AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells

Abstract The study of primary glucagon-secreting α-cells is hampered by their low abundance and scattered distribution in rodent pancreatic islets. We have designed a double-stranded adeno-associated virus containing a rat proglucagon promoter (700 bp) driving enhanced green fluorescent protein (AAV...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Eva Tudurí, Maria M. Glavas, Ali Asadi, Robert K. Baker, Cara E. Ellis, Galina Soukhatcheva, Marjolaine Philit, Frank K. Huynh, James D. Johnson, C. Bruce Verchere, Timothy J. Kieffer
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2019
Materias:
R
Q
Acceso en línea:https://doaj.org/article/556a5308d1314702b2cd07d70fc68443
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:556a5308d1314702b2cd07d70fc68443
record_format dspace
spelling oai:doaj.org-article:556a5308d1314702b2cd07d70fc684432021-12-02T16:08:05ZAAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells10.1038/s41598-019-46735-22045-2322https://doaj.org/article/556a5308d1314702b2cd07d70fc684432019-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-019-46735-2https://doaj.org/toc/2045-2322Abstract The study of primary glucagon-secreting α-cells is hampered by their low abundance and scattered distribution in rodent pancreatic islets. We have designed a double-stranded adeno-associated virus containing a rat proglucagon promoter (700 bp) driving enhanced green fluorescent protein (AAV GCG-EGFP), to specifically identify α-cells. The administration of AAV GCG-EGFP by intraperitoneal or intraductal injection led to EGFP expression selectively in the α-cell population. AAV GCG-EGFP delivery to mice followed by islet isolation, dispersion and separation by FACS for EGFP resulted in an 86% pure population of α-cells. Furthermore, the administration of AAV GCG-EGFP at various doses to adult wild type mice did not significantly alter body weight, blood glucose, plasma insulin or glucagon levels, glucose tolerance or arginine tolerance. In vitro experiments in transgene positive α-cells demonstrated that EGFP expression did not alter the intracellular Ca2+ pattern in response to glucose or adrenaline. This approach may be useful for studying purified primary α-cells and for the in vivo delivery of other genes selectively to α-cells to further probe their function or to manipulate them for therapeutic purposes.Eva TuduríMaria M. GlavasAli AsadiRobert K. BakerCara E. EllisGalina SoukhatchevaMarjolaine PhilitFrank K. HuynhJames D. JohnsonC. Bruce VerchereTimothy J. KiefferNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 9, Iss 1, Pp 1-11 (2019)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Eva Tudurí
Maria M. Glavas
Ali Asadi
Robert K. Baker
Cara E. Ellis
Galina Soukhatcheva
Marjolaine Philit
Frank K. Huynh
James D. Johnson
C. Bruce Verchere
Timothy J. Kieffer
AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
description Abstract The study of primary glucagon-secreting α-cells is hampered by their low abundance and scattered distribution in rodent pancreatic islets. We have designed a double-stranded adeno-associated virus containing a rat proglucagon promoter (700 bp) driving enhanced green fluorescent protein (AAV GCG-EGFP), to specifically identify α-cells. The administration of AAV GCG-EGFP by intraperitoneal or intraductal injection led to EGFP expression selectively in the α-cell population. AAV GCG-EGFP delivery to mice followed by islet isolation, dispersion and separation by FACS for EGFP resulted in an 86% pure population of α-cells. Furthermore, the administration of AAV GCG-EGFP at various doses to adult wild type mice did not significantly alter body weight, blood glucose, plasma insulin or glucagon levels, glucose tolerance or arginine tolerance. In vitro experiments in transgene positive α-cells demonstrated that EGFP expression did not alter the intracellular Ca2+ pattern in response to glucose or adrenaline. This approach may be useful for studying purified primary α-cells and for the in vivo delivery of other genes selectively to α-cells to further probe their function or to manipulate them for therapeutic purposes.
format article
author Eva Tudurí
Maria M. Glavas
Ali Asadi
Robert K. Baker
Cara E. Ellis
Galina Soukhatcheva
Marjolaine Philit
Frank K. Huynh
James D. Johnson
C. Bruce Verchere
Timothy J. Kieffer
author_facet Eva Tudurí
Maria M. Glavas
Ali Asadi
Robert K. Baker
Cara E. Ellis
Galina Soukhatcheva
Marjolaine Philit
Frank K. Huynh
James D. Johnson
C. Bruce Verchere
Timothy J. Kieffer
author_sort Eva Tudurí
title AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
title_short AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
title_full AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
title_fullStr AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
title_full_unstemmed AAV GCG-EGFP, a new tool to identify glucagon-secreting α-cells
title_sort aav gcg-egfp, a new tool to identify glucagon-secreting α-cells
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/556a5308d1314702b2cd07d70fc68443
work_keys_str_mv AT evatuduri aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT mariamglavas aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT aliasadi aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT robertkbaker aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT caraeellis aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT galinasoukhatcheva aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT marjolainephilit aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT frankkhuynh aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT jamesdjohnson aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT cbruceverchere aavgcgegfpanewtooltoidentifyglucagonsecretingacells
AT timothyjkieffer aavgcgegfpanewtooltoidentifyglucagonsecretingacells
_version_ 1718384595049644032