Skeletal stem cell and bone implant interactions are enhanced by LASER titanium modification

被引:21
作者
Sisti, Karin E. [1 ,2 ,3 ]
de Andres, Maria C. [1 ]
Johnston, David [1 ]
Almeida-Filho, Edson [2 ]
Guastaldi, Antonio C. [2 ]
Oreffo, Richard O. C. [1 ]
机构
[1] Univ Southampton, Inst Dev Sci, Ctr Human Dev Stem Cells & Regenerat, Bone & Joint Res Grp, Southampton SO16 6YD, Hants, England
[2] Sao Paulo State Univ UNESP, Inst Chem, Biomat Grp, Box 355, Araraquara, Brazil
[3] Fed Univ Mato Grosso Sul UFMS, Campo Grande, Brazil
基金
英国生物技术与生命科学研究理事会;
关键词
Titanium surface; Skeletal stem cell; Tissue regeneration; Bone formation; LASER; SURFACE MODIFICATION; IN-VIVO; OSTEOBLAST; OSTEOCALCIN; ADHESION; OSSEOINTEGRATION; DIFFERENTIATION; OSTEOPONTIN; MECHANISMS; EXPRESSION;
D O I
10.1016/j.bbrc.2015.10.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: To evaluate the osteo-regenerative potential of Titanium (Ti) modified by Light Amplification by Stimulated Emission of Radiation (LASER) beam (Yb-YAG) upon culture with human Skeletal Stem Cells (hSSCs(1)). Methods: Human skeletal cell populations were isolated from the bone marrow of haematologically normal patients undergoing primary total hip replacement following appropriate consent. STRO-1(+) hSSC(1) function was examined for 10 days across four groups using Ti discs: i) machined Ti surface group in basal media (Mb(2)), ii) machined Ti surface group in osteogenic media (Mo-3), iii) LASER-modified Ti group in basal media (Lb(4)) and, iv) LASER-modified Ti group in osteogenic media (Lo(5)). Molecular analysis and qRT-PCR as well as functional analysis including biochemistry (DNA, Alkaline Phosphatase (ALP(6)) specific activity), live/dead immunostaining (Cell Tracker Green (CTG(7))/Ethidium Homodimer-1 (EH-1(8))), and fluorescence staining (for vinculin and phalloidin) were undertaken. Inverted, confocal and Scanning Electron Microscopy (SEM) approaches were used to characterise cell adherence, proliferation, and phenotype. Results: Enhanced cell spreading and morphological rearrangement, including focal adhesions were observed following culture of hSSCs(1) on LASER surfaces in both basal and osteogenic conditions. Biochemical analysis demonstrated enhanced ALP6 specific activity on the hSSCs(1)-seeded on LASER-modified surface in basal culture media. Molecular analysis demonstrated enhanced ALP(6) and osteopontin expression on titanium LASER treated surfaces in basal conditions. SEM, inverted microscopy and confocal laser scanning microscopy confirmed extensive proliferation and migration of human bone marrow stromal cells on all surfaces evaluated. Conclusions: LASER-modified Ti surfaces modify the behaviour of hSSCs.(1) In particular, SSC1 adhesion, osteogenic gene expression, cell morphology and cytoskeleton structure were affected. The current studies show Ti LASER modification can enhance the osseointegration between Ti and skeletal cells, with important implications for orthopaedic application. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:719 / 725
页数:7
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