Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS
Abstract Background Microglia, the primary resident myeloid cells of the brain, play critical roles in immune defense by maintaining tissue homeostasis and responding to injury or disease. However, microglial activation and dysfunction has been implicated in a number of central nervous system (CNS)...
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BMC
2020-09-01
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Series: | Journal of Neuroinflammation |
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Online Access: | http://link.springer.com/article/10.1186/s12974-020-01931-0 |
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author | Lindsay A. Hohsfield Allison R. Najafi Yasamine Ghorbanian Neelakshi Soni Edna E. Hingco Sung Jin Kim Ayer Darling Jue Vivek Swarup Mathew A. Inlay Kim N. Green |
author_facet | Lindsay A. Hohsfield Allison R. Najafi Yasamine Ghorbanian Neelakshi Soni Edna E. Hingco Sung Jin Kim Ayer Darling Jue Vivek Swarup Mathew A. Inlay Kim N. Green |
author_sort | Lindsay A. Hohsfield |
collection | DOAJ |
description | Abstract Background Microglia, the primary resident myeloid cells of the brain, play critical roles in immune defense by maintaining tissue homeostasis and responding to injury or disease. However, microglial activation and dysfunction has been implicated in a number of central nervous system (CNS) disorders, thus developing tools to manipulate and replace these myeloid cells in the CNS is of therapeutic interest. Methods Using whole body irradiation, bone marrow transplant, and colony-stimulating factor 1 receptor inhibition, we achieve long-term and brain-wide (~ 80%) engraftment and colonization of peripheral bone marrow-derived myeloid cells (i.e., monocytes) in the brain parenchyma and evaluated the long-term effects of their colonization in the CNS. Results Here, we identify a monocyte signature that includes an upregulation in Ccr1, Ms4a6b, Ms4a6c, Ms4a7, Apobec1, Lyz2, Mrc1, Tmem221, Tlr8, Lilrb4a, Msr1, Nnt, and Wdfy1 and a downregulation of Siglech, Slc2a5, and Ccl21a/b. We demonstrate that irradiation and long-term (~ 6 months) engraftment of the CNS by monocytes induces brain region-dependent alterations in transcription profiles, astrocytes, neuronal structures, including synaptic components, and cognition. Although our results show that microglial replacement with peripherally derived myeloid cells is feasible and that irradiation-induced changes can be reversed by the replacement of microglia with monocytes in the hippocampus, we also observe that brain-wide engraftment of peripheral myeloid cells (relying on irradiation) can result in cognitive and synaptic deficits. Conclusions These findings provide insight into better understanding the role and complexity of myeloid cells in the brain, including their regulation of other CNS cells and functional outcomes. |
first_indexed | 2024-12-17T03:46:12Z |
format | Article |
id | doaj.art-2730dc4d642e42c2be9436563f4a7612 |
institution | Directory Open Access Journal |
issn | 1742-2094 |
language | English |
last_indexed | 2024-12-17T03:46:12Z |
publishDate | 2020-09-01 |
publisher | BMC |
record_format | Article |
series | Journal of Neuroinflammation |
spelling | doaj.art-2730dc4d642e42c2be9436563f4a76122022-12-21T22:04:53ZengBMCJournal of Neuroinflammation1742-20942020-09-0117112010.1186/s12974-020-01931-0Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNSLindsay A. Hohsfield0Allison R. Najafi1Yasamine Ghorbanian2Neelakshi Soni3Edna E. Hingco4Sung Jin Kim5Ayer Darling Jue6Vivek Swarup7Mathew A. Inlay8Kim N. Green9Department of Neurobiology and Behavior, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaSue and Bill Gross Stem Cell Research Center, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaSue and Bill Gross Stem Cell Research Center, University of CaliforniaDepartment of Neurobiology and Behavior, University of CaliforniaAbstract Background Microglia, the primary resident myeloid cells of the brain, play critical roles in immune defense by maintaining tissue homeostasis and responding to injury or disease. However, microglial activation and dysfunction has been implicated in a number of central nervous system (CNS) disorders, thus developing tools to manipulate and replace these myeloid cells in the CNS is of therapeutic interest. Methods Using whole body irradiation, bone marrow transplant, and colony-stimulating factor 1 receptor inhibition, we achieve long-term and brain-wide (~ 80%) engraftment and colonization of peripheral bone marrow-derived myeloid cells (i.e., monocytes) in the brain parenchyma and evaluated the long-term effects of their colonization in the CNS. Results Here, we identify a monocyte signature that includes an upregulation in Ccr1, Ms4a6b, Ms4a6c, Ms4a7, Apobec1, Lyz2, Mrc1, Tmem221, Tlr8, Lilrb4a, Msr1, Nnt, and Wdfy1 and a downregulation of Siglech, Slc2a5, and Ccl21a/b. We demonstrate that irradiation and long-term (~ 6 months) engraftment of the CNS by monocytes induces brain region-dependent alterations in transcription profiles, astrocytes, neuronal structures, including synaptic components, and cognition. Although our results show that microglial replacement with peripherally derived myeloid cells is feasible and that irradiation-induced changes can be reversed by the replacement of microglia with monocytes in the hippocampus, we also observe that brain-wide engraftment of peripheral myeloid cells (relying on irradiation) can result in cognitive and synaptic deficits. Conclusions These findings provide insight into better understanding the role and complexity of myeloid cells in the brain, including their regulation of other CNS cells and functional outcomes.http://link.springer.com/article/10.1186/s12974-020-01931-0MicrogliaMonocytesCSF1R inhibitionIrradiationBone marrow transplantBrain |
spellingShingle | Lindsay A. Hohsfield Allison R. Najafi Yasamine Ghorbanian Neelakshi Soni Edna E. Hingco Sung Jin Kim Ayer Darling Jue Vivek Swarup Mathew A. Inlay Kim N. Green Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS Journal of Neuroinflammation Microglia Monocytes CSF1R inhibition Irradiation Bone marrow transplant Brain |
title | Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS |
title_full | Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS |
title_fullStr | Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS |
title_full_unstemmed | Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS |
title_short | Effects of long-term and brain-wide colonization of peripheral bone marrow-derived myeloid cells in the CNS |
title_sort | effects of long term and brain wide colonization of peripheral bone marrow derived myeloid cells in the cns |
topic | Microglia Monocytes CSF1R inhibition Irradiation Bone marrow transplant Brain |
url | http://link.springer.com/article/10.1186/s12974-020-01931-0 |
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