Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.

<h4>Background and purpose</h4>Microglia are resident immunocompetent and phagocytic cells of central nervous system (CNS), which produce various cytokines and growth factors in response to injury and thereby regulate disease pathology. The purpose of this study is to investigate the eff...

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Main Authors: Dashdemberel Narantuya, Atsushi Nagai, Abdullah Md Sheikh, Junichi Masuda, Shotai Kobayashi, Shuhei Yamaguchi, Seung U Kim
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-07-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20668522/?tool=EBI
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author Dashdemberel Narantuya
Atsushi Nagai
Abdullah Md Sheikh
Junichi Masuda
Shotai Kobayashi
Shuhei Yamaguchi
Seung U Kim
author_facet Dashdemberel Narantuya
Atsushi Nagai
Abdullah Md Sheikh
Junichi Masuda
Shotai Kobayashi
Shuhei Yamaguchi
Seung U Kim
author_sort Dashdemberel Narantuya
collection DOAJ
description <h4>Background and purpose</h4>Microglia are resident immunocompetent and phagocytic cells of central nervous system (CNS), which produce various cytokines and growth factors in response to injury and thereby regulate disease pathology. The purpose of this study is to investigate the effects of microglial transplantation on focal cerebral ischemia model in rat.<h4>Methods</h4>Transient middle cerebral artery occlusion (MCAO) in rats was induced by the intraluminal filament technique. HMO6 cells, human microglial cell line, were transplanted intravenously at 48 hours after MCAO. Functional tests were performed and the infarct volume was measured at 7 and 14 days after MCAO. Migration and cell survival of transplanted microglial cells and host glial reaction in the brain were studied by immunohistochemistry. Gene expression of neurotrophic factors, cytokines and chemokines in transplanted cells and host rat glial cells was determined by laser capture microdissection (LCM) and quantitative real time-PCR.<h4>Results</h4>HMO6 human microglial cells transplantation group demonstrated significant functional recovery compared with control group. At 7 and 14 days after MCAO, infarct volume was significantly reduced in the HMO group. In the HMO6 group, number of apoptotic cells was time-dependently reduced in the infarct core and penumbra. In addition, number of host rat microglia/macrophages and reactive astrocytes was significantly decreased at 7 and 14 days after MCAO in the penumbra. Gene expression of various neurotrophic factors (GDNF, BDNF, VEGF and BMP7) and anti-inflammatory cytokines (IL4 and IL5) was up-regulated in transplanted HMO6 cells of brain tissue compared with those in culture. The expression of GDNF and VEGF in astrocytes in penumbra was significantly up-regulated in the HMO6 group.<h4>Conclusions</h4>Our results indicate that transplantation of HMO6 human microglial cells reduces ischemic deficits and apoptotic events in stroke animals. The results were mediated by modulation of gliosis and neuroinflammation, and neuroprotection provided by neurotrophic factors of endogenous and transplanted cells-origin.
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spelling doaj.art-ffa54785354e4f9384ac05d2ff9cb8bb2022-12-21T20:37:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-07-0157e1174610.1371/journal.pone.0011746Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.Dashdemberel NarantuyaAtsushi NagaiAbdullah Md SheikhJunichi MasudaShotai KobayashiShuhei YamaguchiSeung U Kim<h4>Background and purpose</h4>Microglia are resident immunocompetent and phagocytic cells of central nervous system (CNS), which produce various cytokines and growth factors in response to injury and thereby regulate disease pathology. The purpose of this study is to investigate the effects of microglial transplantation on focal cerebral ischemia model in rat.<h4>Methods</h4>Transient middle cerebral artery occlusion (MCAO) in rats was induced by the intraluminal filament technique. HMO6 cells, human microglial cell line, were transplanted intravenously at 48 hours after MCAO. Functional tests were performed and the infarct volume was measured at 7 and 14 days after MCAO. Migration and cell survival of transplanted microglial cells and host glial reaction in the brain were studied by immunohistochemistry. Gene expression of neurotrophic factors, cytokines and chemokines in transplanted cells and host rat glial cells was determined by laser capture microdissection (LCM) and quantitative real time-PCR.<h4>Results</h4>HMO6 human microglial cells transplantation group demonstrated significant functional recovery compared with control group. At 7 and 14 days after MCAO, infarct volume was significantly reduced in the HMO group. In the HMO6 group, number of apoptotic cells was time-dependently reduced in the infarct core and penumbra. In addition, number of host rat microglia/macrophages and reactive astrocytes was significantly decreased at 7 and 14 days after MCAO in the penumbra. Gene expression of various neurotrophic factors (GDNF, BDNF, VEGF and BMP7) and anti-inflammatory cytokines (IL4 and IL5) was up-regulated in transplanted HMO6 cells of brain tissue compared with those in culture. The expression of GDNF and VEGF in astrocytes in penumbra was significantly up-regulated in the HMO6 group.<h4>Conclusions</h4>Our results indicate that transplantation of HMO6 human microglial cells reduces ischemic deficits and apoptotic events in stroke animals. The results were mediated by modulation of gliosis and neuroinflammation, and neuroprotection provided by neurotrophic factors of endogenous and transplanted cells-origin.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20668522/?tool=EBI
spellingShingle Dashdemberel Narantuya
Atsushi Nagai
Abdullah Md Sheikh
Junichi Masuda
Shotai Kobayashi
Shuhei Yamaguchi
Seung U Kim
Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
PLoS ONE
title Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
title_full Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
title_fullStr Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
title_full_unstemmed Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
title_short Human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement.
title_sort human microglia transplanted in rat focal ischemia brain induce neuroprotection and behavioral improvement
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20668522/?tool=EBI
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