Hypopituitarism in Sox3 null mutants correlates with altered NG2-glia in the median eminence and is influenced by aspirin and gut microbiota

The median eminence (ME), located at the base of the hypothalamus, is an essential centre of information exchange between the brain and the pituitary. We and others previously showed that mutations and duplications affecting the transcription factor SOX3/Sox3 result in hypopituitarism, and this is likely of hypothalamic origin. We demonstrate here that the absence of Sox3 predominantly affects the ME with phenotypes that first occur in juvenile animals, despite the embryonic onset of SOX3 expression. In the pituitary, reduction in hormone levels correlates with a lack of endocrine cell maturation. In parallel, ME NG2-glia renewal and oligodendrocytic differentiation potential are affected. We further show that low-dose aspirin treatment, which is known to affect NG2-glia, or changes in gut microbiota, rescue both proliferative defects and hypopituitarism in Sox3 mutants. Our study highlights a central role of NG2-glia for ME function during a transitional period of post-natal development and indicates their sensitivity to extrinsic signals.

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Publication Details

Journal
PLoS Genetics
Published
2024-09-26
DOI
https://doi.org/10.1371/journal.pgen.1011395
Citations
2
Primary Topic
Regulation of Appetite and Obesity
Type
article
Field-Weighted Citation Impact
0.27

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article

Hypopituitarism in Sox3 null mutants correlates with altered NG2-glia in the median eminence and is influenced by aspirin and gut microbiota

Robin Lovell‐Badge, Christophe Galichet, Karine Rizzoti
2 citations
PLoS Genetics
Regulation of Appetite and Obesity
0.27
article

Hypopituitarism in Sox3 null mutants correlates with altered NG2-glia in the median eminence and is influenced by aspirin and gut microbiota

Robin Lovell‐Badge, Christophe Galichet, Karine Rizzoti
article en
2 citations

Abstract

The median eminence (ME), located at the base of the hypothalamus, is an essential centre of information exchange between the brain and the pituitary. We and others previously showed that mutations and duplications affecting the transcription factor SOX3/Sox3 result in hypopituitarism, and this is likely of hypothalamic origin. We demonstrate here that the absence of Sox3 predominantly affects the ME with phenotypes that first occur in juvenile animals, despite the embryonic onset of SOX3 expression. In the pituitary, reduction in hormone levels correlates with a lack of endocrine cell maturation. In parallel, ME NG2-glia renewal and oligodendrocytic differentiation potential are affected. We further show that low-dose aspirin treatment, which is known to affect NG2-glia, or changes in gut microbiota, rescue both proliferative defects and hypopituitarism in Sox3 mutants. Our study highlights a central role of NG2-glia for ME function during a transitional period of post-natal development and indicates their sensitivity to extrinsic signals.

PLoS GeneticsVol. 20(9)
Sainsbury Laboratory (GB), The Francis Crick Institute (GB), University College London (GB)
Wellcome Trust, Francis Crick Institute, Cancer Research UK, University College London, School of Medicine, Indiana University, Medical Research Council
Good health and well-being
Openalex Percentile: Top 44%
Regulation of Appetite and Obesity
0.27
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Hypopituitarism in Sox3 null mutants correlates with altered NG2-glia in the median eminence and is influenced by aspirin and gut microbiota — Robin Lovell‐Badge, Christophe Galichet, et al. · PLoS Genetics (2024) | TGRS Research Map | TGRS