Farnesylated RhoB inhibits radiation-induced mitotic cell death and controls radiation-induced centrosome overduplication

被引:0
|
作者
J Milia
F Teyssier
F Dalenc
I Ader
C Delmas
A Pradines
I Lajoie-Mazenc
R Baron
J Bonnet
E Cohen-Jonathan
G Favre
C Toulas
机构
[1] INSERM U563,Département de Radiothérapie
[2] CPTP,undefined
[3] Département d'Innovation Thérapeutique et d'Oncologie Moléculaire,undefined
[4] Institut Claudius Regaud,undefined
[5] Institut Claudius Regaud,undefined
来源
Cell Death & Differentiation | 2005年 / 12卷
关键词
mitotic cell death; ionizing radiation; Rho B; centrosome duplication; radioresistance;
D O I
暂无
中图分类号
学科分类号
摘要
Our previous results demonstrated that expressing the GTPase ras homolog gene family, member B (RhoB) in radiosensitive NIH3T3 cells increases their survival following 2 Gy irradiation (SF2). We have first demonstrated here that RhoB expression inhibits radiation-induced mitotic cell death. RhoB is present in both a farnesylated and a geranylgeranylated form in vivo. By expressing RhoB mutants encoding for farnesylated (RhoB-F cells), geranylgeranylated or the CAAX deleted form of RhoB, we have then shown that only RhoB-F expression was able to increase the SF2 value by reducing the sensitivity of these cells to radiation-induced mitotic cell death. Moreover, RhoB-F cells showed an increased G2 arrest and an inhibition of centrosome overduplication following irradiation mediated by the Rho-kinase, strongly suggesting that RhoB-F may control centrosome overduplication during the G2 arrest after irradiation. Overall, our results for the first time clearly implicate farnesylated RhoB as a crucial protein in mediating cellular resistance to radiation-induced nonapoptotic cell death.
引用
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页码:492 / 501
页数:9
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