Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.

Newly synthesized hormones have been suggested to be preferentially secreted by various neuroendocrine cells. This observation indicates that there is a distinct population of secretory granules containing new and old hormones. Recent development of fluorescent timer proteins used in bovine adrenal...

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Main Authors: Ni Hou, Hideo Mogami, Chisato Kubota-Murata, Meng Sun, Toshiyuki Takeuchi, Seiji Torii
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3485036?pdf=render
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spelling doaj-adca35bd9bbf40b2bd0a8a2ed84413e42020-11-24T22:08:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4792110.1371/journal.pone.0047921Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.Ni HouHideo MogamiChisato Kubota-MurataMeng SunToshiyuki TakeuchiSeiji ToriiNewly synthesized hormones have been suggested to be preferentially secreted by various neuroendocrine cells. This observation indicates that there is a distinct population of secretory granules containing new and old hormones. Recent development of fluorescent timer proteins used in bovine adrenal chromaffin cells revealed that secretory vesicles segregate into distinct age-dependent populations. Here, we verify the preferential release of newly synthesized insulin in the pancreatic β-cell line, MIN6, using a combination of multi-labeling reporter systems with both fluorescent and biochemical procedures. This system allows hormones or granules of any age to be labeled, in contrast to the timer proteins, which require fluorescence shift time. Pulse-chase labeling with different color probes distinguishes insulin secretory granules by age, with younger granules having a predominantly intracellular localization rather than at the cell periphery.http://europepmc.org/articles/PMC3485036?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ni Hou
Hideo Mogami
Chisato Kubota-Murata
Meng Sun
Toshiyuki Takeuchi
Seiji Torii
spellingShingle Ni Hou
Hideo Mogami
Chisato Kubota-Murata
Meng Sun
Toshiyuki Takeuchi
Seiji Torii
Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
PLoS ONE
author_facet Ni Hou
Hideo Mogami
Chisato Kubota-Murata
Meng Sun
Toshiyuki Takeuchi
Seiji Torii
author_sort Ni Hou
title Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
title_short Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
title_full Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
title_fullStr Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
title_full_unstemmed Preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line MIN6.
title_sort preferential release of newly synthesized insulin assessed by a multi-label reporter system using pancreatic β-cell line min6.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Newly synthesized hormones have been suggested to be preferentially secreted by various neuroendocrine cells. This observation indicates that there is a distinct population of secretory granules containing new and old hormones. Recent development of fluorescent timer proteins used in bovine adrenal chromaffin cells revealed that secretory vesicles segregate into distinct age-dependent populations. Here, we verify the preferential release of newly synthesized insulin in the pancreatic β-cell line, MIN6, using a combination of multi-labeling reporter systems with both fluorescent and biochemical procedures. This system allows hormones or granules of any age to be labeled, in contrast to the timer proteins, which require fluorescence shift time. Pulse-chase labeling with different color probes distinguishes insulin secretory granules by age, with younger granules having a predominantly intracellular localization rather than at the cell periphery.
url http://europepmc.org/articles/PMC3485036?pdf=render
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