How do reactive oxygen species and calcium trigger mitochondrial membrane permeabilisation?

Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS...

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Published inBiochimica et biophysica acta Vol. 1860; no. 6; pp. 1079 - 1088
Main Author Tajeddine, Nicolas
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.06.2016
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Abstract Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS) and Ca2+ were the prominent inducers of MMP. However, the mechanisms connecting ROS and Ca2+ to the players of MMP are still a matter of debate. The aim of this review is to summarise the various studies related to the mechanisms of ROS- and Ca2+-induced MMP. Several lines of evidence suggest that ROS and Ca2+ cooperate to induce MMP but the molecular details of the ROS–Ca2+-MMP network remain controversial. We then discuss recent data depicting this topic. Cytotoxic stimuli may be transduced within the cell by ROS and Ca2+ increases. In most models, Ca2+ and ROS can cooperate to induce MMP. Moreover, several data suggest that MMP increases mitochondrial Ca2+ and ROS which therefore amplify the cytotoxic signal. Intriguingly, many reports have identified players of MMP as direct ROS targets. On the contrary, direct targets of Ca2+ remain elusive. At the same time, the mechanisms by which mitochondrial Ca2+ overload induces ROS generation are well documented. Upon these observations, we hypothesise that Ca2+ cannot directly induce MMP and requires ROS production as a mandatory step. Given the importance of Ca2+- and ROS-induced MMP in diseases, we expect that a better understanding of this process will lead to the development of novel therapies. •Mitochondrial membrane permeabilisation (MMP) is a crucial step leading to cell death.•In most models, ROS and mitochondrial Ca2+ cooperate to induce MMP.•ROS directly target several components involved in MMP.•However, the mechanisms by which mitochondrial Ca2+ induces MMP remain obscure.•Ca2+ might require mitochondrial ROS generation as a mandatory step to trigger MMP.
AbstractList Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS) and Ca(2+) were the prominent inducers of MMP. However, the mechanisms connecting ROS and Ca(2+) to the players of MMP are still a matter of debate. The aim of this review is to summarise the various studies related to the mechanisms of ROS- and Ca(2+)-induced MMP. Several lines of evidence suggest that ROS and Ca(2+) cooperate to induce MMP but the molecular details of the ROS-Ca(2+)-MMP network remain controversial. We then discuss recent data depicting this topic. Cytotoxic stimuli may be transduced within the cell by ROS and Ca(2+) increases. In most models, Ca(2+) and ROS can cooperate to induce MMP. Moreover, several data suggest that MMP increases mitochondrial Ca(2+) and ROS which therefore amplify the cytotoxic signal. Intriguingly, many reports have identified players of MMP as direct ROS targets. On the contrary, direct targets of Ca(2+) remain elusive. At the same time, the mechanisms by which mitochondrial Ca(2+) overload induces ROS generation are well documented. Upon these observations, we hypothesise that Ca(2+) cannot directly induce MMP and requires ROS production as a mandatory step. Given the importance of Ca(2+)- and ROS-induced MMP in diseases, we expect that a better understanding of this process will lead to the development of novel therapies.
BACKGROUNDMitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS) and Ca(2+) were the prominent inducers of MMP. However, the mechanisms connecting ROS and Ca(2+) to the players of MMP are still a matter of debate.SCOPE OF REVIEWThe aim of this review is to summarise the various studies related to the mechanisms of ROS- and Ca(2+)-induced MMP. Several lines of evidence suggest that ROS and Ca(2+) cooperate to induce MMP but the molecular details of the ROS-Ca(2+)-MMP network remain controversial. We then discuss recent data depicting this topic.MAJOR CONCLUSIONSCytotoxic stimuli may be transduced within the cell by ROS and Ca(2+) increases. In most models, Ca(2+) and ROS can cooperate to induce MMP. Moreover, several data suggest that MMP increases mitochondrial Ca(2+) and ROS which therefore amplify the cytotoxic signal. Intriguingly, many reports have identified players of MMP as direct ROS targets. On the contrary, direct targets of Ca(2+) remain elusive. At the same time, the mechanisms by which mitochondrial Ca(2+) overload induces ROS generation are well documented. Upon these observations, we hypothesise that Ca(2+) cannot directly induce MMP and requires ROS production as a mandatory step.GENERAL SIGNIFICANCEGiven the importance of Ca(2+)- and ROS-induced MMP in diseases, we expect that a better understanding of this process will lead to the development of novel therapies.
Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS) and Ca2+ were the prominent inducers of MMP. However, the mechanisms connecting ROS and Ca2+ to the players of MMP are still a matter of debate. The aim of this review is to summarise the various studies related to the mechanisms of ROS- and Ca2+-induced MMP. Several lines of evidence suggest that ROS and Ca2+ cooperate to induce MMP but the molecular details of the ROS–Ca2+-MMP network remain controversial. We then discuss recent data depicting this topic. Cytotoxic stimuli may be transduced within the cell by ROS and Ca2+ increases. In most models, Ca2+ and ROS can cooperate to induce MMP. Moreover, several data suggest that MMP increases mitochondrial Ca2+ and ROS which therefore amplify the cytotoxic signal. Intriguingly, many reports have identified players of MMP as direct ROS targets. On the contrary, direct targets of Ca2+ remain elusive. At the same time, the mechanisms by which mitochondrial Ca2+ overload induces ROS generation are well documented. Upon these observations, we hypothesise that Ca2+ cannot directly induce MMP and requires ROS production as a mandatory step. Given the importance of Ca2+- and ROS-induced MMP in diseases, we expect that a better understanding of this process will lead to the development of novel therapies. •Mitochondrial membrane permeabilisation (MMP) is a crucial step leading to cell death.•In most models, ROS and mitochondrial Ca2+ cooperate to induce MMP.•ROS directly target several components involved in MMP.•However, the mechanisms by which mitochondrial Ca2+ induces MMP remain obscure.•Ca2+ might require mitochondrial ROS generation as a mandatory step to trigger MMP.
Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous diseases such as cancer, neurodegenerative disorders or ischemia/reperfusion injuries. Many studies established that reactive oxygen species (ROS) and Ca²⁺ were the prominent inducers of MMP. However, the mechanisms connecting ROS and Ca²⁺ to the players of MMP are still a matter of debate.The aim of this review is to summarise the various studies related to the mechanisms of ROS- and Ca²⁺-induced MMP. Several lines of evidence suggest that ROS and Ca²⁺ cooperate to induce MMP but the molecular details of the ROS–Ca²⁺-MMP network remain controversial. We then discuss recent data depicting this topic.Cytotoxic stimuli may be transduced within the cell by ROS and Ca²⁺ increases. In most models, Ca²⁺ and ROS can cooperate to induce MMP. Moreover, several data suggest that MMP increases mitochondrial Ca²⁺ and ROS which therefore amplify the cytotoxic signal. Intriguingly, many reports have identified players of MMP as direct ROS targets. On the contrary, direct targets of Ca²⁺ remain elusive. At the same time, the mechanisms by which mitochondrial Ca²⁺ overload induces ROS generation are well documented. Upon these observations, we hypothesise that Ca²⁺ cannot directly induce MMP and requires ROS production as a mandatory step.Given the importance of Ca²⁺- and ROS-induced MMP in diseases, we expect that a better understanding of this process will lead to the development of novel therapies.
