Affiliation:
1. Department of Health Informatics Niigata University of Health of Welfare Niigata Japan
2. Department of Immunology, Faculty of Medicine Kindai University Osaka Japan
Abstract
AbstractObjectivesGalectin‐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.MethodsThe BM cells in adult C57BL/6J (B6) mice were collected and analysed in vitro.ResultsIn 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.ConclusionsThese results may stimulate further investigation of the role of Gal‐9 in haematopoiesis.
Funder
Japan Society for the Promotion of Science
Kindai University
Mochida Memorial Foundation for Medical and Pharmaceutical Research
Children's Cancer Association of Japan