Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity

Low vitamin D during childhood is associated with an increased risk of developing multiple sclerosis (MS) as an adult. Given that vitamin D has anti-inflammatory properties, it has been postulated that the relationship between MS and low vitamin D is due to immune dysregulation. Since the vitamin D...

Full description

Bibliographic Details
Main Authors: Priscilla W. Lee, Amanda Selhorst, Sara Gombash Lampe, Yue Liu, Yuhong Yang, Amy E. Lovett-Racke
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-01-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2020.00019/full
id doaj-05d07390515342daaa5d8d3ff6dd1ffb
record_format Article
spelling doaj-05d07390515342daaa5d8d3ff6dd1ffb2020-11-25T00:11:29ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-01-011110.3389/fneur.2020.00019495999Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS AutoimmunityPriscilla W. Lee0Amanda Selhorst1Sara Gombash Lampe2Yue Liu3Yuhong Yang4Yuhong Yang5Amy E. Lovett-Racke6Amy E. Lovett-Racke7Department of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Microbial Infection and Immunity, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesDepartment of Neuroscience, The Ohio State University Wexner Medical Center, Columbus, OH, United StatesLow vitamin D during childhood is associated with an increased risk of developing multiple sclerosis (MS) as an adult. Given that vitamin D has anti-inflammatory properties, it has been postulated that the relationship between MS and low vitamin D is due to immune dysregulation. Since the vitamin D receptor (VDR) is expressed in many cell types, this study investigated an alternative hypothesis—neuron-specific VDR signaling induces anti-inflammatory molecules that protect the central nervous system from autoimmunity. Using media from neurons treated with calcitriol, the active form of vitamin D3, LPS-activated microglia had a reduction in pro-inflammatory molecules, and a reciprocal induction of anti-inflammatory molecules. Since IL-34 is critical to the homeostasis of microglia, and was previously shown to be induced in endothelial cells by vitamin D, we investigated IL-34 as the potential anti-inflammatory molecule induced in neurons by vitamin D. Treatment of LPS-activated microglia with IL-34 reduced pro-inflammatory cytokine production and enhanced the expression of anti-inflammatory transcripts. However, neutralizing IL-34 in vitamin D neuronal conditioned media only impacted IL-6 and not the broader anti-inflammatory phenotype of microglia. To mimic low vitamin D in children, we used a neuron-specific inducible mouse model in which VDR was partially deleted in juvenile mice. Partial deletion of VDR in neurons during early life resulted in exacerbated CNS autoimmunity in adult mice. Overall, the study illustrated that vitamin D signaling in neurons promotes an anti-inflammatory state in microglia, and low vitamin D in early life may enhance CNS autoimmunity.https://www.frontiersin.org/article/10.3389/fneur.2020.00019/fullmultiple sclerosisexperimental autoimmune encephalomyelitisvitamin Dneuronsmicroglia
collection DOAJ
language English
format Article
sources DOAJ
author Priscilla W. Lee
Amanda Selhorst
Sara Gombash Lampe
Yue Liu
Yuhong Yang
Yuhong Yang
Amy E. Lovett-Racke
Amy E. Lovett-Racke
spellingShingle Priscilla W. Lee
Amanda Selhorst
Sara Gombash Lampe
Yue Liu
Yuhong Yang
Yuhong Yang
Amy E. Lovett-Racke
Amy E. Lovett-Racke
Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
Frontiers in Neurology
multiple sclerosis
experimental autoimmune encephalomyelitis
vitamin D
neurons
microglia
author_facet Priscilla W. Lee
Amanda Selhorst
Sara Gombash Lampe
Yue Liu
Yuhong Yang
Yuhong Yang
Amy E. Lovett-Racke
Amy E. Lovett-Racke
author_sort Priscilla W. Lee
title Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
title_short Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
title_full Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
title_fullStr Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
title_full_unstemmed Neuron-Specific Vitamin D Signaling Attenuates Microglia Activation and CNS Autoimmunity
title_sort neuron-specific vitamin d signaling attenuates microglia activation and cns autoimmunity
publisher Frontiers Media S.A.
series Frontiers in Neurology
issn 1664-2295
publishDate 2020-01-01
description Low vitamin D during childhood is associated with an increased risk of developing multiple sclerosis (MS) as an adult. Given that vitamin D has anti-inflammatory properties, it has been postulated that the relationship between MS and low vitamin D is due to immune dysregulation. Since the vitamin D receptor (VDR) is expressed in many cell types, this study investigated an alternative hypothesis—neuron-specific VDR signaling induces anti-inflammatory molecules that protect the central nervous system from autoimmunity. Using media from neurons treated with calcitriol, the active form of vitamin D3, LPS-activated microglia had a reduction in pro-inflammatory molecules, and a reciprocal induction of anti-inflammatory molecules. Since IL-34 is critical to the homeostasis of microglia, and was previously shown to be induced in endothelial cells by vitamin D, we investigated IL-34 as the potential anti-inflammatory molecule induced in neurons by vitamin D. Treatment of LPS-activated microglia with IL-34 reduced pro-inflammatory cytokine production and enhanced the expression of anti-inflammatory transcripts. However, neutralizing IL-34 in vitamin D neuronal conditioned media only impacted IL-6 and not the broader anti-inflammatory phenotype of microglia. To mimic low vitamin D in children, we used a neuron-specific inducible mouse model in which VDR was partially deleted in juvenile mice. Partial deletion of VDR in neurons during early life resulted in exacerbated CNS autoimmunity in adult mice. Overall, the study illustrated that vitamin D signaling in neurons promotes an anti-inflammatory state in microglia, and low vitamin D in early life may enhance CNS autoimmunity.
topic multiple sclerosis
experimental autoimmune encephalomyelitis
vitamin D
neurons
microglia
url https://www.frontiersin.org/article/10.3389/fneur.2020.00019/full
work_keys_str_mv AT priscillawlee neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT amandaselhorst neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT saragombashlampe neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT yueliu neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT yuhongyang neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT yuhongyang neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT amyelovettracke neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
AT amyelovettracke neuronspecificvitamindsignalingattenuatesmicrogliaactivationandcnsautoimmunity
_version_ 1725403709040492544