Journal of Shandong University (Health Sciences) ›› 2018, Vol. 56 ›› Issue (12): 19-25.doi: 10.6040/j.issn.1671-7554.0.2018.338

Previous Articles    

Effect of adipose-derived stem cells on intrinsic skin aging

ZHANG Kun1,2, YAN Bing3, LI Fang1,2, XIAO Dongjie1,2, WANG Yunshan1,2, LIU Hua1,2   

  1. 1. Laboratory of Cell Therapy and Translational Medicine, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, Shandong, China;
    2. Shandong Research Center of Transplantation and Tissue, Jinan 250013, Shandong, China;
    3. Department of Gastrointestinal Surgery, Jinan Central Hospital Affiliated to Shandong University, Jinan 250013, Shandong, China
  • Published:2022-09-27

Abstract: Objective To observe the effects of adipose-derived stem cells(ADSCs)on intrinsic skin aging, and investigate the underlying mechanisms. Methods Mouse skin fibroblast cells(MSFCs)and human ADSCs were primarily cultured. MSFCs cells were randomly divided into control group, model group, ADSCs conditioned medium(ADSCs-CM)group. MSFCs were treated with D-galactose(D-gal)and ADSCs-CM. The changes of ROS and β-galactosidase were tested by microscopy and flow cytometry, the expressions of caspase3, p53 and sirt1 were detected by RT-PCR, and the expression of Sirt1 protein was detected by Western blotting. Results The level of ROS in model group was higher than that in control group(P<0.001), and the β-galactosidase staining was deepened. The level of ROS in ADSCs-CM group was lower than that in model group(P<0.001), and the β-galactosidase staining was lighter. RT-PCR showed that the expressions of caspase3(P<0.001)and p53(P=0.001)were increased while the expression of sirt1(P<0.001)was decreased in model group compared with those in control group. The expressions of caspase3 山 东 大 学 学 报 (医 学 版)56卷12期 -张坤,等.脂肪源性干细胞对内源性皮肤老化的治疗作用 \=-(P<0.001)and p53(P=0.001)were decreased while the expression of sirt1 (P<0.001)was increased in ADSCs-CM group compared with that in model group. Western blotting showed that the Sirt1 protein expression was decreased in model group compared with that in control group(P<0.001)and increased in ADSCs-CM group compared with that in model group(P=0.006). Conclusion ADSCs show a protective effect on intrinsic skin aging induced by D-gal via Sirt1 signal pathway.

Key words: Adipose-derived stem cells, D-galactose, Skin aging

CLC Number: 

