骨髓生成
抑制器
髓样
髓系细胞
氨基葡萄糖
细胞生物学
髓源性抑制细胞
化学
免疫学
癌症研究
生物
造血
生物化学
干细胞
基因
作者
Eric Chang-Yi Lin,Shuoh-Wen Chen,Luen-Kui Chen,Ting‐An Lin,Yuxuan Wu,Chi‐Chang Juan,Yuan‐I Chang
标识
DOI:10.3389/fnut.2021.762363
摘要
Glucosamine (GlcN) is the most widely consumed dietary supplement and exhibits anti-inflammatory effects. However, the influence of GlcN on immune cell generation and function is largely unclear. In this study, GlcN was delivered into mice to examine its biological function in hematopoiesis. We found that GlcN promoted the production of immature myeloid cells, known as myeloid-derived suppressor cells (MDSCs), both in vivo and in vitro . Additionally, GlcN upregulated the expression of glucose transporter 1 in hematopoietic stem and progenitor cells (HSPCs), influenced HSPC functions, and downregulated key genes involved in myelopoiesis. Furthermore, GlcN increased the expression of arginase 1 and inducible nitric oxide synthase to produce high levels of reactive oxygen species, which was regulated by the STAT3 and ERK1/2 pathways, to increase the immunosuppressive ability of MDSCs. We revealed a novel role for GlcN in myelopoiesis and MDSC activity involving a potential link between GlcN and immune system, as well as the new therapeutic benefit.
科研通智能强力驱动
Strongly Powered by AbleSci AI