Overexpression of sigma-1 receptor inhibits ADAM10 and ADAM17 mediated shedding in vitro.

Abstract:

:The sigma-1 receptor is a molecular chaperone protein highly enriched in the brain. Recent studies linked it to many diseases, such as drug addition, Alzheimer's disease, stroke, depression, and even cancer. Sigma-1 receptor is enriched in lipid rafts, which are membrane microdomains essential in signaling processes. One of those signaling processes is ADAM17- and ADAM10-dependent ectodomain shedding. By using an alkaline phosphatase tagged substrate reporter system, we have shown that ADAM10-dependent BTC shedding was very sensitive to both membrane lipid component change and sigma-1 receptor agonist DHEAS treatment while ADAM17-dependent HB-EGF shedding was not; and overexpression of sigma-1 receptor diminished ADAM17- and ADAM10-dependent shedding. Our results indicate that sigma-1 receptor plays an important role in modifying the function of transmembrane proteases.

journal_name

Protein Cell

journal_title

Protein & cell

authors

Li J,Liu B,Gao X,Ma Z,CaoSong T,Mei YA,Zheng Y

doi

10.1007/s13238-012-2006-9

subject

Has Abstract

pub_date

2012-02-01 00:00:00

pages

153-9

issue

2

eissn

1674-800X

issn

1674-8018

journal_volume

3

pub_type

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