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Sonic Hedgehog receptor Patched deficiency in astrocytes enhances glucose metabolism in mice
- Source :
- Molecular Metabolism, Molecular metabolism, Molecular metabolism, Elsevier, 2021, 47, pp.101172. ⟨10.1016/j.molmet.2021.101172⟩, Molecular metabolism, Elsevier, 2021, pp.101172. ⟨10.1016/j.molmet.2021.101172⟩, Molecular metabolism, 2021, 47, pp.101172. ⟨10.1016/j.molmet.2021.101172⟩, Molecular Metabolism, Vol 47, Iss, Pp 101172-(2021)
- Publication Year :
- 2020
-
Abstract
- Objective Astrocytes are glial cells proposed as the main Sonic hedgehog (Shh)-responsive cells in the adult brain. Their roles in mediating Shh functions are still poorly understood. In the hypothalamus, astrocytes support neuronal circuits implicated in the regulation of energy metabolism. In this study, we investigated the impact of genetic activation of Shh signaling on hypothalamic astrocytes and characterized its effects on energy metabolism. Methods We analyzed the distribution of gene transcripts of the Shh pathway (Ptc, Gli1, Gli2, and Gli3) in astrocytes using single molecule fluorescence in situ hybridization combined with immunohistofluorescence of Shh peptides by Western blotting in the adult mouse hypothalamus. Based on the metabolic phenotype, we characterized Glast-CreERT2-YFP-Ptc−/− (YFP-Ptc−/−) mice and their controls over time and under a high-fat diet (HFD) to investigate the potential effects of conditional astrocytic deletion of the Shh receptor Patched (Ptc) on metabolic efficiency, insulin sensitivity, and systemic glucose metabolism. Molecular and biochemical assays were used to analyze the alteration of key pathways modulating energy metabolism, insulin sensitivity, glucose uptake, and inflammation. Primary astrocyte cultures were used to evaluate a potential role of Shh signaling in astrocytic glucose uptake. Results Shh peptides were the highest in the hypothalamic extracts of adult mice and a large population of hypothalamic astrocytes expressed Ptc and Gli1-3 mRNAs. Characterization of Shh signaling after conditional Ptc deletion in the YFP-Ptc−/− mice revealed heterogeneity in hypothalamic astrocyte populations. Interestingly, activation of Shh signaling in Glast+ astrocytes enhanced insulin responsiveness as evidenced by glucose and insulin tolerance tests. This effect was maintained over time and associated with lower blood insulin levels and also observed under a HFD. The YFP-Ptc−/− mice exhibited a lean phenotype with the absence of body weight gain and a marked reduction of white and brown adipose tissues accompanied by increased whole-body fatty acid oxidation. In contrast, food intake, locomotor activity, and body temperature were not altered. At the cellular level, Ptc deletion did not affect glucose uptake in primary astrocyte cultures. In the hypothalamus, activation of the astrocytic Shh pathway was associated with the upregulation of transcripts coding for the insulin receptor and liver kinase B1 (LKB1) after 4 weeks and the glucose transporter GLUT-4 after 32 weeks. Conclusions Here, we define hypothalamic Shh action on astrocytes as a novel master regulator of energy metabolism. In the hypothalamus, astrocytic Shh signaling could be critically involved in preventing both aging- and obesity-related metabolic disorders.<br />Highlights • Astrocytes exhibit differences in regulating the hedgehog signaling pathway. • Deletion of Ptc in Glast+ cells prevents body weight gain and insulin resistance. • Deletion of Ptc in Glast+ cells increases β oxidation. • Central hedgehog signaling participates in the regulation of whole-body metabolism.
- Subjects :
- 0301 basic medicine
Patched
Patched Receptors
Transcriptional Activation
Aging
Glucose uptake
[SDV]Life Sciences [q-bio]
Hypothalamus
030209 endocrinology & metabolism
03 medical and health sciences
Mice
0302 clinical medicine
Downregulation and upregulation
GLI3
medicine
Animals
Humans
Hedgehog Proteins
Obesity
Sonic hedgehog
Internal medicine
Molecular Biology
In Situ Hybridization, Fluorescence
2. Zero hunger
Neurons
biology
Chemistry
Glucose transporter
Cell Biology
RC31-1245
Cell biology
[SDV] Life Sciences [q-bio]
Mice, Inbred C57BL
Insulin receptor
030104 developmental biology
medicine.anatomical_structure
Glucose
HEK293 Cells
Astrocytes
biology.protein
NIH 3T3 Cells
Original Article
Energy Metabolism
Astrocyte
Hedgehog
Signal Transduction
Subjects
Details
- ISSN :
- 22128778
- Volume :
- 47
- Database :
- OpenAIRE
- Journal :
- Molecular metabolism
- Accession number :
- edsair.doi.dedup.....11fb5ff972201183f9a6e9a8ee475cd0