Different Metabolic Responses in Alpha-, Beta-, and Delta-cells of the Islet of Langerhans Monitored by Redox Confocal Microscopy.
From: Institute of Bioengineering, Miguel Hernandez University, Sant Joan d’ Alacant, Spain. ivanq@umh.es
Biophysical journal
- Publish Date: Apr 2006
- ISSN: 0006-3495
- Volume: 90
- Issue: 7
- Pages: 2641-50
- Medium: Print
- Language: English
- Citation (JAMA): Quesada Ivan, Todorova Mariana G, Soria Bernat, et al. Different Metabolic Responses in Alpha-, Beta-, and Delta-cells of the Islet of Langerhans Monitored by Redox Confocal Microscopy.. Biophys. J. Apr 2006;90:2641-50
Abstract
Blood glucose homeostasis is mainly achieved by the coordinated function of pancreatic alpha-, beta-, and delta-cells, which secrete glucagon, insulin, and somatostatin, respectively. Each cell type responds to glucose changes with different secretion patterns. Currently, considerable information can be found about the signal transduction mechanisms that lead to glucose-mediated insulin release in the pancreatic beta-cell, mitochondrial activation being an essential step. Increases in glucose stimulate the mitochondrial metabolism, activating the tricarboxylic acid cycle and raising the source of redox electron carrier molecules needed for respiratory ATP synthesis. However, little is known about the glucose-induced mitochondrial response of non-beta-cells and its role in the stimulus-secretion coupling process. This limited information is probably a result of the scarcity of these cells in the islet, the lack of identification patterns, and the technical limitations of conventional methods. In this study, we used flavin adenine dinucleotide redox confocal microscopy as a noninvasive technique to specifically monitor mitochondrial redox responses in immunoidentified alpha-, beta-, and delta-cells in freshly isolated intact islets and in dispersed cultured cells. We have shown that glucose provokes metabolic changes in beta- and delta-cell populations in a dose-dependent manner. Conversely, no significant responses were observed in alpha-cells, despite the sensitivity of their metabolism to drugs acting on the mitochondrial function, and their intact ability to develop Ca2+ signals. Identical results were obtained in islets and in cultures of dispersed cells. Our findings indicate metabolic differences in glucose utilization among the alpha-, beta-, and delta-cell populations, which might be important in the signal transduction events that lead to hormone release.
Mesh Headings (Keywords): Adenosine Triphosphate, Animals, Argon, Blood Glucose, Calcium, Cell Survival, Cells, Cultured, Dose-Response Relationship, Drug, Electrons, Glucose, Immunohistochemistry, Insulin, Insulin-Secreting Cells, Islets of Langerhans, Kinetics, Lasers, Mice, Microscopy, Confocal, Microscopy, Fluorescence, Oxidation-Reduction, Signal Transduction, Somatostatin-Secreting Cells, Time Factors, Tricarboxylic Acids
Check for Full Text / PubMed Unique Identifier (PMID): 16399832
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