1 556

Cited 344 times in

Nano-fibrous scaffolding promotes osteoblast differentiation and biomineralization

DC Field Value Language
dc.contributor.author전지혜-
dc.date.accessioned2014-12-21T16:26:50Z-
dc.date.available2014-12-21T16:26:50Z-
dc.date.issued2007-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/95709-
dc.description.abstractNano-fibrous poly(l-lactic acid) (PLLA) scaffolds with interconnected pores were developed under the hypothesis that nano-fibrous scaffolding would mimic a morphological function of collagen fibrils to create a more favorable microenvironment for cells versus solid-walled scaffolds. In this study, an in vitro system was used to examine biological properties of the nano-fibrous scaffolds compared with those of solid-walled scaffolds for their potential use in bone tissue engineering. Biomineralization was enhanced substantially on the nano-fibous scaffolds compared to solid-walled scaffolds, and this was confirmed by von Kossa staining, measurement of calcium contents, and transmission electron microscopy. In support of this finding, osteoblasts cultured on the nano-fibrous scaffolds exhibited higher alkaline phosphatase activity and an earlier and enhanced expression of the osteoblast phenotype versus solid-walled scaffolds. Most notable were the increases in runx2 protein and in bone sialoprotein mRNA in cells cultured on nano-fibrous scaffolds versus solid-walled scaffolds. At the day 1 of culture, α2 and β1 integrins as well as αv and β3 integrins were highly expressed on the surface of cells seeded on nano-fibrous scaffolds, and linked to this were higher levels of phospho-Paxillin and phospho-FAK in cell lysates. In contrast, cells seeded on solid-walled scaffolds expressed significantly lower levels of these integrins, phospho-Paxillin, and phospho-FAK. To further examine the role of nano-fibrous architecture, we inhibited the formation of collagen fibrils by adding 3,4-dehydroproline to cultures and then assayed cells for expression of α2 integrin. Cells seeded on nano-fibrous scaffolds sustained expression of α2 integrin in the presence of dehydroproline, while suppression of α2 integrin was evident in cells seeded on solid-walled scaffolds. These results provide initial evidence that synthetic nano fibers may exhibit certain properties that are comparable to natural collagen fibers, and thus, the nano-fibrous architecture may serve as a superior scaffolding versus solid-walled architecture for promoting osteoblast differentiation and biomineralization.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfBIOMATERIALS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleNano-fibrous scaffolding promotes osteoblast differentiation and biomineralization-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Life Science (의생명과학부)-
dc.contributor.googleauthorKyung Mi Woo-
dc.contributor.googleauthorJi-Hae Jun-
dc.contributor.googleauthorPeter X. Ma-
dc.contributor.googleauthorMartha J. Somerman-
dc.contributor.googleauthorGwan-Shik Kim-
dc.contributor.googleauthorHyun-Mo Ryoo-
dc.contributor.googleauthorJeong-Hwa Baek-
dc.contributor.googleauthorJihye Seo-
dc.contributor.googleauthorVictor J. Chen-
dc.identifier.doi10.1016/j.biomaterials.2006.06.013-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03551-
dc.relation.journalcodeJ00312-
dc.identifier.eissn1878-5905-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0142961206005680-
dc.contributor.alternativeNameJun, Ji Hae-
dc.contributor.affiliatedAuthorJun, Ji Hae-
dc.rights.accessRightsnot free-
dc.citation.volume28-
dc.citation.number2-
dc.citation.startPage335-
dc.citation.endPage343-
dc.identifier.bibliographicCitationBIOMATERIALS, Vol.28(2) : 335-343, 2007-
dc.identifier.rimsid45038-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers

qrcode

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