Cargando…

Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas

The leptin deficient ob/ob mouse is a widely used model for studies on initial aspects of metabolic disturbances leading to type 2 diabetes, including insulin resistance and obesity. Although it is generally accepted that ob/ob mice display a dramatic increase in β-cell mass to compensate for increa...

Descripción completa

Detalles Bibliográficos
Autores principales: Parween, Saba, Kostromina, Elena, Nord, Christoffer, Eriksson, Maria, Lindström, Per, Ahlgren, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054357/
https://www.ncbi.nlm.nih.gov/pubmed/27713548
http://dx.doi.org/10.1038/srep34885
_version_ 1782458580896579584
author Parween, Saba
Kostromina, Elena
Nord, Christoffer
Eriksson, Maria
Lindström, Per
Ahlgren, Ulf
author_facet Parween, Saba
Kostromina, Elena
Nord, Christoffer
Eriksson, Maria
Lindström, Per
Ahlgren, Ulf
author_sort Parween, Saba
collection PubMed
description The leptin deficient ob/ob mouse is a widely used model for studies on initial aspects of metabolic disturbances leading to type 2 diabetes, including insulin resistance and obesity. Although it is generally accepted that ob/ob mice display a dramatic increase in β-cell mass to compensate for increased insulin demand, the spatial and quantitative dynamics of β-cell mass distribution in this model has not been assessed by modern optical 3D imaging techniques. We applied optical projection tomography and ultramicroscopy imaging to extract information about individual islet β-cell volumes throughout the volume of ob/ob pancreas between 4 and 52 weeks of age. Our data show that cystic lesions constitute a significant volume of the hyperplastic ob/ob islets. We propose that these lesions are formed by a mechanism involving extravasation of red blood cells/plasma due to increased islet vessel blood flow and vessel instability. Further, our data indicate that the primary lobular compartments of the ob/ob pancreas have different potentials for expanding their β-cell population. Unawareness of the characteristics of β-cell expansion in ob/ob mice presented in this report may significantly influence ex vivo and in vivo assessments of this model in studies of β-cell adaptation and function.
format Online
Article
Text
id pubmed-5054357
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-50543572016-10-19 Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas Parween, Saba Kostromina, Elena Nord, Christoffer Eriksson, Maria Lindström, Per Ahlgren, Ulf Sci Rep Article The leptin deficient ob/ob mouse is a widely used model for studies on initial aspects of metabolic disturbances leading to type 2 diabetes, including insulin resistance and obesity. Although it is generally accepted that ob/ob mice display a dramatic increase in β-cell mass to compensate for increased insulin demand, the spatial and quantitative dynamics of β-cell mass distribution in this model has not been assessed by modern optical 3D imaging techniques. We applied optical projection tomography and ultramicroscopy imaging to extract information about individual islet β-cell volumes throughout the volume of ob/ob pancreas between 4 and 52 weeks of age. Our data show that cystic lesions constitute a significant volume of the hyperplastic ob/ob islets. We propose that these lesions are formed by a mechanism involving extravasation of red blood cells/plasma due to increased islet vessel blood flow and vessel instability. Further, our data indicate that the primary lobular compartments of the ob/ob pancreas have different potentials for expanding their β-cell population. Unawareness of the characteristics of β-cell expansion in ob/ob mice presented in this report may significantly influence ex vivo and in vivo assessments of this model in studies of β-cell adaptation and function. Nature Publishing Group 2016-10-07 /pmc/articles/PMC5054357/ /pubmed/27713548 http://dx.doi.org/10.1038/srep34885 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Parween, Saba
Kostromina, Elena
Nord, Christoffer
Eriksson, Maria
Lindström, Per
Ahlgren, Ulf
Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title_full Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title_fullStr Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title_full_unstemmed Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title_short Intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3D imaging of intact pancreas
title_sort intra-islet lesions and lobular variations in β-cell mass expansion in ob/ob mice revealed by 3d imaging of intact pancreas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054357/
https://www.ncbi.nlm.nih.gov/pubmed/27713548
http://dx.doi.org/10.1038/srep34885
work_keys_str_mv AT parweensaba intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas
AT kostrominaelena intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas
AT nordchristoffer intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas
AT erikssonmaria intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas
AT lindstromper intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas
AT ahlgrenulf intraisletlesionsandlobularvariationsinbcellmassexpansioninobobmicerevealedby3dimagingofintactpancreas