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Lucienne, M.* ; Gerlini, R. ; Rathkolb, B. ; Calzada-Wack, J. ; Forny, P.* ; Wueest, S.* ; Kaech, A.* ; Traversi, F.* ; Forny, M.* ; Bürer, C.* ; Aguilar-Pimentel, J.A. ; Irmler, M. ; Beckers, J. ; Sauer, S.* ; Kölker, S.* ; Dewulf, J.P.* ; Bommer, G.T.* ; Hoces, D.* ; Gailus-Durner, V. ; Fuchs, H. ; Rozman, J. ; Froese, D.S.* ; Baumgartner, M.R.* ; Hrabě de Angelis, M.

Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria.

Hum. Mol. Genet. 32, 2717-2734 (2023)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Inherited disorders of mitochondrial metabolism, including isolated methylmalonic aciduria, present unique challenges to energetic homeostasis by disrupting energy-producing pathways. To better understand global responses to energy shortage, we investigated a hemizygous mouse model of methylmalonyl-CoA mutase (Mmut)-type methylmalonic aciduria. We found Mmut mutant mice to have reduced appetite, energy expenditure and body mass compared with littermate controls, along with a relative reduction in lean mass but increase in fat mass. Brown adipose tissue showed a process of whitening, in line with lower body surface temperature and lesser ability to cope with cold challenge. Mutant mice had dysregulated plasma glucose, delayed glucose clearance and a lesser ability to regulate energy sources when switching from the fed to fasted state, while liver investigations indicated metabolite accumulation and altered expression of peroxisome proliferator-activated receptor and Fgf21-controlled pathways. Together, these shed light on the mechanisms and adaptations behind energy imbalance in methylmalonic aciduria and provide insight into metabolic responses to chronic energy shortage, which may have important implications for disease understanding and patient management.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Multiple Oxphos Deficiency; Ppar-alpha; Insulin-resistance; Mitochondrial Dysfunction; Body-temperature; Lipid-metabolism; Adipose-tissue; Brown Fat; Liver; Fgf21
ISSN (print) / ISBN 0964-6906
e-ISSN 1460-2083
Zeitschrift Human Molecular Genetics
Quellenangaben Band: 32, Heft: 17, Seiten: 2717-2734 Artikelnummer: , Supplement: ,
Verlag Oxford University Press
Verlagsort Great Clarendon St, Oxford Ox2 6dp, England
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Experimental Genetics (IEG)