Muscles types can produce medium enduring forces and or high peak forces followed by quick fatigue. The energy fuelling their contractile motors is largely supplied by their mitochondria. By combining genetics in the fruit fly Drosophila with state-of-the-art imaging and deep-learning, researchers at the Developmental Biology Institute of Marseille have found that mitochondria coordinate their formation with myofibril development to match the correct muscle type. To do so, mitochondria and myofibrils undergo highly orchestrated physical interactions that instruct how each of them progresses through development. These findings show that mitochondria and myofibril morphogenesis are tied mechanically to define the correct muscle fate. These results are now published in Nature Communications.
Most animals have different muscle types dedicated for specific tasks. These can twitch slowly and involuntary, such as the ones that ensheath our gut or keep our heart beating, or be fast and quickly exhausted, like the ones we use to generate maximum force for escaping or lifting heavy objects. Mitochondria are the power houses of all muscles and generate most of their energy by converting nutrients from food into ATP, which fuels the muscle motor proteins. Mitochondria adopt different shapes and localisations in different cell types, in particular in different muscle types. How this is achieved is largely unknown. Now, a multidisciplinary project led by Nuno Luis and Frank Schnorrer at the Developmental Biology Institute of Marseille (IBDM) of the CNRS & Aix-Marseille University, has found that the force producing myofibrils coordinate their development closely with their mitochondria by generating a mechanical feedback mechanism that instructs their final morphology and function.
The flight muscle of the fruit fly Drosophila melanogaster is a “stretch-activated” fibrillar muscle type, similar to the mammalian heart. One group of muscles mechanically senses when stretched by the other group, and then contracts. Hence, wings can oscillate 200 times per second to enable flight. These oscillations require an extensive amount of ATP. Thus, the mitochondria are located in intimate contact to and squeezed in between the individual myofibrils, to quickly deliver ATP to the motor proteins. In contrast, the slower leg muscles of the fly used for walking display a different mitochondrial morphology by forming complex shapes above or below the myofibril layer.
By using state-of-the-art 3D imaging and deep-learning algorithms, Jerome Avellaneda, PhD student and first author of this study, discovered that the muscle-type specific mitochondrial morphology is already instructed during the early stages of flight muscle development. Initially, mitochondria are clustered together. However, as soon as the myofibrils assemble mitochondria intercalate in between them to insulate one from its neighbours. In the following steps, myofibrils grow in size and diameter and push their surrounding mitochondria into elongated ellipsoid shapes. The authors found that the mitochondrial fusion and fission machinery is crucial for this dynamic “mitochondrial-myofibril-dance” with fission being necessary for the mitochondria to intercalate between the myofibrils. Surprisingly, a failure in intercalation results in a myofibril organisation resembling the ones in the slow leg muscle. Even more surprisingly, these flight muscles express leg muscle specific contractile proteins suggesting that the mitochondrial morphology directly feeds back on muscle type choice. These results suggest that in force producing muscle tissue the morphogenesis of the different cellular components and organelles is highly coordinated. Interfering with one, may dramatically change the other. This may have important consequences for treatment of muscle and in particular heart disease in human.
To know more :
- Avellaneda, J., Rodier, C., Daian, F. et al. Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle. Nat Commun 12, 2091 (2021). https://doi.org/10.1038/s41467-021-22058-7
Frank Schnorrer - frank.SCHNORRER@univ-amu.fr