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Calcium-stimulated disassembly of focal adhesions mediated by an ORP3/IQSec1 complex

Coordinated assembly and disassembly of integrin-mediated focal adhesions (FAs) is essential for cell migration. Many studies have shown that FA disassembly requires Ca(2+) influx, however our understanding of this process remains incomplete. Here, we show that Ca(2+) influx via STIM1/Orai1 calcium...

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Detalles Bibliográficos
Autores principales: D'Souza, Ryan S, Lim, Jun Y, Turgut, Alper, Servage, Kelly, Zhang, Junmei, Orth, Kim, Sosale, Nisha G, Lazzara, Matthew J, Allegood, Jeremy, Casanova, James E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159923/
https://www.ncbi.nlm.nih.gov/pubmed/32234213
http://dx.doi.org/10.7554/eLife.54113
Descripción
Sumario:Coordinated assembly and disassembly of integrin-mediated focal adhesions (FAs) is essential for cell migration. Many studies have shown that FA disassembly requires Ca(2+) influx, however our understanding of this process remains incomplete. Here, we show that Ca(2+) influx via STIM1/Orai1 calcium channels, which cluster near FAs, leads to activation of the GTPase Arf5 via the Ca(2+)-activated GEF IQSec1, and that both IQSec1 and Arf5 activation are essential for adhesion disassembly. We further show that IQSec1 forms a complex with the lipid transfer protein ORP3, and that Ca(2+) influx triggers PKC-dependent translocation of this complex to ER/plasma membrane (PM) contact sites adjacent to FAs. In addition to allosterically activating IQSec1, ORP3 also extracts PI4P from the PM, in exchange for phosphatidylcholine. ORP3-mediated lipid exchange is also important for FA turnover. Together, these findings identify a new pathway that links calcium influx to FA turnover during cell migration.