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Glycosylation modification of human prion protein provokes apoptosis in HeLa cells in vitro
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  • Glycosylation modification of human prion protein provokes apoptosis in HeLa cells in vitro
  • Glycosylation modification of human prion protein provokes apoptosis in HeLa cells in vitro
저자명
Yang. Yang,Chen. Lan,Pan. Hua-Zhen,Kou. Yi,Xu. Cai-Min
간행물명
BMB reports
권/호정보
2009년|42권 6호|pp.331-337 (7 pages)
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생화학분자생물학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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We investigate the correlation between the glycosylation modified prion proteins and apoptosis. The wild-type PRNP gene and four PRNP gene glycosylated mutants were transiently expressed in HeLa cells. The effect of apoptosis induced by PrP mutants was confirmed by MTT assay, Hochest staining, Annexin-V staining and PI staining. ROS test detected ROS generation within the cells. The mitochondrial membrane potential was analyzed by the flow cytometry. The expression levels of Bcl-xL, Bax, cleaved Caspase-9 proteins were analyzed by Western Blot. The results indicated that the expressed non-glycosylated PrP in HeLa cells obviously induced apoptosis, inhibited the growth of cells and reduced the mitochondrial membrane potential, and more ROS generation and low levels of the apoptosis-related proteins Bcl-xL, the activated the cleaved Caspase-9 proteins were found. The apoptosis induced by non-glycosylated PrP demonstrates that its underlying mechanism correlates with the mitochondria-mediated signal transduction pathway.