Prion protein protects human neurons against Bax-mediated apoptosis

被引:293
作者
Bounhar, Y
Zhang, Y
Goodyer, CG
LeBlanc, A
机构
[1] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Bloomfield Ctr Res Aging, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2T5, Canada
[3] McGill Univ, Dept Pediat, Montreal, PQ H3A 2T5, Canada
关键词
D O I
10.1074/jbc.C100443200
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
The function of the cellular prion protein (PrP) is still poorly understood. We present here an unprecedented role for PrP against Bax-mediated neuronal apoptosis and show that PrP potently inhibits Bax-induced cell death in human primary neurons. Deletion of four octapeptide repeats of PrP (PrP Delta OR) and familial D178N and T183A PrP mutations completely or partially eliminate the neuroprotective effect of PrP. PrP remains anti-apoptotic despite truncation of the glycosylphosphatidylinositol (GPI) anchor signal peptide, indicating that the neuroprotective form of PrP does not require the abundant cell surface GPI-anchored PrP. Our results implicate PrP as a potent and novel anti-apoptotic protein against Bax-mediated cell death.
引用
收藏
页码:39145 / 39149
页数:5
相关论文
共 42 条
[1]   The Bcl-2 protein family: Arbiters of cell survival [J].
Adams, JM ;
Cory, S .
SCIENCE, 1998, 281 (5381) :1322-1326
[2]   SCRAPIE AND CELLULAR PRION PROTEINS DIFFER IN THEIR KINETICS OF SYNTHESIS AND TOPOLOGY IN CULTURED-CELLS [J].
BORCHELT, DR ;
SCOTT, M ;
TARABOULOS, A ;
STAHL, N ;
PRUSINER, SB .
JOURNAL OF CELL BIOLOGY, 1990, 110 (03) :743-752
[3]   Normal prion protein has an activity like that of superoxide dismutase [J].
Brown, DR ;
Wong, BS ;
Hafiz, F ;
Clive, C ;
Haswell, SJ ;
Jones, IM .
BIOCHEMICAL JOURNAL, 1999, 344 :1-5
[4]   Prion protein-deficient cells show altered response to oxidative stress due to decreased SOD-1 activity [J].
Brown, DR ;
SchulzSchaeffer, WJ ;
Schmidt, B ;
Kretzschmar, HA .
EXPERIMENTAL NEUROLOGY, 1997, 146 (01) :104-112
[5]   NORMAL DEVELOPMENT AND BEHAVIOR OF MICE LACKING THE NEURONAL CELL-SURFACE PRP PROTEIN [J].
BUELER, H ;
FISCHER, M ;
LANG, Y ;
BLUETHMANN, H ;
LIPP, HP ;
DEARMOND, SJ ;
PRUSINER, SB ;
AGUET, M ;
WEISSMANN, C .
NATURE, 1992, 356 (6370) :577-582
[6]   CELLULAR ISOFORM OF THE SCRAPIE AGENT PROTEIN PARTICIPATES IN LYMPHOCYTE-ACTIVATION [J].
CASHMAN, NR ;
LOERTSCHER, R ;
NALBANTOGLU, J ;
SHAW, I ;
KASCSAK, RJ ;
BOLTON, DC ;
BENDHEIM, PE .
CELL, 1990, 61 (01) :185-192
[7]   Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation [J].
Chiesa, R ;
Drisaldi, B ;
Quaglio, E ;
Migheli, A ;
Piccardo, P ;
Ghetti, B ;
Harris, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5574-5579
[8]   PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION [J].
COLLINGE, J ;
WHITTINGTON, MA ;
SIDLE, KCL ;
SMITH, CJ ;
PALMER, MS ;
CLARKE, AR ;
JEFFERYS, JGR .
NATURE, 1994, 370 (6487) :295-297
[9]   Golgi-disturbing agents [J].
Dinter, A ;
Berger, EG .
HISTOCHEMISTRY AND CELL BIOLOGY, 1998, 109 (5-6) :571-590
[10]   A NEUROTOXIC PRION PROTEIN-FRAGMENT INDUCES RAT ASTROGLIAL PROLIFERATION AND HYPERTROPHY [J].
FORLONI, G ;
DELBO, R ;
ANGERETTI, N ;
CHIESA, R ;
SMIROLDO, S ;
DONI, R ;
GHIBAUDI, E ;
SALMONA, M ;
PORRO, M ;
VERGA, L ;
GIACCONE, G ;
BUGIANI, O ;
TAGLIAVINI, F .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (09) :1415-1422