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Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism
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 Ca(2+) fluxes. Human GAAP is expressed in all human tissues, i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838802/ https://www.ncbi.nlm.nih.gov/pubmed/31693977 http://dx.doi.org/10.1016/j.redox.2019.101361 |
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author | Almeida, Nuno Carrara, Guia Palmeira, Carlos M. Fernandes, Ana S. Parsons, Maddy Smith, Geoffrey L. Saraiva, Nuno |
author_facet | Almeida, Nuno Carrara, Guia Palmeira, Carlos M. Fernandes, Ana S. Parsons, Maddy Smith, Geoffrey L. Saraiva, Nuno |
author_sort | Almeida, Nuno |
collection | PubMed |
description | 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 Ca(2+) 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 Ca(2+) 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 Ca(2+) and reactive oxygen species signaling contribute to cell invasion and to the role of the GA in these processes. |
format | Online Article Text |
id | pubmed-6838802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68388022019-11-12 Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism Almeida, Nuno Carrara, Guia Palmeira, Carlos M. Fernandes, Ana S. Parsons, Maddy Smith, Geoffrey L. Saraiva, Nuno Redox Biol Research Paper 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 Ca(2+) 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 Ca(2+) 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 Ca(2+) and reactive oxygen species signaling contribute to cell invasion and to the role of the GA in these processes. Elsevier 2019-10-22 /pmc/articles/PMC6838802/ /pubmed/31693977 http://dx.doi.org/10.1016/j.redox.2019.101361 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Paper Almeida, Nuno Carrara, Guia Palmeira, Carlos M. Fernandes, Ana S. Parsons, Maddy Smith, Geoffrey L. Saraiva, Nuno Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title | Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title_full | Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title_fullStr | Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title_full_unstemmed | Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title_short | Stimulation of cell invasion by the Golgi Ion Channel GAAP/TMBIM4 via an H(2)O(2)-Dependent Mechanism |
title_sort | stimulation of cell invasion by the golgi ion channel gaap/tmbim4 via an h(2)o(2)-dependent mechanism |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838802/ https://www.ncbi.nlm.nih.gov/pubmed/31693977 http://dx.doi.org/10.1016/j.redox.2019.101361 |
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