Serotonin regulates adult β-cell mass by stimulating perinatal β-cell proliferation

  • Joon Ho Moon
  • , Yeong Gi Kim
  • , Kyuho Kim
  • , Sho Osonoi
  • , Shuang Wang
  • , Diane C. Saunders
  • , Juehu Wang
  • , Katherine Yang
  • , Hyeongseok Kim
  • , Junguee Lee
  • , Ji Seon Jeong
  • , Ronadip R. Banerjee
  • , Seung K. Kim
  • , Yingjie Wu
  • , Hiroki Mizukami
  • , Alvin C. Powers
  • , Michael S. German
  • , Hail Kim

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

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 Tph1 knockout (Tph1 bKO) mice, perinatal β-cell proliferation was reduced along with the loss of serotonin production in β-cells. Adult Tph1 bKO mice exhibited glucose intolerance with decreased β-cell mass. Disruption of Htr2b 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.

Original languageEnglish
Pages (from-to)205-214
Number of pages10
JournalDiabetes
Volume69
Issue number2
DOIs
StatePublished - 1 Feb 2020

Bibliographical note

Publisher Copyright:
© 2019 by the American Diabetes Association.

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