Vitamin D Promotes Protein Homeostasis and Longevity via the Stress Response Pathway Genes skn-1, ire-1, and xbp-1

Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases, including Alzheimer’s disease, Parkinson’s disease, cognitive impa...

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Published inCell reports (Cambridge) Vol. 17; no. 5; pp. 1227 - 1237
Main Authors Mark, Karla A., Dumas, Kathleen J., Bhaumik, Dipa, Schilling, Birgit, Davis, Sonnet, Oron, Tal Ronnen, Sorensen, Dylan J., Lucanic, Mark, Brem, Rachel B., Melov, Simon, Ramanathan, Arvind, Gibson, Bradford W., Lithgow, Gordon J.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 25.10.2016
Elsevier
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Abstract Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases, including Alzheimer’s disease, Parkinson’s disease, cognitive impairment, and cancer. In this study, we utilized Caenorhabditis elegans to examine the mechanism by which vitamin D influences aging. We found that vitamin-D3-induced lifespan extension requires the stress response pathway genes skn-1, ire-1, and xbp-1. Vitamin D3 (D3) induced expression of SKN-1 target genes but not canonical targets of XBP-1. D3 suppressed an important molecular pathology of aging, that of widespread protein insolubility, and prevented toxicity caused by human β-amyloid. Our observation that D3 improves protein homeostasis and slows aging highlights the importance of maintaining appropriate vitamin D serum levels and may explain why such a wide variety of human age-related diseases are associated with vitamin D deficiency. [Display omitted] •Vitamin D metabolism is conserved between nematodes and mammals•Vitamin D prevents the age-dependent accumulation of SDS-insoluble proteins•Vitamin D enhances lifespan and protein homeostasis via IRE-1, XBP-1, and SKN-1 Maintenance of protein homeostasis is crucial to cellular health and contributes significantly to the lifespan of organisms. Mark et al. demonstrate that vitamin D supplementation promotes protein homeostasis and slows aging in the nematode, C. elegans. These findings identify a mechanism by which vitamin D influences aging.
AbstractList Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases, including Alzheimer’s disease, Parkinson’s disease, cognitive impairment, and cancer. In this study, we utilized Caenorhabditis elegans to examine the mechanism by which vitamin D influences aging. We found that vitamin-D3-induced lifespan extension requires the stress response pathway genes skn-1, ire-1, and xbp-1. Vitamin D3 (D3) induced expression of SKN-1 target genes but not canonical targets of XBP-1. D3 suppressed an important molecular pathology of aging, that of widespread protein insolubility, and prevented toxicity caused by human β-amyloid. Our observation that D3 improves protein homeostasis and slows aging highlights the importance of maintaining appropriate vitamin D serum levels and may explain why such a wide variety of human age-related diseases are associated with vitamin D deficiency. [Display omitted] •Vitamin D metabolism is conserved between nematodes and mammals•Vitamin D prevents the age-dependent accumulation of SDS-insoluble proteins•Vitamin D enhances lifespan and protein homeostasis via IRE-1, XBP-1, and SKN-1 Maintenance of protein homeostasis is crucial to cellular health and contributes significantly to the lifespan of organisms. Mark et al. demonstrate that vitamin D supplementation promotes protein homeostasis and slows aging in the nematode, C. elegans. These findings identify a mechanism by which vitamin D influences aging.
Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases, including Alzheimer's disease, Parkinson's disease, cognitive impairment, and cancer. In this study, we utilized Caenorhabditis elegans to examine the mechanism by which vitamin D influences aging. We found that vitamin-D3-induced lifespan extension requires the stress response pathway genes skn-1, ire-1, and xbp-1. Vitamin D3 (D3) induced expression of SKN-1 target genes but not canonical targets of XBP-1. D3 suppressed an important molecular pathology of aging, that of widespread protein insolubility, and prevented toxicity caused by human β-amyloid. Our observation that D3 improves protein homeostasis and slows aging highlights the importance of maintaining appropriate vitamin D serum levels and may explain why such a wide variety of human age-related diseases are associated with vitamin D deficiency.
