Responses of adipose-derived stem cells during hypoxia: enhanced skin-regenerative potential

被引:100
作者
Chung, Hyung-Min [1 ,2 ,3 ]
Won, Chong-Hyun [4 ]
Sung, Jong-Hyuk [1 ,2 ]
机构
[1] CHA Stem Cell Inst, Stem Cell Res Lab, Seoul, South Korea
[2] CHA Univ, Dept Biomed Sci, Seoul 135081, South Korea
[3] CHA Bio & Diostech Co Ltd, Seoul, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Dermatol, Seoul, South Korea
关键词
adipose-derived stem cell; growth factor; hypoxia; skin regeneration; HUMAN BONE-MARROW; ACUTE MYOCARDIAL-INFARCTION; HUMAN DERMAL FIBROBLASTS; UMBILICAL-CORD BLOOD; STROMAL CELLS; PROGENITOR CELLS; SECRETORY FACTORS; SKELETAL-MUSCLE; POSTNATAL NEOVASCULARIZATION; GENE-EXPRESSION;
D O I
10.1517/14712590903307362
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Mesenchymal stem cells within the stromal-vascular fraction of subcutaneous adipose tissue (i.e., adipose-derived stem cells (ASCs)), have been used for tissue engineering. In addition to serving a building-block function, ASCs are reported to secrete growth factors that are essential for their function. Increasing evidence indicates that ASCs play a significant role in skin regeneration, a function that is enhanced by hypoxia through upregulating secretion of growth factors. Although the anatomical sites of ASCs in the body are relatively oxygen-deficient, ASCs are usually cultured under normoxic conditions (i.e., atmospheric oxygen levels). Culturing ASCs under physiologically relevant low-oxygen-tension conditions may uniquely benefit the expansion, differentiation, adhesion, growth factor secretion and regenerative potential of ASCs. Therefore, understanding the response and adaptation of ASCs to hypoxia may be invaluable for developing novel cell- and cyto-therapy strategies. This review highlights our current understanding of cellular and molecular responses of ASCs to hypoxia, focusing on the enhancement of ASC function and secretory activity by hypoxic culture conditions.
引用
收藏
页码:1499 / 1508
页数:10
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