Distinct hsp70 Domains Mediate Apoptosis-inducing Factor Release and Nuclear Accumulation

• Published in: The Journal of biological chemistry 2006-03, Vol.281 (12), p.7873-7880
• Main Authors: Ruchalski, Kathleen, Mao, Haiping, Li, Zhijian, Wang, Zhiyong, Gillers, Sara, Wang, Yihan, Mosser, Dick D., Gabai, Vladimir, Schwartz, John H., Borkan, Steven C.
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphatases - metabolism; Adenosine Triphosphate - chemistry; Adenoviridae - metabolism; Animals; Apoptosis; Apoptosis Inducing Factor - metabolism; bcl-2-Associated X Protein - metabolism; Cell Membrane - metabolism; Cell Nucleus - metabolism; Cytosol - metabolism; Dithiothreitol - chemistry; Gene Deletion; HSP70 Heat-Shock Proteins - chemistry; Humans; Hydrolysis; Immunoblotting; Immunoprecipitation; Kidney; Membrane Proteins - metabolism; Mice; Mitochondria - metabolism; Models, Statistical; Molecular Chaperones - metabolism; Opossums; Protein Structure, Tertiary
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M513728200

Although hsp70 antagonizes apoptosis-inducing factor (AIF)-mediated cell death, the relative importance of preventing its release from mitochondria versus sequestering leaked AIF in the cytosol remains controversial. To dissect these two protective mechanisms, hsp70 deletion mutants lacking either the chaperone function (hsp70-ΔEEVD) or ATPase function (hsp70-ΔATPase) were selectively overexpressed before exposing cells to a metabolic inhibitor, an insult sufficient to cause mitochondrial AIF release, nuclear AIF accumulation, and apoptosis. Compared with empty vector, overexpression of wild type human hsp70 inhibited bax activation and reduced mitochondrial AIF release after injury. In contrast, mutants lacking either the chaperone function (hsp70-ΔEEVD) or the ATP hydrolytic domain (hsp70-ΔATPase) failed to prevent mitochondrial AIF release. Although hsp70-ΔEEVD did not inhibit bax activation or mitochondrial membrane injury after cell stress, this hsp70 mutant co-immunoprecipitated with leaked AIF in injured cells and decreased nuclear AIF accumulation. In contrast, hsp70-ΔATPase did not interact with AIF either in intact cells or in a cell-free system and furthermore, failed to prevent nuclear AIF accumulation. These results demonstrate that mitochondrial protection against bax-mediated injury requires both intact chaperone and ATPase functions, whereas the ATPase domain is critical for sequestering AIF in the cytosol.