The Bardet-Biedl syndrome complex component BBS1 controls T cell polarity during immune synapse assembly

0554522 - ÚMG 2022 RIV GB eng J - Článek v odborném periodiku
Cassioli, C. - Onnis, A. - Finetti, F. - Capitani, N. - Brunetti, J. - Compeer, E. - Niederlová, Veronika - Štěpánek, Ondřej - Dustin, M. - Baldari, C.
The Bardet-Biedl syndrome complex component BBS1 controls T cell polarity during immune synapse assembly.
Journal of Cell Science. Roč. 134, č. 16 (2021), č. článku jcs258462. ISSN 0021-9533. E-ISSN 1477-9137
Grant CEP: GA ČR GJ19-03435Y
Institucionální podpora: RVO:68378050
Klíčová slova: Immune synapse * Primary cilium * Bardet-Biedl syndrome * Centrosome * Proteasome * Dynein
Obor OECD: Cell biology
Impakt faktor: 5.235, rok: 2021
Způsob publikování: Omezený přístup
https://journals.biologists.com/jcs/article/134/16/jcs258462/271909/The-Bardet-Biedl-syndrome-complex-component-BBS1

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.
Trvalý link: http://hdl.handle.net/11104/0329233