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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Jiang, Junjun Li, Liyuan Xie, Mingchao Fuji, Ryosuke Liu, Shangfeng Yin, Xiaobei Li, Genlin Wang, Zhao |
| Description | Author Affiliation: Jiang J ( MOE Key Laboratory of Protein Sciences, Department of Pharmacology, School of Medicine, Tsinghua University.) |
| Abstract | Spermatogenesis associated 4 (SPATA4) is a testis-specific gene first cloned by our laboratory, and plays an important role in maintaining the physiological function of germ cells. Accumulated evidence suggests that SPATA4 might be associated with apoptosis. Here we established HeLa cells that stably expressed SPATA4 to investigate the function of SPATA4 in apoptosis. SPATA4 protected HeLa cells from etoposide-induced apoptosis through the mitochondrial apoptotic pathway, in the way that SPATA4 suppressed decrease of the mitochondrial membrane potential, the release of cytochrome c, and subsequent activation of caspase-9 and -3. We further demonstrated that SPATA4 upregulated anti-apoptotic members of Bcl-2 family proteins, Bcl-2, and downregulated the pro-apoptotic member of Bcl-2 family proteins, Bax. Knockdown of SPATA4 in HeLa/SPATA4 cells could partially rescue expression levels of bcl-2 and bax. In conclusion, SPATA4 protects HeLa cells against etoposide-induced apoptosis through the mitochondrial apoptotic pathway. Our findings provide further evidence that SPATA4 plays a role in regulating apoptosis. |
| File Format | HTM / HTML |
| ISSN | 09186158 |
| e-ISSN | 13475215 |
| Journal | Biological & Pharmaceutical Bulletin |
| Issue Number | 10 |
| Volume Number | 38 |
| Language | English |
| Publisher | The Pharmaceutical Society of Japan J-STAGE |
| Publisher Date | 2015-01-01 |
| Publisher Place | Japan |
| Access Restriction | Open |
| Subject Keyword | Discipline Biochemistry Discipline Pharmacology Apoptosis Physiology Proteins Metabolism Proto-oncogene Proteins C-bcl-2 Drug Effects Caspase 3 Caspase 9 Cytochromes c Etoposide Hela Cells Membrane Potential, Mitochondrial Mitochondria Genetics Topoisomerase Ii Inhibitors Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine Pharmacology Pharmaceutical Science |
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