DSpace

DSpace at RU >    University Library >    Academic bibliography >

SFX Query

Files in This Item:

File Description SizeFormat
publisher's version819.11 kBAdobe PDFUnder Embargo

Title: FGF-2-loaded collagen scaffolds attract cells and blood vessels in rat oral mucosa.
Author(s): Jansen, R.G. (314433651)
Kuppevelt, A.H.M.S.M. van (07255150X)
Daamen, W.F. (29137378X)
Kuijpers-Jagtman, A.M. (068355343)
Hoff, J.W. von den (112259634)
Publication year: 2009
Document type: Article / Letter to editor
Journal: Journal of Oral Pathology & Medicine
ISSN: 0904-2512
Volume: vol. 38
Issue: iss. 8
Start page: p. 630
End page: p. 638
Abstract: BACKGROUND: Wound contraction and scar formation after cleft palate repair impair the growth of the maxilla. The implantation of a growth factor-loaded scaffold might solve these problems. METHODS: The tissue response to fibroblast growth factor (FGF)-2 loaded collagen scaffolds was evaluated after implantation in the palate of rats. Scaffolds, with and without FGF-2, were implanted submucoperiosteally in the palate of 25 rats and evaluated after up to 16 weeks. On hematoxylin and eosin (H&E)-stained sections, the cell density and the number of giant cells within the scaffolds were quantified. Infiltration of inflammatory cells, myofibroblasts, and the number of blood vessels were quantified after immunohistochemistry. RESULTS: The cell density was significantly higher in the FGF-2 group up to 4 weeks after implantation (102% at 2 weeks, P < 0.001). The number of blood vessels was also significantly higher in the FGF-2 group at 1 and 2 weeks (316% at 1 week, P = 0.003), but the myofibroblast score was lower (100% at 2 weeks, P = 0.008). A comparable mild and rapidly subsiding inflammatory response and foreign body reaction were found in both groups. CONCLUSION: FGF-2-loaded scaffolds displayed a faster influx of host cells, an increased rate of vascularization, and a reduced differentiation of myofibroblasts. These scaffolds might therefore be highly suitable for intra-oral reconstructions, such as cleft palate repair.
Subject: NCMLS 1C: Tissue engineering and pathology
Organization: Biochemistry (UMCN)
Dentistry
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/80714

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

 

  DSpace Software Copyright © 2002-2011  Duraspace - Feedback