Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0014070 (
encephalomyelitis
)
13,017
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
SKAP-HOM
is a cytosolic adaptor protein representing a specific substrate for the Src family protein tyrosine kinase Fyn. Previously, several groups have provided experimental evidence that
SKAP-HOM
(most likely in cooperation with the cytosolic adaptor protein ADAP) is involved in regulating leukocyte adhesion. To further assess the physiological role of
SKAP-HOM
, we investigated the immune system of
SKAP-HOM
-deficient mice. Our data show that T-cell responses towards a variety of stimuli are unaffected in the absence of
SKAP-HOM
. Similarly, B-cell receptor (BCR)-mediated total tyrosine phosphorylation and phosphorylation of Erk, p38, and JNK, as well as immunoreceptor-mediated Ca(2+) responses, are normal in
SKAP-HOM
(-/-) animals. However, despite apparently normal membrane-proximal signaling events, BCR-mediated proliferation is strongly attenuated in the absence of
SKAP-HOM
(-/-). In addition, adhesion of activated B cells to fibronectin (a ligand for beta1 integrins) as well as to ICAM-1 (a ligand for beta2 integrins) is strongly reduced. In vivo, the loss of
SKAP-HOM
results in a less severe clinical course of experimental autoimmune
encephalomyelitis
following immunization of mice with the encephalitogenic peptide of MOG (myelin oligodendrocyte glycoprotein). This is accompanied by strongly reduced serum levels of MOG-specific antibodies and lower MOG-specific T-cell responses. In summary, our data suggest that
SKAP-HOM
is required for proper activation of the immune system, likely by regulating the cross-talk between immunoreceptors and integrins.
...
PMID:Regulation of in vitro and in vivo immune functions by the cytosolic adaptor protein SKAP-HOM. 1613 97