NOD小鼠自然杀伤细胞功能成熟和细胞溶解功能的解耦

IF 3.2 4区 医学 Q3 CELL BIOLOGY Immunology & Cell Biology Pub Date : 2023-08-03 DOI:10.1111/imcb.12676
Capucine Bourel, Victor Mullins-Dansereau, Maher Al Khaldi, Geneviève Chabot-Roy, Félix Lombard-Vadnais, Sylvie Lesage
{"title":"NOD小鼠自然杀伤细胞功能成熟和细胞溶解功能的解耦","authors":"Capucine Bourel,&nbsp;Victor Mullins-Dansereau,&nbsp;Maher Al Khaldi,&nbsp;Geneviève Chabot-Roy,&nbsp;Félix Lombard-Vadnais,&nbsp;Sylvie Lesage","doi":"10.1111/imcb.12676","DOIUrl":null,"url":null,"abstract":"<p>NK cells are innate immune cells that target infected and tumor cells. Mature NK (mNK) cells undergo functional maturation characterized by four distinct stages, during which they acquire their cytotoxic properties. mNK cells from non-obese diabetic (NOD) mice exhibit a defect in functional maturation and have impaired cytotoxic functions. Hence, we tested whether the impaired cytotoxic function observed in mNK cells from NOD mice can be explained by their defect in functional maturation. By comparing the function of mNK cells from B6, B6<sup>g7</sup> and NOD mice, we show that the expression of granzyme B is severely impaired in mNK cells from NOD mice, agreeing with their inability to control tumor growth <i>in vivo</i>. The low level of granzyme B expression in mNK cells from NOD mice is found at all stages of functional maturation and is therefore independent of their functional maturation defect. Consequently, this study demonstrates that phenotypic functional maturation of mNK cells can be uncoupled from the acquisition of cytotoxic functions.</p>","PeriodicalId":179,"journal":{"name":"Immunology & Cell Biology","volume":"101 9","pages":"867-874"},"PeriodicalIF":3.2000,"publicationDate":"2023-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/imcb.12676","citationCount":"0","resultStr":"{\"title\":\"Uncoupling of Natural Killer cell functional maturation and cytolytic function in NOD mice\",\"authors\":\"Capucine Bourel,&nbsp;Victor Mullins-Dansereau,&nbsp;Maher Al Khaldi,&nbsp;Geneviève Chabot-Roy,&nbsp;Félix Lombard-Vadnais,&nbsp;Sylvie Lesage\",\"doi\":\"10.1111/imcb.12676\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>NK cells are innate immune cells that target infected and tumor cells. Mature NK (mNK) cells undergo functional maturation characterized by four distinct stages, during which they acquire their cytotoxic properties. mNK cells from non-obese diabetic (NOD) mice exhibit a defect in functional maturation and have impaired cytotoxic functions. Hence, we tested whether the impaired cytotoxic function observed in mNK cells from NOD mice can be explained by their defect in functional maturation. By comparing the function of mNK cells from B6, B6<sup>g7</sup> and NOD mice, we show that the expression of granzyme B is severely impaired in mNK cells from NOD mice, agreeing with their inability to control tumor growth <i>in vivo</i>. The low level of granzyme B expression in mNK cells from NOD mice is found at all stages of functional maturation and is therefore independent of their functional maturation defect. Consequently, this study demonstrates that phenotypic functional maturation of mNK cells can be uncoupled from the acquisition of cytotoxic functions.</p>\",\"PeriodicalId\":179,\"journal\":{\"name\":\"Immunology & Cell Biology\",\"volume\":\"101 9\",\"pages\":\"867-874\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2023-08-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/imcb.12676\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Immunology & Cell Biology\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/imcb.12676\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunology & Cell Biology","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/imcb.12676","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

NK细胞是针对感染细胞和肿瘤细胞的先天免疫细胞。成熟的NK(mNK)细胞经历以四个不同阶段为特征的功能成熟,在这四个阶段中,它们获得了细胞毒性特性。来自非肥胖糖尿病(NOD)小鼠的mNK细胞表现出功能成熟缺陷并且具有受损的细胞毒性功能。因此,我们测试了在NOD小鼠的mNK细胞中观察到的细胞毒性功能受损是否可以用其功能成熟缺陷来解释。通过比较B6、B6g7和NOD小鼠的mNK细胞的功能,我们发现颗粒酶B在NOD小鼠mNK细胞中的表达严重受损,这与它们在体内无法控制肿瘤生长一致。来自NOD小鼠的mNK细胞中颗粒酶B的低水平表达在功能成熟的所有阶段都被发现,因此与它们的功能成熟缺陷无关。因此,本研究表明,mNK细胞的表型功能成熟可以与细胞毒性功能的获得脱钩。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Uncoupling of Natural Killer cell functional maturation and cytolytic function in NOD mice

NK cells are innate immune cells that target infected and tumor cells. Mature NK (mNK) cells undergo functional maturation characterized by four distinct stages, during which they acquire their cytotoxic properties. mNK cells from non-obese diabetic (NOD) mice exhibit a defect in functional maturation and have impaired cytotoxic functions. Hence, we tested whether the impaired cytotoxic function observed in mNK cells from NOD mice can be explained by their defect in functional maturation. By comparing the function of mNK cells from B6, B6g7 and NOD mice, we show that the expression of granzyme B is severely impaired in mNK cells from NOD mice, agreeing with their inability to control tumor growth in vivo. The low level of granzyme B expression in mNK cells from NOD mice is found at all stages of functional maturation and is therefore independent of their functional maturation defect. Consequently, this study demonstrates that phenotypic functional maturation of mNK cells can be uncoupled from the acquisition of cytotoxic functions.

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
Immunology & Cell Biology
Immunology & Cell Biology 医学-免疫学
CiteScore
7.50
自引率
2.50%
发文量
98
审稿时长
4-8 weeks
期刊介绍: The Australasian Society for Immunology Incorporated (ASI) was created by the amalgamation in 1991 of the Australian Society for Immunology, formed in 1970, and the New Zealand Society for Immunology, formed in 1975. The aim of the Society is to encourage and support the discipline of immunology in the Australasian region. It is a broadly based Society, embracing clinical and experimental, cellular and molecular immunology in humans and animals. The Society provides a network for the exchange of information and for collaboration within Australia, New Zealand and overseas. ASI members have been prominent in advancing biological and medical research worldwide. We seek to encourage the study of immunology in Australia and New Zealand and are active in introducing young scientists to the discipline.
期刊最新文献
Prenatal Skin Cell Atlas reveals macrophages' role beyond immunity. The journey of young scientists in Brazil: challenges and perspectives. When academia met industry: working toward a needle-free vaccination future in the sunshine state. Issue Information Choose your own T-cell fate: creation of a narrative-based, decision-making activity to engage students in immunology.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1