  • R751
[1] Ruetze M, Richter W. Adipose-derived stromal cells for osteoarticular repair: trophic function versus stem cell activity [J]. Expert Rev Mol Med, 2014, 16: e9. doi: 10.1017/erm.2014.9.
[2] Chung MT, Zimmermann AS, Paik KJ, et al. Isolation of human adipose-derived stromal cells using laser-assisted liposuction and their therapeutic potential in regenerative medicine [J]. Stem Cells Transl Med, 2013, 2(10): 808-817.
[3] 黄平,张坤,李芳,等.脐带和脂肪源性间充质干细胞生物学特性比较[J].山东大学学报(医学版),2018, 56(3): 72-78. HUANG Ping, ZHANG Kun, LI Fang, et al. Comparative study on biological characteristics of mesenchymal stem cellsfrom human umbilical cord and adipose[J]. Journal of Shandong University(Health Sciences), 2018, 56(3): 72-78.
[4] Naylor EC, Watson RE, Sherratt MJ. Molecular aspects of skin ageing[J]. Maturitas, 2011, 69(3): 249-256.
[5] Bonta M, Daina L, Mutiu G. The process of ageing reflected by histological changes in the skin[J]. Rom J Morphol Embryol, 2013, 54(3): 797-804.
[6] Quan C, Cho MK, Perry D, et al. Age-associated reduction of cell spreading induces mitochondrial DNA common deletion by oxidative stress in human skin dermal fibroblasts: implication for human skin connective tissue aging[J]. J Biomed Sci, 2015, 22: 62. doi: 10.1186/s12929-015-0167-6.
[7] Gaur M, Dobke M, Lunyak VV. Mesenchymal stem cells from adipose tissue in clinical applications for dermatological indications and skin aging[J]. Int J Mol Sci, 2017, 18(1). pii: E208. doi: 10.3390/ijms18010208.
[8] Tabatabaei Qomi R, Sheykhhasan M. Adipose-derived stromal cell in regenerative medicine: a review [J]. World J Stem Cells, 2017, 9(8): 107-117.
[9] Couto PS, Bersenev A, Verter F. The first decade of advanced cell therapy clinical trials using perinatal cells(2005-2015)[J]. Regen Med, 2017, 12(8): 953-968.
[10] Paschos NK, Sennett ML. Update on mesenchymal stem cell therapies for cartilage disorders[J]. World J Orthop, 2017, 8(12): 853-860.
[11] Sun Z, Luo B, Liu ZH, et al. Adipose-derived Sstromal cells protect intervertebral disc cells in compression: implications for stem cell regenerative disc therapy [J]. Int J Biol Sci, 2015, 11(2): 133-143.
[12] Condé-Green A, Marano AA, Lee ES, et al. Fat grafting and adipose-derived regenerative cells in burn wound healing and scarring: a systematic review of the literature [J]. Plast Reconstr Surg, 2016, 137(1): 302-312.
[13] Shingyochi Y, Orbay H, Mizuno H. Adipose-derived stem cells for wound repair and regeneration[J]. Expert Opin Biol Ther, 2015, 15(9):1285-1292.
[14] Lee JH, Fisher DE. Melanocyte stem cells as potential therapeutics in skin disorders[J]. Expert Opin Biol Ther, 2014, 14(11): 1569-1579.
[15] Pu CM, Liu CW, Liang CJ, et al. Adipose-derived stem cells protect skin flaps against ischemia/reperfusion injury via IL-6 expression [J]. J Invest Dermatol, 2017, 137(6): 1353-1362.
[16] Iser IC, Ceschini SM, Onzi GR, et al. Conditioned medium from adipose-derived stem cells(ADSCs)promotes epithelial-to-mesenchymal-like transition(EMT-Like)in glioma cells in vitro [J]. Mol Neurobiol, 2016, 53(10): 7184-7199.
[17] Fukuoka H, Suga H. Hair regeneration treatment using adipose-derived stem cell conditioned medium: follow-up with trichograms [J]. Eplasty, 2015, 15: e10.
[18] Ramdasi S, Tiwari SK. Human mesenchymal stem cell-derived conditioned media for hair regeneration applications [J].J Stem Cells, 2016, 11(4): 201-211.
[19] Maynard S, Fang EF, Scheibye-Knudsen M, et al. DNA damage, DNA repair, aging, and neurodegeneration [J]. Cold Spring Harb Perspect Med, 2015, 5(10). pii:a025130. doi: 10.1101/cshperspect.a025130.
[20] H(¨overo)hn A, Weber D, Jung T, et al. Happily(n)ever after: aging in the context of oxidative stress, proteostasis loss and cellular senescence [J]. Redox Biol, 2017, 11: 482-501. doi: 10.1016/j.redox.2016.12.001.
[21] Edrey YH, Salmon AB. Salmon. Revisiting an age-old question regarding oxidative stress [J]. Free Radic Biol Med, 2014, 71: 368-378. doi: 10.1016/j.freeradbiomed.2014.03.038.
[22] 林映雪,庄朋伟,张金保,等. D-半乳糖剂量及小鼠性别对衰老模型的影响[J].天津中医药大学学报, 2013, 32(3): 144-147. LIN Yingxue, ZHUANG Pengwei, ZHANG Jinbao, et al. Impact of D-galactoses dose and gender of mice on aging model[J]. Journal of Tianjin University of Traditional Chinese Medicine, 2013, 32(3): 144-147.
[23] Li J, Cai D, Yao X, et al. Protective effect of ginsenoside Rg1 on ehmatopoietic stem/progenitor cells through attenuating oxidative stress and the Wnt/β-catenin signaling pathway in a mouse model of d-galactose-induced aging[J]. Int J Mol Sci, 2016, 17(6). pii:E849. doi: 10.3390/ijms17060849.
[24] Mortuza R, Chen S, Feng B, et al. High glucose induced alteration of SIRTs in endothelial cells causes rapid aging in a p300 and FOXO regulated pathway [J]. PLoS One, 2013, 8(1): e54514. doi: 10.1371/journal.pone.0054514.
[25] Salminen A, Kaarniranta K, Kauppinen A. Crosstalk between oxi-dative stress and SIRT1: impact on the aging process [J]. Int JMol Sci, 2013, 14(2): 3834-3859.
[1] ZHANG Zhengduo, WU Hong, QI Shaojun, TANG Yanjin, GAO Xibao. Preventive effects of oral 5-methyltetrahydrofolate on Alzheimers disease in rats [J]. Journal of Shandong University (Health Sciences), 2022, 60(3): 13-23.
[2] SHI Yehua, CHEN Zhipeng, MA Qikui, JU Ruihua, WANG Qirong. A new method of inducing adipose-derived stem cells into cartilage tissue [J]. JOURNAL OF SHANDONG UNIVERSITY (HEALTH SCIENCES), 2014, 52(12): 45-49.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!