Early cell response of osteogenic cells on differently modified implant surfaces: Sequences of cell proliferation, adherence and differentiation. Issue 3 (March 2018)
- Record Type:
- Journal Article
- Title:
- Early cell response of osteogenic cells on differently modified implant surfaces: Sequences of cell proliferation, adherence and differentiation. Issue 3 (March 2018)
- Main Title:
- Early cell response of osteogenic cells on differently modified implant surfaces: Sequences of cell proliferation, adherence and differentiation
- Authors:
- Blatt, Sebastian
Pabst, Andreas Max
Schiegnitz, Eik
Hosang, Marco
Ziebart, Thomas
Walter, Christian
Al-Nawas, Bilal
Klein, Marcus Oliver - Abstract:
- Abstract: Objectives: Osseointegration of dental implants is a crucial prerequisite for long-term survival. Therefore, surface modifications are needed to interact with the extracellular environment and to trigger osteogenic cell responses such as cell proliferation, adherence, and differentiation. The purpose of this study was to investigate different surface modifications in vitro over 2 weeks. Materials and methods: Commercially available cells from a human osteogenic cell line (HHOB-c) were cultivated on the following surfaces: titanium with smooth surfaces (polished titanium (P), machined titanium (M), polyetheretherketone (Peek)), titanium with rough and hydrophilised surfaces (acid etched titanium (A), sandblasted acid etched titanium (SA and SA2), sandblasted acid etched hydrophilised (SAH), titanium plasma painted titanium (TPS)), titanium with calcium phosphate-containing surfaces (titanium plasma painted calcium phosphate modified titanium (TPS-CaP), sandblasted calcium phosphate modified titanium (S-CaP), sandblasted acid etched calcium phosphate modified titanium (SA-CaP)), and zirconium-oxide (yttrium amplified zirconium (Z), yttrium amplified Ca 2+ delivering zirconium (Z-Ca)). Tissue culture polystyrene (TCPS) served as a control. Cell count was assessed after 24 h, 48 h, 72 h, 7 d, and 14 d; osteogenic cell adherence and differentiation were analysed by using cellular Quantitative Immuno-Cytochemistry (QIC) assay for alkaline phosphatase (AP), osteocalcinAbstract: Objectives: Osseointegration of dental implants is a crucial prerequisite for long-term survival. Therefore, surface modifications are needed to interact with the extracellular environment and to trigger osteogenic cell responses such as cell proliferation, adherence, and differentiation. The purpose of this study was to investigate different surface modifications in vitro over 2 weeks. Materials and methods: Commercially available cells from a human osteogenic cell line (HHOB-c) were cultivated on the following surfaces: titanium with smooth surfaces (polished titanium (P), machined titanium (M), polyetheretherketone (Peek)), titanium with rough and hydrophilised surfaces (acid etched titanium (A), sandblasted acid etched titanium (SA and SA2), sandblasted acid etched hydrophilised (SAH), titanium plasma painted titanium (TPS)), titanium with calcium phosphate-containing surfaces (titanium plasma painted calcium phosphate modified titanium (TPS-CaP), sandblasted calcium phosphate modified titanium (S-CaP), sandblasted acid etched calcium phosphate modified titanium (SA-CaP)), and zirconium-oxide (yttrium amplified zirconium (Z), yttrium amplified Ca 2+ delivering zirconium (Z-Ca)). Tissue culture polystyrene (TCPS) served as a control. Cell count was assessed after 24 h, 48 h, 72 h, 7 d, and 14 d; osteogenic cell adherence and differentiation were analysed by using cellular Quantitative Immuno-Cytochemistry (QIC) assay for alkaline phosphatase (AP), osteocalcin (OC), integrin alpha V (ITGAV), and talin (T). Results: All tested surfaces showed a positive influence on the differentiation and adherence of osteogenic cells, especially P, M, A, TCPS, and Peek. After 48 h, the surfaces M, SA and SAH had induced a positive influence on adherence, whereas SA2, SA, and SAH triggered proliferation after 14 d. Conclusions: Rough and hydrophilised surface modifications, such as SAH, trigger osteogenic cell responses. These in vitro results highlight the potential use of SAH surface modifications of dental implants and indicate further clinical studies are warranted. … (more)
- Is Part Of:
- Journal of cranio-maxillofacial surgery. Volume 46:Issue 3(2018)
- Journal:
- Journal of cranio-maxillofacial surgery
- Issue:
- Volume 46:Issue 3(2018)
- Issue Display:
- Volume 46, Issue 3 (2018)
- Year:
- 2018
- Volume:
- 46
- Issue:
- 3
- Issue Sort Value:
- 2018-0046-0003-0000
- Page Start:
- 453
- Page End:
- 460
- Publication Date:
- 2018-03
- Subjects:
- Dental implant -- Surface modification -- Osseointegration -- Primary stability
Skull -- Surgery -- Periodicals
Maxilla -- Surgery -- Periodicals
Face -- Surgery -- Periodicals
Surgery, Plastic -- Periodicals
Maxilla -- surgery -- Periodicals
Face -- surgery -- Periodicals
Skull -- surgery -- Periodicals
Oral Surgical Procedures -- Periodicals
Reconstructive Surgical Procedures -- Periodicals
Surgery, Plastic -- Periodicals
Surgery, Oral -- Periodicals
Electronic journals
617.514 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10105182 ↗
http://firstsearch.oclc.org ↗
http://www.clinicalkey.com/dura/browse/journalIssue/10105182 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jcms.2017.12.021 ↗
- Languages:
- English
- ISSNs:
- 1010-5182
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4965.482000
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