Mito.newsMito.news
← All articlesEditorial brief · abstract-levelScore 91/100Confidence high
biorxiv2026-09-03cardiologymetabolismautophagycalcium

Adult cardiomyocyte prohibitin knockout unleashes mTORC1, Warburg-like amino-acid synthesis, and fatal DCM

Delete the PHB1/2 complex in adult mouse cardiomyocytes and mTORC1 runs unrestrained. Glucose carbon swings toward de novo amino acids, mitochondrial calcium handling breaks, autophagy fails, the heart dilates, and the animals die within 12 weeks. mTORC1 inhibition eases remodeling only in females.

Mito.news · at a glance

Signal profile (abstract-level)

cardiology · metabolism · autophagy · calcium

Score 91/100BIORXIVhigh confidencecardiology
91
Importance
62
Mito signal
95
Dysfunction
75
Evidence
30
Translational

Editorial signal profile from the abstract (importance score, mito keywords, dysfunction tags, evidence density, translational cues). Not a figure reproduced from the preprint PDF.

Finding. Prohibitins keep a heart's carbon honest. Huo, Anderson and colleagues wipe the PHB complex out of adult cardiomyocytes. mTORC1 will not sit down. Glucose is spent on new amino acids, a Warburg-like biosynthetic turn. Mitochondrial calcium handling breaks. Autophagy fails. The ventricle dilates. Mice are gone inside 12 weeks. Block mTORC1 and only the females remodel less.

Why this paper matters DCM papers often end at 'energy failure.' This one starts at a mitochondrial scaffold and walks through a growth-kinase and a carbon-allocation error. The female-only rescue is a trial-design warning, not a footnote.

Score 91. Scaffold, mTORC1, mito-Ca2+, autophagy, sex, lethality. High confidence for the mouse phenomenology.

Free HTML is above. Bots pay for JSON at /api/v1/papers/10-64898-2026-09-01-748696. Optional wallet tester: MetaMask ($0.005).

Source preprint

Cardiomyocyte prohibitin ablation reprograms cardiac metabolism revealing a pathogenic role for mTORC1 in dilated cardiomyopathy

10.64898/2026.09.01.748696

Huo R, Torrence SE, Berns KA, Crawford RM, Alowaisi AA, Mahoney JC, Chen B, Shi Q, Darbro BW, Song L, Anderson EJ.

Related briefs