The mitochondrial ATP-dependent potassium channel (mitoK
Journal
Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092
Informations de publication
Date de publication:
17 Jan 2024
17 Jan 2024
Historique:
received:
19
06
2023
accepted:
02
01
2024
revised:
20
12
2023
medline:
18
1
2024
pubmed:
18
1
2024
entrez:
17
1
2024
Statut:
epublish
Résumé
MitoK
Identifiants
pubmed: 38233399
doi: 10.1038/s41419-024-06426-x
pii: 10.1038/s41419-024-06426-x
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
58Subventions
Organisme : Ministero della Salute (Ministry of Health, Italy)
ID : RF-2016-02363566
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research)
ID : PRIN 2020R2BP2E_002
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research)
ID : PRIN 2017YF9FBS
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research)
ID : PRIN 2020RRJP5L
Organisme : AFM-Téléthon (French Muscular Dystrophy Association)
ID : 22493
Informations de copyright
© 2024. The Author(s).
Références
Checchetto V, Leanza L, De Stefani D, Rizzuto R, Gulbins E, Szabo I. Mitochondrial K+ channels and their implications for disease mechanisms. Pharm Ther. 2021;227:107874.
doi: 10.1016/j.pharmthera.2021.107874
Malinska D, Mirandola SR, Kunz WS. Mitochondrial potassium channels and reactive oxygen species. FEBS Lett. 2010;584:2043–8.
doi: 10.1016/j.febslet.2010.01.013
pubmed: 20080090
Kowaltowski AJ, Seetharaman S, Paucek P, Garlid KD. Bioenergetic consequences of opening the ATP-sensitive K(+) channel of heart mitochondria. Am J Physiol Heart Circ Physiol. 2001;280:H649–57.
doi: 10.1152/ajpheart.2001.280.2.H649
pubmed: 11158963
Minners J, Van Den Bos EJ, Yellon DM, Schwalb H, Opie LH, Sack MN. Dinitrophenol, cyclosporin A, and trimetazidine modulate preconditioning in the isolated rat heart: Support for a mitochondrial role in cardioprotection. Cardiovasc Res. 2000;47:68–73.
doi: 10.1016/S0008-6363(00)00069-9
pubmed: 10869531
Paggio A, Checchetto V, Campo A, Menabò R, Di Marco G, Di Lisa F, et al. Identification of an ATP-sensitive potassium channel in mitochondria. Nature. 2019;572:609–13.
doi: 10.1038/s41586-019-1498-3
pubmed: 31435016
pmcid: 6726485
Debska G, Kicinska A, Skalska J, Szewczyk A, May R, Elger CE, et al. Opening of potassium channels modulates mitochondrial function in rat skeletal muscle. Biochim et Biophys Acta (BBA) - Bioenerg. 2002;1556:97–105.
doi: 10.1016/S0005-2728(02)00340-7
Montoya-Pérez R, Saavedra-Molina A, Trujillo X, Huerta M, Andrade F, Sánchez-Pastor E, et al. Inhibition of oxygen consumption in skeletal muscle-derived mitochondria by pinacidil, diazoxide, and glibenclamide, but not by 5-hydroxydecanoate. J Bioenerg Biomembr. 2010;42:21–27.
doi: 10.1007/s10863-009-9265-z
pubmed: 20066482
García MC, Hernández A, Sánchez JA. Role of mitochondrial ATP-sensitive potassium channels on fatigue in mouse muscle fibers. Biochem Biophys Res Commun. 2009;385:28–32.
doi: 10.1016/j.bbrc.2009.05.019
pubmed: 19427835
Sánchez-Duarte E, Trujillo X, Huerta M, Ortiz-Mesina M, Cortés-Rojo C, Manzo-Ávalos S, et al. Mitochondrial KATP channels in skeletal muscle: are protein kinases C and G, and nitric oxide synthase involved in the fatigue process? Open Access Anim Physiol. 2012;4:21–28.
Luévano-Martínez LA, Kowaltowski AJ. Phosphatidylglycerol-derived phospholipids have a universal, domain-crossing role in stress responses. Arch Biochem Biophys. 2015;585:90–97.
doi: 10.1016/j.abb.2015.09.015
pubmed: 26391924
Romanello V, Sandri M. The connection between the dynamic remodeling of the mitochondrial network and the regulation of muscle mass. Cell Mol Life Sci. 2020;78:1305–28.
doi: 10.1007/s00018-020-03662-0
pubmed: 33078210
pmcid: 7904552
Sartori R, Romanello V, Sandri M. Mechanisms of muscle atrophy and hypertrophy: implications in health and disease. Nat Commun 2021 12:1. 2021;12:1–12.
