Cargando…
Rapamycin Regulates iTreg Function through CD39 and Runx1 Pathways
It has been shown that rapamycin is able to significantly increase the expression of FoxP3 and suppress activity in induced Treg (iTreg) cells in vivo and in vitro. CD39 is a newly determined Treg marker that relates to cell suppression. Runx1, a regulator of FoxP3, controls the expression of adenos...
Autores principales: | Lu, Yunjie, Wang, Jirong, Gu, Jian, Lu, Hao, Li, Xiangcheng, Qian, Xiaofeng, Liu, Xiaoshan, Wang, Xuehao, Zhang, Feng, Lu, Ling |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988749/ https://www.ncbi.nlm.nih.gov/pubmed/24741640 http://dx.doi.org/10.1155/2014/989434 |
Ejemplares similares
-
In-vitro inhibition of IFNγ(+) iTreg mediated by monoclonal antibodies against cell surface determinants essential for iTreg function
por: Daniel, Volker, et al.
Publicado: (2012) -
CD8+CD103+ iTregs Inhibit Chronic Graft-versus-Host Disease with Lupus Nephritis by the Increased Expression of CD39
por: Zhang, Xiao, et al.
Publicado: (2019) -
Cholesterol suppresses human iTreg differentiation and nTreg function through mitochondria-related mechanisms
por: Zhang, Huanzhi, et al.
Publicado: (2023) -
Efficient induction of CD25(- )iTreg by co-immunization requires strongly antigenic epitopes for T cells
por: Geng, Shuang, et al.
Publicado: (2011) -
P38 MAP Kinase Signaling Is Required for the Conversion of CD4+CD25− T Cells into iTreg
por: Huber, Samuel, et al.
Publicado: (2008)