Light-modulated stem cells in the camera-type eye of an annelid model for adult brain plasticity

Camera-type eyes in vertebrates and cephalopods are striking examples of parallel evolution of a complex structure. While comparisons have focused on these two groups, camera-type eyes with likely high functionality are also found in other invertebrate phyla with simpler brains. Employing single-cell RNA sequencing, we identify neurogenic cells in the adult eyes and brain of the marine annelid worm Platynereis dumerilii. Distinct neural stem cells in the camera-type adult eyes, located at the edge of the cup-shaped retina, and adjacent to the glass body/lens, produce radial lines of cells, reminiscent of stem cells in ciliary marginal zones of vertebrate eyes exhibiting life-long growth. Normal proliferation in the eye depends on ambient light, a phenomenon that depends on the integrity of the photoreceptor gene c-opsin1, which is present in emerging rhabdomeric photoreceptors, and impacts on their differentiation. During reproductive maturation, proliferation in the eye as well as the entire brain sharply declines, while cells upregulate molecular characteristics of mammalian adult neural stem cell quiescence. Our data provide insights into the development and modulation of annelid head and brain cells, revealing similarities and differences to vertebrate eye development, neurogenesis and brain plasticity.

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Publication Details

Journal
Nature Communications
Published
2025-12-01
DOI
https://doi.org/10.1038/s41467-025-65631-0
Citations
2
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
1.61

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article

Light-modulated stem cells in the camera-type eye of an annelid model for adult brain plasticity

Camila Lissett Velastegui Gamboa, Pedro Ozório Brum, Kristin Tessmar‐Raible, Nadja Milivojev et al.
2 citations
Nature Communications
Developmental Biology and Gene Regulation
1.61
article

Light-modulated stem cells in the camera-type eye of an annelid model for adult brain plasticity

Camila Lissett Velastegui Gamboa, Pedro Ozório Brum, Kristin Tessmar‐Raible, Nadja Milivojev, Gabriele Andreatta, Florian Raible, Federico Scaramuzza
article en
2 citations

Abstract

Camera-type eyes in vertebrates and cephalopods are striking examples of parallel evolution of a complex structure. While comparisons have focused on these two groups, camera-type eyes with likely high functionality are also found in other invertebrate phyla with simpler brains. Employing single-cell RNA sequencing, we identify neurogenic cells in the adult eyes and brain of the marine annelid worm Platynereis dumerilii. Distinct neural stem cells in the camera-type adult eyes, located at the edge of the cup-shaped retina, and adjacent to the glass body/lens, produce radial lines of cells, reminiscent of stem cells in ciliary marginal zones of vertebrate eyes exhibiting life-long growth. Normal proliferation in the eye depends on ambient light, a phenomenon that depends on the integrity of the photoreceptor gene c-opsin1, which is present in emerging rhabdomeric photoreceptors, and impacts on their differentiation. During reproductive maturation, proliferation in the eye as well as the entire brain sharply declines, while cells upregulate molecular characteristics of mammalian adult neural stem cell quiescence. Our data provide insights into the development and modulation of annelid head and brain cells, revealing similarities and differences to vertebrate eye development, neurogenesis and brain plasticity.

Nature CommunicationsVol. 16(1)
Institute of Molecular Biotechnology (AT), Alfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung (DE), University of Vienna (AT), Carl von Ossietzky Universität Oldenburg (DE), Austrian Academy of Sciences (AT), University of Padua (IT), Institute of Science and Technology Austria (AT), Vienna Biocenter (AT), Medical University of Vienna (AT), BOKU University (AT)
Austrian Science Fund, Universität Wien, Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research, Horizon 2020 Framework Programme, H2020 European Research Council
Openalex Percentile: Top 14%
Developmental Biology and Gene Regulation
1.61
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