The expression of Galectin-9 correlates with mTOR and AMPK in murine colony-forming erythroid progenitors

IF 2.3 3区 医学 Q2 HEMATOLOGY European Journal of Haematology Pub Date : 2024-06-10 DOI:10.1111/ejh.14249
Tetsuo Tsukamoto
{"title":"The expression of Galectin-9 correlates with mTOR and AMPK in murine colony-forming erythroid progenitors","authors":"Tetsuo Tsukamoto","doi":"10.1111/ejh.14249","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objectives</h3>\n \n <p>Galectin-9 (Gal-9) is an immune checkpoint ligand for T-cell immunoglobulin and mucin domain 3. Although the roles of Gal-9 in regulating immune responses have been well investigated, their biological roles have yet to be fully documented. This study aimed to analyse the expression of Gal-9 bone marrow (BM) cells in C57BL/6J (B6) mice. Furthermore, the co-expression of Gal-9 with the mammalian target of rapamycin (mTOR) and AMP-activated protein kinase (AMPK) was investigated.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>The BM cells in adult C57BL/6J (B6) mice were collected and analysed in vitro.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>In a flow cytometric analysis of BM cells, Gal-9 was highly expressed in c-Kit<sup>hi</sup>Sca-1<sup>−</sup>CD34<sup>−</sup>CD71<sup>+</sup> erythroid progenitors (EPs), whereas it was downregulated in more differentiated c-Kit<sup>lo</sup>CD71<sup>+</sup>TER119<sup>+</sup> cells. Subsequently, a negative selection of CD3<sup>−</sup>B220<sup>−</sup>Sca-1<sup>−</sup>CD34<sup>−</sup>CD41<sup>−</sup>CD16/32<sup>−</sup> EPs was performed. This resulted in substantial enrichment of Kit<sup>hi</sup>CD71<sup>+</sup>Gal-9<sup>+</sup> cells and erythroid colony-forming units (CFU-Es), suggesting that the colony-forming subset of EPs are included in the Kit<sup>hi</sup>CD71<sup>+</sup>Gal-9<sup>+</sup> population. Furthermore, we found that EPs had lower mTOR and AMPK expression levels in Gal-9 knockout B6 mice than in wild-type B6 mice.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>These results may stimulate further investigation of the role of Gal-9 in haematopoiesis.</p>\n </section>\n </div>","PeriodicalId":11955,"journal":{"name":"European Journal of Haematology","volume":"113 4","pages":"416-425"},"PeriodicalIF":2.3000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Haematology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejh.14249","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives

Galectin-9 (Gal-9) is an immune checkpoint ligand for T-cell immunoglobulin and mucin domain 3. Although the roles of Gal-9 in regulating immune responses have been well investigated, their biological roles have yet to be fully documented. This study aimed to analyse the expression of Gal-9 bone marrow (BM) cells in C57BL/6J (B6) mice. Furthermore, the co-expression of Gal-9 with the mammalian target of rapamycin (mTOR) and AMP-activated protein kinase (AMPK) was investigated.

Methods

The BM cells in adult C57BL/6J (B6) mice were collected and analysed in vitro.

Results

In a flow cytometric analysis of BM cells, Gal-9 was highly expressed in c-KithiSca-1CD34CD71+ erythroid progenitors (EPs), whereas it was downregulated in more differentiated c-KitloCD71+TER119+ cells. Subsequently, a negative selection of CD3B220Sca-1CD34CD41CD16/32 EPs was performed. This resulted in substantial enrichment of KithiCD71+Gal-9+ cells and erythroid colony-forming units (CFU-Es), suggesting that the colony-forming subset of EPs are included in the KithiCD71+Gal-9+ population. Furthermore, we found that EPs had lower mTOR and AMPK expression levels in Gal-9 knockout B6 mice than in wild-type B6 mice.

Conclusions

These results may stimulate further investigation of the role of Gal-9 in haematopoiesis.

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
小鼠集落形成红细胞祖细胞中 Galectin-9 的表达与 mTOR 和 AMPK 相关。
目的Galectin-9(Gal-9)是T细胞免疫球蛋白和粘蛋白域3的免疫检查点配体。尽管 Gal-9 在调节免疫反应中的作用已得到了深入研究,但其生物学作用仍有待充分证实。本研究旨在分析C57BL/6J(B6)小鼠骨髓(BM)细胞中Gal-9的表达。此外,还研究了Gal-9与哺乳动物雷帕霉素靶标(mTOR)和AMP激活蛋白激酶(AMPK)的共同表达:方法:收集成年 C57BL/6J (B6) 小鼠的骨髓细胞并进行体外分析:结果:在对BM细胞进行的流式细胞分析中,Gal-9在c-KithiSca-1-CD34-CD71+红系祖细胞(EPs)中高表达,而在分化程度较高的c-KitloCD71+TER119+细胞中则下调。随后,对 CD3-B220-Sca-1-CD34-CD41-CD16/32- EPs 进行了阴性选择。这导致 KithiCD71+Gal-9+ 细胞和红细胞集落形成单位(CFU-Es)大量富集,表明集落形成亚群 EPs 包含在 KithiCD71+Gal-9+ 群体中。此外,我们还发现,在 Gal-9 基因敲除的 B6 小鼠中,EPs 的 mTOR 和 AMPK 表达水平低于野生型 B6 小鼠:这些结果可能会促使人们进一步研究 Gal-9 在造血过程中的作用。
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
CiteScore
5.50
自引率
0.00%
发文量
168
审稿时长
4-8 weeks
期刊介绍: European Journal of Haematology is an international journal for communication of basic and clinical research in haematology. The journal welcomes manuscripts on molecular, cellular and clinical research on diseases of the blood, vascular and lymphatic tissue, and on basic molecular and cellular research related to normal development and function of the blood, vascular and lymphatic tissue. The journal also welcomes reviews on clinical haematology and basic research, case reports, and clinical pictures.
期刊最新文献
An Overview of Chronic Myeloid Leukemia Treatment: From Tyrosine Kinase Inhibitors to Novel and Emerging Therapies. Whole Blood Transcriptomic Analysis of Sickle Cell Trait. Polycythemia Vera and Essential Thrombocythemia: A Nationwide Population-Based Study on Treatment Patterns, Vascular Complications and Survival. Survival and Renal Recovery in Newly Diagnosed Multiple Myeloma Patients Presenting With Dialysis-Requiring Severe Renal Impairment. VULVO-Vaginal Chronic Graft-Versus-Host Disease Assessment: A Single-Center Prospective Observational Study.
×
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:604180095
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