Corps Anthony N, Jones Gavin C, Harrall Rebecca L, Curry Valerie A, Hazleman Brian L, Riley Graham P
Rheumatology Research Unit, Addenbrooke's Hospital, Cambridge, UK.
Matrix Biol. 2008 Jun;27(5):393-401. doi: 10.1016/j.matbio.2008.02.002. Epub 2008 Apr 2.
Several members of the ADAMTS (A Disintegrin And Metalloproteinase with ThromboSpondin motifs) family have been identified as aggrecanases, whose substrates include versican, the principal large proteoglycan in the tendon extracellular matrix. We have characterized the expression of ADAMTS-4 in human Achilles tendon and tendon-derived cells. ADAMTS-4 mRNA levels were higher in ruptured tendon compared with normal tendon or chronic painful tendinopathy. In tissue extracts probed by Western blotting, mature ADAMTS-4 (68 kDa) was detected only in ruptured tendons, while processed ADAMTS-4 (53 kDa) was detected also in chronic painful tendinopathy and in normal tendon. In cultured Achilles tendon cells, transforming growth factor-beta (TGF-beta) stimulated ADAMTS-4 mRNA expression (typically 20-fold after 24 h), while interleukin-1 induced a smaller, shorter-term stimulation which synergised markedly with that induced by TGF-beta. Increased levels of immunoreactive proteins consistent with mature and processed forms of ADAMTS-4 were detected in TGF-beta-stimulated cells. ADAMTS-4 mRNA was expressed at higher levels by tendon cells in collagen gels than in monolayer cultures. In contrast, the expression of ADAMTS-1 and -5 mRNA was lower in collagen gels compared with monolayers, and these mRNA showed smaller or opposite responses to growth factors and cytokines compared with that of ADAMTS-4 mRNA. We conclude that both ADAMTS-4 mRNA and ADAMTS-4 protein processing may be differentially regulated in normal and damaged tendons and that both the matrix environment and growth factors such as TGF-beta are potentially important factors controlling ADAMTS aggrecanase activities in tendon pathology.
ADAMTS(含血小板反应蛋白基序的解聚素和金属蛋白酶)家族的多个成员已被鉴定为聚集蛋白聚糖酶,其底物包括多功能蛋白聚糖,它是肌腱细胞外基质中的主要大型蛋白聚糖。我们已对ADAMTS-4在人跟腱及肌腱衍生细胞中的表达进行了表征。与正常肌腱或慢性疼痛性肌腱病相比,ADAMTS-4 mRNA水平在断裂肌腱中更高。在Western印迹检测的组织提取物中,仅在断裂肌腱中检测到成熟的ADAMTS-4(68 kDa),而在慢性疼痛性肌腱病和正常肌腱中也检测到加工后的ADAMTS-4(53 kDa)。在培养的跟腱细胞中,转化生长因子-β(TGF-β)刺激ADAMTS-4 mRNA表达(通常在24小时后增加20倍),而白细胞介素-1诱导较小的短期刺激,且与TGF-β诱导的刺激有明显协同作用。在TGF-β刺激的细胞中检测到与成熟和加工形式的ADAMTS-4一致的免疫反应性蛋白水平升高。与单层培养相比,肌腱细胞在胶原凝胶中ADAMTS-4 mRNA表达水平更高。相反,与单层培养相比,胶原凝胶中ADAMTS-1和-5 mRNA的表达较低,并且这些mRNA对生长因子和细胞因子的反应与ADAMTS-4 mRNA相比更小或相反。我们得出结论,在正常和受损肌腱中,ADAMTS-4 mRNA和ADAMTS-4蛋白加工可能受到不同调节,并且基质环境和生长因子如TGF-β都是控制肌腱病理中ADAMTS聚集蛋白聚糖酶活性的潜在重要因素。