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4Pi microscopy reveals an impaired three-dimensional mitochondrial network of pancreatic islet beta-cells, an experimental model of type-2 diabetes
Andrea Dlasková, Tomáš Špaček, Jitka Šantorová, Lydie Plecitá-Hlavatá, Zuzana Berková, František Saudek, Mark Lessard, Joerg Bewersdorf, Petr Ježek
Jazyk angličtina Země Nizozemsko
Typ dokumentu práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.
Grantová podpora
NR9183
MZ0
CEP - Centrální evidence projektů
- MeSH
- beta-buňky * patologie ultrastruktura MeSH
- diabetes mellitus 2. typu * patologie MeSH
- inzulinom patologie MeSH
- konfokální mikroskopie * metody MeSH
- krysa rodu rattus MeSH
- mitochondrie * patologie ultrastruktura MeSH
- modely nemocí na zvířatech MeSH
- nádorové buněčné linie MeSH
- nádory slinivky břišní patologie MeSH
- potkani Wistar MeSH
- rekombinantní fúzní proteiny genetika MeSH
- techniky in vitro MeSH
- transfekce MeSH
- zelené fluorescenční proteiny genetika MeSH
- zobrazování trojrozměrné MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
- Publikační typ
- práce podpořená grantem MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
Insulin production in pancreatic beta-cells is critically linked to mitochondrial oxidative phosphorylation. Increased ATP production triggered by blood glucose represents the beta-cells' glucose sensor. Type-2 diabetes mellitus results from insulin resistance in peripheral tissues and impaired insulin secretion. Pathology of diabetic beta-cells might be reflected by the altered morphology of mitochondrial network. Its characterization is however hampered by the complexity and density of the three-dimensional (3D) mitochondrial tubular networks in these cell types. Conventional confocal microscopy does not provide sufficient axial resolution to reveal the required details; electron tomography reconstruction of these dense networks is still difficult and time consuming. However, mitochondrial network morphology in fixed cells can also be studied by 4Pi microscopy, a laser scanning microscopy technique which provides an approximately 7-fold improved axial resolution (approximately 100 nm) over conventional confocal microscopy. Here we present a quantitative study of these networks in insulinoma INS-1E cells and primary beta-cells in Langerhans islets. The former were a stably-transfected cell line while the latter were transfected with lentivirus, both expressing mitochondrial matrix targeted redox-sensitive GFP. The mitochondrial networks and their partial disintegration and fragmentation are revealed by carefully created iso-surface plots and their quantitative analysis. We demonstrate that beta-cells within the Langerhans islets from diabetic Goto Kakizaki rats exhibited a more disintegrated mitochondrial network compared to those from control Wistar rats and model insulinoma INS-1E cells. Standardization of these patterns may lead to development of morphological diagnostics for Langerhans islets, for the assessment of beta-cell condition, before their transplantations. Copyright 2010 Elsevier B.V. All rights reserved.
Deparment of Cell Biology Yale University New Haven Connecticut USA
Imaging Science Services Tha Jackson Laboratory Bar Harbor Maine USA
Institute of Clinical and Experimental Medicine Prague Czech Republic
Citace poskytuje Crossref.org
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