CD45 functions as a signaling gatekeeper in T cells
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F19%3A00511337" target="_blank" >RIV/68378050:_____/19:00511337 - isvavai.cz</a>
Result on the web
<a href="https://stke.sciencemag.org/content/12/604/eaaw8151" target="_blank" >https://stke.sciencemag.org/content/12/604/eaaw8151</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1126/scisignal.aaw8151" target="_blank" >10.1126/scisignal.aaw8151</a>
Alternative languages
Result language
angličtina
Original language name
CD45 functions as a signaling gatekeeper in T cells
Original language description
T cells require the protein tyrosine phosphatase CD45 to detect and respond to antigen because it activates the Src family kinase Lck, which phosphorylates the T cell antigen receptor (TCR) complex. CD45 activates Lck by opposing the negative regulatory kinase Csk. Paradoxically, CD45 has also been implicated in suppressing TCR signaling by dephosphorylating the same signaling motifs within the TCR complex upon which Lck acts. We sought to reconcile these observations using chemical and genetic perturbations of the Csk/CD45 regulatory axis incorporated with computational analyses. Specifically, we titrated the activities of Csk and CD45 and assessed their influence on Lck activation, TCR-associated.-chain phosphorylation, and more downstream signaling events. Acute inhibition of Csk revealed that CD45 suppressed zeta-chain phosphorylation and was necessary for a regulatable pool of active Lck, thereby interconnecting the activating and suppressive roles of CD45 that tune antigen discrimination. CD45 suppressed signaling events that were antigen independent or induced by low-affinity antigen but not those initiated by high-affinity antigen. Together, our findings reveal that CD45 acts as a signaling ´gatekeeper,´ enabling graded signaling outputs while filtering weak or spurious signaling events.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30102 - Immunology
Result continuities
Project
<a href="/en/project/GJ16-09208Y" target="_blank" >GJ16-09208Y: T cell receptor signaling and fate decisions made by peripheral T cells in homeostasis and during inflammation</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Science Signaling
ISSN
1945-0877
e-ISSN
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Volume of the periodical
12
Issue of the periodical within the volume
604
Country of publishing house
US - UNITED STATES
Number of pages
15
Pages from-to
aaw8151
UT code for WoS article
000492378200002
EID of the result in the Scopus database
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