Yamasaki Keiichiro, Nakasa Tomoyuki, Miyaki Shigeru, Ishikawa Masakazu, Deie Masataka, Adachi Nobuo, Yasunaga Yuji, Asahara Hiroshi, Ochi Mitsuo
Hiroshima University, Hiroshima, Japan.
Arthritis Rheum. 2009 Apr;60(4):1035-41. doi: 10.1002/art.24404.
A role of microRNA, which are approximately 22-nucleotide noncoding RNAs, has recently been recognized in human diseases. The objective of this study was to identify the expression pattern of microRNA-146a (miR-146a) in cartilage from patients with osteoarthritis (OA).
The expression of miR-146a in cartilage from 15 patients with OA was analyzed by quantitative reverse transcription-polymerase chain reaction (RT-PCR) and by in situ hybridization. Induction of the expression of miR-146a by cultures of normal human articular chondrocytes following stimulation with interleukin-1beta (IL-1beta) was examined by quantitative RT-PCR.
All cartilage samples were divided into 3 groups according to a modification of the Mankin score (grade I = mild OA scored 0-5, grade II = moderate OA scored 6-10, and grade III = severe OA scored 11-14). In grade I OA cartilage samples, the expression of miR-146a and COL2A1 was significantly higher than that in the other groups (P < 0.05). In grades II and III OA cartilage, the expression of miR-146a and COL2A1 was decreased, whereas the expression of matrix metalloproteinase 13 (MMP-13) was elevated in grade II OA cartilage. These data showed that miR-146a is expressed intensely in cartilage with a low Mankin grade and that miR-146a expression decreases in parallel with the level of MMP-13 expression. Tissue section in situ hybridization of primary miR-146a (pri-miR-146a) revealed that pri-miR-146a was expressed in chondrocytes residing in all tissue layers, especially in the superficial layer, where it was intensely expressed. The expression of miR-146 was markedly elevated by IL-1beta stimulation in human chondrocytes in vitro.
This study shows that miR-146 is intensely expressed in low-grade OA cartilage and that its expression is induced by stimulation of IL-1beta. Thus, miR-146 might play a role in OA cartilage pathogenesis.
微小RNA是一类长度约为22个核苷酸的非编码RNA,其在人类疾病中的作用最近已得到认可。本研究的目的是确定骨关节炎(OA)患者软骨中微小RNA - 146a(miR - 146a)的表达模式。
采用定量逆转录 - 聚合酶链反应(RT - PCR)和原位杂交技术分析15例OA患者软骨中miR - 146a的表达。通过定量RT - PCR检测白细胞介素 - 1β(IL - 1β)刺激后正常人关节软骨细胞培养物中miR - 146a表达的诱导情况。
根据改良的曼金评分将所有软骨样本分为3组(I级 = 轻度OA评分为0 - 5分,II级 = 中度OA评分为6 - 10分,III级 = 重度OA评分为11 - 14分)。在I级OA软骨样本中,miR - 146a和COL2A1的表达显著高于其他组(P < 0.05)。在II级和III级OA软骨中,miR - 146a和COL2A1的表达降低,而II级OA软骨中基质金属蛋白酶13(MMP - 13)的表达升高。这些数据表明,miR - 146a在曼金分级低的软骨中强烈表达,且miR - 146a表达与MMP - 13表达水平平行下降。初级miR - 146a(pri - miR - 146a)的组织切片原位杂交显示,pri - miR - 146a在所有组织层的软骨细胞中表达,尤其是在表层,表达强烈。体外IL - 1β刺激可显著提高人软骨细胞中miR - 146的表达。
本研究表明,miR - 146在低度OA软骨中强烈表达,且其表达受IL - 1β刺激诱导。因此,miR - 146可能在OA软骨发病机制中起作用。