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Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers

The morphology of microglial cells is often closely related to their functions. The mechanisms that regulate microglial ramification are not well understood. Here we reveal the biological mechanisms by which astrocytes regulate microglial ramification. Morphological variation in mouse microglial cul...

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Detalles Bibliográficos
Autores principales: Zhang, Jinqiang, Zhang, Lijuan, Yi, Saini, Jiang, Xue, Qiao, Yan, Zhang, Yue, Xiao, Chenghong, Zhou, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366495/
https://www.ncbi.nlm.nih.gov/pubmed/32754014
http://dx.doi.org/10.3389/fncel.2020.00195
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author Zhang, Jinqiang
Zhang, Lijuan
Yi, Saini
Jiang, Xue
Qiao, Yan
Zhang, Yue
Xiao, Chenghong
Zhou, Tao
author_facet Zhang, Jinqiang
Zhang, Lijuan
Yi, Saini
Jiang, Xue
Qiao, Yan
Zhang, Yue
Xiao, Chenghong
Zhou, Tao
author_sort Zhang, Jinqiang
collection PubMed
description The morphology of microglial cells is often closely related to their functions. The mechanisms that regulate microglial ramification are not well understood. Here we reveal the biological mechanisms by which astrocytes regulate microglial ramification. Morphological variation in mouse microglial cultures was measured in terms of cell area as well as branch number and length. Effects on microglial ramification were analyzed after microinjecting the toxin L-alpha-aminoadipic acid (L-AAA) in the mouse cortex or hippocampus to ablate astrocytes, and after culturing microglia on their own in an astrocyte-conditioned medium (ACM) or together with astrocytes in coculture. TGF-β expression was determined by Western blotting, immunohistochemistry, and ELISA. The TGF-β signaling pathway was blocked by the TGF-β antibody to assess the role of TGF-β on microglial ramification. The results showed that microglia had more and longer branches and smaller cell bodies in brain areas where astrocytes were abundant. In the mouse cortex and hippocampus, ablation of astrocytes by L-AAA decreased number and length of microglial branches and increased the size of cell bodies. Similar results were obtained with isolated microglia in culture. However, isolated microglia were able to maintain their multibranched structure for a long time when cultured on astrocyte monolayers. Ameboid microglia isolated from P0 to P3 mice showed increased ramification when cultured in ACM or on astrocyte monolayers. Microglia cultured on astrocyte monolayers showed more complex branching structures than those cultured in ACM. Blocking astrocyte-derived TGF-β decreased microglial ramification. Astrocytes induced the formation of protuberances on branches of microglia by forming glial fibers that increased traction. These experiments in mice suggest that astrocytes promote microglial ramification by forming glial fibers to create traction and by secreting soluble factors into the surroundings. For example, astrocyte-secreted TGF-β promotes microglia to generate primitive branches, whose ramification is refined by glial fibers.
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spelling pubmed-73664952020-08-03 Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers Zhang, Jinqiang Zhang, Lijuan Yi, Saini Jiang, Xue Qiao, Yan Zhang, Yue Xiao, Chenghong Zhou, Tao Front Cell Neurosci Cellular Neuroscience The morphology of microglial cells is often closely related to their functions. The mechanisms that regulate microglial ramification are not well understood. Here we reveal the biological mechanisms by which astrocytes regulate microglial ramification. Morphological variation in mouse microglial cultures was measured in terms of cell area as well as branch number and length. Effects on microglial ramification were analyzed after microinjecting the toxin L-alpha-aminoadipic acid (L-AAA) in the mouse cortex or hippocampus to ablate astrocytes, and after culturing microglia on their own in an astrocyte-conditioned medium (ACM) or together with astrocytes in coculture. TGF-β expression was determined by Western blotting, immunohistochemistry, and ELISA. The TGF-β signaling pathway was blocked by the TGF-β antibody to assess the role of TGF-β on microglial ramification. The results showed that microglia had more and longer branches and smaller cell bodies in brain areas where astrocytes were abundant. In the mouse cortex and hippocampus, ablation of astrocytes by L-AAA decreased number and length of microglial branches and increased the size of cell bodies. Similar results were obtained with isolated microglia in culture. However, isolated microglia were able to maintain their multibranched structure for a long time when cultured on astrocyte monolayers. Ameboid microglia isolated from P0 to P3 mice showed increased ramification when cultured in ACM or on astrocyte monolayers. Microglia cultured on astrocyte monolayers showed more complex branching structures than those cultured in ACM. Blocking astrocyte-derived TGF-β decreased microglial ramification. Astrocytes induced the formation of protuberances on branches of microglia by forming glial fibers that increased traction. These experiments in mice suggest that astrocytes promote microglial ramification by forming glial fibers to create traction and by secreting soluble factors into the surroundings. For example, astrocyte-secreted TGF-β promotes microglia to generate primitive branches, whose ramification is refined by glial fibers. Frontiers Media S.A. 2020-07-10 /pmc/articles/PMC7366495/ /pubmed/32754014 http://dx.doi.org/10.3389/fncel.2020.00195 Text en Copyright © 2020 Zhang, Zhang, Yi, Jiang, Qiao, Zhang, Xiao and Zhou. http://creativecommons.org/licenses/by/4.0/ 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.
spellingShingle Cellular Neuroscience
Zhang, Jinqiang
Zhang, Lijuan
Yi, Saini
Jiang, Xue
Qiao, Yan
Zhang, Yue
Xiao, Chenghong
Zhou, Tao
Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title_full Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title_fullStr Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title_full_unstemmed Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title_short Mouse Astrocytes Promote Microglial Ramification by Releasing TGF-β and Forming Glial Fibers
title_sort mouse astrocytes promote microglial ramification by releasing tgf-β and forming glial fibers
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366495/
https://www.ncbi.nlm.nih.gov/pubmed/32754014
http://dx.doi.org/10.3389/fncel.2020.00195
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