缺血性卒中后干细胞和小胶质细胞/巨噬细胞中CD44的表达。

Q1 Biochemistry, Genetics and Molecular Biology
Stem cell investigation Pub Date : 2020-03-10 eCollection Date: 2020-01-01 DOI:10.21037/sci.2020.02.02
Rikako Sawada, Akiko Nakano-Doi, Tomohiro Matsuyama, Nami Nakagomi, Takayuki Nakagomi
{"title":"缺血性卒中后干细胞和小胶质细胞/巨噬细胞中CD44的表达。","authors":"Rikako Sawada,&nbsp;Akiko Nakano-Doi,&nbsp;Tomohiro Matsuyama,&nbsp;Nami Nakagomi,&nbsp;Takayuki Nakagomi","doi":"10.21037/sci.2020.02.02","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>CD44, an adhesion molecule in the hyaluronate receptor family, plays diverse and important roles in multiple cell types and organs. Increasing evidence is mounting for CD44 expression in various types of stem cells and niche cells surrounding stem cells. However, the precise phenotypes of CD44<sup>+</sup> cells in the brain under pathologic conditions, such as after ischemic stroke, remain unclear.</p><p><strong>Methods: </strong>In the present study, using a mouse model for cerebral infarction by middle cerebral artery (MCA) occlusion, we examined the localization and traits of CD44<sup>+</sup> cells.</p><p><strong>Results: </strong>In sham-mice operations, CD44 was rarely observed in the cortex of MCA regions. Following ischemic stroke, CD44<sup>+</sup> cells emerged in ischemic areas of the MCA cortex during the acute phase. Although CD44 at ischemic areas was, in part, expressed in stem cells, it was also expressed in hematopoietic lineages, including activated microglia/macrophages, surrounding the stem cells. CD44 expression in microglia/macrophages persisted through the chronic phase following ischemic stroke.</p><p><strong>Conclusions: </strong>These data demonstrate that CD44 is expressed in stem cells and cells in the niches surrounding them, including inflammatory cells, suggesting that CD44 may play an important role in reparative processes within ischemic areas under neuroinflammatory conditions; in particular, strokes.</p>","PeriodicalId":21938,"journal":{"name":"Stem cell investigation","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.21037/sci.2020.02.02","citationCount":"11","resultStr":"{\"title\":\"CD44 expression in stem cells and niche microglia/macrophages following ischemic stroke.\",\"authors\":\"Rikako Sawada,&nbsp;Akiko Nakano-Doi,&nbsp;Tomohiro Matsuyama,&nbsp;Nami Nakagomi,&nbsp;Takayuki Nakagomi\",\"doi\":\"10.21037/sci.2020.02.02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>CD44, an adhesion molecule in the hyaluronate receptor family, plays diverse and important roles in multiple cell types and organs. Increasing evidence is mounting for CD44 expression in various types of stem cells and niche cells surrounding stem cells. However, the precise phenotypes of CD44<sup>+</sup> cells in the brain under pathologic conditions, such as after ischemic stroke, remain unclear.</p><p><strong>Methods: </strong>In the present study, using a mouse model for cerebral infarction by middle cerebral artery (MCA) occlusion, we examined the localization and traits of CD44<sup>+</sup> cells.</p><p><strong>Results: </strong>In sham-mice operations, CD44 was rarely observed in the cortex of MCA regions. Following ischemic stroke, CD44<sup>+</sup> cells emerged in ischemic areas of the MCA cortex during the acute phase. Although CD44 at ischemic areas was, in part, expressed in stem cells, it was also expressed in hematopoietic lineages, including activated microglia/macrophages, surrounding the stem cells. CD44 expression in microglia/macrophages persisted through the chronic phase following ischemic stroke.</p><p><strong>Conclusions: </strong>These data demonstrate that CD44 is expressed in stem cells and cells in the niches surrounding them, including inflammatory cells, suggesting that CD44 may play an important role in reparative processes within ischemic areas under neuroinflammatory conditions; in particular, strokes.</p>\",\"PeriodicalId\":21938,\"journal\":{\"name\":\"Stem cell investigation\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-03-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.21037/sci.2020.02.02\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Stem cell investigation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21037/sci.2020.02.02\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem cell investigation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/sci.2020.02.02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 11

摘要

背景:CD44是透明质酸受体家族中的粘附分子,在多种细胞类型和器官中发挥着多样而重要的作用。越来越多的证据表明,CD44在各种类型的干细胞和干细胞周围的小生境细胞中表达。然而,在病理条件下,如缺血性中风后,大脑中CD44+细胞的确切表型仍不清楚。方法:采用大脑中动脉闭塞性脑梗死小鼠模型,观察CD44+细胞的定位及特征。结果:在假小鼠手术中,在MCA区皮层中很少观察到CD44。缺血性卒中后,急性期MCA皮质缺血区域出现CD44+细胞。尽管缺血区域的CD44部分在干细胞中表达,但它也在造血谱系中表达,包括干细胞周围活化的小胶质细胞/巨噬细胞。在缺血性脑卒中后的慢性期,小胶质细胞/巨噬细胞中的CD44表达持续存在。结论:这些数据表明,CD44在干细胞及其周围小生境细胞中表达,包括炎症细胞,这表明CD44可能在神经炎症条件下缺血区域的修复过程中发挥重要作用;特别是中风。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CD44 expression in stem cells and niche microglia/macrophages following ischemic stroke.

Background: CD44, an adhesion molecule in the hyaluronate receptor family, plays diverse and important roles in multiple cell types and organs. Increasing evidence is mounting for CD44 expression in various types of stem cells and niche cells surrounding stem cells. However, the precise phenotypes of CD44+ cells in the brain under pathologic conditions, such as after ischemic stroke, remain unclear.

Methods: In the present study, using a mouse model for cerebral infarction by middle cerebral artery (MCA) occlusion, we examined the localization and traits of CD44+ cells.

Results: In sham-mice operations, CD44 was rarely observed in the cortex of MCA regions. Following ischemic stroke, CD44+ cells emerged in ischemic areas of the MCA cortex during the acute phase. Although CD44 at ischemic areas was, in part, expressed in stem cells, it was also expressed in hematopoietic lineages, including activated microglia/macrophages, surrounding the stem cells. CD44 expression in microglia/macrophages persisted through the chronic phase following ischemic stroke.

Conclusions: These data demonstrate that CD44 is expressed in stem cells and cells in the niches surrounding them, including inflammatory cells, suggesting that CD44 may play an important role in reparative processes within ischemic areas under neuroinflammatory conditions; in particular, strokes.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Stem cell investigation
Stem cell investigation Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
5.80
自引率
0.00%
发文量
9
期刊介绍: The Stem Cell Investigation (SCI; Stem Cell Investig; Online ISSN: 2313-0792) is a free access, peer-reviewed online journal covering basic, translational, and clinical research on all aspects of stem cells. It publishes original research articles and reviews on embryonic stem cells, induced pluripotent stem cells, adult tissue-specific stem/progenitor cells, cancer stem like cells, stem cell niche, stem cell technology, stem cell based drug discovery, and regenerative medicine. Stem Cell Investigation is indexed in PubMed/PMC since April, 2016.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信