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author Buchanan, JoAnn
Elabbady, Leila
Collman, Forrest
Jorstad, Nikolas L.
Bakken, Trygve E.
Ott, Carolyn
Glatzer, Jenna
Bleckert, Adam A.
Bodor, Agnes L.
Brittain, Derrick
Bumbarger, Daniel J.
Mahalingam, Gayathri
Seshamani, Sharmishtaa
Schneider-Mizell, Casey
Takeno, Marc M.
Torres, Russel
Yin, Wenjing
Hodge, Rebecca D.
Castro, Manuel
Dorkenwald, Sven
Ih, Dodam
Jordan, Chris S.
Kemnitz, Nico
Lee, Kisuk
Lu, Ran
Macrina, Thomas
Mu, Shang
Popovych, Sergiy
Silversmith, William M.
Tartavull, Ignacio
Turner, Nicholas L.
Wilson, Alyssa M.
Wong, William
Wu, Jingpeng
Zlateski, Aleksandar
Zung, Jonathan
Lippincott-Schwartz, Jennifer
Lein, Ed S.
Seung, H. Sebastian
Bergles, Dwight E.
Reid, R. Clay
da Costa, Nuno Maçarico
author_facet Buchanan, JoAnn
Elabbady, Leila
Collman, Forrest
Jorstad, Nikolas L.
Bakken, Trygve E.
Ott, Carolyn
Glatzer, Jenna
Bleckert, Adam A.
Bodor, Agnes L.
Brittain, Derrick
Bumbarger, Daniel J.
Mahalingam, Gayathri
Seshamani, Sharmishtaa
Schneider-Mizell, Casey
Takeno, Marc M.
Torres, Russel
Yin, Wenjing
Hodge, Rebecca D.
Castro, Manuel
Dorkenwald, Sven
Ih, Dodam
Jordan, Chris S.
Kemnitz, Nico
Lee, Kisuk
Lu, Ran
Macrina, Thomas
Mu, Shang
Popovych, Sergiy
Silversmith, William M.
Tartavull, Ignacio
Turner, Nicholas L.
Wilson, Alyssa M.
Wong, William
Wu, Jingpeng
Zlateski, Aleksandar
Zung, Jonathan
Lippincott-Schwartz, Jennifer
Lein, Ed S.
Seung, H. Sebastian
Bergles, Dwight E.
Reid, R. Clay
da Costa, Nuno Maçarico
author_sort Buchanan, JoAnn
collection PubMed
description Neurons in the developing brain undergo extensive structural refinement as nascent circuits adopt their mature form. This physical transformation of neurons is facilitated by the engulfment and degradation of axonal branches and synapses by surrounding glial cells, including microglia and astrocytes. However, the small size of phagocytic organelles and the complex, highly ramified morphology of glia have made it difficult to define the contribution of these and other glial cell types to this crucial process. Here, we used large-scale, serial section transmission electron microscopy (TEM) with computational volume segmentation to reconstruct the complete 3D morphologies of distinct glial types in the mouse visual cortex, providing unprecedented resolution of their morphology and composition. Unexpectedly, we discovered that the fine processes of oligodendrocyte precursor cells (OPCs), a population of abundant, highly dynamic glial progenitors, frequently surrounded small branches of axons. Numerous phagosomes and phagolysosomes (PLs) containing fragments of axons and vesicular structures were present inside their processes, suggesting that OPCs engage in axon pruning. Single-nucleus RNA sequencing from the developing mouse cortex revealed that OPCs express key phagocytic genes at this stage, as well as neuronal transcripts, consistent with active axon engulfment. Although microglia are thought to be responsible for the majority of synaptic pruning and structural refinement, PLs were ten times more abundant in OPCs than in microglia at this stage, and these structures were markedly less abundant in newly generated oligodendrocytes, suggesting that OPCs contribute substantially to the refinement of neuronal circuits during cortical development.
