The tyrosine phosphatase CD148 is excluded from the immunologic synapse and down-regulates prolonged T cell signaling (Q24314787)

negative regulation of T cell receptor signaling pathway

GOA release 2020-03-11

1 reference

Protein tyrosine phosphatase, receptor type, J

GOA release 2020-03-11

1 reference

Protein tyrosine phosphatase CD148-mediated inhibition of T-cell receptor signal transduction is associated with reduced LAT and phospholipase Cgamma1 phosphorylation

GOA release 2020-03-11

Arthur Weiss

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author name string

Joseph Lin

series ordinal

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language of work or name

English

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publication date

18 August 2003

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published in

Journal of Cell Biology

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volume

162

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issue

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page(s)

673-82

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cites work

1 reference

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Negative regulation of human T cell activation by the receptor-type protein tyrosine phosphatase CD148

19 March 2017

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LAT: the ZAP-70 tyrosine kinase substrate that links T cell receptor to cellular activation

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Ezrin/radixin/moesin (ERM) proteins bind to a positively charged amino acid cluster in the juxta-membrane cytoplasmic domain of CD44, CD43, and ICAM-2

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CD45 ectodomain controls interaction with GEMs and Lck activity for optimal TCR signaling

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T cell receptor signaling precedes immunological synapse formation

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Exclusion of CD43 from the immunological synapse is mediated by phosphorylation-regulated relocation of the cytoskeletal adaptor moesin

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Essential role of LAT in T cell development

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LAT is required for TCR-mediated activation of PLCgamma1 and the Ras pathway

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CD148: a receptor-type protein tyrosine phosphatase involved in the regulation of human T cell activation

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A novel adaptor protein orchestrates receptor patterning and cytoskeletal polarity in T-cell contacts

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Rat protein tyrosine phosphatase eta physically interacts with the PDZ domains of syntenin

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Dependence of T cell antigen recognition on the dimensions of an accessory receptor-ligand complex

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T cell receptor signalling

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The membrane-microfilament linker ezrin is involved in the formation of the immunological synapse and in T cell activation

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