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CD38 is critical for social behaviour by regulating oxytocin secretion
Authors:Jin Duo  Liu Hong-Xiang  Hirai Hirokazu  Torashima Takashi  Nagai Taku  Lopatina Olga  Shnayder Natalia A  Yamada Kiyofumi  Noda Mami  Seike Toshihiro  Fujita Kyota  Takasawa Shin  Yokoyama Shigeru  Koizumi Keita  Shiraishi Yoshitake  Tanaka Shigenori  Hashii Minako  Yoshihara Toru  Higashida Kazuhiro  Islam Mohammad Saharul  Yamada Nobuaki  Hayashi Kenshi  Noguchi Naoya  Kato Ichiro  Okamoto Hiroshi  Matsushima Akihiro  Salmina Alla  Munesue Toshio  Shimizu Nobuaki  Mochida Sumiko  Asano Masahide  Higashida Haruhiro
Institution:Kanazawa University 21st Century COE Program on Innovative Brain Science on Development, Learning and Memory, Kanazawa 920-8640, Japan.
Abstract:CD38, a transmembrane glycoprotein with ADP-ribosyl cyclase activity, catalyses the formation of Ca2+ signalling molecules, but its role in the neuroendocrine system is unknown. Here we show that adult CD38 knockout (CD38-/-) female and male mice show marked defects in maternal nurturing and social behaviour, respectively, with higher locomotor activity. Consistently, the plasma level of oxytocin (OT), but not vasopressin, was strongly decreased in CD38-/- mice. Replacement of OT by subcutaneous injection or lentiviral-vector-mediated delivery of human CD38 in the hypothalamus rescued social memory and maternal care in CD38-/- mice. Depolarization-induced OT secretion and Ca2+ elevation in oxytocinergic neurohypophysial axon terminals were disrupted in CD38-/- mice; this was mimicked by CD38 metabolite antagonists in CD38+/+ mice. These results reveal that CD38 has a key role in neuropeptide release, thereby critically regulating maternal and social behaviours, and may be an element in neurodevelopmental disorders.
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