McCarthy G M, Cheung H S
Department of Medicine, Medical College of Wisconsin, Milwaukee 53226.
Biochim Biophys Acta. 1994 Apr 12;1226(1):97-104. doi: 10.1016/0925-4439(94)90064-7.
Synovial fluid basic calcium phosphate (BCP) crystals are associated with severe destructive arthropathies characterised by synovial proliferation and non-inflammatory degradation of intra-articular collagenous structures. BCP crystals stimulate fibroblast and chondrocyte mitogenesis, metalloprotease secretion and prostaglandin production. As a tissue protective effect of prostaglandins has been suggested, we recently studied the effect of PGE1 on BCP crystal-induced mitogenesis and collagenase mRNA accumulation in human fibroblasts (HF). We demonstrated a dose-dependent inhibition of BCP crystal-induced mitogenesis and collagenase mRNA accumulation. The mechanism of PGE1 inhibition of BCP crystal-induced mitogenesis and collagenase mRNA accumulation was therefore explored. PGE1 (100 ng/ml) increased HF intracellular cAMP 40-fold over control. BCP alone caused no such change but inhibited the PGE1-induced increase in intracellular cAMP by at least 60%. The PGE1-induced increase in intracellular cAMP was also blocked by the adenyl cyclase inhibitor, 2',5'-dideoxyadenosine (ddA) (10 microM) and ddA reversed the PGE1-mediated inhibition of BCP crystal-induced mitogenesis. Dibutyryl cAMP also inhibited BCP crystal-induced mitogenesis in a concentration-dependent manner. Agents which increase intracellular cAMP levels such as the adenyl cyclase activator forskolin and the phosphodiesterase, inhibitor 3-isobutyl-1-methylxanthine (IBMX) mimicked the effect of PGE1 on HF collagenase mRNA levels. PGE1 inhibits the biologic effects of BCP crystals through the cAMP signal transduction pathway and such inhibition may have significant therapeutic implications.
滑膜液碱性磷酸钙(BCP)晶体与严重的破坏性关节病相关,其特征为滑膜增生和关节内胶原结构的非炎性降解。BCP晶体刺激成纤维细胞和软骨细胞的有丝分裂、金属蛋白酶分泌以及前列腺素生成。由于已表明前列腺素具有组织保护作用,我们最近研究了前列腺素E1(PGE1)对BCP晶体诱导的人成纤维细胞(HF)有丝分裂和胶原酶mRNA积累的影响。我们证明了PGE1对BCP晶体诱导的有丝分裂和胶原酶mRNA积累具有剂量依赖性抑制作用。因此,我们探索了PGE1抑制BCP晶体诱导的有丝分裂和胶原酶mRNA积累的机制。PGE1(100 ng/ml)使HF细胞内cAMP水平比对照增加了40倍。单独的BCP不会引起这种变化,但至少抑制了PGE1诱导的细胞内cAMP增加的60%。腺苷酸环化酶抑制剂2',5'-二脱氧腺苷(ddA)(10 microM)也阻断了PGE1诱导的细胞内cAMP增加,并且ddA逆转了PGE1介导的对BCP晶体诱导的有丝分裂的抑制作用。二丁酰cAMP也以浓度依赖性方式抑制BCP晶体诱导的有丝分裂。增加细胞内cAMP水平的试剂,如腺苷酸环化酶激活剂福斯可林和磷酸二酯酶抑制剂3-异丁基-1-甲基黄嘌呤(IBMX),模拟了PGE1对HF胶原酶mRNA水平的影响。PGE1通过cAMP信号转导途径抑制BCP晶体的生物学效应,这种抑制可能具有重要的治疗意义。