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Cellular transcriptional response to zirconia-based implant materials

Altmann, Brigitte (author)
University Medical Center Freiburg, Germany
Rabel, Kerstin (author)
University Medical Center Freiburg, Germany
Kohal, Ralf J. (author)
University Medical Center Freiburg, Germany
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Proksch, Susanne (author)
University Medical Center Freiburg, Germany
Tomakidi, Pascal (author)
University Medical Center Freiburg, Germany
Adolfsson, Erik (author)
RISE,IVF
Bernsmann, Falk (author)
NTTF Coatings GmbH, Germany
Palmero, Paola (author)
Politecnico di Torino, Italy
Fürderer, Tobias (author)
MOESCHTER GROUP Holding GmbH, Germany
Steinberg, Thorsten (author)
University Medical Center Freiburg, Germany
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 (creator_code:org_t)
Elsevier BV, 2017
2017
English.
In: Dental Materials. - : Elsevier BV. - 0109-5641 .- 1879-0097. ; 33:2, s. 241-255
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective To adequately address clinically important issues such as osseointegration and soft tissue integration, we screened for the direct biological cell response by culturing human osteoblasts and gingival fibroblasts on novel zirconia-based dental implant biomaterials and subjecting them to transcriptional analysis. Methods Biomaterials used for osteoblasts involved micro-roughened surfaces made of a new type of ceria-stabilized zirconia composite with two different topographies, zirconium dioxide, and yttria-stabilized zirconia (control). For fibroblasts smooth ceria- and yttria-stabilized zirconia surface were used. The expression of 90 issue-relevant genes was determined on mRNA transcription level by real-time PCR Array technology after growth periods of 1 and 7 days. Results Generally, modulation of gene transcription exhibited a dual dependence, first by time and second by the biomaterial, whereas biomaterial-triggered changes were predominantly caused by the biomaterials’ chemistry rather than surface topography. Per se, modulated genes assigned to regenerative tissue processes such as fracture healing and wound healing and in detail included colony stimulating factors (CSF2 and CSF3), growth factors, which regulate bone matrix properties (e.g. BMP3 and TGFB1), osteogenic BMPs (BMP2/4/6/7) and transcription factors (RUNX2 and SP7), matrix collagens and osteocalcin, laminins as well as integrin ß1 and MMP-2. Significance With respect to the biomaterials under study, the screening showed that a new zirconia-based composite stabilized with ceria may be promising to provide clinically desired periodontal tissue integration. Moreover, by detecting biomarkers modulated in a time- and/or biomaterial-dependent manner, we identified candidate genes for the targeted analysis of cell-implant bioresponse during biomaterial research and development.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Materialteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Medicinteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Medical Engineering (hsv//eng)

Keyword

Alveolar bone osteoblasts
Gingiva fibroblasts
Gene profiling
Zirconia composite
Dental implants

Publication and Content Type

ref (subject category)
art (subject category)

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