Your browser doesn't support javascript.
loading
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.
Afiliação
  • Buchanan J; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Elabbady L; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Collman F; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Jorstad NL; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Bakken TE; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Ott C; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
  • Glatzer J; The Solomon H. Snyder Department of Neuroscience, John Hopkins University School of Medicine, Baltimore, MD 21205.
  • Bleckert AA; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Bodor AL; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Brittain D; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Bumbarger DJ; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Mahalingam G; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Seshamani S; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Schneider-Mizell C; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Takeno MM; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Torres R; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Yin W; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Hodge RD; Allen Institute for Brain Sciences, Seattle, WA 98109.
  • Castro M; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Dorkenwald S; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Ih D; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Jordan CS; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Kemnitz N; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Lee K; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Lu R; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Macrina T; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Mu S; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Popovych S; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Silversmith WM; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Tartavull I; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Turner NL; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Wilson AM; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Wong W; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Wu J; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Zlateski A; Computer Science Department, Princeton University, Princeton, NJ 08554.
  • Zung J; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Lippincott-Schwartz J; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Lein ES; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Seung HS; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Bergles DE; Princeton Neuroscience Institute, Princeton University, Princeton, NJ 08540.
  • Reid RC; Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147.
  • da Costa NM; Allen Institute for Brain Sciences, Seattle, WA 98109.
Proc Natl Acad Sci U S A ; 119(48): e2202580119, 2022 11 29.
Article em En | MEDLINE | ID: mdl-36417438
ABSTRACT
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.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neocórtex / Células Precursoras de Oligodendrócitos Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neocórtex / Células Precursoras de Oligodendrócitos Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article