Full metadata record
DC FieldValueLanguage
dc.contributor.authorRashid, Rafi-
dc.contributor.authorLim, Natalie Sheng Jie-
dc.contributor.authorChee, Stella Min Ling-
dc.contributor.authorPng, Si Ning-
dc.contributor.authorWohland, Thorsten-
dc.contributor.authorRaghunath, Michael-
dc.date.accessioned2018-10-26T14:42:36Z-
dc.date.available2018-10-26T14:42:36Z-
dc.date.issued2014-
dc.identifier.issn1937-3392de_CH
dc.identifier.issn1937-3384de_CH
dc.identifier.urihttps://digitalcollection.zhaw.ch/handle/11475/12205-
dc.description.abstractMacromolecular crowding (MMC) is a biophysical effect that governs biochemical processes inside and outside of cells. Since standard cell culture media lack this effect, the physiological performance of differentiated and progenitor cells, including extracellular matrix (ECM) deposition, is impaired in vitro. To bring back physiological crowdedness to in vitro systems, we have previously introduced carbohydrate-based macromolecules to culture media and have achieved marked improvements with mixed MMC in terms of ECM deposition and differentiation of mesenchymal stem cells (MSCs). We show here that although this system is successful, it is limited, due to viscosity, to only 33% of the fractional volume occupancy (FVO) of full serum, which we calculated to have an FVO of approximately 54% v/v. We show here that full-serum FVO can be achieved using polyvinylpyrrolidone (PVP) 360 kDa. Under these conditions, ECM deposition in human fibroblasts and MSCs is on par, if not stronger than, with original MMC protocols using carbohydrates, but with a viscosity that is not significantly changed. In addition, we have found that the proliferation rate for bone marrow-derived MSCs and fibroblasts increases slightly in the presence of PVP360, similar to that observed with carbohydrate-based crowders. A palette of MMC compounds is now emerging that enables us to tune the crowdedness of culture media seamlessly from interstitial fluid (9% FVO), in which the majority of tissue cells might be based, to serum environments mimicking intravascular conditions. Despite identical FVO's, individual crowder size effects play a role and different cell types appear to have preferences in terms of FVO and the crowder that this is achieved with. However, in the quest of crowders that we have predicted to have a smoother regulatory approval path, PVP is a highly interesting compound, as it has been widely used in the medical and food industries and shows a novel promising use in cell culture and tissue engineering.de_CH
dc.language.isoende_CH
dc.publisherMary Ann Liebertde_CH
dc.relation.ispartofTissue Engineering - Part C: Methodsde_CH
dc.rightsLicence according to publishing contractde_CH
dc.subject.ddc571: Physiologie und verwandte Themende_CH
dc.subject.ddc572: Biochemiede_CH
dc.titleNovel use for polyvinylpyrrolidone as a macromolecular crowder for enhanced extracellular matrix deposition and cell proliferationde_CH
dc.typeBeitrag in wissenschaftlicher Zeitschriftde_CH
dcterms.typeTextde_CH
zhaw.departementLife Sciences und Facility Managementde_CH
zhaw.organisationalunitInstitut für Chemie und Biotechnologie (ICBT)de_CH
dc.identifier.doi10.1089/ten.tec.2013.0733de_CH
zhaw.funding.euNode_CH
zhaw.issue12de_CH
zhaw.originated.zhawNode_CH
zhaw.publication.statuspublishedVersionde_CH
zhaw.volume20de_CH
zhaw.publication.reviewPeer review (Publikation)de_CH
zhaw.webfeedMetabolic Tissue Engineeringde_CH
Appears in collections:Publikationen Life Sciences und Facility Management

Files in This Item:
There are no files associated with this item.
Show simple item record
Rashid, R., Lim, N. S. J., Chee, S. M. L., Png, S. N., Wohland, T., & Raghunath, M. (2014). Novel use for polyvinylpyrrolidone as a macromolecular crowder for enhanced extracellular matrix deposition and cell proliferation. Tissue Engineering - Part C: Methods, 20(12). https://doi.org/10.1089/ten.tec.2013.0733
Rashid, R. et al. (2014) ‘Novel use for polyvinylpyrrolidone as a macromolecular crowder for enhanced extracellular matrix deposition and cell proliferation’, Tissue Engineering - Part C: Methods, 20(12). Available at: https://doi.org/10.1089/ten.tec.2013.0733.
R. Rashid, N. S. J. Lim, S. M. L. Chee, S. N. Png, T. Wohland, and M. Raghunath, “Novel use for polyvinylpyrrolidone as a macromolecular crowder for enhanced extracellular matrix deposition and cell proliferation,” Tissue Engineering - Part C: Methods, vol. 20, no. 12, 2014, doi: 10.1089/ten.tec.2013.0733.
RASHID, Rafi, Natalie Sheng Jie LIM, Stella Min Ling CHEE, Si Ning PNG, Thorsten WOHLAND und Michael RAGHUNATH, 2014. Novel use for polyvinylpyrrolidone as a macromolecular crowder for enhanced extracellular matrix deposition and cell proliferation. Tissue Engineering - Part C: Methods. 2014. Bd. 20, Nr. 12. DOI 10.1089/ten.tec.2013.0733
Rashid, Rafi, Natalie Sheng Jie Lim, Stella Min Ling Chee, Si Ning Png, Thorsten Wohland, and Michael Raghunath. 2014. “Novel Use for Polyvinylpyrrolidone as a Macromolecular Crowder for Enhanced Extracellular Matrix Deposition and Cell Proliferation.” Tissue Engineering - Part C: Methods 20 (12). https://doi.org/10.1089/ten.tec.2013.0733.
Rashid, Rafi, et al. “Novel Use for Polyvinylpyrrolidone as a Macromolecular Crowder for Enhanced Extracellular Matrix Deposition and Cell Proliferation.” Tissue Engineering - Part C: Methods, vol. 20, no. 12, 2014, https://doi.org/10.1089/ten.tec.2013.0733.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.