大鼠软骨的蛋白质组学分析:骨关节炎早期差异表达蛋白的鉴定
Proteomic analysis of rat cartilage: the identification of differentially expressed proteins in the early stages of osteoarthritis.
作者信息
Parra-Torres Nancy Marbella, Cázares-Raga Febe Elena, Kouri Juan Bautista
机构信息
Departamento de Infectómica y Patogénesis Molecular, Centro de Investigación y de Estudios Avanzados, Instituto Politécnico Nacional (CINVESTAV-IPN), México, DF México.
出版信息
Proteome Sci. 2014 Nov 18;12(1):55. doi: 10.1186/s12953-014-0055-0. eCollection 2014.
BACKGROUND
Osteoarthritis (OA) is a chronic degenerative disease of the articular cartilage, and its diagnosis is based on symptoms and radiological signs that are only present in the late stages of the disease. Due to the limitations in diagnosing OA before the onset of symptoms, such as pain, little is known about the molecular mechanisms involved in the pathogenesis of OA. Experimental OA models are often used to study the kinetics of the progression of this disease. In this report, we conducted a proteomic study of osteoarthritic cartilage during the early stages of OA using an experimental rat model.
RESULTS
Ten proteins that are differentially expressed under early OA conditions were identified by 2-DE and MALDI-TOF/MS. These proteins mediated many processes, such as glycolysis and energy production (Nme2 and Pnp), cartilage matrix (Col2a1), transcription and protein synthesis (Eef1a1 and DJ-1), signal transduction (CaM and Pebp1), transport (Alb and Hba1), and latexin (Lxn). In addition, changes in Lxn expression in early OA were observed and validated by western blot and immunofluorescence analysis.
CONCLUSIONS
The proteins that we identified indicate that energy metabolism, cartilage matrix remodelling, and protective cellular mechanisms are associated with early OA. In addition, latexin expression during the early stages of OA could be implicated in cartilage repair.
背景
骨关节炎(OA)是一种关节软骨的慢性退行性疾病,其诊断基于仅在疾病晚期才出现的症状和放射学征象。由于在症状出现前诊断OA存在局限性,例如疼痛,因此对于OA发病机制中涉及的分子机制知之甚少。实验性OA模型常用于研究该疾病进展的动力学。在本报告中,我们使用实验性大鼠模型对OA早期阶段的骨关节炎软骨进行了蛋白质组学研究。
结果
通过二维电泳(2-DE)和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF/MS)鉴定出在OA早期条件下差异表达的10种蛋白质。这些蛋白质介导了许多过程,如糖酵解和能量产生(Nme2和Pnp)、软骨基质(Col2a1)、转录和蛋白质合成(Eef1a1和DJ-1)、信号转导(CaM和Pebp1)、转运(Alb和Hba1)以及乳清酸蛋白(Lxn)。此外,通过蛋白质免疫印迹和免疫荧光分析观察并验证了OA早期Lxn表达的变化。
结论
我们鉴定出的蛋白质表明能量代谢、软骨基质重塑和细胞保护机制与OA早期相关。此外,OA早期阶段的乳清酸蛋白表达可能与软骨修复有关。