Engulfing astrocytes protect neurons from contact-induced apoptosis following injury
Clearing of dead cells is a fundamental process to limit tissue damage following brain injury. Engulfment has classically been believed to be performed by professional phagocytes, but recent data show that non-professional phagocytes are highly involved in the removal of cell corpses in various situ...
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description | Clearing of dead cells is a fundamental process to limit tissue damage following brain injury. Engulfment has classically been believed to be performed by professional phagocytes, but recent data show that non-professional phagocytes are highly involved in the removal of cell corpses in various situations. The role of astrocytes in cell clearance following trauma has however not been studied in detail. We have found that astrocytes actively collect and engulf whole dead cells in an in vitro model of brain injury and thereby protect healthy neurons from bystander cell death. Time-lapse experiments showed that migrating neurons that come in contact with free-floating cell corpses induced apoptosis, while neurons that migrate through groups of dead cells, garnered by astrocytes, remain unaffected. Furthermore, apoptotic cells are present within astrocytes in the mouse brain following traumatic brain injury (TBI), indicating a possible role for astrocytes in engulfment of apoptotic cells in vivo. qRT-PCR analysis showed that members of both ced pathways and Megf8 are expressed in the cell culture, indicating their possible involvement in astrocytic engulfment. Moreover, addition of dead cells had a positive effect on the protein expression of MEGF10, an ortholog to CED1, known to initiate phagocytosis by binding to phosphatidylserine. Although cultured astrocytes have an immense capacity for engulfment, seemingly without adverse effects, the ingested material is stored rather than degraded. This finding might explain the multinuclear astrocytes that are found at the lesion site in patients with various brain disorders. |
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Engulfment has classically been believed to be performed by professional phagocytes, but recent data show that non-professional phagocytes are highly involved in the removal of cell corpses in various situations. The role of astrocytes in cell clearance following trauma has however not been studied in detail. We have found that astrocytes actively collect and engulf whole dead cells in an in vitro model of brain injury and thereby protect healthy neurons from bystander cell death. Time-lapse experiments showed that migrating neurons that come in contact with free-floating cell corpses induced apoptosis, while neurons that migrate through groups of dead cells, garnered by astrocytes, remain unaffected. Furthermore, apoptotic cells are present within astrocytes in the mouse brain following traumatic brain injury (TBI), indicating a possible role for astrocytes in engulfment of apoptotic cells in vivo. qRT-PCR analysis showed that members of both ced pathways and Megf8 are expressed in the cell culture, indicating their possible involvement in astrocytic engulfment. Moreover, addition of dead cells had a positive effect on the protein expression of MEGF10, an ortholog to CED1, known to initiate phagocytosis by binding to phosphatidylserine. Although cultured astrocytes have an immense capacity for engulfment, seemingly without adverse effects, the ingested material is stored rather than degraded. This finding might explain the multinuclear astrocytes that are found at the lesion site in patients with various brain disorders.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0033090</identifier><identifier>PMID: 22461890</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animals ; Apoptosis ; Apoptosis - physiology ; Astrocytes ; Astrocytes - metabolism ; Astrocytes - physiology ; Astrocytes - ultrastructure ; Biology ; Blotting, Western ; Brain ; Brain damage ; Brain injuries ; Brain Injuries - physiopathology ; Caenorhabditis elegans ; Cell Communication - physiology ; Cell culture ; Cell death ; Cell migration ; Cell Movement - physiology ; Cells, Cultured ; Chemokines ; Clearing ; Female ; Floating ; Glial Fibrillary Acidic Protein - genetics ; Glial Fibrillary Acidic Protein - metabolism ; Head injuries ; Injury prevention ; Male ; Medicine ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mice ; Mice, Inbred C57BL ; Microscopy ; Microscopy, Confocal ; Microscopy, Electron, Transmission ; Neurons ; Neurons - physiology ; Oligodendroglia - physiology ; Phagocytes ; Phagocytosis ; Phagocytosis - physiology ; Phosphatidylserine ; Reverse Transcriptase Polymerase Chain Reaction ; Rodents ; Stress, Mechanical ; Studies ; Traumatic brain injury</subject><ispartof>PloS one, 2012-03, Vol.7 (3), p.e33090-e33090</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Lööv et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Engulfment has classically been believed to be performed by professional phagocytes, but recent data show that non-professional phagocytes are highly involved in the removal of cell corpses in various situations. The role of astrocytes in cell clearance following trauma has however not been studied in detail. We have found that astrocytes actively collect and engulf whole dead cells in an in vitro model of brain injury and thereby protect healthy neurons from bystander cell death. Time-lapse experiments showed that migrating neurons that come in contact with free-floating cell corpses induced apoptosis, while neurons that migrate through groups of dead cells, garnered by astrocytes, remain unaffected. Furthermore, apoptotic cells are present within astrocytes in the mouse brain following traumatic brain injury (TBI), indicating a possible role for astrocytes in engulfment of apoptotic cells in vivo. qRT-PCR analysis showed that members of both ced pathways and Megf8 are expressed in the cell culture, indicating their possible involvement in astrocytic engulfment. Moreover, addition of dead cells had a positive effect on the protein expression of MEGF10, an ortholog to CED1, known to initiate phagocytosis by binding to phosphatidylserine. Although cultured astrocytes have an immense capacity for engulfment, seemingly without adverse effects, the ingested material is stored rather than degraded. This finding might explain the multinuclear astrocytes that are found at the lesion site in patients with various brain disorders.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22461890</pmid><doi>10.1371/journal.pone.0033090</doi><tpages>e33090</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Apoptosis Apoptosis - physiology Astrocytes Astrocytes - metabolism Astrocytes - physiology Astrocytes - ultrastructure Biology Blotting, Western Brain Brain damage Brain injuries Brain Injuries - physiopathology Caenorhabditis elegans Cell Communication - physiology Cell culture Cell death Cell migration Cell Movement - physiology Cells, Cultured Chemokines Clearing Female Floating Glial Fibrillary Acidic Protein - genetics Glial Fibrillary Acidic Protein - metabolism Head injuries Injury prevention Male Medicine Membrane Proteins - genetics Membrane Proteins - metabolism Mice Mice, Inbred C57BL Microscopy Microscopy, Confocal Microscopy, Electron, Transmission Neurons Neurons - physiology Oligodendroglia - physiology Phagocytes Phagocytosis Phagocytosis - physiology Phosphatidylserine Reverse Transcriptase Polymerase Chain Reaction Rodents Stress, Mechanical Studies Traumatic brain injury |
title | Engulfing astrocytes protect neurons from contact-induced apoptosis following injury |
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