Acta Biochimica et Biophysica Sinica Advance Access originally published online on August 1, 2009
Acta Biochimica et Biophysica Sinica 2009 41(9):800-807; doi:10.1093/abbs/gmp069
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
The role of MAPK and FAS death receptor pathways in testicular germ cell apoptosis induced by lead
1 Institute of Public Health, Harbin Medical University, Harbin 150086, China
2 Hangzhou Dianzi University, Hangzhou 310000, China
* Correspondence address. Tel: +86-571-86878632; E-mail: liangduoping{at}hdu.edu.cn
| Abstract |
|---|
The aim of the present study is to investigate gene expression involved in the signal pathway of MAPK and death signal receptor pathway of FAS in lead-induced apoptosis of testicular germ cells. First, cell viabilities were determined by MTT assay. Second, using single cell gel-electrophoresis test (comet assay) and TUNEL staining technique, apoptotic rate and cell apoptosis localization of testicular germ cells were measured in mice treated with 0.15%, 0.3%, and 0.6% lead, respectively. Third, the immunolocalization of K-ras, c-fos, Fas, and active caspase-3 proteins was determined by immunohistochemistry. Finally, changes in the translational levels of K-ras, c-fos, Fas, and active caspase-3 were further detected by western blot analysis. Our results showed that lead could significantly induce testicular germ cell apoptosis in a dose-dependent manner (P < 0.01). The mechanisms were closely related to the increased expressions of K-ras, c-fos, Fas, and active caspase-3 in apoptotic germ cells. In conclusion, K-ras/c-fos and Fas/caspase-3 death signaling receptor pathways were involved in the lead-induced apoptosis of the testicular germ cells in mice.
Keywords lead acetate; testis; cell apoptosis; K-ras; c-fos; Fas; caspase-3
Received: April 1, 2009; Accepted: June 21, 2009
![]()
CiteULike
Connotea
Del.icio.us What's this?