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Multifaceted control of T cell differentiation by STIM1

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TRENDS IN BIOCHEMICAL SCIENCES
卷 48, 期 12, 页码 1083-1097

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CELL PRESS
DOI: 10.1016/j.tibs.2023.08.006

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This review focuses on the novel mechanisms through which STIM controls Ca2+ signals in T cell activation, and its impact on mitochondrial function and transcriptional activation for T cell differentiation and function. It also highlights areas that require further research, including the roles of PMCA and POST in controlling Orai function, and the independence of T cell development from STIM and Orai. Resolving these issues will contribute to the advancement of this field.
In T cells, stromal interaction molecule (STIM) and Orai are dispensable for conventional T cell development, but critical for activation and differentiation. This review focuses on novel STIM-dependent mechanisms for control of Cat+ signals during T cell activation and its impact on mitochondrial function and transcriptional activation for control of T cell differentiation and function. We highlight areas that require further work including the roles of plasma membrane Cat+ ATPase (PMCA) and partner of STIM1 (POST) in controlling Orai function. A major knowledge gap also exists regarding the independence of T cell development from STIM and Orai, despite compelling evidence that it requires Cat+ signals. Resolving these and other outstanding questions ensures that the field will remain active for many years to come.

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