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Aberrant fetal macrophage/microglial reactions to cytomegalovirus infection
http://hdl.handle.net/10271/3145
http://hdl.handle.net/10271/3145ab74604b-5f33-418e-8d13-4bb21b0a148f
名前 / ファイル | ライセンス | アクション |
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Item type | 学位論文 / Thesis or Dissertation(1) | |||||||
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公開日 | 2017-01-28 | |||||||
タイトル | ||||||||
タイトル | Aberrant fetal macrophage/microglial reactions to cytomegalovirus infection | |||||||
言語 | en | |||||||
言語 | ||||||||
言語 | eng | |||||||
資源タイプ | ||||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_db06 | |||||||
資源タイプ | doctoral thesis | |||||||
アクセス権 | ||||||||
アクセス権 | open access | |||||||
アクセス権URI | http://purl.org/coar/access_right/c_abf2 | |||||||
その他のタイトル | ||||||||
その他のタイトル | サイトメガロウイルス感染に対する胎生期マクロファージ/ミクログリア異常反応 | |||||||
著者 |
Suzuki, Makiko
× Suzuki, Makiko
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書誌情報 |
en : Annals of Clinical and Translational Neurology 巻 1, 号 8, p. 570-588, 発行日 2014-07-28 |
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出版者 | ||||||||
出版者 | American Neurological Association | |||||||
言語 | en | |||||||
抄録 | ||||||||
内容記述タイプ | Abstract | |||||||
内容記述 | Objective: Congenital cytomegalovirus (CMV) infection is the leading viral cause of neurodevelopmental disorders in humans, with the most severe and permanent sequelae being those affecting the cerebrum. As the fetal immune reactions to congenital CMV infection in the brain and their effects on cerebral development remain elusive, our aim was to investigate primitive innate immunity to CMV infection and its effects on cerebral corticogenesis in a mouse model for congenital CMV infection using a precise intraplacental inoculation method. Methods: At 13.5 embryonic days (E13.5), pregnant C57BL/6 mice were intraplacentally infected with murine CMV (MCMV). Placentas and fetal organs were collected at 1, 3, and 5 days postinfection and analyzed. Results: MCMV antigens were found frequently in perivascular macrophages, and subsequently in neural stem/progenitor cells (NSPCs). With increased expression of inducible nitric oxide synthase and proinflammatory cytokines, activated macrophages infiltrated into the infectious foci. In addition to the infected area, the numbers of both meningeal macrophages and parenchymal microglia increased even in the uninfected areas of MCMV-infected brain due to recruitment of their precursors from other sites. A bromodeoxyuridine (BrdU) incorporation experiment demonstrated that MCMV infection globally disrupted the self-renewal of NSPCs. Furthermore, BrdU-labeled neurons, particularly Brn2+ neurons of upper layers II/III in the cortical plate, decreased in number significantly in the MCMV-infected E18.5 cerebrum. Interpretation: Brain macrophages are crucial for innate immunity during MCMV infection in the fetal brain, while their aberrant recruitment and activation may adversely impact on the stemness of NSPCs, resulting in neurodevelopmental disorders. | |||||||
言語 | en | |||||||
学位名 | ||||||||
学位名 | 博士(医学) | |||||||
学位の区分 | ||||||||
内容記述 | doctoral | |||||||
学位の分野 | ||||||||
内容記述 | 医学系研究科 | |||||||
学位授与機関 | ||||||||
学位授与機関識別子Scheme | kakenhi | |||||||
学位授与機関識別子 | 13802 | |||||||
学位授与機関名 | 浜松医科大学 | |||||||
学位授与年月日 | ||||||||
学位授与年月日 | 2016-03-14 | |||||||
学位授与番号 | ||||||||
学位授与番号 | 甲第723号 | |||||||
ISSN | ||||||||
収録物識別子タイプ | PISSN | |||||||
収録物識別子 | 2328-9503 | |||||||
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収録物識別子タイプ | EISSN | |||||||
収録物識別子 | 2328-9503 | |||||||
PubMed番号 | ||||||||
識別子タイプ | PMID | |||||||
関連識別子 | 25356429 | |||||||
出版社DOI | ||||||||
識別子タイプ | DOI | |||||||
関連識別子 | https://doi.org/10.1002/acn3.88 | |||||||
著者版フラグ | ||||||||
出版タイプ | VoR | |||||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 |