{"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-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.
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.