Vitamin D has multiple roles including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases including Alzheimer’s disease, Parkinson’s disease, cognitive impairment, and cancer. In this study, we utilized Caenorhabditis elegans to examine the mechanism by which vitamin D influences aging. We found that Vitamin D3-induced lifespan extension requires the stress response pathway genes SKN-1, IRE-1, and XBP-1. Vitamin D3 (D3) induced expression of SKN-1 target genes, but not canonical targets of IRE-1/XBP-1. D3 suppressed an important molecular pathology of aging, that of widespread protein insolubility, and prevented toxicity caused by human β-amyloid. Our observation that D3 improves protein homeostasis and slows aging highlights the importance of maintaining appropriate vitamin D serum levels, and may explain why such a wide variety of human age-related diseases are associated with vitamin D deficiency. Maintenance of protein homeostasis is crucial to cellular health, and contributes significantly to the lifespan of the organism. Mark et al. demonstrate that vitamin D supplementation promotes protein homeostasis and slows aging in the nematode, C. elegans . These findings identify a mechanism by which Vitamin D influences aging.
Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin D, is associated with an increased risk of age-related chronic diseases, including Alzheimer’s disease, Parkinson’s disease, cognitive impairment, and cancer. In this study, we utilized Caenorhabditis elegans to examine the mechanism by which vitamin D influences aging. We found that vitamin-D3-induced lifespan extension requires the stress response pathway genes skn-1, ire-1, and xbp-1. Vitamin D3 (D3) induced expression of SKN-1 target genes but not canonical targets of XBP-1. D3 suppressed an important molecular pathology of aging, that of widespread protein insolubility, and prevented toxicity caused by human β-amyloid. Our observation that D3 improves protein homeostasis and slows aging highlights the importance of maintaining appropriate vitamin D serum levels and may explain why such a wide variety of human age-related diseases are associated with vitamin D deficiency. : Maintenance of protein homeostasis is crucial to cellular health and contributes significantly to the lifespan of organisms. Mark et al. demonstrate that vitamin D supplementation promotes protein homeostasis and slows aging in the nematode, C. elegans. These findings identify a mechanism by which vitamin D influences aging. Keywords: Ceanorhabditis elegans, vitamin D, lifespan. aging, insoluble protein, SKN-1, XBP-1, IRE-1, proteostasis, protein aggregation, Alzheimer’s disease
Author Bhaumik, Dipa
Mark, Karla A.
Lucanic, Mark
Schilling, Birgit
Oron, Tal Ronnen
Ramanathan, Arvind
Melov, Simon
Brem, Rachel B.
Davis, Sonnet
Sorensen, Dylan J.
Gibson, Bradford W.
Lithgow, Gordon J.
Dumas, Kathleen J.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27783938$$D View this record in MEDLINE/PubMed
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Issue 5
Keywords Alzheimer’s disease
lifespan. aging
vitamin D
protein aggregation
insoluble protein
IRE-1
proteostasis
Ceanorhabditis elegans
XBP-1
SKN-1
Language English
License This is an open access article under the CC BY-NC-ND license.
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Snippet Vitamin D has multiple roles, including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of...
Vitamin D has multiple roles including the regulation of bone and calcium homeostasis. Deficiency of 25-hydroxyvitamin D, the major circulating form of vitamin...
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SubjectTerms Alzheimer’s disease
Animals
Caenorhabditis elegans - drug effects
Caenorhabditis elegans - genetics
Caenorhabditis elegans - physiology
Caenorhabditis elegans Proteins - genetics
Caenorhabditis elegans Proteins - metabolism
Calcitriol - metabolism
Carrier Proteins - genetics
Carrier Proteins - metabolism
Ceanorhabditis elegans
Cholecalciferol - metabolism
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
Endoplasmic Reticulum - drug effects
Endoplasmic Reticulum - metabolism
Homeostasis - drug effects
insoluble protein
IRE-1
lifespan. aging
Longevity - physiology
Protein Aggregates
protein aggregation
Protein-Serine-Threonine Kinases - genetics
Protein-Serine-Threonine Kinases - metabolism
proteostasis
SKN-1
Solubility
Stress, Physiological - genetics
Transcription Factors - genetics
Transcription Factors - metabolism
Unfolded Protein Response - drug effects
vitamin D
Vitamin D - pharmacology
XBP-1
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Title Vitamin D Promotes Protein Homeostasis and Longevity via the Stress Response Pathway Genes skn-1, ire-1, and xbp-1
URI https://dx.doi.org/10.1016/j.celrep.2016.09.086
https://www.ncbi.nlm.nih.gov/pubmed/27783938
https://pubmed.ncbi.nlm.nih.gov/PMC5689451
https://doaj.org/article/3f8a22d43d664bb88d686bd3cb8a33a3
Volume 17
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