TOPK inhibits TNF-a-induced granulosa cell apoptosis via regulation of SIRT1/p53

被引:5
|
作者
Joo, Na-Rae [1 ]
Park, Sang-Ah [1 ]
Park, Jung-Hwan [1 ]
Oh, Sang-Muk [1 ,2 ]
机构
[1] Konyang Univ, Coll Med, Dept Biochem, Daejeon 35365, South Korea
[2] Konyang Univ, Myunggok Med Res Inst, Coll Med, Prior Res Ctr, Daejeon 35365, South Korea
基金
新加坡国家研究基金会;
关键词
TNF-a; Granulosa cell; TOPK; Apoptosis; NECROSIS-FACTOR-ALPHA; ESTRADIOL SECRETION; FOLLICULAR ATRESIA; EXPRESSION; PBK/TOPK; KINASE; PROLIFERATION; INVOLVEMENT; MODULATION; DEPENDENCE;
D O I
10.1016/j.bbrc.2023.04.113
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
T-LAK cell originated protein kinase (TOPK) has been shown to regulate proliferation, invasion or migration of various cancer cells. However, the role of TOPK in follicle environments remains unknown. Here we reveal that TOPK inhibits TNF-a-induced human granulosa COV434 cell apoptosis. The expression of TOPK were increased in COV434 cells in response to TNF-a. TOPK inhibition also decreased TNF-a-induced SIRT1 expression but promoted TNF-a-induced p53 acetylation and expression of PUMA or NOXA. Accordingly, TOPK inhibition attenuated TNF-a-mediated SIRT1 transcriptional activity. In addition, SIRT1 inhibition augmented acetylation of p53 or expression of PUMA and NOXA in response to TNF-a, leading to COV434 cell apoptosis. We conclude that TOPK suppresses TNF-a-induced COV434 granulosa cell apoptosis via regulation of p53/SIRT1 axis, suggesting a potential role of TOPK in regu-lation of ovarian follicular development.(c) 2023 Published by Elsevier Inc.
引用
收藏
页码:128 / 135
页数:8
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