Dogan 2014 Cell Metab

From Bioblast
Publications in the MiPMap
Dogan SA, Pujol C, Maiti P, Kukat A, Wang S, Hermans S, Senft K, Wibom R, Rugarli EI, Trifunovic A (2014) Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart. Cell Metab 19:458-69.

Β» PMID: 24606902 Open Access

Dogan Sukru Anil, Pujol Claire, Maiti Priyanka, Kukat Alexandra, Wang Shuaiyu, Hermans Steffen, Senft Katharina, Wibom Rofl, Rugarli Elena I, Trifunovic Aleksandra (2014) Cell Metab

Abstract: Adaptive stress responses activated upon mitochondrial dysfunction are assumed to arise in order to counteract respiratory chain deficiency. Here, we demonstrate that loss of DARS2 (mitochondrial aspartyl-tRNA synthetase) leads to the activation of various stress responses in a tissue-specific manner independently of respiratory chain deficiency. DARS2 depletion in heart and skeletal muscle leads to the severe deregulation of mitochondrial protein synthesis followed by a strong respiratory chain deficit in both tissues, yet the activation of adaptive responses is observed predominantly in cardiomyocytes. We show that the impairment of mitochondrial proteostasis in the heart activates the expression of mitokine FGF21, which acts as a signal for cell-autonomous and systemic metabolic changes. Conversely, skeletal muscle has an intrinsic mechanism relying on the slow turnover of mitochondrial transcripts and higher proteostatic buffering capacity. Our results show that mitochondrial dysfunction is sensed independently of respiratory chain deficiency, questioning the current view on the role of stress responses in mitochondrial diseases.

Copyright Β© 2014 Elsevier Inc. All rights reserved.

β€’ Bioblast editor: Plangger M β€’ O2k-Network Lab: TR Istanbul Dogan SA, DE Cologne Trifunovic A

Labels: MiParea: Respiration, Genetic knockout;overexpression 

Organism: Mouse  Tissue;cell: Heart, Skeletal muscle, Liver  Preparation: Permeabilized tissue, Isolated mitochondria 

Coupling state: LEAK, OXPHOS, ET  Pathway: N, S  HRR: Oxygraph-2k 


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