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Retrograde ERK activation waves drive base-to-apex multicellular flow in murine cochlear duct morphogenesis.


ABSTRACT: A notable example of spiral architecture in organs is the mammalian cochlear duct, where the morphology is critical for hearing function. Genetic studies have revealed necessary signaling molecules, but it remains unclear how cellular dynamics generate elongating, bending, and coiling of the cochlear duct. Here, we show that extracellular signal-regulated kinase (ERK) activation waves control collective cell migration during the murine cochlear duct development using deep tissue live-cell imaging, Förster resonance energy transfer (FRET)-based quantitation, and mathematical modeling. Long-term FRET imaging reveals that helical ERK activation propagates from the apex duct tip concomitant with the reverse multicellular flow on the lateral side of the developing cochlear duct, resulting in advection-based duct elongation. Moreover, model simulations, together with experiments, explain that the oscillatory wave trains of ERK activity and the cell flow are generated by mechanochemical feedback. Our findings propose a regulatory mechanism to coordinate the multicellular behaviors underlying the duct elongation during development.

SUBMITTER: Ishii M 

PROVIDER: S-EPMC7935486 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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Retrograde ERK activation waves drive base-to-apex multicellular flow in murine cochlear duct morphogenesis.

Ishii Mamoru M   Tateya Tomoko T   Matsuda Michiyuki M   Hirashima Tsuyoshi T  

eLife 20210305


A notable example of spiral architecture in organs is the mammalian cochlear duct, where the morphology is critical for hearing function. Genetic studies have revealed necessary signaling molecules, but it remains unclear how cellular dynamics generate elongating, bending, and coiling of the cochlear duct. Here, we show that extracellular signal-regulated kinase (ERK) activation waves control collective cell migration during the murine cochlear duct development using deep tissue live-cell imagin  ...[more]

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