A novel paraptosis pathway involving LEI/L-DNasell for EGF-induced cell death in somato-lactotrope pituitary cells

被引:42
作者
Fombonne, J
Padrón, L
Enjalbert, A
Krantic, S
Torriglia, A
机构
[1] INSERM, Inst Neurobiol Mediterranee INMED, U29, F-13273 Marseille 09, France
[2] Univ Mediterranee, CNRS, Inst Jean Roche, UMR6544,Fac Med Nord, F-13916 Marseille, France
[3] INSERM, U598, F-75005 Paris, France
关键词
AIP-1/Alix; caspase-independent pathway; L-DNasell; paraptosis;
D O I
10.1007/s10495-006-4568-6
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
We have recently reported that EGF triggers an original form of cell death in pituitary cell line (GH4C1) with a phenotype sharing some characteristics of both apoptosis (internucleosomal DNA fragmentation) and paraptosis (caspase-independence and cytoplasmic vacuolization). However, the endonuclease involved in EGF-induced DNA fragmentation has not been assessed so far. In the present work we therefore further explored the putative paraptosis involvement in EGF-induced cell death and asked whether L-DNasell might be involved. Indeed, this endonuclease is known to mediate internucleosomal DNA fragmentation in caspase independent manner. Our Western blot, immunocytochemistry and enzymatic measurement assays show that EGF triggers a cleavage of Leukocyte Elastase Inhibitor (LEI) precursor into L-DNasell, its subsequent enzymatic activation and nuclear translocation thus pointing to the involvement of this endonuclease pathway in caspase-independent DNA fragmentation. In addition, EGF-induced cell death can be blocked by paraptosis inhibitor AIP-1/Alix, but not with its anti-apoptotic C-terminal fragment (Alix-CT). Altogether these data suggest that EGF-induced cell death defines a novel, L-DNasell-mediated form of paraptosis.
引用
收藏
页码:367 / 375
页数:9
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