Ebert SM, Monteys AM, Fox DK, Bongers KS, Shields BE, Malmberg SE, et al. The Transcription Factor ATF4 Promotes Skeletal Myofiber Atrophy during Fasting. Mol Endocrinol. 2010;24:790–9.
doi: 10.1210/me.2009-0345
pubmed: 20197309
pmcid: 2852358
Ebert SM, Dyle MC, Kunkel SD, Bullard SA, Bongers KS, Fox DK, et al. Stress-induced Skeletal Muscle Gadd45a Expression Reprograms Myonuclei and Causes Muscle Atrophy. J Biol Chem. 2012;287:27290–301.
doi: 10.1074/jbc.M112.374777
pubmed: 22692209
pmcid: 3431665
Bongers KS, Fox DK, Kunkel SD, Stebounova LV, Murry DJ, Pufall MA, et al. Spermine oxidase maintains basal skeletal muscle gene expression and fiber size and is strongly repressed by conditions that cause skeletal muscle atrophy. Am J Physiol Endocrinol Metab. 2015;308:E144–E158.
doi: 10.1152/ajpendo.00472.2014
pubmed: 25406264
Fox DK, Ebert SM, Bongers KS, Dyle MC, Bullard SA, Dierdorff JM, et al. p53 and ATF4 mediate distinct and additive pathways to skeletal muscle atrophy during limb immobilization. Am J Physiol Endocrinol Metab. 2014;307:E245–E261.
doi: 10.1152/ajpendo.00010.2014
pubmed: 24895282
pmcid: 4121573
Thada V, Greenberg RA. Unpaved roads: How the DNA damage response navigates endogenous genotoxins. DNA Repair (Amst). 2022;118:103383.
doi: 10.1016/j.dnarep.2022.103383
pubmed: 35939975
pmcid: 9703833
Fennel ZJ, Amorim FT, Deyhle MR, Hafen PS, Mermier CM. The heat shock connection: skeletal muscle hypertrophy and atrophy. Am J Physiol Regul Integr Comp Physiol. 2022;323:R133–R148.
doi: 10.1152/ajpregu.00048.2022
pubmed: 35536704
Cramer AAW, Prasad V, Eftestøl E, Song T, Hansson KA, Dugdale HF, et al. Nuclear numbers in syncytial muscle fibers promote size but limit the development of larger myonuclear domains. Nat Commun. 2020;11:6287.
doi: 10.1038/s41467-020-20058-7
pubmed: 33293533
pmcid: 7722938
Hansson KA, Eftestøl E, Bruusgaard JC, Juvkam I, Cramer AW, Malthe-Sørenssen A, et al. Myonuclear content regulates cell size with similar scaling properties in mice and humans. Nat Commun. 2020;11:6288.
doi: 10.1038/s41467-020-20057-8
pubmed: 33293572
pmcid: 7722898
Vega-Moreno J, Tirado-Cortes A, Álvarez R, Irles C, Mas-Oliva J, Ortega A. Cholesterol Depletion Uncouples β-dystroglycans from Discrete Sarcolemmal Domains, Reducing the Mechanical Activity of Skeletal Muscle. Cell Physiol Biochem. 2012;29:905–18.
doi: 10.1159/000186933
pubmed: 22613990
Kohin S, Stary CM, Howlett RA, Hogan MC. Preconditioning improves function and recovery of single muscle fibers during severe hypoxia and reoxygenation. Am J Physiol-Cell Physiol. 2001;281:C142–C146.
doi: 10.1152/ajpcell.2001.281.1.C142
pubmed: 11401836
Masiero E, Agatea L, Mammucari C, Blaauw B, Loro E, Komatsu M, et al. Autophagy is required to maintain muscle mass. Cell Metab. 2009;10:507–15.
doi: 10.1016/j.cmet.2009.10.008
pubmed: 19945408
Ebert SM, Bullard SA, Basisty N, Marcotte GR, Skopec ZP, Dierdorff JM, et al. Activating transcription factor 4 (ATF4) promotes skeletal muscle atrophy by forming a heterodimer with the transcriptional regulator C/EBPβ. J Biol Chem. 2020;295:2787–803.
doi: 10.1074/jbc.RA119.012095
pubmed: 31953319
pmcid: 7049960
Bongers KS, Fox DK, Ebert SM, Kunkel SD, Dyle MC, Bullard SA, et al. Skeletal muscle denervation causes skeletal muscle atrophy through a pathway that involves both Gadd45a and HDAC4. Am J Physiol Endocrinol Metab. 2013;305:907–15.
doi: 10.1152/ajpendo.00380.2013
Schindelin J, Arganda-Carreras I, Frise E, Kaynig V, Longair M, Pietzsch T, et al. Fiji: an open-source platform for biological-image analysis. Nat Methods. 2012;9:676–82.
doi: 10.1038/nmeth.2019
pubmed: 22743772
Pendin D, Norante R, De Nadai A, Gherardi G, Vajente N, Basso E, et al. A Synthetic Fluorescent Mitochondria-Targeted Sensor for Ratiometric Imaging of Calcium in Live Cells. Angew Chem Int Ed. 2019;58:9917–22.
doi: 10.1002/anie.201902272
Blaauw B, Mammucari C, Toniolo L, Agatea L, Abraham R, Sandri M, et al. Akt activation prevents the force drop induced by eccentric contractions in dystrophin-deficient skeletal muscle. Hum Mol Genet. 2008;17:3686–96.
doi: 10.1093/hmg/ddn264
pubmed: 18753145
Ju JS, Varadhachary AS, Miller SE, Weihl CC. Quantitation of ‘autophagic flux’ in mature skeletal muscle. Autophagy. 2010;6:929–35.
doi: 10.4161/auto.6.7.12785
pubmed: 20657169
pmcid: 3039739
Rozen S, Skaletsky H Primer3 on the WWW for General Users and for Biologist Programmers. In: Bioinformatics Methods and Protocols. Humana Press: New Jersey, 2000, pp 365–86.