Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+
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Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+
Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+
解放军医学杂志(英文版)2002年第3期 页码:181-187
Affiliations:
1. Institute of Combined Injury
2. Third Military Medical University
3. ,Japan
4. Department of Environmental Toxicology
5. University of Occupational and Environmental Health
6. Kitakyushu 5,807-8555
Author bio:
Funds:
in part by Natural Sciences Foundation of China (No. 39870239);by the Sasagawa Fellowship,Japan.
DOI:
中图分类号:R363
纸质出版:2002
Accepted:
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Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+[J]. 解放军医学杂志(英文版), 2002,(3):181-187.
[1]周舟,王小华,Igisu Hideki,林远,楼淑芬,Matsuoka Masato,程天民,余争平.Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca~(2+)[J].Journal of Medical Colleges of PLA,2002(03):181-187.
Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+[J]. 解放军医学杂志(英文版), 2002,(3):181-187.DOI:
[1]周舟,王小华,Igisu Hideki,林远,楼淑芬,Matsuoka Masato,程天民,余争平.Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca~(2+)[J].Journal of Medical Colleges of PLA,2002(03):181-187.DOI:
Differential activation of mitogen-activated protein kinases by γ-irradi-ation in IEC-6 cells: Role of intracellular Ca2+
摘要
Abstract
<正> Objective: To explore the effects of γ-irradiation on mitogen-activated protein kinases (MAPKs) and role of intracellular calcium in this event in intestinal epithelial cell line 6 (IEC-6 cells). Methods: After cultured rat IIEC-6 cells with or without the pretreatment of intracellular Ca2+ chelator were exposed to Y-ir-radiation of 6 Gy
the total and phosphorylated MAPKs in the cells were determined with Western blotting and apoptosis was examined with flow cytometry. Activities of Extracellular signal-regulated protein kinase (ERK) and p38 MAPK were determined by using immuoprecipitation followed by Western blotting. Results: In response to γ-irradiation
phosphorylation of ERK was not significantly observed
while the levels of phosphorylated c-Jun NH2-terminal kinase (JNK) and p38 MAPK were increased in 30 min and reached the peak 2 h after exposure to 6 Gy γ-irradiation
though the cell viability was significantly lowered 12 h. On the other hand
no obvious changes were seen in the total protei
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