Increased lamina propria B cells play roles in fructose-induced hypertension of Dahl salt-sensitive rats.

IF 5.2 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Life sciences Pub Date : 2024-12-14 DOI:10.1016/j.lfs.2024.123314
Sungmin Jang, Cheong-Wun Kim, Zainab Yetunde Olarinoye, Sadia Akter, Inkyeom Kim
{"title":"Increased lamina propria B cells play roles in fructose-induced hypertension of Dahl salt-sensitive rats.","authors":"Sungmin Jang, Cheong-Wun Kim, Zainab Yetunde Olarinoye, Sadia Akter, Inkyeom Kim","doi":"10.1016/j.lfs.2024.123314","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>Although the immune system participates in the development of hypertension, the proportional contributions of distinct immune cells remain poorly understood. With the development of transcriptomics, we can profile the transcriptomes of individual immune cells and assess the relative contribution of each immune cell to the development of hypertension. So, we tested the hypothesis that increased lamina propria B cells play roles in fructose-induced hypertension of Dahl salt-sensitive (SS) rats.</p><p><strong>Materials and methods: </strong>Eight-week-old Dahl SS and Dahl salt-resistant (SR) male rats were divided into four groups; each group received either tap water (TW) or a 20 % fructose solution (HFS) for 4 weeks. Systolic blood pressure was measured using the tail-cuff method. Single-cell RNA sequencing (scRNA-seq) analysis was performed on lamina propria (LP) cells and peripheral blood mononuclear cells (PBMCs) obtained from the SS and SR rats subjected to either TW or HFS.</p><p><strong>Key findings: </strong>Results revealed that high-fructose intake induced hypertension in the SS rats but not in the SR rats. It also increased B cells in LPs but not in PBMCs of the SS rats; their subsets showed increased follicular and naïve B cells. Increased lamina propria B cells play roles in fructose-induced hypertension of SS rats.</p><p><strong>Significance: </strong>This finding suggest that targeting B cells could be a potential strategy to mitigate high blood pressure in fructose-induced hypertension.</p>","PeriodicalId":18122,"journal":{"name":"Life sciences","volume":" ","pages":"123314"},"PeriodicalIF":5.2000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Life sciences","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.lfs.2024.123314","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Aims: Although the immune system participates in the development of hypertension, the proportional contributions of distinct immune cells remain poorly understood. With the development of transcriptomics, we can profile the transcriptomes of individual immune cells and assess the relative contribution of each immune cell to the development of hypertension. So, we tested the hypothesis that increased lamina propria B cells play roles in fructose-induced hypertension of Dahl salt-sensitive (SS) rats.

Materials and methods: Eight-week-old Dahl SS and Dahl salt-resistant (SR) male rats were divided into four groups; each group received either tap water (TW) or a 20 % fructose solution (HFS) for 4 weeks. Systolic blood pressure was measured using the tail-cuff method. Single-cell RNA sequencing (scRNA-seq) analysis was performed on lamina propria (LP) cells and peripheral blood mononuclear cells (PBMCs) obtained from the SS and SR rats subjected to either TW or HFS.

Key findings: Results revealed that high-fructose intake induced hypertension in the SS rats but not in the SR rats. It also increased B cells in LPs but not in PBMCs of the SS rats; their subsets showed increased follicular and naïve B cells. Increased lamina propria B cells play roles in fructose-induced hypertension of SS rats.

Significance: This finding suggest that targeting B cells could be a potential strategy to mitigate high blood pressure in fructose-induced hypertension.

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
目的:尽管免疫系统参与了高血压的发病,但人们对不同免疫细胞的作用比例仍然知之甚少。随着转录组学的发展,我们可以分析单个免疫细胞的转录组,评估每个免疫细胞对高血压发生的相对贡献。因此,我们测试了固有层 B 细胞增加在果糖诱导的 Dahl 盐敏感(SS)大鼠高血压中发挥作用的假设:将8周大的Dahl SS和Dahl耐盐(SR)雄性大鼠分为4组,每组接受自来水(TW)或20%果糖溶液(HFS)4周。采用尾袖法测定收缩压。对从接受 TW 或 HFS 的 SS 和 SR 大鼠体内获得的固有层(LP)细胞和外周血单核细胞(PBMC)进行了单细胞 RNA 测序(scRNA-seq)分析:研究结果表明,高果糖摄入会诱发 SS 大鼠的高血压,但不会诱发 SR 大鼠的高血压。高果糖还增加了 SS 大鼠固有层 B 细胞的数量,但没有增加 SS 大鼠 PBMCs 中的 B 细胞数量。固有层 B 细胞的增加在果糖诱导的 SS 大鼠高血压中发挥作用:这一发现表明,针对 B 细胞可能是缓解果糖诱导的高血压的一种潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Life sciences
Life sciences 医学-药学
CiteScore
12.20
自引率
1.60%
发文量
841
审稿时长
6 months
期刊介绍: Life Sciences is an international journal publishing articles that emphasize the molecular, cellular, and functional basis of therapy. The journal emphasizes the understanding of mechanism that is relevant to all aspects of human disease and translation to patients. All articles are rigorously reviewed. The Journal favors publication of full-length papers where modern scientific technologies are used to explain molecular, cellular and physiological mechanisms. Articles that merely report observations are rarely accepted. Recommendations from the Declaration of Helsinki or NIH guidelines for care and use of laboratory animals must be adhered to. Articles should be written at a level accessible to readers who are non-specialists in the topic of the article themselves, but who are interested in the research. The Journal welcomes reviews on topics of wide interest to investigators in the life sciences. We particularly encourage submission of brief, focused reviews containing high-quality artwork and require the use of mechanistic summary diagrams.
期刊最新文献
The crosstalks between vascular endothelial cells, vascular smooth muscle cells, and adventitial fibroblasts in vascular remodeling. Increased lamina propria B cells play roles in fructose-induced hypertension of Dahl salt-sensitive rats. Emerging insights on the role of Elovl6 in human diseases: Therapeutic challenges and opportunities. Enhancing the anti-tumor activity and reprogramming M2 macrophages by delivering siRNAs against SIRPα and STAT6 via M1 exosomes and combining with anti-PD-L1. TMP: A dual modulator of apoptosis and autophagy via SHP-1 regulation in hepatocellular carcinoma.
×
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