Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum

Summary: Pancreatic β-cell mass expands during pregnancy and regresses in the postpartum period in conjunction with dynamic metabolic demands on maternal glucose homeostasis. To understand transcriptional changes driving these adaptations in β-cells and other islet cell types, we performed single-ce...

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Main Authors: Jin-Yong Chung, Yongjie Ma, Dingguo Zhang, Hayden H. Bickerton, Eric Stokes, Sweta B. Patel, Hubert M. Tse, Joseph Feduska, Rob S. Welner, Ronadip R. Banerjee
Format: Article
Language:English
Published: Elsevier 2023-04-01
Series:iScience
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Online Access:http://www.sciencedirect.com/science/article/pii/S2589004223005163
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author Jin-Yong Chung
Yongjie Ma
Dingguo Zhang
Hayden H. Bickerton
Eric Stokes
Sweta B. Patel
Hubert M. Tse
Joseph Feduska
Rob S. Welner
Ronadip R. Banerjee
author_facet Jin-Yong Chung
Yongjie Ma
Dingguo Zhang
Hayden H. Bickerton
Eric Stokes
Sweta B. Patel
Hubert M. Tse
Joseph Feduska
Rob S. Welner
Ronadip R. Banerjee
author_sort Jin-Yong Chung
collection DOAJ
description Summary: Pancreatic β-cell mass expands during pregnancy and regresses in the postpartum period in conjunction with dynamic metabolic demands on maternal glucose homeostasis. To understand transcriptional changes driving these adaptations in β-cells and other islet cell types, we performed single-cell RNA sequencing on islets from virgin, late gestation, and early postpartum mice. We identified transcriptional signatures unique to gestation and the postpartum in β-cells, including induction of the AP-1 transcription factor subunits and other genes involved in the immediate-early response (IEGs). In addition, we found pregnancy and postpartum-induced changes differed within each endocrine cell type, and in endothelial cells and antigen-presenting cells within islets. Together, our data reveal insights into cell type–specific transcriptional changes responsible for adaptations by islet cells to pregnancy and their resolution postpartum.
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spelling doaj.art-e462455c24ea41eba113a99958e8fbf92023-04-01T08:51:08ZengElsevieriScience2589-00422023-04-01264106439Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartumJin-Yong Chung0Yongjie Ma1Dingguo Zhang2Hayden H. Bickerton3Eric Stokes4Sweta B. Patel5Hubert M. Tse6Joseph Feduska7Rob S. Welner8Ronadip R. Banerjee9Division of Endocrinology, Diabetes & Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USADepartment of Pharmacology, the University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, The University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, The University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADepartment of Pharmacology, University of Colorado Denver/Anschutz, Aurora, CO 80045, USADivision of Hematology and Oncology, Department of Medicine, The University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADepartment of Microbiology, the University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADepartment of Microbiology, the University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADivision of Hematology and Oncology, Department of Medicine, The University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294, USADivision of Endocrinology, Diabetes & Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA; Corresponding authorSummary: Pancreatic β-cell mass expands during pregnancy and regresses in the postpartum period in conjunction with dynamic metabolic demands on maternal glucose homeostasis. To understand transcriptional changes driving these adaptations in β-cells and other islet cell types, we performed single-cell RNA sequencing on islets from virgin, late gestation, and early postpartum mice. We identified transcriptional signatures unique to gestation and the postpartum in β-cells, including induction of the AP-1 transcription factor subunits and other genes involved in the immediate-early response (IEGs). In addition, we found pregnancy and postpartum-induced changes differed within each endocrine cell type, and in endothelial cells and antigen-presenting cells within islets. Together, our data reveal insights into cell type–specific transcriptional changes responsible for adaptations by islet cells to pregnancy and their resolution postpartum.http://www.sciencedirect.com/science/article/pii/S2589004223005163PregnancyMolecular physiologyTranscriptomics
spellingShingle Jin-Yong Chung
Yongjie Ma
Dingguo Zhang
Hayden H. Bickerton
Eric Stokes
Sweta B. Patel
Hubert M. Tse
Joseph Feduska
Rob S. Welner
Ronadip R. Banerjee
Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
iScience
Pregnancy
Molecular physiology
Transcriptomics
title Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
title_full Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
title_fullStr Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
title_full_unstemmed Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
title_short Pancreatic islet cell type–specific transcriptomic changes during pregnancy and postpartum
title_sort pancreatic islet cell type specific transcriptomic changes during pregnancy and postpartum
topic Pregnancy
Molecular physiology
Transcriptomics
url http://www.sciencedirect.com/science/article/pii/S2589004223005163
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