Inositol 1,4,5-tripshosphate receptor, calcium signalling and huntington’s disease

Abstract

Huntington’s disease (HD) is an autosomal-dominant neurodegenerative disorder that has no cure. HD primarily affects medium spiny striatal neurons (MSN). HD is caused by polyglutamine (polyQ) expansion (exp) in the amino-terminal region of a protein huntingtin (Htt). The connection between polyQ expansion in Htt ^Expand MSN neurodegeneration remains elusive. My laboratory discovered that mutant Htt^Exp protein specifically binds to the carboxy-terminal region of the type 1 inositol 1,4,5-trisphosphatereceptor (InsP₃R1), an intracellular Ca²⁺ release channel. Moreover, we found thatHtt^Exp association with InsP₃R1 causes sensitization of InsP₃R1 to activation by InsP₃ in planar lipid bilayers and in primary MSN. Mutant Htt^Exp has also been shown to activate Ca²⁺-permeable NR2B-containing NMDA receptors. All these results suggested that deranged neuronal Ca²⁺ signaling may play an important role in pathogenesis of HDIn support of this idea, we demonstrated a connection between abnormal Ca²⁺ signaling and apoptosis of MSN cultured from YAC128 HD mouse model. These results indicate that InsP₃R and other Ca²⁺ signaling proteins should be considered as potential therapeutic targets for treatment of HD