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2003 Volume No 6 -
pages 22-27
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Title: Osteoblasts generate an osteogenic microenvironment
when grown on surfaces with rough microtopographies
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Authors: B.D. Boyan, S. Lossdörfer, L. Wang,
G. Zhao, C.H. Lohmann, D.L. Cochran & Z. Schwartz
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Address: Dept. of Biomedical Engineering, Georgia
Institute of Technology, Atlanta, USA
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E-mail: barbara.Boyan at bme.gatech.edu
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Key Words: Osteoblasts, titanium, surfaces, microtopography,
osteoprotegerin (OPG), osteogenesis.
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Publication date: October 24th 2003
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Abstract: Osteoblasts respond to microarchitectural
features of their substrate. On smooth surfaces (tissue culture
plastic, tissue culture glass, and titanium), the cells attach
and proliferate but they exhibit relatively low expression
of differentiation markers in monolayer cultures, even when
confluent. When grown on microrough Ti surfaces with an average
roughness (Ra) of 4-7 µm, proliferation is reduced but
differentiation is enhanced and in some cases, is synergistic
with the effects of surface microtopography. In addition,
cells on microrough Ti substrates form hydroxyapatite in a
manner that is more typical of bone than do cells cultured
on smooth surfaces. Osteoblasts also respond to growth factors
and cytokines in a surface-dependent manner. On rougher surfaces,
the effects of regulatory factors like 1α,25(OH)2D3
or 17ß-estradiol are enhanced. The response to the surface
is mediated by integrins, which signal to the cell through
many of the same mechanisms used by growth factors and hormones.
Studies using PEG-modified surfaces indicate that increased
differentiation may be related to altered attachment to the
surface. When osteoblasts are grown on surfaces with chemistries
or microarchitectures that reduce cell attachment and proliferation,
and enhance differentiation, the cells tend to increase production
of factors like TGF- ß1 that promote osteogenesis while
decreasing osteoclastic activity. Thus, on microrough Ti surface,
osteoblasts create a microenvironment conducive to new bone
formation.
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