The Role of Chemokines in Proangiogenic Action Induced by Human Adipose Tissue-Derived Mesenchymal Stem Cells in the Murine Model of Hindlimb Ischemia

被引:21
作者
Cho, Hyun Hwa [1 ,2 ]
Kim, Yeon Jeong [1 ,2 ]
Kim, Jong Tae [1 ]
Song, Ji Sun [1 ,2 ,3 ]
Shin, Keun Koo [1 ,2 ,3 ]
Bae, Yong Chan [4 ]
Jung, Jin Sup [1 ,2 ,3 ,5 ]
机构
[1] Pusan Natl Univ, Sch Med, Dept Physiol, Yangsan, Kyungsangnamdo, South Korea
[2] Pusan Natl Univ, Med Res Ctr Ischem Tissue Regenerat, Yangsan, Kyungsangnamdo, South Korea
[3] Pusan Natl Univ, Sch Med, Med Sci Educ Ctr BK21, Yangsan, Kyungsangnamdo, South Korea
[4] Pusan Natl Univ, Sch Med, Dept Plast Surg, Yangsan, Kyungsangnamdo, South Korea
[5] Pusan Natl Univ, Med Res Inst, Yangsan, Kyungsangnamdo, South Korea
关键词
hASCs; GCP2; MCP1; Capillary-like structure formation; Proangiogenic action; IMPROVE POSTNATAL NEOVASCULARIZATION; ENDOTHELIAL GROWTH-FACTOR; FEMORAL-ARTERY OCCLUSION; STROMAL CELLS; BONE-MARROW; OSTEOGENIC DIFFERENTIATION; TUMOR ANGIOGENESIS; CXC CHEMOKINES; LIMB ISCHEMIA; IN-VITRO;
D O I
10.1159/000257495
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The proangiogenic action of human adipose tissue-derived mesenchymal stem cells (hASCs) transplantation has been shown to be mediated by secretory factors. In this study, we determined if human granulocyte chemotactic protein-2(GCP2) or monocyte chemoattractant protein-1(MCP1) is involved in the proangiogenic action of hASCs transplantation in the hindlimb ischemia model. hASCs secrete GCP2 and MCP1, which leads to increased tubule formation. The downregulation of GCP2 or MCP1 decreased MCP1 and GCP2 secretion, respectively, whereas the external addition of GCP2 or MCP1 increased MCP1 and GCP2, respectively. Additionally, the treatment of GCP2 and MCP1 increased VEGF secretion, while the downregulation of GCP2 and MCP1 showed the opposite effect on VEGF secretion. Downregulation of GCP2 and MCP1 expression also inhibited hASCs-induced proangiogenic action, while the overexpression of GCP2 increased it. Finally, the downregulation of MCP1 or VEGF inhibited the GCP2 overexpression-induced increase in blood flow recovery. Taken together, these data indicate that the proangiogenic action of hASCs transplantation is mediated by the interaction between GCP2, MCP1 and VEGF, which are secreted from the transplanted cells. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:511 / 518
页数:8
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