Astrocyte apoptosis induced by HIV-1 transactivation of the c-kit protooncogene

被引:49
作者
He, JL
deCastro, CM
Vandenbark, GR
Busciglio, J
Gabuzda, D
机构
[1] HARVARD UNIV, SCH MED, DANA FARBER CANC INST, DIV HUMAN RETROVIROL, BOSTON, MA 02115 USA
[2] HARVARD UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02115 USA
[3] HARVARD UNIV, SCH MED, DEPT NEUROL, BOSTON, MA 02115 USA
[4] DUKE UNIV, MED CTR, DEPT MED, DIV HEMATOL ONCOL, DURHAM, NC 27710 USA
[5] CHILDRENS HOSP, DEPT NEUROL, MED CTR, BOSTON, MA 02115 USA
关键词
D O I
10.1073/pnas.94.8.3954
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
HIV-1 infection of the central nervous system (CNS) frequently causes dementia and other neurological disorders. The mechanisms of CNS injury in HIV-1 infection are poorly understood. Apoptosis of neurons and astrocytes is induced by HIV-1 infection ira vitro and in brain tissue from AIDS patients, but the apoptotic stimuli have not been identified. We report herein that HIV-1 infection of primary brain cultures induces the receptor tyrosine kinase protooncogene c-kit and that high levels of c-Kit expression are associated with astrocyte apoptosis. Overexpression of c-Kit in an astrocyte-derived cell line in the absence of HIV-1 induces rapid apoptotic death. The apoptotic mechanism requires the c-Kit tyrosine kinase domain. The mechanism of c-kit induction by HIV-1 involves transactivation of the c-kit promoter by the HIV-1 Nef protein. These studies demonstrate that c-Kit can induce astrocyte apoptosis and suggest that this mechanism may play a role in CNS injury caused by HIV-1 infection. We propose that c-Kit can serve dual functions as a growth factor receptor or apoptosis inducer.
引用
收藏
页码:3954 / 3959
页数:6
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