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Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats

Microglia, as the resident immune cells in the central nervous system, play important roles in regulating neuronal processes, such as neural excitability, synaptic activity, and apoptotic cell clearance. Growth factors can activate multiple signaling pathways in central nervous system microglia and...

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Autores principales: Liu, Ruo-Xu, Ma, Jie, Guo, Ning, Liu, Shao-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437599/
https://www.ncbi.nlm.nih.gov/pubmed/32209776
http://dx.doi.org/10.4103/1673-5374.276342
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author Liu, Ruo-Xu
Ma, Jie
Guo, Ning
Liu, Shao-Jun
author_facet Liu, Ruo-Xu
Ma, Jie
Guo, Ning
Liu, Shao-Jun
author_sort Liu, Ruo-Xu
collection PubMed
description Microglia, as the resident immune cells in the central nervous system, play important roles in regulating neuronal processes, such as neural excitability, synaptic activity, and apoptotic cell clearance. Growth factors can activate multiple signaling pathways in central nervous system microglia and can regulate their immune effects, but whether growth factors can affect the morphological characteristics and ultrastructure of microglia has not been reported. After microinjecting 300 nL of a growth factor cocktail, including 10 μg/mL epidermal growth factor, 10 μg/mL basic fibroblast growth factor, 10 μg/mL hepatocyte growth factor and 10 μg/mL insulin-like growth factor into adult rat cortex, we found that the number of IBA1-positive microglia around the injection area increased significantly, indicating local activation of microglia. All CD68-positive labeling co-localized with IBA1 in microglia. Cell bodies and protrusions of CD68-positive cells were strongly attached to or were engulfing neurons. Characteristic huge phagosomes were observed in activated phagocytes by electron microscopy. The phagosomes generally included non-degraded neuronal protrusions and mitochondria, yet they contained no myelin membrane or remnants, which might indicate selective phagocytosis by the phagocytes. The remnant myelin sheath after phagocytosis still had regenerative ability and formed “myelin-like” structures around phagocytes. These results show that microinjection of a growth factor cocktail into the cerebral cortex of rodents can locally activate microglia and induce selective phagocytosis of neural structures by phagocytes. The study was approved by the Institute of Laboratory Animal Science, Beijing Institute of Basic Medical Sciences (approval No. IACUC-AMMS-2014-501) on June 30, 2014.
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spelling pubmed-74375992020-08-28 Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats Liu, Ruo-Xu Ma, Jie Guo, Ning Liu, Shao-Jun Neural Regen Res Research Article Microglia, as the resident immune cells in the central nervous system, play important roles in regulating neuronal processes, such as neural excitability, synaptic activity, and apoptotic cell clearance. Growth factors can activate multiple signaling pathways in central nervous system microglia and can regulate their immune effects, but whether growth factors can affect the morphological characteristics and ultrastructure of microglia has not been reported. After microinjecting 300 nL of a growth factor cocktail, including 10 μg/mL epidermal growth factor, 10 μg/mL basic fibroblast growth factor, 10 μg/mL hepatocyte growth factor and 10 μg/mL insulin-like growth factor into adult rat cortex, we found that the number of IBA1-positive microglia around the injection area increased significantly, indicating local activation of microglia. All CD68-positive labeling co-localized with IBA1 in microglia. Cell bodies and protrusions of CD68-positive cells were strongly attached to or were engulfing neurons. Characteristic huge phagosomes were observed in activated phagocytes by electron microscopy. The phagosomes generally included non-degraded neuronal protrusions and mitochondria, yet they contained no myelin membrane or remnants, which might indicate selective phagocytosis by the phagocytes. The remnant myelin sheath after phagocytosis still had regenerative ability and formed “myelin-like” structures around phagocytes. These results show that microinjection of a growth factor cocktail into the cerebral cortex of rodents can locally activate microglia and induce selective phagocytosis of neural structures by phagocytes. The study was approved by the Institute of Laboratory Animal Science, Beijing Institute of Basic Medical Sciences (approval No. IACUC-AMMS-2014-501) on June 30, 2014. Wolters Kluwer - Medknow 2020-02-28 /pmc/articles/PMC7437599/ /pubmed/32209776 http://dx.doi.org/10.4103/1673-5374.276342 Text en Copyright: © 2020 Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/4.0 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.
spellingShingle Research Article
Liu, Ruo-Xu
Ma, Jie
Guo, Ning
Liu, Shao-Jun
Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title_full Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title_fullStr Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title_full_unstemmed Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title_short Microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
title_sort microinjection of a growth factor cocktail affects activated microglia in the neocortex of adult rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437599/
https://www.ncbi.nlm.nih.gov/pubmed/32209776
http://dx.doi.org/10.4103/1673-5374.276342
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