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血清剥夺诱导的ZrchI朊蛋白(PrP)基因缺陷神经元细胞系凋亡被PrP抑制,且不依赖于多配体蛋白聚糖。

Serum withdrawal-induced apoptosis in ZrchI prion protein (PrP) gene-deficient neuronal cell line is suppressed by PrP, independent of Doppel.

作者信息

Nishimura Takuya, Sakudo Akikazu, Hashiyama Yoriko, Yachi Akiko, Saeki Keiichi, Matsumoto Yoshitsugu, Ogawa Masaharu, Sakaguchi Suehiro, Itohara Shigeyoshi, Onodera Takashi

机构信息

Department of Molecular Immunology, School of Agricultural and Life Sciences, University of Tokyo, Tokyo, Japan.

出版信息

Microbiol Immunol. 2007;51(4):457-66. doi: 10.1111/j.1348-0421.2007.tb03920.x.

Abstract

Previous studies have shown that cellular prion protein (PrP(C)) plays anti-apoptotic and antioxidative role against cell death induced by serum-deprivation (SDP) in an immortalized prion protein gene-deficient neuronal cell line derived from Rikn prion protein (PrP) gene-deficient (Prnp(-/-)) mice, which ectopically produce excess Doppel (Dpl) (PrP-like glycoprotein). To investigate whether PrP(C) inhibits apoptotic neuronal cell death without Dpl, an immortalized cell line was established from the brain of ZrchI Prnp(-/-) mice, which do not show ectopic expression of Dpl. The results using a ZrchI neuronal Prnp(-/-) cell line (NpL2) showed that PrP(C) potently inhibited SDP-induced apoptotic cell death. Furthermore, PrP(C) expression enhanced the superoxide dismutase (SOD) activity in NpL2 cells. These results indicate that Dpl production did not affect anti-apoptotic and anti-oxidative functions of PrP, suggesting that PrP(C) may be directly correlated with protection against oxidative stress.

摘要

先前的研究表明,在源自里肯朊病毒蛋白(PrP)基因缺陷(Prnp(-/-))小鼠的永生化朊病毒蛋白基因缺陷神经元细胞系中,细胞朊病毒蛋白(PrP(C))对血清剥夺(SDP)诱导的细胞死亡发挥抗凋亡和抗氧化作用,该细胞系异位产生过量的多普蛋白(Dpl)(PrP样糖蛋白)。为了研究PrP(C)是否在没有Dpl的情况下抑制凋亡性神经元细胞死亡,从ZrchI Prnp(-/-)小鼠的大脑中建立了一个永生化细胞系,该小鼠不显示Dpl的异位表达。使用ZrchI神经元Prnp(-/-)细胞系(NpL2)的结果表明,PrP(C)有力地抑制了SDP诱导的凋亡细胞死亡。此外,PrP(C)的表达增强了NpL2细胞中的超氧化物歧化酶(SOD)活性。这些结果表明,Dpl的产生并不影响PrP的抗凋亡和抗氧化功能,提示PrP(C)可能与抵抗氧化应激直接相关。

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