Abolished InsP(3)R2 function inhibits sweat secretion in both humans and mice

作者：Klar Joakim; Hisatsune Chihiro; Baig Shahid M; Tariq Muhammad; Johansson Anna C V; Rasool Mahmood; Malik Naveed Altaf; Ameur Adam; Sugiura Kotomi; Feuk Lars; Mikoshiba Katsuhiko; Dahl Niklas^*

来源：Journal of Clinical Investigation, 2014, 124(11): 4773-4780.

DOI：10.1172/JCI70720

There are 3 major sweat-producing glands present in skin; eccrine, apocrine, and apoeccrine glands. Due to the high rate of secretion, eccrine sweating is a vital regulator of body temperature in response to thermal stress in humans; therefore, an inability to sweat (anhidrosis) results in heat intolerance that may cause impaired consciousness and death. Here, we have reported 5 members of a consanguineous family with generalized, isolated anhidrosis, but morphologically normal eccrine sweat glands. Whole-genome analysis identified the presence of a homozygous missense mutation in ITPR2, which encodes the type 2 inositol 1,4,5-trisphosphate receptor (InsP(3)R2), that was present in all affected family members. We determined that the mutation is localized within the pore forming region of InsP(3)R2 and abrogates Ca2+ release from the endoplasmic reticulum, which suggests that intracellular Ca2+ release by InsP(3)R2 in clear cells of the sweat glands is important for eccrine sweat production. Itpr2(-/-) mice exhibited a marked reduction in sweat secretion, and evaluation of sweat glands from Itpr2(-/-) animals revealed a decrease in Ca2+ response compared with controls. Together, our data indicate that loss of InsP(3)R2-mediated Ca2+ release causes isolated anhidrosis in humans and suggest that specific InsP(3)R inhibitors have the potential to reduce sweat production in hyperhidrosis.

• 出版日期2014-11
• 单位RIKEN