Diabetes Center of Excellence; Program in Molecular Medicine; Department of Microbiology and Physiological Systems; Department of Medicine; Program in Bioinformatics and Integrative Biology; Garber Lab
Cellular and Molecular Physiology | Endocrine System Diseases | Endocrinology | Endocrinology, Diabetes, and Metabolism | Hormones, Hormone Substitutes, and Hormone Antagonists | Nucleic Acids, Nucleotides, and Nucleosides | Nutritional and Metabolic Diseases
Human pancreatic islets engrafted into immunodeficient mice serve as an important model for in vivo human diabetes studies. Following engraftment, islet function can be monitored in vivo by measuring circulating glucose and human insulin; however, it will be important to recover viable cells for more complex graft analyses. Moreover, RNA analyses of dissected grafts have not distinguished which hormone-specific cell types contribute to gene expression. We developed a method for recovering live cells suitable for fluorescence-activated cell sorting from human islets engrafted in mice. Although yields of recovered islet cells were relatively low, the ratios of bulk-sorted beta, alpha, and delta cells and their respective hormone-specific RNA-Seq transcriptomes are comparable pretransplant and posttransplant, suggesting that the cellular characteristics of islet grafts posttransplant closely mirror the original donor islets. Single-cell RNA-Seq transcriptome analysis confirms the presence of appropriate beta, alpha, and delta cell subsets. In addition, ex vivo perifusion of recovered human islet grafts demonstrated glucose-stimulated insulin secretion. Viable cells suitable for patch-clamp analysis were recovered from transplanted human embryonic stem cell-derived beta cells. Together, our functional and hormone-specific transcriptome analyses document the broad applicability of this system for longitudinal examination of human islet cells undergoing developmental/metabolic/pharmacogenetic manipulation in vivo and may facilitate the discovery of treatments for diabetes.
L‐type voltage‐gated calcium channel, RNA‐Seq, graft recovery, insulin, β cell
Rights and Permissions
© 2019 The Authors. The FASEB Journal published by Wiley Periodicals, Inc. on behalf of Federation of American Societies for Experimental Biology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
DOI of Published Version
Redick SD, Leehy L, Rittenhouse AR, Blodgett DM, Derr AG, Kucukural A, Garber MG, Shultz LD, Greiner DL, Wang JP, Harlan DM, Bortell R, Jurczyk A. Recovery of viable endocrine-specific cells and transcriptomes from human pancreatic islet-engrafted mice. FASEB J. 2020 Jan;34(1):1901-1911. doi: 10.1096/fj.201901022RR. Epub 2019 Dec 10. PMID: 31914605; PMCID: PMC6972551. Link to article on publisher's site
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Redick SD, Leehy L, Rittenhouse AR, Blodgett DM, Derr AG, Kucukural A, Garber M, Shultz LD, Greiner DL, Wang JP, Harlan DM, Bortell R, Jurczyk A. (2020). Recovery of viable endocrine-specific cells and transcriptomes from human pancreatic islet-engrafted mice. Program in Molecular Medicine Publications. https://doi.org/10.1096/fj.201901022RR. Retrieved from https://escholarship.umassmed.edu/pmm_pp/142
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
Cellular and Molecular Physiology Commons, Endocrine System Diseases Commons, Endocrinology Commons, Endocrinology, Diabetes, and Metabolism Commons, Hormones, Hormone Substitutes, and Hormone Antagonists Commons, Nucleic Acids, Nucleotides, and Nucleosides Commons, Nutritional and Metabolic Diseases Commons