• Neuroscience · Jul 2020

    Response to Hypoxic Preconditioning of Glial Cells from the Roof of the Fourth Ventricle.

    • Marymar Becerra-González, Ragu Varman Durairaj, Aline Ostos Valverde, Emilio J Gualda, Pablo Loza-Alvarez, Wendy Portillo Martínez, Gómez-González Gabriela Berenice GB Instituto de Neurobiología, Departamento de Neurobiología Celular y Molecular, Laboratorio de Neurobiología Molecular y Celular, Unive, Annalisa Buffo, and Ataúlfo Martínez-Torres.
    • Instituto de Neurobiología, Departamento de Neurobiología Celular y Molecular, Laboratorio de Neurobiología Molecular y Celular, Universidad Nacional Autónoma de México, Juriquilla, Querétaro 76230, Mexico.
    • Neuroscience. 2020 Jul 15; 439: 211-229.

    AbstractThe cerebellum harbors a specialized area on the roof of the fourth ventricle that is composed of glial cells and neurons that interface with the cerebrospinal fluid. This region includes the so-called ventromedial cord (VMC), which is composed of cells that are glial fibrillary acidic protein (GFAP)-positive and nestin-positive and distributes along the midline in association with blood vessels. We hypothesized that these cells should compare to GFAP and nestin-positive cells that are known to exist in other areas of the brain, which undergo proliferation and differentiation under hypoxic conditions. Thus, we tested whether cells of the VMC would display a similar reaction to hypoxic preconditioning (HPC). Indeed, we found that the VMC does respond to HPC by reorganizing its cellular components before it gradually returns to its basal state after about a week. This response we documented by monitoring global changes in the expression of GFAP-EGFP in transgenic mice, using light-sheet fluorescence microscopy (LSFM) revealed a dramatic loss of EGFP upon HPC, and was paralleled by retraction of Bergmann glial cell processes. This EGFP loss was supported by western blot analysis, which also showed a loss in the astrocyte-markers GFAP and ALDH1L1. On the other hand, other cell-markers appeared to be upregulated in the blots (including nestin, NeuN, and Iba1). Finally, we found that HPC does not remarkably affect the incorporation of BrdU into cells on the cerebellum, but strongly augments BrdU incorporation into periventricular cells on the floor of the fourth ventricle over the adjacent medulla.Copyright © 2019 IBRO. Published by Elsevier Ltd. All rights reserved.

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