Yamanishi Yuji, Boyle David L, Clark Melody, Maki Rich A, Tortorella Micky D, Arner Elizabeth C, Firestein Gary S
Division of Rheumatology, Allergy, and Immunology, University of California at San Diego School of Medicine, 9500 Gilman Drive, La Jolla, CA 92093, USA.
J Immunol. 2002 Feb 1;168(3):1405-12. doi: 10.4049/jimmunol.168.3.1405.
Aggrecanases are key matrix-degrading enzymes that act by cleaving aggrecan at the Glu(373)-Ala(374) site. While these fragments have been detected in osteoarthritis (OA) and rheumatoid arthritis (RA) cartilage and synovial fluid, no information is available on the regulation or expression of the two key aggrecanases (aggrecanase-1 and aggrecanase-2) in synovial tissue (ST) or fibroblast-like synoviocytes (FLS). The aggrecanase-1 gene was constitutively expressed by both RA and OA FLS. Real-time PCR demonstrated that TGF-beta significantly increased aggrecanase-1 gene expression in FLS. Aggrecanase-1 induction peaked after 24 h of TGF-beta stimulation. The expression of aggrecanase-1 mRNA was significantly greater in RA ST than in OA or nonarthritis ST. Aggrecanase-2 mRNA and protein were constitutively produced by nonarthritis, OA, and RA FLS but were not increased by IL-1, TNF-alpha, or TGF-beta. Furthermore, OA, RA, and nonarthritis ST contained similar amounts of immunoreactive aggrecanase-2. The major form of the aggrecanase-2 enzyme was 70 kDa in nonarthritis ST, whereas a processed 53-kDa form was abundant in RA ST. Therefore, aggrecanase-1 and -2 are differentially regulated in FLS. Both are constitutively expressed, but aggrecanase-1 is induced by cytokines, especially TGF-beta. In contrast, aggrecanase-2 protein may be regulated by a post-translational mechanism in OA and RA ST. Synovial and FLS production of aggrecanase can contribute to cartilage degradation in RA and OA.
聚集蛋白聚糖酶是关键的基质降解酶,通过在Glu(373)-Ala(374)位点切割聚集蛋白聚糖发挥作用。虽然这些片段已在骨关节炎(OA)和类风湿关节炎(RA)的软骨及滑液中被检测到,但关于滑膜组织(ST)或成纤维细胞样滑膜细胞(FLS)中两种关键聚集蛋白聚糖酶(聚集蛋白聚糖酶-1和聚集蛋白聚糖酶-2)的调节或表达情况尚无相关信息。RA和OA的FLS均组成性表达聚集蛋白聚糖酶-1基因。实时PCR表明,转化生长因子-β(TGF-β)显著增加FLS中聚集蛋白聚糖酶-1基因的表达。TGF-β刺激24小时后,聚集蛋白聚糖酶-1的诱导达到峰值。RA滑膜组织中聚集蛋白聚糖酶-1 mRNA的表达显著高于OA或非关节炎滑膜组织。非关节炎、OA和RA的FLS组成性产生聚集蛋白聚糖酶-2 mRNA和蛋白,但白细胞介素-1(IL-1)、肿瘤坏死因子-α(TNF-α)或TGF-β不会使其增加。此外,OA、RA和非关节炎滑膜组织中免疫反应性聚集蛋白聚糖酶-2的含量相似。非关节炎滑膜组织中聚集蛋白聚糖酶-2酶的主要形式为70 kDa,而在RA滑膜组织中大量存在加工后的53-kDa形式。因此,聚集蛋白聚糖酶-1和-2在FLS中的调节存在差异。两者均组成性表达,但聚集蛋白聚糖酶-1由细胞因子尤其是TGF-β诱导。相比之下,聚集蛋白聚糖酶-2蛋白在OA和RA滑膜组织中可能受翻译后机制调节。滑膜和FLS产生聚集蛋白聚糖酶可导致RA和OA中的软骨降解。