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Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function
Vitamin D, a fat-soluble vitamin, plays a critical role in calcium homeostasis, the immune system, and normal development. Many epidemiological cohort studies globally have found high prevalence rates of vitamin D deficiency and insufficiency, recognized as an important health issue that needs to be...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133936/ https://www.ncbi.nlm.nih.gov/pubmed/35634491 http://dx.doi.org/10.3389/fendo.2022.860286 |
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author | Lundy, Kassidy Greally, John F. Essilfie-Bondzie, Grace Olivier, Josephine B. Doña-Termine, Reanna Greally, John M. Suzuki, Masako |
author_facet | Lundy, Kassidy Greally, John F. Essilfie-Bondzie, Grace Olivier, Josephine B. Doña-Termine, Reanna Greally, John M. Suzuki, Masako |
author_sort | Lundy, Kassidy |
collection | PubMed |
description | Vitamin D, a fat-soluble vitamin, plays a critical role in calcium homeostasis, the immune system, and normal development. Many epidemiological cohort studies globally have found high prevalence rates of vitamin D deficiency and insufficiency, recognized as an important health issue that needs to be solved. In particular, reproductive age and pregnant women low in vitamin D status may confer risks of diseases like obesity on their offspring. While observational studies have suggested associations between prenatal vitamin D deficiency and metabolic phenotypes in offspring, not yet determined is whether prenatal vitamin D deficiency permanently alters the development of the liver, a major metabolic organ. We tested the histopathology and the transcriptomic profiles of livers from male C57BL/6J mice exposed to prenatal vitamin D deficiency through a maternal dietary intervention model. We found that prenatal vitamin D deficiency increases the prevalence of histopathological changes in the liver, and alters its gene expression profile. Cell subtype proportion analysis showed that the liver of prenatal vitamin D deficiency alters non-parenchymal cells of the liver, specifically macrophages, a subset of endothelial cells, and dendritic cells. Our results indicate the long-term memory of prenatal vitamin D deficiency exposure in the adult liver, a potential contributor to offspring health risks. |
format | Online Article Text |
id | pubmed-9133936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91339362022-05-27 Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function Lundy, Kassidy Greally, John F. Essilfie-Bondzie, Grace Olivier, Josephine B. Doña-Termine, Reanna Greally, John M. Suzuki, Masako Front Endocrinol (Lausanne) Endocrinology Vitamin D, a fat-soluble vitamin, plays a critical role in calcium homeostasis, the immune system, and normal development. Many epidemiological cohort studies globally have found high prevalence rates of vitamin D deficiency and insufficiency, recognized as an important health issue that needs to be solved. In particular, reproductive age and pregnant women low in vitamin D status may confer risks of diseases like obesity on their offspring. While observational studies have suggested associations between prenatal vitamin D deficiency and metabolic phenotypes in offspring, not yet determined is whether prenatal vitamin D deficiency permanently alters the development of the liver, a major metabolic organ. We tested the histopathology and the transcriptomic profiles of livers from male C57BL/6J mice exposed to prenatal vitamin D deficiency through a maternal dietary intervention model. We found that prenatal vitamin D deficiency increases the prevalence of histopathological changes in the liver, and alters its gene expression profile. Cell subtype proportion analysis showed that the liver of prenatal vitamin D deficiency alters non-parenchymal cells of the liver, specifically macrophages, a subset of endothelial cells, and dendritic cells. Our results indicate the long-term memory of prenatal vitamin D deficiency exposure in the adult liver, a potential contributor to offspring health risks. Frontiers Media S.A. 2022-05-12 /pmc/articles/PMC9133936/ /pubmed/35634491 http://dx.doi.org/10.3389/fendo.2022.860286 Text en Copyright © 2022 Lundy, Greally, Essilfie-Bondzie, Olivier, Doña-Termine, Greally and Suzuki https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Lundy, Kassidy Greally, John F. Essilfie-Bondzie, Grace Olivier, Josephine B. Doña-Termine, Reanna Greally, John M. Suzuki, Masako Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title | Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title_full | Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title_fullStr | Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title_full_unstemmed | Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title_short | Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function |
title_sort | vitamin d deficiency during development permanently alters liver cell composition and function |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133936/ https://www.ncbi.nlm.nih.gov/pubmed/35634491 http://dx.doi.org/10.3389/fendo.2022.860286 |
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