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spelling pubmed-98898862023-02-02 Oligodendrocyte precursor cells ingest axons in the mouse neocortex Buchanan, JoAnn Elabbady, Leila Collman, Forrest Jorstad, Nikolas L. Bakken, Trygve E. Ott, Carolyn Glatzer, Jenna Bleckert, Adam A. Bodor, Agnes L. Brittain, Derrick Bumbarger, Daniel J. Mahalingam, Gayathri Seshamani, Sharmishtaa Schneider-Mizell, Casey Takeno, Marc M. Torres, Russel Yin, Wenjing Hodge, Rebecca D. Castro, Manuel Dorkenwald, Sven Ih, Dodam Jordan, Chris S. Kemnitz, Nico Lee, Kisuk Lu, Ran Macrina, Thomas Mu, Shang Popovych, Sergiy Silversmith, William M. Tartavull, Ignacio Turner, Nicholas L. Wilson, Alyssa M. Wong, William Wu, Jingpeng Zlateski, Aleksandar Zung, Jonathan Lippincott-Schwartz, Jennifer Lein, Ed S. Seung, H. Sebastian Bergles, Dwight E. Reid, R. Clay da Costa, Nuno Maçarico Proc Natl Acad Sci U S A Biological Sciences Neurons in the developing brain undergo extensive structural refinement as nascent circuits adopt their mature form. This physical transformation of neurons is facilitated by the engulfment and degradation of axonal branches and synapses by surrounding glial cells, including microglia and astrocytes. However, the small size of phagocytic organelles and the complex, highly ramified morphology of glia have made it difficult to define the contribution of these and other glial cell types to this crucial process. Here, we used large-scale, serial section transmission electron microscopy (TEM) with computational volume segmentation to reconstruct the complete 3D morphologies of distinct glial types in the mouse visual cortex, providing unprecedented resolution of their morphology and composition. Unexpectedly, we discovered that the fine processes of oligodendrocyte precursor cells (OPCs), a population of abundant, highly dynamic glial progenitors, frequently surrounded small branches of axons. Numerous phagosomes and phagolysosomes (PLs) containing fragments of axons and vesicular structures were present inside their processes, suggesting that OPCs engage in axon pruning. Single-nucleus RNA sequencing from the developing mouse cortex revealed that OPCs express key phagocytic genes at this stage, as well as neuronal transcripts, consistent with active axon engulfment. Although microglia are thought to be responsible for the majority of synaptic pruning and structural refinement, PLs were ten times more abundant in OPCs than in microglia at this stage, and these structures were markedly less abundant in newly generated oligodendrocytes, suggesting that OPCs contribute substantially to the refinement of neuronal circuits during cortical development. National Academy of Sciences 2022-11-23 2022-11-29 /pmc/articles/PMC9889886/ /pubmed/36417438 http://dx.doi.org/10.1073/pnas.2202580119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Buchanan, JoAnn
Elabbady, Leila
Collman, Forrest
Jorstad, Nikolas L.
Bakken, Trygve E.
Ott, Carolyn
Glatzer, Jenna
Bleckert, Adam A.
Bodor, Agnes L.
Brittain, Derrick
Bumbarger, Daniel J.
Mahalingam, Gayathri
Seshamani, Sharmishtaa
Schneider-Mizell, Casey
Takeno, Marc M.
Torres, Russel
Yin, Wenjing
Hodge, Rebecca D.
Castro, Manuel
Dorkenwald, Sven
Ih, Dodam
Jordan, Chris S.
Kemnitz, Nico
Lee, Kisuk
Lu, Ran
Macrina, Thomas
Mu, Shang
Popovych, Sergiy
Silversmith, William M.
Tartavull, Ignacio
Turner, Nicholas L.
Wilson, Alyssa M.
Wong, William
Wu, Jingpeng
Zlateski, Aleksandar
Zung, Jonathan
Lippincott-Schwartz, Jennifer
Lein, Ed S.
Seung, H. Sebastian
Bergles, Dwight E.
Reid, R. Clay
da Costa, Nuno Maçarico
Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title_full Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title_fullStr Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title_full_unstemmed Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title_short Oligodendrocyte precursor cells ingest axons in the mouse neocortex
title_sort oligodendrocyte precursor cells ingest axons in the mouse neocortex
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9889886/
https://www.ncbi.nlm.nih.gov/pubmed/36417438
http://dx.doi.org/10.1073/pnas.2202580119
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