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Irx3 and Irx5-Novel Regulatory Factors of Postnatal Hypothalamic Neurogenesis

期刊

FRONTIERS IN NEUROSCIENCE
卷 15, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2021.763856

关键词

FTO (Fat Mass and Obesity-Associated) Gene; obesity; metabolic regulation; neural stem cell (NSC); tanycyte; neurogenesis; IRX3 gene; IRX5 gene

资金

  1. Canadian Institutes of Health Research [PJT-178147]
  2. Canada Research Chairs program
  3. Diabetes Canada

向作者/读者索取更多资源

The hypothalamus, a highly conserved brain region, plays a crucial role in regulating physiological processes like energy balance. Neurons in the arcuate nucleus sense peripheral signals and regulate food intake and energy expenditure. Postnatal neurogenesis in the mouse hypothalamus, particularly in the first two postnatal weeks, contributes to remodeling and energy balance regulation. Radial glia-like cells, including RGL-NSCs, play a key role in this neurogenesis process, with genetic factors such as Irx3 and Irx5 influencing their properties. Understanding these mechanisms provides insights into hypothalamic remodeling and energy balance control.
The hypothalamus is a brain region that exhibits highly conserved anatomy across vertebrate species and functions as a central regulatory hub for many physiological processes such as energy homeostasis and circadian rhythm. Neurons in the arcuate nucleus of the hypothalamus are largely responsible for sensing of peripheral signals such as leptin and insulin, and are critical for the regulation of food intake and energy expenditure. While these neurons are mainly born during embryogenesis, accumulating evidence have demonstrated that neurogenesis also occurs in postnatal-adult mouse hypothalamus, particularly in the first two postnatal weeks. This second wave of active neurogenesis contributes to the remodeling of hypothalamic neuronal populations and regulation of energy homeostasis including hypothalamic leptin sensing. Radial glia cell types, such as tanycytes, are known to act as neuronal progenitors in the postnatal mouse hypothalamus. Our recent study unveiled a previously unreported radial glia-like neural stem cell (RGL-NSC) population that actively contributes to neurogenesis in the postnatal mouse hypothalamus. We also identified Irx3 and Irx5, which encode Iroquois homeodomain-containing transcription factors, as genetic determinants regulating the neurogenic property of these RGL-NSCs. These findings are significant as IRX3 and IRX5 have been implicated in FTO-associated obesity in humans, illustrating the importance of postnatal hypothalamic neurogenesis in energy homeostasis and obesity. In this review, we summarize current knowledge regarding postnatal-adult hypothalamic neurogenesis and highlight recent findings on the radial glia-like cells that contribute to the remodeling of postnatal mouse hypothalamus. We will discuss characteristics of the RGL-NSCs and potential actions of Irx3 and Irx5 in the regulation of neural stem cells in the postnatal-adult mouse brain. Understanding the behavior and regulation of neural stem cells in the postnatal-adult hypothalamus will provide novel mechanistic insights in the control of hypothalamic remodeling and energy homeostasis.

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