High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice

Abstract Osteoporosis is associated with reduced density and quality of bone leading to weakened skeleton thereby increasing the risk of fractures responsible for increased morbidity and mortality. Due to preference for western food style the consumption of salt intake in our diets has increased man...

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Autores principales: Hamid Y. Dar, Anjali Singh, Prashant Shukla, Rajaneesh Anupam, Rajesh K. Mondal, Pradyumna K. Mishra, Rupesh K. Srivastava
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/d8ec2faffb614dd29ceab10a7343e8c0
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spelling oai:doaj.org-article:d8ec2faffb614dd29ceab10a7343e8c02021-12-02T15:08:26ZHigh dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice10.1038/s41598-018-20896-y2045-2322https://doaj.org/article/d8ec2faffb614dd29ceab10a7343e8c02018-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-20896-yhttps://doaj.org/toc/2045-2322Abstract Osteoporosis is associated with reduced density and quality of bone leading to weakened skeleton thereby increasing the risk of fractures responsible for increased morbidity and mortality. Due to preference for western food style the consumption of salt intake in our diets has increased many folds. High dietary salt intake has recently been linked with induction of Th17 cells along with impairment of Treg cells. Also, Th17 cells have been one of major players in the pathophysiology of various bone pathologies including osteoporosis. We thus hypothesized that high salt diet (HSD) intake would lead to enhanced bone loss by modulating Th17-Treg cell balance. In the present study, we report for the first time that HSD intake in male mice impairs both trabecular and cortical bone microarchitecture along with decreasing the mineral density and heterogeneity of bones. The HSD modulates host immune system and skews Treg-Th17 balance by promoting osteoclastogenic Th17 cells and inhibiting development of anti-osteoclastogenic Treg cells in mice. HSD also enhanced expression of proinflammatory cytokines (IL-6, TNF-α, RANKL and IL-17) and decreased the expression of anti-inflammatory cytokines (IL-10, IFN-γ). Taken together the present study for the first time establishes a strong correlation between high dietary salt intake and bone health via interplay between Th17-Treg cells.Hamid Y. DarAnjali SinghPrashant ShuklaRajaneesh AnupamRajesh K. MondalPradyumna K. MishraRupesh K. SrivastavaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hamid Y. Dar
Anjali Singh
Prashant Shukla
Rajaneesh Anupam
Rajesh K. Mondal
Pradyumna K. Mishra
Rupesh K. Srivastava
High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
description Abstract Osteoporosis is associated with reduced density and quality of bone leading to weakened skeleton thereby increasing the risk of fractures responsible for increased morbidity and mortality. Due to preference for western food style the consumption of salt intake in our diets has increased many folds. High dietary salt intake has recently been linked with induction of Th17 cells along with impairment of Treg cells. Also, Th17 cells have been one of major players in the pathophysiology of various bone pathologies including osteoporosis. We thus hypothesized that high salt diet (HSD) intake would lead to enhanced bone loss by modulating Th17-Treg cell balance. In the present study, we report for the first time that HSD intake in male mice impairs both trabecular and cortical bone microarchitecture along with decreasing the mineral density and heterogeneity of bones. The HSD modulates host immune system and skews Treg-Th17 balance by promoting osteoclastogenic Th17 cells and inhibiting development of anti-osteoclastogenic Treg cells in mice. HSD also enhanced expression of proinflammatory cytokines (IL-6, TNF-α, RANKL and IL-17) and decreased the expression of anti-inflammatory cytokines (IL-10, IFN-γ). Taken together the present study for the first time establishes a strong correlation between high dietary salt intake and bone health via interplay between Th17-Treg cells.
format article
author Hamid Y. Dar
Anjali Singh
Prashant Shukla
Rajaneesh Anupam
Rajesh K. Mondal
Pradyumna K. Mishra
Rupesh K. Srivastava
author_facet Hamid Y. Dar
Anjali Singh
Prashant Shukla
Rajaneesh Anupam
Rajesh K. Mondal
Pradyumna K. Mishra
Rupesh K. Srivastava
author_sort Hamid Y. Dar
title High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
title_short High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
title_full High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
title_fullStr High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
title_full_unstemmed High dietary salt intake correlates with modulated Th17-Treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
title_sort high dietary salt intake correlates with modulated th17-treg cell balance resulting in enhanced bone loss and impaired bone-microarchitecture in male mice
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/d8ec2faffb614dd29ceab10a7343e8c0
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