Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/6862
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dc.contributor.authorChen, D-
dc.contributor.authorNorris, D-
dc.contributor.authorVentikos, Y-
dc.contributor.author2nd Micro and Nano Flows Conference (MNF2009)-
dc.date.accessioned2012-10-05T13:50:00Z-
dc.date.available2012-10-05T13:50:00Z-
dc.date.issued2009-
dc.identifier.citation2nd Micro and Nano Flows Conference, Brunel University, West London, UK, 01-02 September 2009en_US
dc.identifier.isbn978-1-902316-72-7-
dc.identifier.issn978-1-902316-73-4-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/6862-
dc.descriptionThis paper was presented at the 2nd Micro and Nano Flows Conference (MNF2009), which was held at Brunel University, West London, UK. The conference was organised by Brunel University and supported by the Institution of Mechanical Engineers, IPEM, the Italian Union of Thermofluid dynamics, the Process Intensification Network, HEXAG - the Heat Exchange Action Group and the Institute of Mathematics and its Applications.en_US
dc.description.abstractThe breaking of left-right symmetry in the mammalian embryo is believed to occur in a transient embryonic structure, the node, when cilia create a leftward flow of liquid. It has been widely confirmed that this nodal flow is the first sign of left-right differentiation; however, the mechanism through which embryonic cilia produce their movement and how the leftward flow confers laterality are still requiring investigation. The ciliary motility in the embryonic node involves complex dynein activations and the handed information is transmitted to the cells by the flow produced by cilia, either mechanically and/or by advection of a chemical species. In this paper, we present a computational model of ciliary ultrastructure (protein-structure model) and discuss the scenarios that incorporate this internal microtubule-dynein system with the external fluidic environment (fluid-structure-protein interaction model, FSPI). By employing computational fluid dynamics, deformable mesh computational techniques and fluid-structure interaction analysis, and solving the three-dimensional unsteady transport equations, the protein-triggered mechanism of nodal ciliary motility has been studied, which is a primary component for the FSPI model. Future work regarding the integrative model is discussed, that will provide more accurate quantitative information on the flow rate, ciliary motion, and molecule/ particle transport in the embryonic node and support the plausibility of hypotheses regarding left-right information transmission.en_US
dc.language.isoenen_US
dc.publisherBrunel Universityen_US
dc.subjectEmbryonic nodeen_US
dc.subjectCiliaen_US
dc.subjectComputational fluid dynamicsen_US
dc.subjectFluid-structure-protein interactionen_US
dc.titleCilia-mediated signalling in the embryonic nodes: A computational fluid-structure-protein interaction (FSPI) modelen_US
dc.typeConference Paperen_US
Appears in Collections:Brunel Institute for Bioengineering (BIB)
The Brunel Collection

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