NEIRID Lab (NeuroEndocrine Interaction in Rheumatology and Inflammatory Diseases), SERGAS, Santiago University Clinical Hospital, Institute of Medical Research (IDIS), Santiago de Compostela, Spain.
PLoS One. 2012;7(12):e52533. doi: 10.1371/journal.pone.0052533. Epub 2012 Dec 19.
Osteoarthritis (OA) and rheumatoid arthritis (RA), the most common rheumatic diseases, are characterized by irreversible degeneration of the joint tissues. There are several factors involved in the pathogenesis of these diseases including pro-inflammatory cytokines, adipokines and adhesion molecules.
Up to now, the relationship between adipokines and adhesion molecules at cartilage level was not explored. Thus, the aim of this article was to study the effect of leptin and adiponectin on the expression of VCAM-1 in human and murine chondrocytes. For completeness, intracellular signal transduction pathway was also explored.
VCAM-1 expression was assessed by quantitative RT-PCR and western blot analysis upon treatment with leptin, adiponectin and other pertinent reagents in cultured human primary chondrocytes. Signal transduction pathways have been explored by using specific pharmacological inhibitors in the adipokine-stimulated human primary chondrocytes and ATDC5 murine chondrocyte cell line.
Herein, we demonstrate, for the first time, that leptin and adiponectin increase VCAM-1 expression in human and murine chondrocytes. In addition, both adipokines have additive effect with IL-1β. Finally, we demonstrate that several kinases, including JAK2, PI3K and AMPK are at a play in the intracellular signalling of VCAM-1 induction.
Taken together, our results suggest that leptin and adiponectin could perpetuate cartilage-degrading processes by inducing also factors responsible of leukocyte and monocyte infiltration at inflamed joints.
骨关节炎(OA)和类风湿关节炎(RA)是最常见的风湿性疾病,其特征是关节组织的不可逆转退化。有几个因素参与这些疾病的发病机制,包括促炎细胞因子、脂肪因子和黏附分子。
到目前为止,脂肪因子和黏附分子在软骨水平的关系尚未被探索。因此,本文的目的是研究瘦素和脂联素对人源和鼠源软骨细胞 VCAM-1 表达的影响。为完整起见,还研究了细胞内信号转导通路。
用瘦素、脂联素和其他相关试剂处理培养的人原代软骨细胞,通过定量 RT-PCR 和 Western blot 分析评估 VCAM-1 的表达。在脂联素刺激的人原代软骨细胞和 ATDC5 鼠源软骨细胞系中,使用特定的药理学抑制剂探索信号转导通路。
本文首次证明,瘦素和脂联素均可增加人源和鼠源软骨细胞 VCAM-1 的表达。此外,两种脂肪因子与 IL-1β 具有相加作用。最后,我们证明了几种激酶,包括 JAK2、PI3K 和 AMPK,在 VCAM-1 诱导的细胞内信号转导中发挥作用。
总之,我们的研究结果表明,瘦素和脂联素可以通过诱导炎症关节中白细胞和单核细胞浸润的因子,使软骨降解过程持续进行。