A Specific Groove Pattern Can Effectively Induce Osteoblast Differentiation

Authors
Kim, Chang-SuKim, Jin-HeeKim, BokyoungPark, Young-SeokKim, Hong-KyunHieu Trung TranKim, Sang HoonJeon, HojeongKim, SangjibSim, Ji HyunShin, Hyun MuKim, GwanghunBaik, Young JooLee, Kee-JoonKim, Hae-YoungYun, Tae JinKim, Youn SangKim, Hang-Rae
Issue Date
2017-11-24
Publisher
WILEY-V C H VERLAG GMBH
Citation
ADVANCED FUNCTIONAL MATERIALS, v.27, no.44
Abstract
Little is known about the principles of surface structure design for orthopedic and dental implants. To find topographical groove patterns that could enhance osteoblast differentiation according to cell type, groove patterns are fabricated with ridges (0.35-7 mu m) and grooves (0.65-6 mu m) of various widths and explored their mechanisms in improving osteoblast differentiation. This study finds that a groove pattern enhancing osteoblast differentiation is associated with the ability of the cell to extend its length and that it is able to overcome the inhibition of osteoblast differentiation that takes place under inflammatory conditions. The groove pattern suppresses the generation of reactive oxygen species, a reaction that is increased in inflammatory conditions. It also modulates the expression of osteogenic factors according to differentiation time. Importantly, specific groove patterns AZ-2 and AZ-4, with ridge width of 2 mu m and groove width of 2 or 4 mu m, respectively, effectively promote bone regeneration in critical-sized calvarial defects without additional factors. This knowledge of groove patterns can be applied to the development of orthopedic and dental devices.
Keywords
MESENCHYMAL STEM-CELLS; IN-VITRO; BONE-FORMATION; OSTEOGENIC DIFFERENTIATION; SURFACE MICROTOPOGRAPHY; EXTRACELLULAR-MATRIX; MC3T3-E1 CELLS; ASCORBIC-ACID; TOPOGRAPHY; COLLAGEN; MESENCHYMAL STEM-CELLS; IN-VITRO; BONE-FORMATION; OSTEOGENIC DIFFERENTIATION; SURFACE MICROTOPOGRAPHY; EXTRACELLULAR-MATRIX; MC3T3-E1 CELLS; ASCORBIC-ACID; TOPOGRAPHY; COLLAGEN; bone regeneration; groove pattern; inflammation; osteoblast; reactive oxygen species
ISSN
1616-301X
URI
https://pubs.kist.re.kr/handle/201004/122044
DOI
10.1002/adfm.201703569
Appears in Collections:
KIST Article > 2017
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