Protective effects of adipose-derived stem cells secretome on human dermal fibroblasts from ageing damages

被引:4
作者
Wang, Ting [1 ]
Guo, Shu [1 ]
Liu, Xuehui [2 ]
Xv, Nan [1 ]
Zhang, Shuangyi [1 ]
机构
[1] China Med Univ, Hosp 1, Dept Plast Surg, 155 North Nanjing St, Shenyang 110001, Peoples R China
[2] Dalian Med Univ, Hosp 2, Dept Hand & Foot Microsurg, Dalian, Peoples R China
基金
中国国家自然科学基金;
关键词
Adipose-derived stem cells; secretory factors; anti-ageing; human dermal fibroblasts; HUMAN-DIPLOID FIBROBLASTS; HUMAN SKIN FIBROBLASTS; PREMATURE SENESCENCE; STROMAL CELLS; IN-VIVO; TISSUE; ACTIVATION; EXPRESSION; THERAPY; UVB;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Combined effects of intrinsic and extrinsic ageing factors on skin tissue and the therapies have been rarely studied before. ADSCs have gained popularity in anti-ageing field, which may provide promising methods to fight against skin ageing. Objective: To find out the fate of HDFs exposed to intrinsic or extrinsic ageing factors or both of them and further examine the impacts of ADSC-CM on the damaged HDFs. Methods: We irradiated HDFs with UVB at different senescent levels, and then treated them with ADSC-CM. After 48 h, we detected cellular proliferative activity, morphology, SA-beta-Gal expression, apoptosis, mRNA expression of collagen I, collagen III and elastin. Results: Intrinsic ageing factors inhibited cellular proliferation, increased senescent ratio and reduced mRNA expression of collagen I, collagen III and elastin, so did UVB, except for its induction of elastin mRNA expression. Furthermore, ADSC-CM treatment can slightly or significantly improve cellular proliferative activity and restore functions both in irradiated and non-irradiated HDFs. Besides, ADSC-CM treatment decreased cellular apoptosis and senescence induced by UVB but had no obvious effect on cellular senescence induced by intrinsic ageing factors. The results were similar in three generations of HDFs, yet in different degrees. Conclusions: The results suggest that ADSCs secretome protect HDFs from ageing damages but with some limitations.
引用
收藏
页码:15739 / 15748
页数:10
相关论文
共 34 条
[1]   Molecular mechanisms of ageing in connective tissues [J].
Bailey, AJ .
MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (07) :735-755
[2]   PROTEIN-TYROSINE PHOSPHATASES TAKE-OFF [J].
BARFORD, D ;
JIA, ZC ;
TONKS, NK .
NATURE STRUCTURAL BIOLOGY, 1995, 2 (12) :1043-1053
[3]   Stromal cells from the adipose tissue-derived stromal vascular fraction and culture expanded adipose tissue-derived stromal/stem cells: a joint statement of the International Federation for Adipose Therapeutics and Science (IFATS) and the International Society for Cellular Therapy (ISCT) [J].
Bourin, Philippe ;
Bunnell, Bruce A. ;
Casteilla, Louis ;
Dominici, Massimo ;
Katz, Adam J. ;
March, Keith L. ;
Redl, Heinz ;
Rubin, J. Peter ;
Yoshimura, Kotaro ;
Gimble, Jeffrey M. .
CYTOTHERAPY, 2013, 15 (06) :641-648
[4]  
Cavaillon JM, 1996, LES CYTOKINES
[5]  
Champion RH, 1998, ROOK WILSON EBLING T
[6]   TGF-β1-treated ADSCs-CM promotes expression of type I collagen and MMP-1, migration of human skin fibroblasts, and wound healing in vitro and in vivo [J].
Cho, Jae-We ;
Kang, Min-Chul ;
Lee, Kyu-Suk .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2010, 26 (06) :901-906
[7]   Repeated exposure of human skin fibroblasts to UVB at subcytotoxic level triggers premature senescence through the TGF-β1 signaling pathway [J].
Debacq-Chainlaux, F ;
Borlon, C ;
Pascal, T ;
Royer, V ;
Eliaers, F ;
Ninane, N ;
Carrard, G ;
Friguet, B ;
de Longueville, F ;
Boffe, S ;
Remacle, J ;
Toussaint, O .
JOURNAL OF CELL SCIENCE, 2005, 118 (04) :743-758
[8]   Connective tissue growth factor induces c-fos gene activation and cell proliferation through p44/42 MAP kinase in primary rat hepatic stellate cells [J].
Gao, RP ;
Ball, DK ;
Perbal, B ;
Brigstock, DR .
JOURNAL OF HEPATOLOGY, 2004, 40 (03) :431-438
[9]   Down-regulation of tissue inhibitor of matrix metalloprotease-1 (TIMP-1) in aged human skin contributes to matrix degradation and impaired cell growth and survival [J].
Hornebeck, W .
PATHOLOGIE BIOLOGIE, 2003, 51 (10) :569-573
[10]  
Huang Hai-chang, 2005, Zhonghua Yi Xue Za Zhi, V85, P1322