Abstract
T cell receptor (TCR) and costimulatory receptor (CD28) signals cooperate in activating T cells, although understanding of how these pathways are themselves regulated is incomplete. We found that Homer2 and Homer3, members of the Homer family of cytoplasmic scaffolding proteins, are negative regulators of T cell activation. This is achieved through binding of nuclear factor of activated T cells (NFAT) and by competing with calcineurin. Homer-NFAT binding was also antagonized by active serine-threonine kinase AKT, thereby enhancing TCR signaling via calcineurin-dependent dephosphorylation of NFAT. This corresponded with changes in cytokine expression and an increase in effector-memory T cell populations in Homer-deficient mice, which also developed autoimmune-like pathology. These results demonstrate a further means by which costimulatory signals are regulated to control self-reactivity.
Publication types
-
Research Support, N.I.H., Extramural
MeSH terms
-
Animals
-
CD28 Antigens / immunology
-
CD3 Complex / immunology
-
Calcineurin / metabolism
-
Calcium / metabolism
-
Carrier Proteins / chemistry
-
Carrier Proteins / metabolism*
-
Cell Line
-
Cells, Cultured
-
Crystallography, X-Ray
-
Homer Scaffolding Proteins
-
Humans
-
Jurkat Cells
-
Lymphocyte Activation*
-
Mice
-
Mice, Knockout
-
NFATC Transcription Factors / chemistry
-
NFATC Transcription Factors / metabolism*
-
Phosphorylation
-
Protein Structure, Tertiary
-
Proto-Oncogene Proteins c-akt / metabolism
-
Recombinant Fusion Proteins / metabolism
-
Signal Transduction
-
T-Lymphocytes / immunology*
-
T-Lymphocytes / metabolism
Substances
-
CD28 Antigens
-
CD3 Complex
-
Carrier Proteins
-
HOMER3 protein, human
-
Homer Scaffolding Proteins
-
Homer2 protein, mouse
-
Homer3 protein, mouse
-
NFATC Transcription Factors
-
NFATC2 protein, human
-
Nfatc2 protein, mouse
-
Recombinant Fusion Proteins
-
Proto-Oncogene Proteins c-akt
-
Calcineurin
-
Calcium