Author Tajeddine, Nicolas
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Issue 6
Keywords NO
HKII
Reactive oxygen species
Intrinsic pathway
IP3R
Calcium
JNK
HTRA2
CypD
RyR
I/R
PTP
CaM
GSK-3β
RIRR
Mitochondria
ΔΨm
Mitochondrial permeabilisation
SMAC
FADD
MIMP
MOMP
MIMS
CAD
SOD
MOM
MAPK
SERCA
MIM
MMP
CaMKII
PC
DISC
ROS
MAM
IAP
Apoptosis
Language English
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PublicationDateYYYYMMDD 2016-06-01
PublicationDate_xml – month: 06
  year: 2016
  text: June 2016
PublicationDecade 2010
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Biochimica et biophysica acta
PublicationTitleAlternate Biochim Biophys Acta
PublicationYear 2016
Publisher Elsevier B.V
Publisher_xml – name: Elsevier B.V
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Scorrano (10.1016/j.bbagen.2016.02.013_bb0625) 2003; 300
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Korytowski (10.1016/j.bbagen.2016.02.013_bb0385) 2011; 286
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Mihara (10.1016/j.bbagen.2016.02.013_bb0345) 2003; 11
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Hengartner (10.1016/j.bbagen.2016.02.013_bb0045) 2000; 407
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De Stefani (10.1016/j.bbagen.2016.02.013_bb0555) 2011; 476
Giorgio (10.1016/j.bbagen.2016.02.013_bb0150) 2010; 1797
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Neuzil (10.1016/j.bbagen.2016.02.013_bb0715) 2013; 13
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Tan (10.1016/j.bbagen.2016.02.013_bb0170) 2015; 6
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Green (10.1016/j.bbagen.2016.02.013_bb0310) 2009; 458
Droge (10.1016/j.bbagen.2016.02.013_bb0185) 2002; 82
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Fang (10.1016/j.bbagen.2016.02.013_bb0460) 2000; 97
Conklin (10.1016/j.bbagen.2016.02.013_bb0205) 2004; 3
Bernardi (10.1016/j.bbagen.2016.02.013_bb0110) 2015; 95
Brookes (10.1016/j.bbagen.2016.02.013_bb0690) 2004; 287
Juhaszova (10.1016/j.bbagen.2016.02.013_bb0470) 2004; 113
Leu (10.1016/j.bbagen.2016.02.013_bb0335) 2004; 6
Arakaki (10.1016/j.bbagen.2016.02.013_bb0575) 2001; 1504
Chipuk (10.1016/j.bbagen.2016.02.013_bb0340) 2004; 303
Majima (10.1016/j.bbagen.2016.02.013_bb0255) 1993; 268
Kamata (10.1016/j.bbagen.2016.02.013_bb0395) 2005; 120
Zamzami (10.1016/j.bbagen.2016.02.013_bb0005) 1995; 182
Csordas (10.1016/j.bbagen.2016.02.013_bb0530) 2006; 174
Chen (10.1016/j.bbagen.2016.02.013_bb0215) 2014; 114
Miyashita (10.1016/j.bbagen.2016.02.013_bb0330) 1995; 80
Odagiri (10.1016/j.bbagen.2016.02.013_bb0685) 2009; 46
Lutter (10.1016/j.bbagen.2016.02.013_bb0375) 2000; 2
Berridge (10.1016/j.bbagen.2016.02.013_bb0505) 2003; 4
Distelhorst (10.1016/j.bbagen.2016.02.013_bb0615) 2011; 50
Spat (10.1016/j.bbagen.2016.02.013_bb0565) 2008; 44
Rasmussen (10.1016/j.bbagen.2016.02.013_bb0700) 2015; 112
Ding (10.1016/j.bbagen.2016.02.013_bb0465) 2005; 19
Webster (10.1016/j.bbagen.2016.02.013_bb0630) 2012; 8
Jonas (10.1016/j.bbagen.2016.02.013_bb0165) 2015; 99
Vieira (10.1016/j.bbagen.2016.02.013_bb0270) 2001; 20
Rexroth (10.1016/j.bbagen.2016.02.013_bb0325) 2012; 1817
Itano (10.1016/j.bbagen.2016.02.013_bb0590) 1986; 13
Kohr (10.1016/j.bbagen.2016.02.013_bb0290) 2011; 300
Hamanaka (10.1016/j.bbagen.2016.02.013_bb0200) 2009; 21
