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Mol Brain. 2016 Apr 14;9:39. doi: 10.1186/s13041-016-0219-1.

Reductions in hypothalamic Gfap expression, glial cells and α-tanycytes in lean and hypermetabolic Gnasxl-deficient mice.

Author information

1
Integrative Genomics of Ageing Group, Institute of Integrative Biology, University of Liverpool, Crown Str, Liverpool, L69 7ZB, UK.
2
Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Crown Str, Liverpool, L69 3BX, UK.
3
Integrative Genomics of Ageing Group, Institute of Integrative Biology, University of Liverpool, Crown Str, Liverpool, L69 7ZB, UK. jp@senescence.info.
4
Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Crown Str, Liverpool, L69 3BX, UK. a.plagge@liverpool.ac.uk.

Abstract

BACKGROUND:

Neuronal and glial differentiation in the murine hypothalamus is not complete at birth, but continues over the first two weeks postnatally. Nutritional status and Leptin deficiency can influence the maturation of neuronal projections and glial patterns, and hypothalamic gliosis occurs in mouse models of obesity. Gnasxl constitutes an alternative transcript of the genomically imprinted Gnas locus and encodes a variant of the signalling protein Gαs, termed XLαs, which is expressed in defined areas of the hypothalamus. Gnasxl-deficient mice show postnatal growth retardation and undernutrition, while surviving adults remain lean and hypermetabolic with increased sympathetic nervous system (SNS) activity. Effects of this knock-out on the hypothalamic neural network have not yet been investigated.

RESULTS:

RNAseq analysis for gene expression changes in hypothalami of Gnasxl-deficient mice indicated Glial fibrillary acid protein (Gfap) expression to be significantly down-regulated in adult samples. Histological analysis confirmed a reduction in Gfap-positive glial cell numbers specifically in the hypothalamus. This reduction was observed in adult tissue samples, whereas no difference was found in hypothalami of postnatal stages, indicating an adaptation in adult Gnasxl-deficient mice to their earlier growth phenotype and hypermetabolism. Especially noticeable was a loss of many Gfap-positive α-tanycytes and their processes, which form part of the ependymal layer that lines the medial and dorsal regions of the 3(rd) ventricle, while β-tanycytes along the median eminence (ME) and infundibular recesses appeared unaffected. This was accompanied by local reductions in Vimentin and Nestin expression. Hypothalamic RNA levels of glial solute transporters were unchanged, indicating a potential compensatory up-regulation in the remaining astrocytes and tanycytes.

CONCLUSION:

Gnasxl deficiency does not directly affect glial development in the hypothalamus, since it is expressed in neurons, and Gfap-positive astrocytes and tanycytes appear normal during early postnatal stages. The loss of Gfap-expressing cells in adult hypothalami appears to be a consequence of the postnatal undernutrition, hypoglycaemia and continued hypermetabolism and leanness of Gnasxl-deficient mice, which contrasts with gliosis observed in obese mouse models. Since α-tanycytes also function as adult neural progenitor cells, these findings might indicate further developmental abnormalities in hypothalamic formations of Gnasxl-deficient mice, potentially including neuronal composition and projections.

KEYWORDS:

Energy homoeostasis; Genomic imprinting; Gfap; Glia; Gnas; Hypothalamus; RNAseq; Tanycyte

PMID:
27080240
PMCID:
PMC4832494
DOI:
10.1186/s13041-016-0219-1
[Indexed for MEDLINE]
Free PMC Article

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