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表面粗糙度可调节成骨样MG-63细胞生长因子和细胞因子的局部产生。

Surface roughness modulates the local production of growth factors and cytokines by osteoblast-like MG-63 cells.

作者信息

Kieswetter K, Schwartz Z, Hummert T W, Cochran D L, Simpson J, Dean D D, Boyan B D

机构信息

Department of Orthopaedics, University of Texas Health Science Center at San Antonio 78284, USA.

出版信息

J Biomed Mater Res. 1996 Sep;32(1):55-63. doi: 10.1002/(SICI)1097-4636(199609)32:1<55::AID-JBM7>3.0.CO;2-O.

Abstract

Titanium (Ti) surface roughness affects proliferation, differentiation, and matrix production of MG-63 osteoblast-like cells. Cytokines and growth factors produced in the milieu surrounding an implant may also be influenced by its surface, thereby modulating the healing process. This study examined the effect of surface roughness on the production of two factors known to have potent effects on bone, prostaglandin E2 (PGE2) and transforming growth factor beta 1 (TGF-beta 1). MG-63 cells were cultured on Ti disks of varying roughness. The surfaces were ranked from smoothest to roughest: electropolished (EP), pretreated with hydrofluoric acid-nitric acid (PT), fine sand-blasted, etched with HCl and H2SO4, and washed (EA), coarse sand-blasted, etched with HCl and H2SO4, and washed (CA), and Ti plasma-sprayed (TPS). Cells were cultured in 24-well polystyrene (plastic) dishes as controls and to determine when confluence was achieved. Media were collected and cell number determined 24 h postconfluence. PGE2 and TGF-beta 1 levels in the conditioned media were determined using commercial radioimmunoassay and enzyme-linked immunosorbent assay kits, respectively. There was an inverse relationship between cell number and Ti surface roughness. Total PGE2 content in the media of cultures grown on the three roughest surfaces (FA, CA, and TPS) was significantly increased 1.5-4.0 times over that found in media of cultures grown on plastic or smooth surfaces. When PGE2 production was expressed per cell number, CA and TPS cultures exhibited six- to eightfold increases compared to cultures on plastic and smooth surfaces. There was a direct relationship between TGF-beta 1 production and surface roughness, both in terms of total TGF-beta 1 per culture and when normalized for cell number. TGF-beta 1 production on rough surfaces (CA and TPS) was three to five times higher than on plastic. These studies indicate that substrate surface roughness affects cytokine and growth factor production by MG-63 cells, suggesting that surface roughness may modulate the activity of cells interacting with an implant, and thereby affect tissue healing and implant success.

摘要

钛(Ti)表面粗糙度会影响MG-63成骨样细胞的增殖、分化和基质生成。植入物周围环境中产生的细胞因子和生长因子也可能受其表面影响,从而调节愈合过程。本研究考察了表面粗糙度对两种已知对骨有强效作用的因子,即前列腺素E2(PGE2)和转化生长因子β1(TGF-β1)产生的影响。将MG-63细胞培养在不同粗糙度的钛盘上。表面从最光滑到最粗糙依次为:电解抛光(EP)、氢氟酸 - 硝酸预处理(PT)、细喷砂、盐酸和硫酸蚀刻并冲洗(EA)、粗喷砂、盐酸和硫酸蚀刻并冲洗(CA)以及钛等离子喷涂(TPS)。将细胞培养在24孔聚苯乙烯(塑料)培养皿中作为对照并确定何时达到汇合。汇合后24小时收集培养基并测定细胞数量。分别使用商业放射免疫测定试剂盒和酶联免疫吸附测定试剂盒测定条件培养基中PGE2和TGF-β1的水平。细胞数量与钛表面粗糙度呈负相关。在三个最粗糙表面(FA、CA和TPS)上生长的培养物培养基中的总PGE2含量比在塑料或光滑表面上生长的培养物培养基中的含量显著增加1.5至4.0倍。当按细胞数量表示PGE2产生量时,CA和TPS培养物与塑料和光滑表面上的培养物相比增加了6至8倍。TGF-β1产生量与表面粗糙度呈正相关,无论是就每个培养物中的总TGF-β1而言,还是在按细胞数量进行归一化时。粗糙表面(CA和TPS)上的TGF-β1产生量比塑料表面高3至5倍。这些研究表明,底物表面粗糙度会影响MG-63细胞的细胞因子和生长因子产生,提示表面粗糙度可能调节与植入物相互作用的细胞的活性,从而影响组织愈合和植入成功率。

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