Fukui Naoshi, Miyamoto Yoshinari, Nakajima Masahiro, Ikeda Yasuko, Hikita Atsuhiko, Furukawa Hiroshi, Mitomi Hiroyuki, Tanaka Nobuho, Katsuragawa Yozo, Yamamoto Seizo, Sawabe Motoji, Juji Takuo, Mori Toshihito, Suzuki Ryuji, Ikegawa Shiro
Clinical Research Center, National Hospital Organization Sagamihara Hospital, Kanagawa, Japan.
Arthritis Rheum. 2008 Dec;58(12):3843-53. doi: 10.1002/art.24036.
To determine the chondrocyte metabolism in respective zones of osteoarthritic (OA) cartilage.
OA cartilage was obtained from macroscopically intact areas of 4 knee joints with end-stage OA. The cartilage was divided into 3 zones, and gene expression profiles were determined in the respective zones by a custom-designed microarray that focused on chondrocyte-related genes. For the genes whose expression was significantly different among the zones, the expression was compared between OA and control cartilage in the respective zones by an analysis using laser capture microdissection and real-time polymerase chain reaction (PCR). For some genes, the correlation of expression was investigated in specific cartilage zones.
A total of 198 genes (approximately 40% of those investigated) were found to be expressed at significantly different levels among the zones. Expression of 26 of those genes was evaluated by laser capture microdissection and real-time PCR, which confirmed the validity of microarray analysis. The expression of cartilage matrix genes was mostly enhanced in OA cartilage, at similar levels across the zones but at different magnitudes among the genes. The expression of bone-related genes was induced either in the superficial zone or in the deep zone, and positive correlations were found among their expression in the respective zones. The expression of 5 proteinase genes was most enhanced in the superficial zone, where their expression was correlated, suggesting the presence of a common regulatory mechanism(s) for their expression.
In OA cartilage, the metabolic activity of chondrocytes differed considerably among zones. Characteristic changes were observed in the superficial and deep zones.
确定骨关节炎(OA)软骨各区域的软骨细胞代谢情况。
从4个终末期OA膝关节宏观完整区域获取OA软骨。将软骨分为3个区域,通过定制的聚焦于软骨细胞相关基因的微阵列测定各区域的基因表达谱。对于各区域间表达有显著差异的基因,使用激光捕获显微切割和实时聚合酶链反应(PCR)分析比较OA软骨和对照软骨在各区域的表达情况。对于一些基因,研究其在特定软骨区域的表达相关性。
共发现198个基因(约占研究基因的40%)在各区域的表达水平有显著差异。通过激光捕获显微切割和实时PCR对其中26个基因的表达进行评估,证实了微阵列分析的有效性。软骨基质基因的表达在OA软骨中大多增强,各区域水平相似但基因间程度不同。骨相关基因的表达在表层区域或深层区域被诱导,且在各区域的表达之间存在正相关。5种蛋白酶基因的表达在表层区域增强最为明显,其表达具有相关性,提示存在共同的调控机制。
在OA软骨中,软骨细胞的代谢活性在各区域有很大差异。在表层和深层区域观察到特征性变化。