Adult hematopoietic stem cells provide functional hemangioblast activity during retinal neovascularization

被引:531
作者
Grant, MB [1 ]
May, WS
Caballero, S
Brown, GAJ
Guthrie, SM
Mames, RN
Byrne, BJ
Vaught, T
Spoerri, PE
Peck, AB
Scott, EW
机构
[1] Univ Florida, Program Stem Cell Biol, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Pharmacol & Therapeut, Gainesville, FL USA
[3] Univ Florida, Shands Canc Ctr, Gainesville, FL USA
[4] Univ Florida, McKnight Brain Inst, Gainesville, FL USA
[5] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
[6] Univ Florida, Dept Mol Genet & Microbiol, Gainesville, FL USA
[7] Retina Ctr, Gainesville, FL USA
关键词
D O I
10.1038/nm0602-607
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adults maintain a reservoir of hematopoietic stem cells that can enter the circulation to reach organs in need of regeneration. We developed a novel model of retinal neovascularization in adult mice to examine the role of hematopoietic stem cells in revascularizing ischemic retinas. Adult mice were durably engrafted with hematopoietic stem cells isolated from transgenic mice expressing green fluorescent protein. We performed serial long-term transplants, to ensure activity arose from self-renewing stem cells, and single hematopoietic stem-cell transplants to show clonality. After durable hematopoietic engraftment was established, retinal ischemia was induced to promote neovascularization. Our results indicate that self-renewing adult hematopoietic stem cells have functional hemangioblast activity, that is, they can clonally differentiate into all hematopoietic cell lineages as well as endothelial cells that revascularize adult retina. We also show that recruitment of endothelial precursors to sites of ischemic injury has a significant role in neovascularization.
引用
收藏
页码:607 / 612
页数:6
相关论文
共 37 条
[1]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[2]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[3]   Vascular development: Cellular and molecular regulation [J].
Beck, L ;
DAmore, PA .
FASEB JOURNAL, 1997, 11 (05) :365-373
[4]   Enhanced endothelialization and microvessel formation in polyester grafts seeded with CD34+ bone marrow cells [J].
Bhattacharya, V ;
McSweeney, PA ;
Shi, Q ;
Bruno, B ;
Ishida, A ;
Nash, R ;
Storb, RF ;
Sauvage, LR ;
Hammond, WP ;
Wu, MHD .
BLOOD, 2000, 95 (02) :581-585
[5]   Hemangioblast development and regulation [J].
Choi, K .
BIOCHEMISTRY AND CELL BIOLOGY, 1998, 76 (06) :947-956
[6]  
Cilloni D, 2000, BLOOD, V96, P3637
[7]   Endothelial cells of hematopoietic origin make a significant contribution to adult blood vessel formation [J].
Crosby, JR ;
Kaminski, WE ;
Schatteman, G ;
Martin, PJ ;
Raines, EW ;
Seifert, RA ;
Bowen-Pope, DF .
CIRCULATION RESEARCH, 2000, 87 (09) :728-730
[8]   Mesenchymal stem cells are capable of homing to the bone marrow of non-human primates following systemic infusion [J].
Devine, SM ;
Bartholomew, AM ;
Mahmud, N ;
Nelson, M ;
Patil, S ;
Hardy, W ;
Sturgeon, C ;
Hewett, T ;
Chung, T ;
Stock, W ;
Sher, D ;
Weissman, S ;
Ferrer, K ;
Mosca, J ;
Deans, R ;
Moseley, A ;
Hoffman, R .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (02) :244-255
[9]   HMG-CoA reductase inhibitors (statins) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway [J].
Dimmeler, S ;
Aicher, A ;
Vasa, M ;
Mildner-Rihm, C ;
Adler, K ;
Tiemann, M ;
Rütten, H ;
Fichtlscherer, S ;
Martin, H ;
Zeiher, AM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) :391-397
[10]  
FOLKMAN J, 1992, J BIOL CHEM, V267, P10931