{"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":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejh.14249","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","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-1−CD34−CD71+ erythroid progenitors (EPs), whereas it was downregulated in more differentiated c-KitloCD71+TER119+ cells. Subsequently, a negative selection of CD3−B220−Sca-1−CD34−CD41−CD16/32− 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.