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Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death

The human gene MRS2L encodes a mitochondrial protein distantly related to CorA Mg(2+) transport proteins. Constitutive shRNA-mediated knockdown of hMRS2 in human HEK-293 cell line was found here to cause death. To further study its role in Mg(2+) transport, we have established stable cell lines with...

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Autores principales: Piskacek, Martin, Zotova, Ludmila, Zsurka, Gábor, Schweyen, Rudolf J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822876/
https://www.ncbi.nlm.nih.gov/pubmed/18384665
http://dx.doi.org/10.1111/j.1582-4934.2008.00328.x
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author Piskacek, Martin
Zotova, Ludmila
Zsurka, Gábor
Schweyen, Rudolf J
author_facet Piskacek, Martin
Zotova, Ludmila
Zsurka, Gábor
Schweyen, Rudolf J
author_sort Piskacek, Martin
collection PubMed
description The human gene MRS2L encodes a mitochondrial protein distantly related to CorA Mg(2+) transport proteins. Constitutive shRNA-mediated knockdown of hMRS2 in human HEK-293 cell line was found here to cause death. To further study its role in Mg(2+) transport, we have established stable cell lines with conditionally expressing shRNAs directed against hMRS2L. The cells expressing shRNA for several generations exhibited lower steady-state levels of free mitochondrial Mg(2+) ([Mg(2+)](m)) and reduced capacity of mitochondrial Mg(2+) uptake than control cells. Long-term expression of shRNAs resulted in loss of mitochondrial respiratory complex I, decreased mitochondrial membrane potential and cell death. We conclude that hMrs2 is the major transport protein for Mg (+) uptake into mitochondria and that expression of hMrs2 is essential for the maintenance of respiratory complex I and cell viability.
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spelling pubmed-38228762015-04-27 Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death Piskacek, Martin Zotova, Ludmila Zsurka, Gábor Schweyen, Rudolf J J Cell Mol Med Articles The human gene MRS2L encodes a mitochondrial protein distantly related to CorA Mg(2+) transport proteins. Constitutive shRNA-mediated knockdown of hMRS2 in human HEK-293 cell line was found here to cause death. To further study its role in Mg(2+) transport, we have established stable cell lines with conditionally expressing shRNAs directed against hMRS2L. The cells expressing shRNA for several generations exhibited lower steady-state levels of free mitochondrial Mg(2+) ([Mg(2+)](m)) and reduced capacity of mitochondrial Mg(2+) uptake than control cells. Long-term expression of shRNAs resulted in loss of mitochondrial respiratory complex I, decreased mitochondrial membrane potential and cell death. We conclude that hMrs2 is the major transport protein for Mg (+) uptake into mitochondria and that expression of hMrs2 is essential for the maintenance of respiratory complex I and cell viability. Blackwell Publishing Ltd 2009-04 2008-03-31 /pmc/articles/PMC3822876/ /pubmed/18384665 http://dx.doi.org/10.1111/j.1582-4934.2008.00328.x Text en © 2009 The Authors Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Piskacek, Martin
Zotova, Ludmila
Zsurka, Gábor
Schweyen, Rudolf J
Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title_full Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title_fullStr Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title_full_unstemmed Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title_short Conditional knockdown of hMRS2 results in loss of mitochondrial Mg (+) uptake and cell death
title_sort conditional knockdown of hmrs2 results in loss of mitochondrial mg (+) uptake and cell death
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822876/
https://www.ncbi.nlm.nih.gov/pubmed/18384665
http://dx.doi.org/10.1111/j.1582-4934.2008.00328.x
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