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dc.contributor.authorLam, M
dc.contributor.authorCalvo, F
dc.date.accessioned2018-12-17T11:21:26Z
dc.date.issued2019-01
dc.identifier.citationCytoskeleton (Hoboken, N.J.), 2019, 76 (1), pp. 115 - 122
dc.identifier.issn1949-3584
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2972
dc.identifier.eissn1949-3592
dc.identifier.doi10.1002/cm.21485
dc.description.abstractCells exist in dynamic three-dimensional environments where they experience variable mechanical forces due to their interaction with the extracellular matrix, neighbouring cells and physical stresses. The ability to constantly and rapidly alter cellular behaviour in response to the mechanical environment is therefore crucial for cell viability, tissue development and homeostasis. Mechanotransduction is the process whereby cells translate mechanical inputs into biochemical signals. These signals in turn adjust cell morphology and cellular functions as diverse as proliferation, differentiation, migration and apoptosis. Here, we provide an overview of the current understanding of mechanotransduction and how septins may participate in it, drawing on their architecture and localization, their ability to directly bind and modify actomyosin networks and membranes, and their associations with the nuclear envelope.
dc.formatPrint-Electronic
dc.format.extent115 - 122
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectExtracellular Matrix
dc.subjectCytoskeleton
dc.subjectAnimals
dc.subjectHumans
dc.subjectMechanotransduction, Cellular
dc.subjectApoptosis
dc.subjectCell Proliferation
dc.subjectCell Movement
dc.subjectSeptins
dc.titleRegulation of mechanotransduction: Emerging roles for septins.
dc.typeJournal Article
dcterms.dateAccepted2018-08-02
rioxxterms.versionofrecord10.1002/cm.21485
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCytoskeleton (Hoboken, N.J.)
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Tumour Microenvironment
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Tumour Microenvironment
pubs.publication-statusPublished
pubs.volume76
pubs.embargo.termsNot known
icr.researchteamTumour Microenvironmenten_US
dc.contributor.icrauthorCalvo, Fernandoen


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