Inositol hexakisphosphate kinases induce cell death in Huntington disease.

نویسندگان

  • Eiichiro Nagata
  • Adolfo Saiardi
  • Hideo Tsukamoto
  • Yoshinori Okada
  • Yoshiko Itoh
  • Tadayuki Satoh
  • Johbu Itoh
  • Russell L Margolis
  • Shunya Takizawa
  • Akira Sawa
  • Shigeharu Takagi
چکیده

Inositol pyrophosphate diphosphoinositol pentakisphosphate is ubiquitously present in mammalian cells and contains highly energetic pyrophosphate bonds. We have previously reported that inositol hexakisphosphate kinase type 2 (InsP(6)K2), which converts inositol hexakisphosphate to inositol pyrophosphate diphosphoinositol pentakisphosphate, mediates apoptotic cell death via its translocation from the nucleus to the cytoplasm. Here, we report that InsP(6)K2 is localized mainly in the cytoplasm of lymphoblast cells from patients with Huntington disease (HD), whereas this enzyme is localized in the nucleus in control lymphoblast cells. The large number of autophagosomes detected in HD lymphoblast cells is consistent with the down-regulation of Akt in response to InsP(6)K2 activation. Consistent with these observations, the overexpression of InsP(6)Ks leads to the depletion of Akt phosphorylation and the induction of cell death. These results suggest that InsP(6)K2 activation is associated with the pathogenesis of HD.

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عنوان ژورنال:
  • The Journal of biological chemistry

دوره 286 30  شماره 

صفحات  -

تاریخ انتشار 2011