Cargando…

Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels

Patients with type 1 diabetes have lower bone mineral density and higher risk of fractures. The role of osteoblasts in diabetes-related osteoporosis is well acknowledged whereas the role of osteoclasts (OCLs) is still unclear. We hypothesize that OCLs participate in pathological bone remodeling. We...

Descripción completa

Detalles Bibliográficos
Autores principales: Reni, Carlotta, Mangialardi, Giuseppe, Meloni, Marco, Madeddu, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965751/
https://www.ncbi.nlm.nih.gov/pubmed/27468810
http://dx.doi.org/10.1038/srep30639
_version_ 1782445308230238208
author Reni, Carlotta
Mangialardi, Giuseppe
Meloni, Marco
Madeddu, Paolo
author_facet Reni, Carlotta
Mangialardi, Giuseppe
Meloni, Marco
Madeddu, Paolo
author_sort Reni, Carlotta
collection PubMed
description Patients with type 1 diabetes have lower bone mineral density and higher risk of fractures. The role of osteoblasts in diabetes-related osteoporosis is well acknowledged whereas the role of osteoclasts (OCLs) is still unclear. We hypothesize that OCLs participate in pathological bone remodeling. We conducted studies in animals (streptozotocin-induced type 1 diabetic mice) and cellular models to investigate canonical and non-canonical mechanisms underlying excessive OCL activation. Diabetic mice show an increased number of active OCLs. In vitro studies demonstrate the involvement of acidosis in OCL activation and the implication of transient receptor potential cation channel subfamily V member 1 (TRPV1). In vivo studies confirm the establishment of local acidosis in the diabetic bone marrow (BM) as well as the ineffectiveness of insulin in correcting the pH variation and osteoclast activation. Conversely, treatment with TRPV1 receptor antagonists re-establishes a physiological OCL availability. These data suggest that diabetes causes local acidosis in the BM that in turn increases osteoclast activation through the modulation of TRPV1. The use of clinically available TRPV1 antagonists may provide a new means to combat bone problems associated with diabetes.
format Online
Article
Text
id pubmed-4965751
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49657512016-08-08 Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels Reni, Carlotta Mangialardi, Giuseppe Meloni, Marco Madeddu, Paolo Sci Rep Article Patients with type 1 diabetes have lower bone mineral density and higher risk of fractures. The role of osteoblasts in diabetes-related osteoporosis is well acknowledged whereas the role of osteoclasts (OCLs) is still unclear. We hypothesize that OCLs participate in pathological bone remodeling. We conducted studies in animals (streptozotocin-induced type 1 diabetic mice) and cellular models to investigate canonical and non-canonical mechanisms underlying excessive OCL activation. Diabetic mice show an increased number of active OCLs. In vitro studies demonstrate the involvement of acidosis in OCL activation and the implication of transient receptor potential cation channel subfamily V member 1 (TRPV1). In vivo studies confirm the establishment of local acidosis in the diabetic bone marrow (BM) as well as the ineffectiveness of insulin in correcting the pH variation and osteoclast activation. Conversely, treatment with TRPV1 receptor antagonists re-establishes a physiological OCL availability. These data suggest that diabetes causes local acidosis in the BM that in turn increases osteoclast activation through the modulation of TRPV1. The use of clinically available TRPV1 antagonists may provide a new means to combat bone problems associated with diabetes. Nature Publishing Group 2016-07-29 /pmc/articles/PMC4965751/ /pubmed/27468810 http://dx.doi.org/10.1038/srep30639 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
Reni, Carlotta
Mangialardi, Giuseppe
Meloni, Marco
Madeddu, Paolo
Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title_full Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title_fullStr Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title_full_unstemmed Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title_short Diabetes Stimulates Osteoclastogenesis by Acidosis-Induced Activation of Transient Receptor Potential Cation Channels
title_sort diabetes stimulates osteoclastogenesis by acidosis-induced activation of transient receptor potential cation channels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965751/
https://www.ncbi.nlm.nih.gov/pubmed/27468810
http://dx.doi.org/10.1038/srep30639
work_keys_str_mv AT renicarlotta diabetesstimulatesosteoclastogenesisbyacidosisinducedactivationoftransientreceptorpotentialcationchannels
AT mangialardigiuseppe diabetesstimulatesosteoclastogenesisbyacidosisinducedactivationoftransientreceptorpotentialcationchannels
AT melonimarco diabetesstimulatesosteoclastogenesisbyacidosisinducedactivationoftransientreceptorpotentialcationchannels
AT madeddupaolo diabetesstimulatesosteoclastogenesisbyacidosisinducedactivationoftransientreceptorpotentialcationchannels