LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 1 of total 1

Search options

Article ; Online: TRPM7 activates m-calpain by stress-dependent stimulation of p38 MAPK and c-Jun N-terminal kinase.

Su, Li-Ting / Chen, Hsiang-Chin / González-Pagán, Omayra / Overton, Jeffrey D / Xie, Jia / Yue, Lixia / Runnels, Loren W

Journal of molecular biology

2010  Volume 396, Issue 4, Page(s) 858–869

Abstract: ... c-Jun N-terminal kinase (JNK). Application of inhibitors of p38 MAPK and JNK blocked TRPM7-induced ... rounding mediated by p38 MAPK/JNK-dependent activation of m-calpain. ... cells produced cell rounding and loss of adhesion, which was dependent on the Ca(2+)-dependent protease m-calpain ...

Abstract TRPM7 is a Ca(2)(+)-permeant and Mg(2)(+)-permeant ion channel in possession of its own kinase domain. In a previous study, we showed that overexpression of the channel-kinase in HEK-293 cells produced cell rounding and loss of adhesion, which was dependent on the Ca(2+)-dependent protease m-calpain. The TRPM7-elicited change in cell morphology was channel-dependent and occurred without any significant increase in cytosolic Ca(2+). Here we demonstrate that overexpression of TRPM7 increased levels of cellular reactive oxygen species (ROS) and nitric oxide, causing the activation of p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK). Application of inhibitors of p38 MAPK and JNK blocked TRPM7-induced cell rounding and activation of m-calpain, without affecting the phosphorylation state of the protease. Overexpression of TRPM7 increased intracellular Mg(2+); however, when the concentration of either external Ca(2+) or Mg(2+) was increased to favor the permeation of one divalent cation over the other, a similar increase in cell rounding and calpain activity was detected, indicating that TRPM7-mediated activation of m-calpain is not dependent on the nature of the divalent conducted by the channel. Application of inhibitors of nitric oxide synthase and mitochondrial-derived ROS reduced TRPM7-induced increases in nitric oxide and ROS production, blocked the change in cell morphology, and reduced cellular calpain activity. Collectively, our data reveal that excessive TRPM7 channel activity causes oxidative and nitrosative stresses, producing cell rounding mediated by p38 MAPK/JNK-dependent activation of m-calpain.
MeSH term(s) Animals ; Calcium/metabolism ; Calpain/metabolism ; Cell Adhesion ; Cell Line ; Cell Shape ; Feedback, Physiological ; Gene Expression ; Humans ; JNK Mitogen-Activated Protein Kinases/metabolism ; MAP Kinase Signaling System ; Mice ; Nitric Oxide/metabolism ; Oxidative Stress ; Protein-Serine-Threonine Kinases ; Reactive Oxygen Species/metabolism ; Recombinant Proteins/genetics ; Recombinant Proteins/metabolism ; TRPM Cation Channels/genetics ; TRPM Cation Channels/metabolism ; p38 Mitogen-Activated Protein Kinases/metabolism
Chemical Substances Reactive Oxygen Species ; Recombinant Proteins ; TRPM Cation Channels ; Nitric Oxide (31C4KY9ESH) ; Trpm7 protein, mouse (EC 2.7.1.-) ; Protein-Serine-Threonine Kinases (EC 2.7.11.1) ; TRPM7 protein, human (EC 2.7.11.1) ; JNK Mitogen-Activated Protein Kinases (EC 2.7.11.24) ; p38 Mitogen-Activated Protein Kinases (EC 2.7.11.24) ; Calpain (EC 3.4.22.-) ; m-calpain (EC 3.4.22.-) ; Calcium (SY7Q814VUP)
Language English
Publishing date 2010-01-11
Publishing country England
Document type Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID 80229-3
ISSN 1089-8638 ; 0022-2836
ISSN (online) 1089-8638
ISSN 0022-2836
DOI 10.1016/j.jmb.2010.01.014
Shelf mark
Zs.A 867: Show issues Location:
Je nach Verfügbarkeit (siehe Angabe bei Bestand)
bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
Jg. 1995 - 2021: Lesesall (1.OG)
ab Jg. 2022: Lesesaal (EG)
Database MEDical Literature Analysis and Retrieval System OnLINE

More links

Kategorien

To top