. Arterioscler Thromb Vasc Biol 28: 1584-1595, 2008
  44. Gehling UM, et al. Blood 95: 3106-3112, 2000
  45. Rehman J, et al. Circulation 107: 1164-1169, 2003
  46. Gill M, et al. Circ Res 88: 167-174, 2001
  47. Prater DN, et al. Leukemia 21: 1141-1149, 2007

Contact STEMCELL Technologies

Our Customer Service, Sales, and Product and Scientific Support departments in North America are available between 6 am and 5 pm Pacific Time (9 am and 8 pm Eastern Time). One of our representatives will be happy to help you by telephone or email. Please complete the form to contact us by email. A representative will get back to you shortly.

StemCell Technologies Inc. and affiliates ("STEMCELL Technologies") does not share your email address with third parties. StemCell Technologies Inc. will use your email address to confirm your identity and send you newsletters, transaction-related emails, promotional and customer service emails in accordance with our privacy policy. You can change your email preferences at any time.