Abstract

Pancreatic β-cell mass is known to be considerably altered during pregnancy and after parturition in rodents and humans. While β-cell mass increases during pregnancy and starts to return toward its original level after parturition, the cellular mechanisms by which β-cell mass during this period is regulated remains unclear. To address this issue in mice, we quantified β-cell mass and investigated the mechanisms underlying its regulation throughout the perinatal and postpartum period. The increased β-cell size and proliferation during pregnancy were significantly reduced shortly after parturition, whereas there was no evidence of β-cell reprogramming or increased apoptosis. Direct RNA sequencing of islets from pregnant and postpartum mice demonstrated dynamic changes in gene expression patterns, showing robust downregulation of cell cycle-related genes 1 day after parturition, and the reupregulation of serotonin metabolism-related genes at postpartum day 7. Serotonin synthesis was activated only in lactating females, accompanied by increased β-cell mass. Taken together, these findings demonstrate that β-cell mass is decreased shortly after parturition owing to reduced β-cell size and proliferation, and is subsequently increased, in association with lactation and serotonin biosynthesis.

Highlights

  • Pancreatic β-cell mass is known to be considerably altered during pregnancy and after parturition in rodents and humans

  • Direct RNA-sequencing data from the islets of pregnant and postpartum female mice revealed the dynamic changes in mRNA profiles during the perinatal periods, showing robust downregulation of cell cycle-related genes shortly after parturition and re-upregulation of serotonin metabolism-related genes at postpartum day 7

  • To investigate temporal changes in total β-cell volume during the perinatal period, β-cell mass was quantified in non-pregnant females (NP), pregnant females at gestational day 18 (G18), and females on postpartum days 1, 7, and 21 (P1, P7, and P21, respectively) in mice on a C57BL/6 J background at 12–13 weeks of age (Fig. 1A)

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Summary

Introduction

Pancreatic β-cell mass is known to be considerably altered during pregnancy and after parturition in rodents and humans. Direct RNA-sequencing data from the islets of pregnant and postpartum female mice revealed the dynamic changes in mRNA profiles during the perinatal periods, showing robust downregulation of cell cycle-related genes shortly after parturition and re-upregulation of serotonin metabolism-related genes at postpartum day 7. Serotonin production is activated only in lactating females, accompanied by increased β-cell mass, suggesting that lactation plays a www.nature.com/scientificreports role in expanding β-cell mass after parturition as well as placental lactogen during pregnancy. Understanding and controlling this process during the perinatal period may provide us with novel methods for expanding β-cell mass to treat diabetes mellitus

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