Cross Talk with Hematopoietic Cells Regulates the Endothelial Progenitor Cell Differentiation of CD34 Positive Cells

被引:38
作者
Kwon, Sang-Mo [1 ]
Lee, Jun-Hee [1 ]
Lee, Sang-Hun [2 ]
Jung, Seok-Yun [1 ]
Kim, Da-Yeon [1 ]
Kang, Song-Hwa [1 ]
Yoo, So-Young [1 ]
Hong, Jong-Kyu [1 ]
Park, Ji-Hye [1 ]
Kim, Jung-Hee [1 ]
Kim, Sung-Wook [1 ]
Kim, Yeon-Ju [1 ]
Lee, Sun-Jin [1 ]
Kim, Hwi-Gon [3 ]
Asahara, Takayuki [4 ]
机构
[1] Pusan Natl Univ, Sch Med, Med Res Inst, Dept Physiol,Lab Vasc Med & Stem Cell Biol, Yangsan, South Korea
[2] Soonchunhyang Univ, Seoul Hosp, Soonchunhyang Med Sci Res Inst, Seoul, South Korea
[3] Pusan Natl Univ, Sch Med, Dept Obstet & Gynecol, Yangsan, South Korea
[4] Tokai Univ, Sch Med, Dept Regenerat Med Sci, Isehara, Kanagawa 25911, Japan
基金
新加坡国家研究基金会;
关键词
BONE-MARROW; THERAPEUTIC ANGIOGENESIS; POSTNATAL VASCULOGENESIS; CLONOGENIC-ASSAY; CD31(+) CELLS; TRANSPLANTATION; NEOVASCULARIZATION; IMPLANTATION; STEM; IDENTIFICATION;
D O I
10.1371/journal.pone.0106310
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Despite the crucial role of endothelial progenitor cells (EPCs) in vascular regeneration, the specific interactions between EPCs and hematopoietic cells remain unclear. Methods: In EPC colony forming assays, we first demonstrated that the formation of EPC colonies was drastically increased in the coculture of CD34(+) and CD34(-) cells, and determined the optimal concentrations of CD34(+) cells and CD34(-) cells for spindle-shaped EPC differentiation. Results: Functionally, the coculture of CD34(+) and CD34(-) cells resulted in a significant enhancement of adhesion, tube formation, and migration capacity compared with culture of CD34(+) cells alone. Furthermore, blood flow recovery and capillary formation were remarkably increased by the coculture of CD34(+) and CD34(-) cells in a murine hind-limb ischemia model. To elucidate further the role of hematopoietic cells in EPC differentiation, we isolated different populations of hematopoietic cells. T lymphocytes (CD3(+)) markedly accelerated the early EPC status of CD34(+) cells, while macrophages (CD11b(+)) or megakaryocytes (CD41(+)) specifically promoted large EPC colonies. Conclusion: Our results suggest that specific populations of hematopoietic cells play a role in the EPC differentiation of CD34(+) cells, a finding that may aid in the development of a novel cell therapy strategy to overcome the quantitative and qualitative limitations of EPC therapy.
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页数:12
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