Literature DB >> 19609875

Tissue engineering of composite grafts: Cocultivation of human oral keratinocytes and human osteoblast-like cells on laminin-coated polycarbonate membranes and equine collagen membranes under different culture conditions.

R Glaum1, M Wiedmann-Al-Ahmad, U Huebner, R Schmelzeisen.   

Abstract

In complex craniomaxillofacial defects, the simultaneous reconstruction of hard and soft tissue is often necessary. Until now, oral keratinocytes and osteoblast-like cells have not been cocultivated on the same carrier. For the first time, the cocultivation of human oral keratinocytes and human osteoblast-like cells has been investigated in this study. Different carriers (laminin-coated polycarbonate and equine collagen membranes) and various culture conditions were examined. Human oral keratinocytes and human osteoblast-like cells from five patients were isolated from tissue samples, seeded on the opposite sides of the carriers and cultivated for 1 and 2 weeks under static conditions in an incubator and in a perfusion chamber. Proliferation and morphology of the cells were analyzed by EZ4U-tests, light microscopy, and scanning electron microscopy. Cocultivation of both cell-types seeded on one carrier was possible. Quantitative and qualitative growth was significantly better on collagen membranes when compared with laminin-coated polycarbonate membranes independent of the culture conditions. Using perfusion culture in comparison to static culture, the increase of cell proliferation after 2 weeks of cultivation when compared with the proliferation after 1 week was significantly lower, independent of the carriers used. In conclusion, the contemporaneous cultivation of human oral keratinocytes and human osteoblast-like cells on the same carrier is possible, a prerequisite for planned in vivo studies. As carrier collagen is superior to laminin-coated polycarbonate membranes. Regarding the development over time, the increase of proliferation rate is lower in perfusion culture. Examinations of cellular differentiation over time under various culture conditions will be subject of further investigations. Copyright 2009 Wiley Periodicals, Inc.

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Year:  2010        PMID: 19609875     DOI: 10.1002/jbm.a.32575

Source DB:  PubMed          Journal:  J Biomed Mater Res A        ISSN: 1549-3296            Impact factor:   4.396


  4 in total

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Authors:  Constanze Nossol; A-K Diesing; N Walk; H Faber-Zuschratter; R Hartig; A Post; J Kluess; H-J Rothkötter; S Kahlert
Journal:  Histochem Cell Biol       Date:  2011-06-17       Impact factor: 4.304

2.  Bridging the gap between traditional cell cultures and bioreactors applied in regenerative medicine: practical experiences with the MINUSHEET perfusion culture system.

Authors:  Will W Minuth; Lucia Denk
Journal:  Cytotechnology       Date:  2015-04-17       Impact factor: 2.058

3.  Projection method as a probe for multiplexing/demultiplexing of magnetically enriched biological tissues.

Authors:  Mohammad Reza Zamani Kouhpanji; Bethanie J H Stadler
Journal:  RSC Adv       Date:  2020-04-01       Impact factor: 4.036

4.  Supportive development of functional tissues for biomedical research using the MINUSHEET® perfusion system.

Authors:  Will W Minuth; Lucia Denk
Journal:  Clin Transl Med       Date:  2012-10-05
  4 in total

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