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Mitochondria in Embryogenesis: An Organellogenesis Perspective.

Frontiers in cell and developmental biology (2019-12-12)
Yoan Arribat, Dogan Grepper, Sylviane Lagarrigue, Joy Richard, Mélanie Gachet, Philipp Gut, Francesca Amati
RESUMEN

Organogenesis is well characterized in vertebrates. However, the anatomical and functional development of intracellular compartments during this phase of development remains unknown. Taking an organellogenesis point of view, we characterize the spatiotemporal adaptations of the mitochondrial network during zebrafish embryogenesis. Using state of the art microscopy approaches, we find that mitochondrial network follows three distinct distribution patterns during embryonic development. Despite of this constant morphological change of the mitochondrial network, electron transport chain supercomplexes occur at early stages of embryonic development and conserve a stable organization throughout development. The remodeling of the mitochondrial network and the conservation of its structural components go hand-in-hand with somite maturation; for example, genetic disruption of myoblast fusion impairs mitochondrial network maturation. Reciprocally, mitochondria quality represents a key factor to determine embryonic progression. Alteration of mitochondrial polarization and electron transport chain halts embryonic development in a reversible manner suggesting developmental checkpoints that depend on mitochondrial integrity. Our findings establish the subtle dialogue and co-dependence between organogenesis and mitochondria in early vertebrate development. They also suggest the importance of adopting subcellular perspectives to understand organelle-organ communications during embryogenesis.

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Sulfito de sodio, ≥98%
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Oligomicina A, ≥99% (HPLC)
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Peróxido de hidrógeno solution, 30% (w/w), puriss. p.a., reag. ISO, reag. Ph. Eur.
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N-Phenylthiourea, ≥98%
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DMH1, ≥98% (HPLC)
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Mdivi-1, ≥98% (HPLC), powder
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SAG dihydrochloride, ≥98% (HPLC)
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Cyclopamine hydrate, ≥98% (HPLC)