Increase in ultraviolet sensitivity by overexpression of calpastatin in ultraviolet-resistant UVr-1 cells derived from ultraviolet-sensitive human RSa cells

被引:16
作者
Hiwasa, T
Arase, Y
Kikuno, K
Hasegawa, R
Sugaya, S
Kita, K
Saido, T
Yamamori, H
Maki, M
Suzuki, N
机构
[1] Chiba Univ, Sch Med, Dept Biochem, Chuo Ku, Chiba 2608670, Japan
[2] Chiba Univ, Sch Med, Dept Radiol, Chuo Ku, Chiba 2608670, Japan
[3] RIKEN, Brain Sci Inst, Lab Proteolyt Neurosci, Wako, Saitama 3510106, Japan
[4] Chiba Univ, Dept Surg, Sch Med, Chuo Ku, Chiba 2608670, Japan
[5] Nagoya Univ, Sch Agr Sci, Dept Appl Biol Sci, Chikusa Ku, Nagoya, Aichi 4648601, Japan
关键词
ultraviolet; signal transduction; down-regulation; calpain; Bax; apoptosis;
D O I
10.1038/sj.cdd.4400685
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human RSa cells are highly sensitive to apoptotic-like cell death by ultraviolet irradiation (UV) while UVr-1 cells are their variant with an increased resistance to UV, Three days after UV at 10 J/m(2), the viability of RSa cells was approximately 17% while that of UVr-1 cells was 65%, This different survival might reflect apoptotic cell death since apoptosis-specific DNA ladder was more clearly observed in RSa cells than in UVr-1 cells after UV, Addition of ALLN/calpain inhibitor I to the culture medium after UV resulted in similar survival (14 -18%) between RSa and UVr-1 cells. Immunoblot analysis showed down-regulation of protein kinase CB, Src, Bax and mu-calpain after UV was more prominent in UVr-1 than in RSa cells. Activated mu-calpain appeared within 1 h post-UV only in UVr-1 cells. The expression of calpastatin, a specific endogenous inhibitor of calpain, was higher in RSa than in UVr-1 cells, To further examine the role of calpain in UV-induced cell death, cDNA of human calpastatin was transfected into UVr-1 cells. The results showed that overexpression of calpastatin suppressed down-regulation of Src, p-calpain and Bax. Concomitantly, colony survival after UV was reduced in calpastatin-transfected cells as compared to vector control cells, Our results suggest that activation of calpain might account for, at least in part, the lower susceptibility to UV-induced cell death in UVr-1 cells.
引用
收藏
页码:531 / 537
页数:7
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