Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106653
Title: Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H2O2-Dependent Mechanism
Authors: Almeida, Nuno
Carrara, Guia
Palmeira, Carlos M. 
Fernandes, Ana S.
Parsons, Maddy
Smith, Geoffrey L.
Saraiva, Nuno 
Keywords: Calcium; Cell invasion; Golgi apparatus; Hydrogen peroxide; Metabolism; TMBIM
Issue Date: Jan-2020
Publisher: Elsevier
Project: UID/DTP/04567/2019 
Isaac Newton grant 
UID/DTP/04567/2016 
STSM grants from EU-ROS (BM1203) and EuroCellNet (CA15214) COST actions 
GLS is a Wellcome Trust Principal Research Fellow [090315/B/09] 
metadata.degois.publication.title: Redox Biology
metadata.degois.publication.volume: 28
Abstract: The mechanisms by which the Golgi apparatus (GA) impacts on cell invasion are poorly understood. The human Golgi Anti-Apoptotic Protein (hGAAP, also known as TMBIM4) is a highly conserved Golgi cation channel that modulates intracellular Ca2+ fluxes. Human GAAP is expressed in all human tissues, is essential for cell viability and provides resistance against a range of apoptotic stresses. Furthermore, hGAAP enhances adhesion and cell migration by increasing the turnover of focal adhesions due to activation of store-operated Ca2+ entry. Here, we describe a GA-derived mechanism that controls cell invasion. The overexpression of hGAAP stimulates 3-dimensional proteolytic cell invasion by a mechanism that is dependent on the accumulation of intracellular hydrogen peroxide, which might be produced by the hGAAP-dependent stimulation of mitochondrial respiration. These findings provide new insight into the complex mechanisms by which Ca2+ and reactive oxygen species signaling contribute to cell invasion and to the role of the GA in these processes.
URI: https://hdl.handle.net/10316/106653
ISSN: 22132317
DOI: 10.1016/j.redox.2019.101361
Rights: openAccess
Appears in Collections:FCTUC Ciências da Vida - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais

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