Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina

Abstract Microglial cells are the primary resident immune cells in the retina. In healthy adults, they are ramified; that is, they have extensive processes that move continually. In adult retinas, microglia maintain the normal structure and function of neurons and other glial cells, but the mechanis...

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Main Authors: Megan Goyal, Andrea S. Bordt, Jay Neitz, David W. Marshak
Format: Article
Language:English
Published: Nature Portfolio 2023-01-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-27453-2
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author Megan Goyal
Andrea S. Bordt
Jay Neitz
David W. Marshak
author_facet Megan Goyal
Andrea S. Bordt
Jay Neitz
David W. Marshak
author_sort Megan Goyal
collection DOAJ
description Abstract Microglial cells are the primary resident immune cells in the retina. In healthy adults, they are ramified; that is, they have extensive processes that move continually. In adult retinas, microglia maintain the normal structure and function of neurons and other glial cells, but the mechanism underlying this process is not well-understood. In the mouse hippocampus, microglia engulf small pieces of axons and presynaptic terminals via a process called trogocytosis. Here we report that microglia in the adult macaque retina also engulf pieces of neurons and glial cells, but not at sites of synapses. We analyzed microglia in a volume of serial, ultrathin sections of central macaque retina in which many neurons that ramify in the inner plexiform layer (IPL) had been reconstructed previously. We surveyed the IPL and identified the somas of microglia by their small size and scant cytoplasm. We then reconstructed the microglia and studied their interactions with other cells. We found that ramified microglia frequently ingested small pieces of each major type of inner retinal neuron and Müller glial cells via trogocytosis. There were a few instances where the interactions took place near synapses, but the synapses, themselves, were never engulfed. If trogocytosis by retinal microglia plays a role in synaptic remodeling, it was not apparent from the ultrastructure. Instead, we propose that trogocytosis enables these microglia to present antigens derived from normal inner retinal cells and, when activated, they would promote antigen-specific tolerance.
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spelling doaj.art-b6598bafbae5425f9074b5d7310e0edc2023-01-15T12:12:43ZengNature PortfolioScientific Reports2045-23222023-01-011311810.1038/s41598-023-27453-2Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retinaMegan Goyal0Andrea S. Bordt1Jay Neitz2David W. Marshak3Department of Neurobiology and Anatomy, McGovern Medical SchoolDepartment of Neurobiology and Anatomy, McGovern Medical SchoolDepartment of Ophthalmology, University of WashingtonDepartment of Neurobiology and Anatomy, McGovern Medical SchoolAbstract Microglial cells are the primary resident immune cells in the retina. In healthy adults, they are ramified; that is, they have extensive processes that move continually. In adult retinas, microglia maintain the normal structure and function of neurons and other glial cells, but the mechanism underlying this process is not well-understood. In the mouse hippocampus, microglia engulf small pieces of axons and presynaptic terminals via a process called trogocytosis. Here we report that microglia in the adult macaque retina also engulf pieces of neurons and glial cells, but not at sites of synapses. We analyzed microglia in a volume of serial, ultrathin sections of central macaque retina in which many neurons that ramify in the inner plexiform layer (IPL) had been reconstructed previously. We surveyed the IPL and identified the somas of microglia by their small size and scant cytoplasm. We then reconstructed the microglia and studied their interactions with other cells. We found that ramified microglia frequently ingested small pieces of each major type of inner retinal neuron and Müller glial cells via trogocytosis. There were a few instances where the interactions took place near synapses, but the synapses, themselves, were never engulfed. If trogocytosis by retinal microglia plays a role in synaptic remodeling, it was not apparent from the ultrastructure. Instead, we propose that trogocytosis enables these microglia to present antigens derived from normal inner retinal cells and, when activated, they would promote antigen-specific tolerance.https://doi.org/10.1038/s41598-023-27453-2
spellingShingle Megan Goyal
Andrea S. Bordt
Jay Neitz
David W. Marshak
Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
Scientific Reports
title Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
title_full Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
title_fullStr Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
title_full_unstemmed Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
title_short Trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
title_sort trogocytosis of neurons and glial cells by microglia in a healthy adult macaque retina
url https://doi.org/10.1038/s41598-023-27453-2
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