posted on 2025-10-17, 14:31authored byZiqi Chen, Magdalena ZakMagdalena Zak, Shuting Xu, Javier de Andrés, Nicolas Daudet
<p dir="ltr">Raw confocal microscopy images (in Zeiss and Velocity formats) and quantification results (Excel files) related to the paper with the same title are provided here. The files are organized according to the corresponding figures in the paper. If you have further questions, please get in touch with the corresponding author.</p><p dir="ltr"><br></p><p dir="ltr">Abstract </p><p dir="ltr">The inner ear contains distinct sensory organs, produced sequentially by segregation from a large sensory-competent domain in the developing otic vesicle. To understand the mechanistic basis of this process, we investigated the changes in prosensory cell patterning, proliferation and character during the segregation of some of the vestibular organs in the mouse and chicken otic vesicle. We discovered a specialized boundary domain, located at the interface of segregating organs. It is composed of prosensory cells that gradually enlarge, elongate and are ultimately diverted from a prosensory fate. Strikingly, the boundary cells align their apical borders and constrict basally at the interface of cells expressing or not the Lmx1a transcription factor, an orthologue of drosophila Apterous. The boundary domain is absent in Lmx1a-deficient mice, which exhibit defects in sensory organ segregation, and is disrupted by the inhibition of ROCK-dependent actomyosin contractility. Altogether, our results suggest that actomyosin-dependent tissue boundaries ensure the proper separation of inner ear sensory organs and uncover striking homologies between this process and the compartmentalization of the drosophila wing disc by lineage-restricted boundaries.</p><p dir="ltr"><br></p>
Funding
Action on Hearing Loss International Research Grant (G76 to ND and MŻ)
Royal National Institute for Deaf People Fellowship (P27 to MŻ)
Medical Research Council MR/S003029/1 and MR/W005123/1 to ND and MŻ)
Biotechnology and Biological Sciences Research Council BB/L003163/1 to ND
for microscopy Biotechnology and Biological Sciences Research Council BB/R000549/1 to Jonathan Gale)