TY - JOUR
T1 - Vitamin D Deficiency During Development Permanently Alters Liver Cell Composition and Function
AU - Lundy, Kassidy
AU - Greally, John F.
AU - Essilfie-Bondzie, Grace
AU - Olivier, Josephine B.
AU - Doña-Termine, Reanna
AU - Greally, John M.
AU - Suzuki, Masako
N1 - Funding Information:
We thank to Analytical Imaging Facility (AIF) of Albert Einstein College of Medicine for their support. All histology slides were scanned with a P250 slide scanner supported by Shared Instrumentation Grant, 1S10OD019961-01. The AIF is partially funded by Cancer Center Support Grant of National Cancer Institutes (P30CA013330).
Funding Information:
This work was supported by the Human Genome Project Pilot Grant of the Department of Genetics at Albert Einstein College of Medicine and partially supported by the National Institutes of Health under award number R01HL145302 (MS).
Funding Information:
We thank to Analytical Imaging Facility (AIF) of Albert Einstein College of Medicine for their support. All histology slides were scanned with a P250 slide scanner supported by Shared Instrumentation Grant, 1S10OD019961-01. The AIF is partially funded by Cancer Center Support Grant of National Cancer Institutes (P30CA013330).
Publisher Copyright:
Copyright © 2022 Lundy, Greally, Essilfie-Bondzie, Olivier, Doña-Termine, Greally and Suzuki.
PY - 2022/5/12
Y1 - 2022/5/12
N2 - 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.
AB - 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.
KW - DOHaD (developmental origins of health and disease)
KW - liver
KW - prenatal environment
KW - transcriptional alterations
KW - vitamin D deficiency
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U2 - 10.3389/fendo.2022.860286
DO - 10.3389/fendo.2022.860286
M3 - Article
AN - SCOPUS:85130729565
SN - 1664-2392
VL - 13
JO - Frontiers in Endocrinology
JF - Frontiers in Endocrinology
M1 - 860286
ER -