Unknown

Dataset Information

0

Gallic acid caused cultured mice TM4 Sertoli cells apoptosis and necrosis.


ABSTRACT: OBJECTIVE:The study was designed to determine the cytotoxic effect of gallic acid (GA), obtained by the hydrolysis of tannins, on mice TM4 Sertoli cells apoptosis. METHODS:In the present study, non-tumorigenic mice TM4 Sertoli cells were treated with different concentrations of GA for 24 h. After treatment, cell viability was evaluated using WST-1, mitochondrial dysfunction, cells apoptosis and necrosis was detected using JC-1, Hoechst 33342 and propidium iodide staining. The expression levels of Cyclin B1, proliferating cell nuclear antigen (PCNA), Bcl-2-associated X protein (BAX), and Caspase-3 were also detected by quantitative real-time polymerase chain reaction and Western-blotting. RESULTS:The results showed that 20 to 400 ?M GA inhibited viability of TM4 Sertoli cells in a dose-dependent manner. Treatment with 400 ?M GA significantly inhibited PCNA and Cyclin B1 expression, however up-regulated BAX and Caspase-3 expression, caused mitochondrial membrane depolarization, activated Caspase-3, and induced DNA damage, thus, markedly increased the numbers of dead cells. CONCLUSION:Our findings showed that GA could disrupt mitochondrial function and caused TM4 cells to undergo apoptosis and necrosis.

SUBMITTER: Li W 

PROVIDER: S-EPMC6502723 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

altmetric image

Publications

Gallic acid caused cultured mice TM4 Sertoli cells apoptosis and necrosis.

Li Wanhong W   Yue Xiangpeng X   Li Fadi F  

Asian-Australasian journal of animal sciences 20181026 5


<h4>Objective</h4>The study was designed to determine the cytotoxic effect of gallic acid (GA), obtained by the hydrolysis of tannins, on mice TM4 Sertoli cells apoptosis.<h4>Methods</h4>In the present study, non-tumorigenic mice TM4 Sertoli cells were treated with different concentrations of GA for 24 h. After treatment, cell viability was evaluated using WST-1, mitochondrial dysfunction, cells apoptosis and necrosis was detected using JC-1, Hoechst 33342 and propidium iodide staining. The expr  ...[more]

Similar Datasets

| S-EPMC6192158 | biostudies-literature
| S-EPMC3051435 | biostudies-literature
2024-05-25 | GSE243503 | GEO
| S-EPMC3247482 | biostudies-literature
| S-EPMC6562321 | biostudies-literature
2024-07-31 | GSE241623 | GEO
| S-EPMC6757565 | biostudies-literature
| S-EPMC4524530 | biostudies-literature