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10.1111/jcmm.16465

http://scihub22266oqcxt.onion/10.1111/jcmm.16465
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33733611!8107092!33733611
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suck abstract from ncbi


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pmid33733611      J+Cell+Mol+Med 2021 ; 25 (10): 4870-4876
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  • Med1 controls CD8 T cell maintenance through IL-7R-mediated cell survival signalling #MMPMID33733611
  • Lei L; Yang X; Su Y; Zheng H; Liu J; Liu H; Zou Y; Jiao A; Wang X; Zhang C; Zhang X; Zhang J; Zhang D; Zhou X; Shi L; Liu E; Bai L; Sun C; Zhang B
  • J Cell Mol Med 2021[May]; 25 (10): 4870-4876 PMID33733611show ga
  • Under steady-state conditions, the pool size of peripheral CD8(+) T cells is maintained through turnover and survival. Beyond TCR and IL-7R signals, the underlying mechanisms are less well understood. In the present study, we found a significant reduction of CD8(+) T cell proportion in spleens but not in thymi of mice with T cell-specific deletion of Mediator Subunit 1 (Med1). A competitive transfer of wild-type (WT) and Med1-deficient CD8(+) T cells reproduced the phenotype in the same recipients and confirmed intrinsic role of Med1. Furthermore, we observed a comparable degree of migration and proliferation but a significant increase of cell death in Med1-deficient CD8(+) T cells compared with WT counterparts. Finally, Med1-deficient CD8(+) T cells exhibited a decreased expression of interleukin-7 receptor alpha (IL-7Ralpha), down-regulation of phosphorylated-STAT5 (pSTAT5) and Bim up-regulation. Collectively, our study reveals a novel role of Med1 in the maintenance of CD8(+) T cells through IL-7Ralpha/STAT5 pathway-mediated cell survival.
  • |*CD8-Positive T-Lymphocytes/cytology/immunology[MESH]
  • |Animals[MESH]
  • |Apoptosis[MESH]
  • |Bone Marrow Cells[MESH]
  • |Cell Proliferation[MESH]
  • |Cell Survival[MESH]
  • |Cells, Cultured[MESH]
  • |Mediator Complex Subunit 1/genetics/*immunology[MESH]
  • |Mice[MESH]
  • |Mice, Knockout[MESH]
  • |Mice, Transgenic[MESH]
  • |Receptors, Interleukin-7/*immunology[MESH]
  • |Signal Transduction[MESH]


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