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      ADAM10 facilitates rapid neural stem cell cycling and proper positioning within the subventricular zone niche via JAMC/RAP1Gap signaling

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          Abstract

          Abstract

          The mechanisms that regulate neural stem cell (NSC) lineage progression and maintain NSCs within different domains of the adult neural stem cell niche, the subventricular zone are not well defined. Quiescent NSCs are arranged at the apical ventricular wall, while mitotically activated NSCs are found in the basal, vascular region of the subventricular zone. Here, we found that ADAM10 (a disintegrin and metalloproteinase 10) is essential in NSC association with the ventricular wall, and via this adhesion to the apical domain, ADAM10 regulates the switch from quiescent and undifferentiated NSC to an actively proliferative and differentiating cell state. Processing of JAMC (junctional adhesion molecule C) by ADAM10 increases Rap1GAP activity. This molecular machinery promotes NSC transit from the apical to the basal compartment and subsequent lineage progression. Understanding the molecular mechanisms responsible for regulating the proper positioning of NSCs within the subventricular zone niche and lineage progression of NSCs could provide new targets for drug development to enhance the regenerative properties of neural tissue.

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          Animal models of necrotizing enterocolitis: review of the literature and state of the art

          Abstract Necrotizing enterocolitis (NEC) remains the leading cause of gastrointestinal surgical emergency in preterm neonates. Over the last five decades, a variety of experimental models have been developed to study the pathophysiology of this disease and to test the effectiveness of novel therapeutic strategies. Experimental NEC is mainly modeled in neonatal rats, mice and piglets. In this review, we focus on these experimental models and discuss the major advantages and disadvantages of each. We also briefly discuss other models that are not as widely used but have contributed to our current knowledge of NEC.
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            Mechanisms and functional implications of adult neurogenesis.

            The generation of new neurons is sustained throughout adulthood in the mammalian brain due to the proliferation and differentiation of adult neural stem cells. In this review, we discuss the factors that regulate proliferation and fate determination of adult neural stem cells and describe recent studies concerning the integration of newborn neurons into the existing neural circuitry. We further address the potential significance of adult neurogenesis in memory, depression, and neurodegenerative disorders such as Alzheimer's and Parkinson's disease.
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              Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system.

              Neurogenesis in the mammalian central nervous system is believed to end in the period just after birth; in the mouse striatum no new neurons are produced after the first few days after birth. In this study, cells isolated from the striatum of the adult mouse brain were induced to proliferate in vitro by epidermal growth factor. The proliferating cells initially expressed nestin, an intermediate filament found in neuroepithelial stem cells, and subsequently developed the morphology and antigenic properties of neurons and astrocytes. Newly generated cells with neuronal morphology were immunoreactive for gamma-aminobutyric acid and substance P, two neurotransmitters of the adult striatum in vivo. Thus, cells of the adult mouse striatum have the capacity to divide and differentiate into neurons and astrocytes.
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                Author and article information

                Journal
                Neural Regen Res
                Neural Regen Res
                NRR
                Neural Regen Res
                Neural Regeneration Research
                Wolters Kluwer - Medknow (India )
                1673-5374
                1876-7958
                November 2022
                01 April 2022
                : 17
                : 11
                : 2472-2483
                Affiliations
                [1 ]Program in Neuroscience and Medical Scientist Training Program, Renaissance School of Medicine at Stony Brook University, Stony Brook, NY, USA
                [2 ]Department of Pharmacological Sciences, Renaissance School of Medicine at Stony Brook University, Stony Brook, NY, USA
                [3 ]Department of Neurology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, USA
                [4 ]Department of Gynecology and Obstetrics, Johns Hopkins Hospital, Baltimore, MD, USA
                Author notes
                [* ] Correspondence to: Stella E. Tsirka, styliani-anna.tsirka@ 123456stonybrook.edu .
                [#]

                These two authors contributed equally to this paper.

                Author contributions: NM and AA devised the experiments. NM, SD, and EX conducted the experiments. NM, GWK, SET, and AA analyzed the data. All authors participated in writing and editing of the manuscript and approved its final version .

                Author information
                https://orcid.org/0000-0003-0022-1770
                Article
                NRR-17-2472
                10.4103/1673-5374.339007
                9120697
                35535899
                964bf13e-fc0c-4e8e-ad14-d3565c3055ce
                Copyright: © Neural Regeneration Research

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : 17 May 2021
                : 01 July 2021
                : 04 August 2021
                Categories
                Research Article

                adam10,adhesion,junctional adhesion molecule c,neural stem cells,neurogenesis,olfactory bulb,rap1gap,sub-ventricular zone

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