Microarray analysis of MC3T3-E1 osteoblastic cell response to machined titanium surface and resorbable blast material titanium surface

Bone ◽  
2011 ◽  
Vol 48 ◽  
pp. S111 ◽  
Author(s):  
H. Lee ◽  
S.-H. Ko
2009 ◽  
Vol 88A (4) ◽  
pp. 841-848 ◽  
Author(s):  
Rosemeire de Lordo Franco ◽  
Roberto Chiesa ◽  
Marcio Mateus Beloti ◽  
Paulo Tambasco de Oliveira ◽  
Adalberto Luiz Rosa

Bone ◽  
2010 ◽  
Vol 47 ◽  
pp. S125
Author(s):  
H. Lee ◽  
L.-R. Cho ◽  
C.-J. Park ◽  
H. Shin

2012 ◽  
Vol 42 (6) ◽  
pp. 248 ◽  
Author(s):  
Bo-Ah Lee ◽  
Choong-Hee Kang ◽  
Mong-Sook Vang ◽  
Young-Suk Jung ◽  
Xing Hui Piao ◽  
...  

2007 ◽  
Vol 361-363 ◽  
pp. 1095-1098
Author(s):  
S.H. Park ◽  
H.H. Kim ◽  
H.S. Lee ◽  
Y.S. Choi ◽  
A.R. Pae ◽  
...  

Because of its high biocompatibility, hydroxyapatite(HA) has been considered as a good blasting material. DNA microarray is a new molecular technology that enables the analysis of gene expression in parallel on a very large number of genes, spanning a significant fraction of the human genome. It is a qualitive analysis (e.g. it can differentiate each single gene) and quantitative, since it has the sensitivity to detect a change of expression level in the investigated cells when compared to normal samples. The aim of this study is to define the cell attachment and the genetic effect of machined surface implant and RBM (resorbable blast media) surface implant on the osteoblastic cell (MC3T3-E1 osteoblastic cell line) by cDNA microarray slide containing 21575 genes. Cells were cultured on machined grade 4 titanium disks(Group 1, machined surface) and disks of RBM (Group 2) and the samples were moved to new dishes and media were added and the plated disks were cultured for 24 hours. Total RNA extraction was performed with Qiagen mini kit (Qiagen, Chatsworth, CA, USA) for microarray assay. Microarray assay after culturing the cells on the machined surface and RBM surface revealed that osteoinductive molecules appeared more prominent on the RBM surface, whereas the adhesion molecules on the biomaterial were higher on the machined surface than RBM surface.


2004 ◽  
Vol 26 (5) ◽  
pp. 399-402 ◽  
Author(s):  
Yeonhee Kim ◽  
Jun-Hyeog Jang ◽  
Young Ku ◽  
Jae-Young Koak ◽  
Ik-Tae Chang ◽  
...  

2005 ◽  
Vol 2 (2) ◽  
pp. 97-108 ◽  
Author(s):  
Jung Yul Lim ◽  
Joshua C Hansen ◽  
Christopher A Siedlecki ◽  
James Runt ◽  
Henry J Donahue

Nanoscale cell–substratum interactions are of significant interest in various biomedical applications. We investigated human foetal osteoblastic cell response to randomly distributed nanoisland topography with varying heights (11, 38 and 85 nm) produced by a polystyrene (PS)/polybromostyrene polymer-demixing technique. Cells displayed island-conforming lamellipodia spreading, and filopodia projections appeared to play a role in sensing the nanotopography. Cells cultured on 11 nm high islands displayed significantly enhanced cell spreading and larger cell dimensions than cells on larger nanoislands or flat PS control, on which cells often displayed a stellate shape. Development of signal transmitting structures such as focal adhesive vinculin protein and cytoskeletal actin stress fibres was more pronounced, as was their colocalization, in cells cultured on smaller nanoisland surfaces. Cell adhesion and proliferation were greater with decreasing island height. Alkaline phosphatase (AP) activity, an early stage marker of bone cell differentiation, also exhibited nanotopography dependence, i.e. higher AP activity on 11 nm islands compared with that on larger islands or flat PS. Therefore, randomly distributed island topography with varying nanoscale heights not only affect adhesion-related cell behaviour but also bone cell phenotype. Our results suggest that modulation of nanoscale topography may be exploited to control cell function at cell–biomaterial interfaces.


2018 ◽  
Vol 33 (3) ◽  
pp. 597-602 ◽  
Author(s):  
Elizabeth Martinez ◽  
Guilherme Ishikawa ◽  
Alexandre de Lemos ◽  
Fábio Bezerra ◽  
Marcelo Sperandio ◽  
...  

2011 ◽  
Vol 49 (3) ◽  
pp. 245
Author(s):  
Min-Su Kim ◽  
Chang-Mo Jeong ◽  
Young-Chan Jeon ◽  
Jae-Jun Ryu ◽  
Jung-Bo Huh ◽  
...  

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