Show simple item record

dc.contributor.authorZhao, Bing
dc.contributor.authorZhang, Changjiang
dc.contributor.authorForsten-Williams, Kimberly
dc.contributor.authorZhang, Jun
dc.contributor.authorFannon, Michael
dc.date.accessioned2018-11-19T18:38:15Z
dc.date.available2018-11-19T18:38:15Z
dc.date.issued2010-10
dc.identifier.issn1553-734X
dc.identifier.othere1000971
dc.identifier.urihttp://hdl.handle.net/10919/85911
dc.description.abstractCirculation is an important delivery method for both natural and synthetic molecules, but microenvironment interactions, regulated by endothelial cells and critical to the molecule's fate, are difficult to interpret using traditional approaches. In this work, we analyzed and predicted growth factor capture under flow using computer modeling and a three-dimensional experimental approach that includes pertinent circulation characteristics such as pulsatile flow, competing binding interactions, and limited bioavailability. An understanding of the controlling features of this process was desired. The experimental module consisted of a bioreactor with synthetic endothelial-lined hollow fibers under flow. The physical design of the system was incorporated into the model parameters. The heparin-binding growth factor fibroblast growth factor-2 (FGF-2) was used for both the experiments and simulations. Our computational model was composed of three parts: (1) media flow equations, (2) mass transport equations and (3) cell surface reaction equations. The model is based on the flow and reactions within a single hollow fiber and was scaled linearly by the total number of fibers for comparison with experimental results. Our model predicted, and experiments confirmed, that removal of heparan sulfate (HS) from the system would result in a dramatic loss of binding by heparin-binding proteins, but not by proteins that do not bind heparin. The model further predicted a significant loss of bound protein at flow rates only slightly higher than average capillary flow rates, corroborated experimentally, suggesting that the probability of capture in a single pass at high flow rates is extremely low. Several other key parameters were investigated with the coupling between receptors and proteoglycans shown to have a critical impact on successful capture. The combined system offers opportunities to examine circulation capture in a straightforward quantitative manner that should prove advantageous for biologicals or drug delivery investigations.en_US
dc.description.sponsorshipThis study was supported by NIH under grant HL086644, and by a Research to Prevent Blindness Challenge Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
dc.format.mimetypeapplication/pdfen_US
dc.language.isoen_US
dc.publisherPLOS
dc.rightsCreative Commons Attribution 4.0 Internationalen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_US
dc.subjectsmooth-muscle-cells
dc.subjectbarrier in-vitro
dc.subjectfibroblast-growth
dc.subjectsulfate proteoglycans
dc.subjectsignal-transduction
dc.subjectangiogenic factors
dc.subjectbfgf binding
dc.subjectmodel
dc.subjectreceptors
dc.subjectfgf
dc.titleEndothelial Cell Capture of Heparin-Binding Growth Factors under Flowen_US
dc.typeArticle - Refereed
dc.title.serialPLOS Computational Biology
dc.identifier.doihttps://doi.org/10.1371/journal.pcbi.1000971
dc.identifier.volume6
dc.identifier.issue10
dc.type.dcmitypeTexten_US
dc.identifier.pmid21060855
dc.identifier.eissn1553-7358


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Creative Commons Attribution 4.0 International
License: Creative Commons Attribution 4.0 International