Abstract

The store-operated Ca(2+)entry-associated regulatory factor (SARAF) has recently been identified as a STIM1 regulatory protein that facilitates slow Ca(2+)-dependent inactivation of store-operated Ca(2+)entry (SOCE). Both the store-operated channels and the store-independent arachidonate-regulated Ca(2+)(ARC) channels are regulated by STIM1. In the present study, we show that, in addition to its location in the endoplasmic reticulum, SARAF is constitutively expressed in the plasma membrane, where it can interact with plasma membrane (PM)-resident ARC forming subunits in the neuroblastoma cell line SH-SY5Y. Using siRNA-based and overexpression approaches we report that SARAF negatively regulates store-independent Ca(2+)entry via the ARC channels. Arachidonic acid (AA) increases the association of PM-resident SARAF with Orai1. Finally, our results indicate that SARAF modulates the ability of AA to promote cell survival in neuroblastoma cells. In addition to revealing new insight into the biology of ARC channels in neuroblastoma cells, these findings provide evidence for an unprecedented location of SARAF in the plasma membrane.

Highlights

  • The store-operated Ca2؉ entry-associated regulatory factor (SARAF) has recently been identified as a STIM1 regulatory protein that facilitates slow Ca2؉-dependent inactivation of store-operated Ca2؉ entry (SOCE)

  • Since STIM1 is required for the activation of Arachidonic acid (AA)-regulated, store-independent, Ca2ϩ entry via the arachidonate-regulated Ca2؉ (ARC) channels, we have explored the possible regulation of Ca2ϩ entry through the ARC channels by SARAF

  • The store-independent, AA-induced, Ca2ϩ influx is mediated via activation of ARC channels, which consists of a combination of Orai1 and Orai3 subunits, with the cooperation of plasma membrane (PM)-resident STIM1 (4 –5)

Read more

Summary

Experimental Procedures

Materials—Fura-2 acetoxymethyl ester (fura-2/AM) and jasplakinolide were from Molecular Probes (Leiden, The Netherlands).

SARAF Regulates ARC Channels
Results
Discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call