LFA-1 and VLA-4 involved in human high proliferative potentialendothelial progenitor cells homing to ischemic tissue
- 1 January 2006
- journal article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 96 (12) , 807-815
- https://doi.org/10.1160/th06-04-0199
Abstract
Cumulative evidences have revealed that endothelial progenitor cell (EPC) transplantation can promote the neovascularization in ischemic tissue, but the mechanism of EPCs homing to the site of ischemia is poorly understood. In this study, to investigate the mechanism of human umbilical cord blood-derived high proliferative potential-endothelial progenitor cells (HPP-EPCs) homing to ischemic tissue we evaluated the expression of lymphocyte function-associated antigen-1 (LFA-1, or CD11a/CD18) and very late antigen-4 (VLA-4, or CD49d/CD29) in EPCs and the changes of expression level of their ligands, intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1), in ischemic tissue and performed the adhesion and migration assays to analyze the interaction between the receptors and ligands. Furthermore, we studied the roles of LFA-1 and VLA-4 in EPC homing in an ischemic model of mice. The results show that LFA-1 andVLA-4 were expressed in HPPEPCs and ICAM-1 and VCAM-1 were expressed in vessel endothelium in ischemic tissues. The pre-incubation of HPP-EPCs with neutralizing antibodies against CD11a or CD49d reduced adhesion and migration of HPP-EPCs in vitro and reduced recovery of hind-limb blood flow, capillary density and incorporation of HPP-EPC into ischemic tissues in vivo. Furthermore, the pre-incubation of HPP-EPCs with the combination of CD11a and CD49d antibodies led to synergistically negative effects on adhesion and transmigration of HPP-EPCs in vitro, and on the homing of HPP-EPCs to ischemic tissue and on neovascularization capacity in vivo. These results indicate that LFA-1 andVLA-4 are involved in HPP-EPC homing to ischemic tissues.Keywords
Funding Information
- the Hi-Tech Research and Development Program of China (863 program No. 2003AA205181)
- The National Key Basic Research Program of China (973 program No. 00CB5101)
- Bureau of Science and Technology Key Project Funds of Hunan province (No. SSY2001)
- The Research Fund for the Doctoral program of Higher Education from the Ministry of Education of China (No. 20030533002)
- the National Natural Science Foundation (No. 3030119)
- Chinese National Science Foundation Major Program (No. 30030070)
This publication has 23 references indexed in Scilit:
- Essential role of endothelial nitric oxide synthase for mobilization of stem and progenitor cellsNature Medicine, 2003
- Therapeutic stem and progenitor cell transplantation for organ vascularization and regenerationNature Medicine, 2003
- Adult hematopoietic stem cells provide functional hemangioblast activity during retinal neovascularizationNature Medicine, 2002
- Impaired recruitment of bone-marrow–derived endothelial and hematopoietic precursor cells blocks tumor angiogenesis and growthNature Medicine, 2001
- Mobilization of Endothelial Progenitor Cells in Patients With Acute Myocardial InfarctionCirculation, 2001
- Neovascularization of ischemic myocardium by human bone-marrow–derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac functionNature Medicine, 2001
- Angiogenesis in cancer and other diseasesNature, 2000
- Bone Marrow Origin of Endothelial Progenitor Cells Responsible for Postnatal Vasculogenesis in Physiological and Pathological NeovascularizationCirculation Research, 1999
- VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cellsThe EMBO Journal, 1999
- Isolation of Putative Progenitor Endothelial Cells for AngiogenesisScience, 1997