作者: Patricia Castro-Sánchez , Rocio Ramirez-Munoz , Pedro Roda-Navarro
DOI: 10.1155/2017/8701042
关键词: Cell biology 、 Cellular differentiation 、 Signal transduction 、 Phosphorylation 、 T cell 、 MAPK/ERK pathway 、 Intracellular 、 Biology 、 Effector 、 Immune system
摘要: Phosphotyrosine phosphatases (PTPs) constitute a complex family of enzymes that control the balance intracellular phosphorylation levels to allow cell responses while avoiding development diseases. Despite relevance CD4 T polarisation and effector function in human autoimmune diseases, expression profile PTPs during helper restimulation at inflammatory sites has not been assessed. Here, systematic analysis carried out Th1-polarising conditions upon PKC activation raise Ca2+ cells. Changes gene suggest previously nonnoted regulatory role several Th1 function. A substantial change spatial compartmentalisation ERK is proposed based on changes dose cytoplasmic nuclear MAPK phosphatases. Our study also suggests autoimmune-related controlling humans. We expect those regulate will potential targets for intervening immune order generate new therapies treatment