Abstract

The vertebrate eye-primordium consists of a pseudostratified neuroepithelium, the optic vesicle (OV), in which cells acquire neural retina or retinal pigment epithelium (RPE) fates. As these fates arise, the OV assumes a cup-shape, influenced by mechanical forces generated within the neural retina. Whether the RPE passively adapts to retinal changes or actively contributes to OV morphogenesis remains unexplored. We generated a zebrafish Tg(E1-bhlhe40:GFP) line to track RPE morphogenesis and interrogate its participation in OV folding. We show that, in virtual absence of proliferation, RPE cells stretch and flatten, thereby matching the retinal curvature and promoting OV folding. Localized interference with the RPE cytoskeleton disrupts tissue stretching and OV folding. Thus, extreme RPE flattening and accelerated differentiation are efficient solutions adopted by fast-developing species to enable timely optic cup formation. This mechanism differs in amniotes, in which proliferation drives RPE expansion with a much-reduced need of cell flattening.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files. Source data files have been provided for all the graphs shown in the study

Article and author information

Author details

  1. Tania Moreno-Mármol

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    Competing interests
    The authors declare that no competing interests exist.
  2. Mario Ledesma-Terrón

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    Competing interests
    The authors declare that no competing interests exist.
  3. Noemi Tabanera

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    Competing interests
    The authors declare that no competing interests exist.
  4. Maria Jesús Martin-Bermejo

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    Competing interests
    The authors declare that no competing interests exist.
  5. Marcos J Cardozo

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    Competing interests
    The authors declare that no competing interests exist.
  6. Florencia Cavodeassi

    Institute of medical and Biomedical Education, St George's University, London, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4609-6258
  7. Paola Bovolenta

    Centro de Biología Molecular Severo Ochoa., CSIC-UAM, Cantoblanco, Spain
    For correspondence
    pbovolenta@cbm.csic.es
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1870-751X

Funding

Agencia Estatal de Investigación (PID2019-104186RB-100)

  • Paola Bovolenta

Ministerio de Economía, Industria y Competitividad, Gobierno de España (RED2018-102553-T)

  • Paola Bovolenta

Ministerio de Economía, Industria y Competitividad, Gobierno de España (BFU2016-75412-R)

  • Paola Bovolenta

Ministerio de Economía, Industria y Competitividad, Gobierno de España (BFU2014-55918-P)

  • Florencia Cavodeassi

BBVA Foundation (N[16]_BBM_BAS_0078)

  • Florencia Cavodeassi

Fundación Ramon Areces-2016 (no number)

  • Paola Bovolenta

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2021, Moreno-Mármol et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 1,977
    views
  • 299
    downloads
  • 16
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Tania Moreno-Mármol
  2. Mario Ledesma-Terrón
  3. Noemi Tabanera
  4. Maria Jesús Martin-Bermejo
  5. Marcos J Cardozo
  6. Florencia Cavodeassi
  7. Paola Bovolenta
(2021)
Stretching of the retinal pigment epithelium contributes to zebrafish optic cup morphogenesis
eLife 10:e63396.
https://doi.org/10.7554/eLife.63396

Share this article

https://doi.org/10.7554/eLife.63396

Further reading

    1. Cell Biology
    2. Developmental Biology
    Sofía Suárez Freire, Sebastián Perez-Pandolfo ... Mariana Melani
    Research Article

    Eukaryotic cells depend on exocytosis to direct intracellularly synthesized material toward the extracellular space or the plasma membrane, so exocytosis constitutes a basic function for cellular homeostasis and communication between cells. The secretory pathway includes biogenesis of secretory granules (SGs), their maturation and fusion with the plasma membrane (exocytosis), resulting in release of SG content to the extracellular space. The larval salivary gland of Drosophila melanogaster is an excellent model for studying exocytosis. This gland synthesizes mucins that are packaged in SGs that sprout from the trans-Golgi network and then undergo a maturation process that involves homotypic fusion, condensation, and acidification. Finally, mature SGs are directed to the apical domain of the plasma membrane with which they fuse, releasing their content into the gland lumen. The exocyst is a hetero-octameric complex that participates in tethering of vesicles to the plasma membrane during constitutive exocytosis. By precise temperature-dependent gradual activation of the Gal4-UAS expression system, we have induced different levels of silencing of exocyst complex subunits, and identified three temporarily distinctive steps of the regulated exocytic pathway where the exocyst is critically required: SG biogenesis, SG maturation, and SG exocytosis. Our results shed light on previously unidentified functions of the exocyst along the exocytic pathway. We propose that the exocyst acts as a general tethering factor in various steps of this cellular process.

    1. Cell Biology
    2. Developmental Biology
    Heungjin Ryu, Kibum Nam ... Jung-Hoon Park
    Research Article

    In most murine species, spermatozoa exhibit a falciform apical hook at the head end. The function of the sperm hook is not yet clearly understood. In this study, we investigate the role of the sperm hook in the migration of spermatozoa through the female reproductive tract in Mus musculus (C57BL/6), using a deep tissue imaging custom-built two-photon microscope. Through live reproductive tract imaging, we found evidence indicating that the sperm hook aids in the attachment of spermatozoa to the epithelium and facilitates interactions between spermatozoa and the epithelium during migration in the uterus and oviduct. We also observed synchronized sperm beating, which resulted from the spontaneous unidirectional rearrangement of spermatozoa in the uterus. Based on live imaging of spermatozoa-epithelium interaction dynamics, we propose that the sperm hook plays a crucial role in successful migration through the female reproductive tract by providing anchor-like mechanical support and facilitating interactions between spermatozoa and the female reproductive tract in the house mouse.