2003•Zhongguo aizheng zazhiRequires access

Role of p38MAPK in mediating TNF-α-induced apoptosis in rat glioma cells

Bi Zhang

Open publisher page 0 citations

Abstract

Purpose:To study the role of p38MAPK in mediating TNF α induced apoptosis in rat glioma cells C6.Methods:The proliferation activity of C6 cells after the treatment by TNF α was observed by MTT assay. The TNF α induced apoptosis was detected by transmission electron microscopy and flow cytometry. The expression of p38MAPK was detected by SABC method and Westernblot. The effect of SB202190, a specific inhibitor of p38MAPK on TNF α induced apoptosis was observed by flow cytometry and SABC method. Results:The inhibitory rate of TNF α (2×10 5 U/L) on C6 cells was 43.75%. In the TNF α treated group, apoptotic cells were observed by transmission electron microscopy and the apoptotic rate was 37.5% by flow cytometry, p38MAPK positive signals were found by SABC method and Westernblot. In the SB202190 treated group, the apoptotic rate was 7.0% and no p38MAPK signals were found.Conclusions:The apoptosis of C6 cells and expression of p38MAPK could be induced by TNF α. The activation of p38MAPK promoted the apoptosis of C6 cells. [

About this research paper

What this paper is about

Purpose:To study the role of p38MAPK in mediating TNF α induced apoptosis in rat glioma cells C6.Methods:The proliferation activity of C6 cells after the treatment by TNF α was observed by MTT assay. The TNF α induced apoptosis was detected by transmission electron microscopy and flow cytometry. The expression of p38MAPK was detected by SABC method and Westernblot. The effect of SB202190, a specific inhibitor of p38MAPK on TNF α induced apoptosis was observed by flow cytometry and SABC method. Results:The inhibitory rate of TNF α (2×10 5 U/L) on C6 cells was 43.75%. In the TNF α treated group, apoptotic cells were observed by transmission electron microscopy and the apoptotic rate was 37.5% by flow cytometry, p38MAPK positive signals were found by SABC method and Westernblot. In the SB202190 treated group, the apoptotic rate was 7.0% and no p38MAPK signals were found.Conclusions:The apoptosis of C6 cells and expression of p38MAPK could be induced by TNF α. The activation of p38MAPK promoted the apoptosis of C6 cells. [

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Purpose:To study the role of p38MAPK in mediating TNF α induced apoptosis in rat glioma cells C6.Methods:The proliferation activity of C6 cells after the treatment by TNF α was observed by MTT assay. The TNF α induced apoptosis was detected by transmission electron microscopy and flow cytometry. The expression of p38MAPK was detected by SABC method and Westernblot. The effect of SB202190, a specific inhibitor of p38MAPK on TNF α induced apoptosis was observed by flow cytometry and SABC method. Results:The inhibitory rate of TNF α (2×10 5 U/L) on C6 cells was 43.75%. In the TNF α treated group, apoptotic cells were observed by transmission electron microscopy and the apoptotic rate was 37.5% by flow cytometry, p38MAPK positive signals were found by SABC method and Westernblot. In the SB202190 treated group, the apoptotic rate was 7.0% and no p38MAPK signals were found.Conclusions:The apoptosis of C6 cells and expression of p38MAPK could be induced by TNF α. The activation of p38MAPK promoted the apoptosis of C6 cells. [

Key concepts: Apoptosis, Flow cytometry, Tumor necrosis factor alpha, MTT assay, Molecular biology, Cytometry, Chemistry, Cell biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Role of p38MAPK in mediating TNF-α-induced apoptosis in rat glioma cells — Research Paper | ScholarLens