4.8 Article

Nutritional regulation of oligodendrocyte differentiation regulates perineuronal net remodeling in the median eminence

期刊

CELL REPORTS
卷 36, 期 2, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2021.109362

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资金

  1. MRC [MR/S011552/1]
  2. Wellcome Trust [108926/B/15/Z, MRC_MC_UU_12012/5, 100574/Z/12/Z, MRC_MC_UU_00014/5, 208363/Z/17/Z]
  3. BBSRC DTP program
  4. ERC [771411]
  5. Wellcome Pathfinder Award [204488/Z/16/Z]
  6. MRC MDU
  7. Adelson Medical Research Foundation
  8. UK MS Society
  9. l'Oreal-UNESCO For Women In Science program
  10. Wellcome Trust [204488/Z/16/Z, 108926/B/15/Z] Funding Source: Wellcome Trust
  11. European Research Council (ERC) [771411] Funding Source: European Research Council (ERC)
  12. MRC [MR/S011552/1] Funding Source: UKRI

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The mediobasal hypothalamus plays an important role in energy balance maintenance, with refeeding triggering proliferation and differentiation of oligodendrocyte progenitors in the median eminence. The remodeling of perineuronal nets in the mediobasal hypothalamus is essential for metabolic functions, and its disruption in obese mice leads to increased food intake and weight gain. These findings highlight the crucial role of oligodendrocyte differentiation in mediating the effects of nutrition on energy balance.
The mediobasal hypothalamus (MBH; arcuate nucleus of the hypothalamus [ARH] and median eminence [ME]) is a key nutrient sensing site for the production of the complex homeostatic feedback responses required for the maintenance of energy balance. Here, we show that refeeding after an overnight fast rapidly triggers proliferation and differentiation of oligodendrocyte progenitors, leading to the production of new oligodendrocytes in the ME specifically. During this nutritional paradigm, ME perineuronal nets (PNNs), emerging regulators of ARH metabolic functions, are rapidly remodeled, and this process requires myelin regulatory factor (Myrf) in oligodendrocyte progenitors. In genetically obese ob/ob mice, nutritional regulations of ME oligodendrocyte differentiation and PNN remodeling are blunted, and enzymatic digestion of local PNN increases food intake and weight gain. We conclude that MBH PNNs are required for the maintenance of energy balance in lean mice and are remodeled in the adult ME by the nutritional control of oligodendrocyte differentiation.

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