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Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells

Small and big mouse islets were compared with special reference to their content of glucagon-producing α-cells and somatostatin-producing δ-cells. Areas stained for glucagon and somatostatin were measured in the largest cross section of small (diameter < 60 μm) and big (diameter > 100 μm) isle...

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Detalles Bibliográficos
Autores principales: Lau, Joey, Grapengiesser, Eva, Hellman, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967688/
https://www.ncbi.nlm.nih.gov/pubmed/27504459
http://dx.doi.org/10.1155/2016/4930741
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author Lau, Joey
Grapengiesser, Eva
Hellman, Bo
author_facet Lau, Joey
Grapengiesser, Eva
Hellman, Bo
author_sort Lau, Joey
collection PubMed
description Small and big mouse islets were compared with special reference to their content of glucagon-producing α-cells and somatostatin-producing δ-cells. Areas stained for glucagon and somatostatin were measured in the largest cross section of small (diameter < 60 μm) and big (diameter > 100 μm) islets. Comparison of the areas indicated proportionally more δ- than α-cells in the small islets. After isolation with collagenase these islets were practically devoid of α-cells. We evaluated the functional importance of the islet size by measuring the Ca(2+) signal for insulin release. A majority of the small islets responded to the hyperpolarization action of somatostatin with periodic decrease of cytoplasmic Ca(2+) when glucose was elevated after tolbutamide blockade of the K(ATP) channels.
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spelling pubmed-49676882016-08-08 Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells Lau, Joey Grapengiesser, Eva Hellman, Bo J Diabetes Res Research Article Small and big mouse islets were compared with special reference to their content of glucagon-producing α-cells and somatostatin-producing δ-cells. Areas stained for glucagon and somatostatin were measured in the largest cross section of small (diameter < 60 μm) and big (diameter > 100 μm) islets. Comparison of the areas indicated proportionally more δ- than α-cells in the small islets. After isolation with collagenase these islets were practically devoid of α-cells. We evaluated the functional importance of the islet size by measuring the Ca(2+) signal for insulin release. A majority of the small islets responded to the hyperpolarization action of somatostatin with periodic decrease of cytoplasmic Ca(2+) when glucose was elevated after tolbutamide blockade of the K(ATP) channels. Hindawi Publishing Corporation 2016 2016-07-18 /pmc/articles/PMC4967688/ /pubmed/27504459 http://dx.doi.org/10.1155/2016/4930741 Text en Copyright © 2016 Joey Lau et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Lau, Joey
Grapengiesser, Eva
Hellman, Bo
Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title_full Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title_fullStr Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title_full_unstemmed Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title_short Small Mouse Islets Are Deficient in Glucagon-Producing Alpha Cells but Rich in Somatostatin-Secreting Delta Cells
title_sort small mouse islets are deficient in glucagon-producing alpha cells but rich in somatostatin-secreting delta cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967688/
https://www.ncbi.nlm.nih.gov/pubmed/27504459
http://dx.doi.org/10.1155/2016/4930741
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