The absence of a single mitochondrial protein causes severe inflammation

Opa1 and inflammation

Opa1 is a mitochondrial fusion protein. It serves to fuse the internal membranes of mitochondria. Although present in all cells and tissues (except white blood cells), mitochondria are particularly abundant in muscle and liver, and their main function is to convert the energy in food into energy for cells. Mitochondria are highly dynamic; they join and separate, and grow and shrink constantly. These processes are known as mitochondrial dynamics.

Mitochondrial dynamics is one of the research lines addressed in Antonio Zorzano's Complex Metabolic Diseases and Mitochondria Lab. To study this process, the scientists examine the proteins involved in mitochondrial membrane fusion, namely Mitofusin 1 and 2, and Opa1.

Authored by 24 researchers from various centres and involving a significant contribution by Aida Rodríguez-Nuevo, Angels Díaz-Ramos and Eduardo Noguera from Zorzano's lab, this study focuses on the protein Opa1. To examine its functions, the researchers generated a mouse deficient in Opa1 only in skeletal muscle. "It was surprising to see how small they were and that they died after only a few months," explains Zorzano.

The article describes the animal phenotype and explains that the removal of Opa1 exclusively from skeletal muscle fibre triggers a severe inflammatory process that spreads from the muscle fibre throughout the body. The inflammatory response halts growth and shortens the lifespan of the animal. The scientists also describe the main molecular components of the cell signalling pathway that activates the inflammatory response in muscle.

"This is the first time that we've seen that the lack of a muscle mitochondrial protein triggers an inflammatory response of this magnitude, and these observations give us further information on the relation between mitochondria and inflammation," says Zorzano.

The head of the study explains that these results are of biomedical relevance. There is a set of diseases known as inflammatory myopathies, of unknown origin, in which patients show chronic muscle inflammation accompanied by muscle weakness. "The results of this study suggest that mitochondrial alterations may underlie inflammatory myopathies. More research is now needed to address this possible link," says the scientist.