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      Metabolic regulation of the neural stem cell fate: Unraveling new connections, establishing new concepts

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          Abstract

          The neural stem cell niche is a key regulator participating in the maintenance, regeneration, and repair of the brain. Within the niche neural stem cells (NSC) generate new neurons throughout life, which is important for tissue homeostasis and brain function. NSCs are regulated by intrinsic and extrinsic factors with cellular metabolism being lately recognized as one of the most important ones, with evidence suggesting that it may serve as a common signal integrator to ensure mammalian brain homeostasis. The aim of this review is to summarize recent insights into how metabolism affects NSC fate decisions in adult neural stem cell niches, with occasional referencing of embryonic neural stem cells when it is deemed necessary. Specifically, we will highlight the implication of mitochondria as crucial regulators of NSC fate decisions and the relationship between metabolism and ependymal cells. The link between primary cilia dysfunction in the region of hypothalamus and metabolic diseases will be examined as well. Lastly, the involvement of metabolic pathways in ependymal cell ciliogenesis and physiology regulation will be discussed.

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          Most cited references168

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          From inflammation to sickness and depression: when the immune system subjugates the brain.

          In response to a peripheral infection, innate immune cells produce pro-inflammatory cytokines that act on the brain to cause sickness behaviour. When activation of the peripheral immune system continues unabated, such as during systemic infections, cancer or autoimmune diseases, the ensuing immune signalling to the brain can lead to an exacerbation of sickness and the development of symptoms of depression in vulnerable individuals. These phenomena might account for the increased prevalence of clinical depression in physically ill people. Inflammation is therefore an important biological event that might increase the risk of major depressive episodes, much like the more traditional psychosocial factors.
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            Mitochondrial TCA cycle metabolites control physiology and disease

            Mitochondria are signaling organelles that regulate a wide variety of cellular functions and can dictate cell fate. Multiple mechanisms contribute to communicate mitochondrial fitness to the rest of the cell. Recent evidence confers a new role for TCA cycle intermediates, generally thought to be important for biosynthetic purposes, as signaling molecules with functions controlling chromatin modifications, DNA methylation, the hypoxic response, and immunity. This review summarizes the mechanisms by which the abundance of different TCA cycle metabolites controls cellular function and fate in different contexts. We will focus on how these metabolites mediated signaling can affect physiology and disease.
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              The cell biology of neurogenesis.

              During the development of the mammalian central nervous system, neural stem cells and their derivative progenitor cells generate neurons by asymmetric and symmetric divisions. The proliferation versus differentiation of these cells and the type of division are closely linked to their epithelial characteristics, notably, their apical-basal polarity and cell-cycle length. Here, we discuss how these features change during development from neuroepithelial to radial glial cells, and how this transition affects cell fate and neurogenesis.
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                Author and article information

                Contributors
                Journal
                Front Neurosci
                Front Neurosci
                Front. Neurosci.
                Frontiers in Neuroscience
                Frontiers Media S.A.
                1662-4548
                1662-453X
                21 October 2022
                2022
                : 16
                : 1009125
                Affiliations
                [1] 1Department of Physiology, Medical School, University of Patras , Patras, Greece
                [2] 2First Department of Psychiatry, Medical School, National and Kapodistrian University of Athens, Eginition Hospital , Athens, Greece
                [3] 3University Mental Health, Neurosciences and Precision Medicine Research Institute “Costas Stefanis” , Athens, Greece
                [4] 4Department of General Biology, School of Medicine, University of Patras , Patras, Greece
                [5] 5Division of Endocrinology, Department of Internal Medicine, University of Patras , Patras, Greece
                Author notes

                Edited by: Paola Tognini, University of Pisa, Italy

                Reviewed by: Joao C. Sousa, University of Minho, Portugal; Ana Catarina Ferreira, Icahn School of Medicine at Mount Sinai, United States

                *Correspondence: Stavros Taraviras, taraviras@ 123456med.upatras.gr

                This article was submitted to Neurodevelopment, a section of the journal Frontiers in Neuroscience

                Article
                10.3389/fnins.2022.1009125
                9634649
                36340763
                c2301358-e258-4735-8f0a-7674dcb10902
                Copyright © 2022 Angelopoulos, Gakis, Birmpas, Kyrousi, Habeos, Kaplani, Lygerou, Habeos and Taraviras.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 August 2022
                : 03 October 2022
                Page count
                Figures: 4, Tables: 0, Equations: 0, References: 169, Pages: 14, Words: 11241
                Categories
                Neuroscience
                Review

                Neurosciences
                metabolism,neural stem cell niche,subventricular zone (svz),ependymal,neural stem cells,cell mechanics,ciliopathies

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