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dc.citation.endPage 201 -
dc.citation.number 1 -
dc.citation.startPage 171 -
dc.citation.title PHYSICA A-STATISTICAL MECHANICS AND ITS APPLICATIONS -
dc.citation.volume 352 -
dc.contributor.author Safran, SA -
dc.contributor.author Gov, N -
dc.contributor.author Nicolas, A -
dc.contributor.author Schwarz, US -
dc.contributor.author Tlusty, T -
dc.date.accessioned 2023-12-22T10:15:46Z -
dc.date.available 2023-12-22T10:15:46Z -
dc.date.created 2020-02-20 -
dc.date.issued 2005-07 -
dc.description.abstract We review recent theoretical work that analyzes experimental measurements of the shape, fluctuations and adhesion properties of biological cells. Particular emphasis is placed on the role of the cytoskeleton and cell elasticity and we contrast the shape and adhesion of elastic cells with fluid-filled vesicles. In red blood cells (RBC), the cytoskeleton consists of a two-dimensional network of spectrin proteins. Our analysis of the wavevector and frequency dependence of the fluctuation spectrum of RBC indicates that the spectrin network acts as a confining potential that reduces the fluctuations of the lipid bilayer membrane. However, since the cytoskeleton is only sparsely connected to the bilayer, one cannot regard the composite cytoskeleton-membrane as a polymerized object with a shear modulus. The sensitivity of RBC fluctuations and shapes to ATP concentration may reflect topological defects induced in the cytoskeleton network by ATP. The shapes of cells that adhere to a substrate are strongly determined by the cytoskeletal elasticity that can be varied experimentally by drugs that depolymerize the cytoskeleton. This leads to a tension-driven retraction of the cell body and a pearling instability of the resulting ray-like protrusions. Recent experiments have shown that adhering cells exert polarized forces on substrates. The interactions of such "force dipoles" in either bulk gels or on surfaces can be used to predict the nature of self-assembly of cell aggregates and may be important in the formation of artificial tissues. Finally, we note that cell adhesion strongly depends on the forces exerted on the adhesion sites by the tension of the cytoskeleton. The size and shape of the adhesion regions are strongly modified as the tension is varied and we present an elastic model that relates this tension to deformations that induce the recruitment of new molecules to the adhesion region. In all these examples, cell shape and adhesion differ from vesicle shape and adhesion due to the presence of the elastic cytoskeleton and to the fact that active processes (ATP, molecular motors) within the cell modify cytoskeletal elasticity and tension. (c) 2005 Elsevier B.V. All rights reserved. -
dc.identifier.bibliographicCitation PHYSICA A-STATISTICAL MECHANICS AND ITS APPLICATIONS, v.352, no.1, pp.171 - 201 -
dc.identifier.doi 10.1016/j.physa.2004.12.035 -
dc.identifier.issn 0378-4371 -
dc.identifier.scopusid 2-s2.0-17844363952 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/31210 -
dc.identifier.url https://www.sciencedirect.com/science/article/pii/S0378437104016206?via%3Dihub -
dc.identifier.wosid 000229193300008 -
dc.language 영어 -
dc.publisher ELSEVIER SCIENCE BV -
dc.title Physics of cell elasticity, shape and adhesion -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Physics, Multidisciplinary -
dc.relation.journalResearchArea Physics -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor elasticity -
dc.subject.keywordAuthor membrane -
dc.subject.keywordAuthor adhesion -
dc.subject.keywordPlus SMOOTH-MUSCLE-CELLS -
dc.subject.keywordPlus ERYTHROCYTE-MEMBRANE -
dc.subject.keywordPlus FOCAL ADHESIONS -
dc.subject.keywordPlus CONTACT GUIDANCE -
dc.subject.keywordPlus MATRIX ADHESIONS -
dc.subject.keywordPlus LATRUNCULIN-A -
dc.subject.keywordPlus ACTIN -
dc.subject.keywordPlus TRACTION -
dc.subject.keywordPlus FORCES -
dc.subject.keywordPlus SUBSTRATE -

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