The Bardet-Biedl syndrome complex component BBS1 controls T cell polarity during immune synapse assembly
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F21%3A00554522" target="_blank" >RIV/68378050:_____/21:00554522 - isvavai.cz</a>
Result on the web
<a href="https://journals.biologists.com/jcs/article/134/16/jcs258462/271909/The-Bardet-Biedl-syndrome-complex-component-BBS1" target="_blank" >https://journals.biologists.com/jcs/article/134/16/jcs258462/271909/The-Bardet-Biedl-syndrome-complex-component-BBS1</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1242/jcs.258462" target="_blank" >10.1242/jcs.258462</a>
Alternative languages
Result language
angličtina
Original language name
The Bardet-Biedl syndrome complex component BBS1 controls T cell polarity during immune synapse assembly
Original language description
Components of the intraflagellar transport (IFT) system that regulates the assembly of the primary cilium are co-opted by the non-ciliated T cell to orchestrate polarized endosome recycling and to sustain signaling during immune synapse formation. Here, we investigated the potential role of Bardet-Biedl syndrome 1 protein (BBS1), an essential core component of the BBS complex that cooperates with the IFT system in ciliary protein trafficking, in the assembly of the T cell synapse. We demonstrated that BBS1 allows for centrosome polarization towards the immune synapse. This function is achieved through the clearance of centrosomal F-actin and its positive regulator WASH1 (also known as WASHC1), a process that we demonstrated to be dependent on the proteasome. We show that BBS1 regulates this process by coupling the 19S proteasome regulatory subunit to the microtubule motor dynein for its transport to the centrosome. Our data identify the ciliopathy-related protein BBS1 as a new player in T cell synapse assembly that functions upstream of the IFT system to set the stage for polarized vesicular trafficking and sustained signaling.
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
10601 - Cell biology
Result continuities
Project
<a href="/en/project/GJ19-03435Y" target="_blank" >GJ19-03435Y: Naïve, memory, and virtual memory T cells in adaptive immune responses</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Cell Science
ISSN
0021-9533
e-ISSN
1477-9137
Volume of the periodical
134
Issue of the periodical within the volume
16
Country of publishing house
GB - UNITED KINGDOM
Number of pages
18
Pages from-to
jcs258462
UT code for WoS article
000692211500011
EID of the result in the Scopus database
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