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Fluorescent protein vectors for pancreatic islet cell identification in live-cell imaging
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
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2016 (English)In: Pflügers Archiv: European Journal of Physiology, ISSN 0031-6768, E-ISSN 1432-2013, Vol. 468, no 10, 1765-1777 p.Article in journal (Refereed) Published
Abstract [en]

The islets of Langerhans contain different types of endocrine cells, which are crucial for glucose homeostasis. beta- and alpha-cells that release insulin and glucagon, respectively, are most abundant, whereas somatostatin-producing delta-cells and particularly pancreatic polypeptide-releasing PP-cells are more scarce. Studies of islet cell function are hampered by difficulties to identify the different cell types, especially in live-cell imaging experiments when immunostaining is unsuitable. The aim of the present study was to create a set of vectors for fluorescent protein expression with cell-type-specific promoters and evaluate their applicability in functional islet imaging. We constructed six adenoviral vectors for expression of red and green fluorescent proteins controlled by the insulin, preproglucagon, somatostatin, or pancreatic polypeptide promoters. After transduction of mouse and human islets or dispersed islet cells, a majority of the fluorescent cells also immunostained for the appropriate hormone. Recordings of the sub-plasma membrane Ca2+ and cAMP concentrations with a fluorescent indicator and a protein biosensor, respectively, showed that labeled cells respond to glucose and other modulators of secretion and revealed a striking variability in Ca2+ signaling among alpha-cells. The measurements allowed comparison of the phase relationship of Ca2+ oscillations between different types of cells within intact islets. We conclude that the fluorescent protein vectors allow easy identification of specific islet cell types and can be used in live-cell imaging together with organic dyes and genetically encoded biosensors. This approach will facilitate studies of normal islet physiology and help to clarify molecular defects and disturbed cell interactions in diabetic islets.

Place, publisher, year, edition, pages
2016. Vol. 468, no 10, 1765-1777 p.
Keyword [en]
Islets, alpha-cell, beta-cell, delta-cell, PP-cell, Insulin, Glucagon, Somatostatin, Pancreatic polypeptide, Ca2+, cAMP
National Category
Physiology
Identifiers
URN: urn:nbn:se:uu:diva-306746DOI: 10.1007/s00424-016-1864-zISI: 000384425500011PubMedID: 27539300OAI: oai:DiVA.org:uu-306746DiVA: diva2:1045429
Funder
Swedish Research Council, 325-2012-6778, 55X-06240Swedish Diabetes AssociationNovo NordiskEXODIAB - Excellence of Diabetes Research in Sweden
Available from: 2016-11-09 Created: 2016-11-03 Last updated: 2016-11-09Bibliographically approved

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Shuai, HongyanXu, YunjianYu, QianGylfe, ErikTengholm, Anders
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