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Cultivation and Imaging of S. latissima Embryo Monolayered Cell Sheets Inside Microfluidic Devices.
Clerc, Thomas; Boscq, Samuel; Attia, Rafaele; Kaminski Schierle, Gabriele S; Charrier, Bénédicte; Läubli, Nino F.
Afiliação
  • Clerc T; Morphogenesis of Macroalgae, Laboratory of Integrative Biology of Marine Models, Station Biologique de Roscoff, CNRS, Sorbonne University, 29680 Roscoff, France.
  • Boscq S; Morphogenesis of Macroalgae, Laboratory of Integrative Biology of Marine Models, Station Biologique de Roscoff, CNRS, Sorbonne University, 29680 Roscoff, France.
  • Attia R; Ecology of Marine Plankton, Laboratory of Adaptation and Diversity in the Marine Environment, Station Biologique de Roscoff, CNRS, Sorbonne University, 29680 Roscoff, France.
  • Kaminski Schierle GS; Molecular Neuroscience Group, Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, UK.
  • Charrier B; Morphogenesis of Macroalgae, Laboratory of Integrative Biology of Marine Models, Station Biologique de Roscoff, CNRS, Sorbonne University, 29680 Roscoff, France.
  • Läubli NF; Molecular Neuroscience Group, Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge CB3 0AS, UK.
Bioengineering (Basel) ; 9(11)2022 Nov 21.
Article em En | MEDLINE | ID: mdl-36421119
ABSTRACT
The culturing and investigation of individual marine specimens in lab environments is crucial to further our understanding of this highly complex ecosystem. However, the obtained results and their relevance are often limited by a lack of suitable experimental setups enabling controlled specimen growth in a natural environment while allowing for precise monitoring and in-depth observations. In this work, we explore the viability of a microfluidic device for the investigation of the growth of the alga Saccharina latissima to enable high-resolution imaging by confining the samples, which usually grow in 3D, to a single 2D plane. We evaluate the specimen's health based on various factors such as its growth rate, cell shape, and major developmental steps with regard to the device's operating parameters and flow conditions before demonstrating its compatibility with state-of-the-art microscopy imaging technologies such as the skeletonisation of the specimen through calcofluor white-based vital staining of its cell contours as well as the immunolocalisation of the specimen's cell wall. Furthermore, by making use of the on-chip characterisation capabilities, we investigate the influence of altered environmental illuminations on the embryonic development using blue and red light. Finally, live tracking of fluorescent microspheres deposited on the surface of the embryo permits the quantitative characterisation of growth at various locations of the organism.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Bioengineering (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Bioengineering (Basel) Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França