Serotonin Regulates Adult β-Cell Mass by Stimulating Perinatal β-Cell Proliferation.

Moon, Joon Ho; Kim, Yeong Gi; Kim, Kyuho; Osonoi, Sho; Wang, Shuang; Saunders, Diane C; Wang, Juehu; Yang, Katherine et al. · Diabetes · 2020

basic_science · Level V

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Abstract

A sufficient β-cell mass is crucial for preventing diabetes, and perinatal β-cell proliferation is important in determining the adult β-cell mass. However, it is not yet known how perinatal β-cell proliferation is regulated. Here, we report that serotonin regulates β-cell proliferation through serotonin receptor 2B (HTR2B) in an autocrine/paracrine manner during the perinatal period. In β-cell-specific <i>Tph1</i> knockout (<i>Tph1</i> βKO) mice, perinatal β-cell proliferation was reduced along with the loss of serotonin production in β-cells. Adult <i>Tph1</i> βKO mice exhibited glucose intolerance with decreased β-cell mass. Disruption of <i>Htr2b</i> in β-cells also resulted in decreased perinatal β-cell proliferation and glucose intolerance in adulthood. Growth hormone (GH) was found to induce serotonin production in β-cells through activation of STAT5 during the perinatal period. Thus, our results indicate that GH-GH receptor-STAT5-serotonin-HTR2B signaling plays a critical role in determining the β-cell mass by regulating perinatal β-cell proliferation, and defects in this pathway affect metabolic phenotypes in adults.

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