BAG3 Protein Regulates Caspase-3 Activation in HIV-1-Infected Human Primary Microglial Cells

被引:34
作者
Rosati, Alessandra [3 ]
Khalili, Kamel [1 ,2 ]
Deshmane, Satish L. [1 ,2 ]
Radhakrishnan, Sujatha [1 ,2 ]
Pascale, Maria [3 ]
Turco, M. Caterina [3 ]
Marzullo, Liberato [3 ]
机构
[1] Temple Univ, Sch Med, Dept Neurosci, Philadelphia, PA 19122 USA
[2] Temple Univ, Sch Med, Ctr Neurovirol, Philadelphia, PA 19122 USA
[3] Univ Salerno, Dept Pharmaceut Sci DiFarma, I-84100 Salerno, Italy
关键词
BCL-2-BINDING PROTEIN; OXIDATIVE STRESS; REACTIVE ASTROCYTES; HIV-INFECTION; APOPTOSIS; SURVIVAL; GENE; EXPRESSION; COMPLEX; DEATH;
D O I
10.1002/jcp.21604
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BAG3, a member of the BAG co-chaperones family, is expressed in several cell types subjected to stressful conditions, such as exposure to high temperature, heavy metals, drugs. Furthermore, it is constitutively expressed in some tumors. Among the biological activities of the protein, there is apoptosis downmodulation; this appears to be exerted through BAG3 interaction with the heat shock protein (Hsp) 70, that influences cell apoptosis at several levels. We recently reported that BAG3 protein was detectable in the cytoplasm of reactive astrocytes in HIV-1-associated encephalopathy biopsies. Here we report that downmodulation of BAG3 protein levels allows caspase-3 activation by HIV-1 infection in human primary microglial cells. This is the first reported evidence of a role for BAG3 in the balance of death versus survival during viral infection.
引用
收藏
页码:264 / 267
页数:4
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