A Rho Kinase (ROCK) Inhibitor, Y-27632, Inhibits the Dissociation-Induced Cell Death of Salivary Gland Stem Cells

被引:10
作者
Kim, Kichul [1 ]
Min, Sol [1 ]
Kim, Daehwan [2 ,3 ]
Kim, Hyewon [4 ]
Roh, Sangho [1 ]
机构
[1] Seoul Natl Univ, Sch Dent, Dent Res Inst, Cellular Reprogramming & Embryo Biotechnol Lab, Seoul 08826, South Korea
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, QB3 Inst, Berkeley, CA 94720 USA
[4] Hanyang Univ, Dept Biomed Engn, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
salivary gland stem cells (SGSCs); ROCK inhibitor; dissociation-induced cell death; EPITHELIAL-CELLS; APOPTOSIS; TRANSPLANTATION; FIBROSIS; SUPPRESSION; HOMEOSTASIS; EXPRESSION; SURVIVAL; STATE;
D O I
10.3390/molecules26092658
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Salivary gland stem cells (SGSCs) are potential cell sources for the treatment of salivary gland diseases. The control of cell survival is an essential factor for applying stem cells to regenerative medicine or stem cell-based research. The purpose of this study was to investigate the effects of the ROCK inhibitor Y-27632 on the survival of SGSCs and its underlying mechanisms. SGSCs were isolated from mouse submandibular glands and cultured in suspension. Treatment with Y-27632 restored the viability of SGSCs that was significantly decreased during isolation and the subsequent culture. Y-27632 upregulated the expression of anti-apoptotic protein BCL-2 in SGSCs and, in the apoptosis assay, significantly reduced apoptotic and necrotic cell populations. Matrigel was used to mimic the extracellular environment of an intact salivary gland. The expression of genes regulating apoptosis and the ROCK signaling pathway was significantly reduced when SGSCs were embedded in Matrigel. SGSCs cultured in Matrigel and treated with Y-27632 showed no difference in the total numbers of spheroids and expression levels of apoptosis-regulating genes. Matrigel-embedded SGSCs treated with Y-27632 increased the number of spheroids with budding structures and the expression of acinar cell-specific marker AQP5. We demonstrate the protective effects of Y-27632 against dissociation-induced apoptosis of SGSCs during their culture in vitro.
引用
收藏
页数:12
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