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Cellular migration, transition and interaction during regeneration of the sponge Hymeniacidon heliophila.


ABSTRACT: Sponges have a high capacity for regeneration and this process improves biomass production in some species, thus contributing to a solution for the biomass supply problem for biotechnological applications. The aim of this work is to characterize the dynamics of cell behavior during the initial stages of sponge regeneration, using bright-field microscopy, confocal microscopy and SEM. We focused on the first 20 h of regeneration, during which blastema formation and epithelium initialization occur. An innovative sponge organotypic culture of the regenerating internal region is described and investigated by confocal microscopy, cell transplantation and vital staining. Cell-cell interaction and cell density are shown to affect events in morphogenesis such as epithelial/mesenchymal and mesenchymal/epithelial transitions as well as distinct cell movements required for regeneration. Extracellular matrix was organized according to the morphogenetic process observed, with evidence for cell-signaling instructions and remodeling. These data and the method of organotypic culture described here provide support for the development of viable sponge biomass production.

SUBMITTER: Coutinho CC 

PROVIDER: S-EPMC5444830 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

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Cellular migration, transition and interaction during regeneration of the sponge Hymeniacidon heliophila.

Coutinho Cristiano C CC   Rosa Ivone de Andrade IA   Teixeira John Douglas de Oliveira JDO   Andrade Leonardo R LR   Costa Manoel Luis ML   Mermelstein Claudia C  

PloS one 20170525 5


Sponges have a high capacity for regeneration and this process improves biomass production in some species, thus contributing to a solution for the biomass supply problem for biotechnological applications. The aim of this work is to characterize the dynamics of cell behavior during the initial stages of sponge regeneration, using bright-field microscopy, confocal microscopy and SEM. We focused on the first 20 h of regeneration, during which blastema formation and epithelium initialization occur.  ...[more]

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