Hexokinase 1 forms rings that regulate mitochondrial fission during energy stress

被引:9
作者
Pilic, Johannes [1 ]
Gottschalk, Benjamin [1 ]
Bourgeois, Benjamin [2 ,3 ]
Habisch, Hansjorg [3 ]
Koshenov, Zhanat [1 ]
Oflaz, Furkan E. [1 ]
Erdogan, Yusuf C. [1 ]
Miri, Seyed M. [4 ,5 ]
Yigit, Esra N. [4 ,6 ]
Aydin, Mehmet S. [4 ]
Ozturk, Gurkan [4 ]
Eroglu, Emrah [4 ,6 ]
Shoshan-Barmatz, Varda [7 ,8 ]
Madl, Tobias
Graier, Wolfgang F. [1 ]
Malli, Roland [1 ,2 ,9 ]
机构
[1] Med Univ Graz, Gottfried Schatz Res Ctr, Mol Biol & Biochem, Neue Stiftingtalstr 6-4, A-8010 Graz, Austria
[2] BioTechMed Graz, Mozartgasse 12-2, A-8010 Graz, Austria
[3] Med Univ Graz, Otto Loewi Res Ctr, Med Chem, A-8010 Graz, Austria
[4] Istanbul Medipol Univ, Res Inst Hlth Sci & Technol SABITA, Regenerat & Restorat Med Res Ctr REMER, TR-34810 Istanbul, Turkiye
[5] Sabanci Univ, Fac Engn & Nat Sci, Mol Biol Genet & Bioengn Program, TR-34956 Istanbul, Turkiye
[6] Istanbul Medipol Univ, Int Sch Med, Dept Physiol, TR-34810 Istanbul, Turkiye
[7] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
[8] Ben Gurion Univ Negev, Natl Inst Biotechnol Negev, IL-84105 Beer Sheva, Israel
[9] Med Univ Graz, Ctr Med Res, CF Bioimaging, Neue Stiftingtalstr 6-6, A-8010 Graz, Austria
基金
奥地利科学基金会;
关键词
BRAIN HEXOKINASE; BINDING-SITE; GLUCOSE; ACTIN; IDENTIFICATION; DEGRADATION; CURVATURE; AFFINITY; DYNAMICS; ENZYMES;
D O I
10.1016/j.molcel.2024.06.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic enzymes can adapt during energy stress, but the consequences of these adaptations remain understudied. Here, we discovered that hexokinase 1 (HK1), a key glycolytic enzyme, forms rings around mitochondria during energy stress. These HK1-rings constrict mitochondria at contact sites with the endoplasmic reticulum (ER) and mitochondrial dynamics protein (MiD51). HK1-rings prevent mitochondrial fission by displacing the dynamin-related protein 1 (Drp1) from mitochondrial fission factor (Mff) and mitochondrial fission 1 protein (Fis1). The disassembly of HK1-rings during energy restoration correlated with mitochondrial fission. Mechanistically, we identified that the lack of ATP and glucose-6-phosphate (G6P) promotes the formation of HK1-rings. Mutations that affect the formation of HK1-rings showed that HK1-rings rewire cellular metabolism toward increased TCA cycle activity. Our findings highlight that HK1 is an energy stress sensor that regulates the shape, connectivity, and metabolic activity of mitochondria. Thus, the formation of HK1rings may affect mitochondrial function in energy-stress-related pathologies.
引用
收藏
页码:2732 / 2746.e5
页数:21
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