Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.addr.2011.03.003
DC FieldValue
dc.titleApplying macromolecular crowding to enhance extracellular matrix deposition and its remodeling in vitro for tissue engineering and cell-based therapies
dc.contributor.authorChen, C.
dc.contributor.authorLoe, F.
dc.contributor.authorBlocki, A.
dc.contributor.authorPeng, Y.
dc.contributor.authorRaghunath, M.
dc.date.accessioned2014-06-18T06:10:06Z
dc.date.available2014-06-18T06:10:06Z
dc.date.issued2011-04-30
dc.identifier.citationChen, C., Loe, F., Blocki, A., Peng, Y., Raghunath, M. (2011-04-30). Applying macromolecular crowding to enhance extracellular matrix deposition and its remodeling in vitro for tissue engineering and cell-based therapies. Advanced Drug Delivery Reviews 63 (4) : 277-290. ScholarBank@NUS Repository. https://doi.org/10.1016/j.addr.2011.03.003
dc.identifier.issn0169409X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/68134
dc.description.abstractWith the advent of multicellular organisms, the exterior of the cells evolved dramatically from highly aqueous surroundings into an extracellular matrix and space crowded with macromolecules. Cell-based therapies require removal of cells from their crowded physiological context and propagating them in dilute culture medium to attain therapeutically relevant numbers whilst preserving their phenotype. However, bereft of their microenvironment, cells under perform and lose functionality. Major efforts currently aim to modify cell culture surfaces and build three dimensional scaffolds to improve this situation. We discuss here alternative strategies that enable cells to re-create their own microenvironment in vitro, using carbohydrate-based macromolecules as culture media additives that create an excluded volume effect at defined fraction volume occupancies. This biophysical approach dramatically enhances extracellular matrix deposition by differentiated cells and stem cells, and boosts progenitor cell differentiation and proliferation. We begin to understand how well cells really can perform ex vivo if given the chance. © 2011 Elsevier B.V.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.addr.2011.03.003
dc.sourceScopus
dc.subjectCollagen assembly
dc.subjectDifferentiated cells
dc.subjectExcluded volume effect
dc.subjectMatrix maturation
dc.subjectMicroenvironment
dc.subjectStem cells
dc.typeReview
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1016/j.addr.2011.03.003
dc.description.sourcetitleAdvanced Drug Delivery Reviews
dc.description.volume63
dc.description.issue4
dc.description.page277-290
dc.description.codenADDRE
dc.identifier.isiut000292433000008
Appears in Collections:Staff Publications

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