Zorov (10.1016/j.bbagen.2016.02.013_bb0210) 2014; 94
Win (10.1016/j.bbagen.2016.02.013_bb0420) 2014; 5
Bonora (10.1016/j.bbagen.2016.02.013_bb0580) 2014; 4
Peng (10.1016/j.bbagen.2016.02.013_bb0670) 2010; 1201
Giorgio (10.1016/j.bbagen.2016.02.013_bb0155) 2013; 110
Xiao (10.1016/j.bbagen.2016.02.013_bb0425) 2004; 23
Gonzalvez (10.1016/j.bbagen.2016.02.013_bb0380) 2005; 12
Gogvadze (10.1016/j.bbagen.2016.02.013_bb0720) 2010; 127
Toledo (10.1016/j.bbagen.2016.02.013_bb0605) 2014; 88
Sanz-Blasco (10.1016/j.bbagen.2016.02.013_bb0705) 2008; 3
Martel (10.1016/j.bbagen.2016.02.013_bb0245) 2014; 19 Pt A
Szabadkai (10.1016/j.bbagen.2016.02.013_bb0550) 2006; 175
Ren (10.1016/j.bbagen.2016.02.013_bb0360) 2014; 55
Schinzel (10.1016/j.bbagen.2016.02.013_bb0130) 2005; 102
Jardin (10.1016/j.bbagen.2016.02.013_bb0655) 2006; 17
Galluzzi (10.1016/j.bbagen.2016.02.013_bb0120) 2008; 27
Kroemer (10.1016/j.bbagen.2016.02.013_bb0055) 2007; 87
Kowaltowski (10.1016/j.bbagen.2016.02.013_bb0240) 1997; 1318
Lippe (10.1016/j.bbagen.2016.02.013_bb0315) 1991; 181
Mattson (10.1016/j.bbagen.2016.02.013_bb0025) 2000; 1
Nakano (10.1016/j.bbagen.2016.02.013_bb0400) 2006; 13
Nishihara (10.1016/j.bbagen.2016.02.013_bb0485) 2007; 43
Pastorino (10.1016/j.bbagen.2016.02.013_bb0475) 2005; 65
Rasola (10.1016/j.bbagen.2016.02.013_bb0495) 2010; 107
Li (10.1016/j.bbagen.2016.02.013_bb0390) 2008; 68
Zundorf (10.1016/j.bbagen.2016.02.013_bb0660) 2011; 14
Vaseva (10.1016/j.bbagen.2016.02.013_bb0295) 2012; 149
Giacomello (10.1016/j.bbagen.2016.02.013_bb0520) 2007; 14
Baughman (10.1016/j.bbagen.2016.02.013_bb0560) 2011; 476
Alavian (10.1016/j.bbagen.2016.02.013_bb0160) 2014; 111
McCubrey (10.1016/j.bbagen.2016.02.013_bb0405) 2006; 8
Sen (10.1016/j.bbagen.2016.02.013_bb0020) 1992; 307
Miura (10.1016/j.bbagen.2016.02.013_bb0445) 2010; 24
Decuypere (10.1016/j.bbagen.2016.02.013_bb0500) 2011; 2011
Brenner (10.1016/j.bbagen.2016.02.013_bb0100) 2012; 111
Orrenius (10.1016/j.bbagen.2016.02.013_bb0510) 1989; 10
Ha (10.1016/j.bbagen.2016.02.013_bb0350) 2013; 288
Chipuk (10.1016/j.bbagen.2016.02.013_bb0305) 2006; 13
Fang (10.1016/j.bbagen.2016.02.013_bb0455) 2002; 22
Galluzzi (10.1016/j.bbagen.2016.02.013_bb0085) 2009; 10
Javadov (10.1016/j.bbagen.2016.02.013_bb0280) 2013; 4
Liu (10.1016/j.bbagen.2016.02.013_bb0610) 2007; 581
Green (10.1016/j.bbagen.2016.02.013_bb0040) 2004; 305
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Snippet Mitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in numerous...
BACKGROUNDMitochondrial membrane permeabilisation (MMP) is classically considered as a point of no return in several forms of cell death and is involved in...
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SubjectTerms Animals
Apoptosis
Calcium
Calcium - metabolism
cell death
cytotoxicity
Humans
Intrinsic pathway
ischemia
Mitochondria
mitochondrial membrane
Mitochondrial Membranes - metabolism
Mitochondrial permeabilisation
neoplasms
neurodegenerative diseases
Permeability
Reactive oxygen species
Reactive Oxygen Species - metabolism
Title How do reactive oxygen species and calcium trigger mitochondrial membrane permeabilisation?
URI https://dx.doi.org/10.1016/j.bbagen.2016.02.013
https://www.ncbi.nlm.nih.gov/pubmed/26922832
https://www.proquest.com/docview/1782216361
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