Lin C W, Phillips S L, Brinckerhoff C E, Georgescu H I, Bandara G, Evans C H
Ferguson Laboratory, University of Pittsburgh, School of Medicine, Pennsylvania 15261.
Arch Biochem Biophys. 1988 Jul;264(1):351-4. doi: 10.1016/0003-9861(88)90605-4.
The cDNA probe H-9, originally constructed to recognize a portion of the mRNA for lapine synovial collagenase, also hybridized with a RNA of the same size (approximately 2.0 kb) isolated from activated lapine articular chondrocytes. Primary, monolayer cultures of lapine articular chondrocytes did not contain detectable amounts of this RNA, nor did they secrete measurable amounts of collagenase into their culture media. Following exposure to synovial factors, the chondrocytes contained high levels of collagenase mRNA, while their conditioned media had considerable collagenolytic activity. Collagenase mRNA started to appear in chondrocytes 3-5 h after treatment with the synovial material. Maximum levels occurred after 12-24 h. Recombinant human interleukin-1 also induced the appearance of this mRNA. We conclude that chondrocyte collagenase is likely to be the same gene product as synovial collagenase, and that its regulation by lapine articular chondrocytes probably occurs at a pretranslational level.
cDNA探针H - 9最初构建用于识别兔滑膜胶原酶的一部分mRNA,它也与从活化的兔关节软骨细胞中分离出的相同大小(约2.0 kb)的RNA杂交。兔关节软骨细胞的原代单层培养物中未检测到这种RNA,它们也没有向培养基中分泌可测量量的胶原酶。暴露于滑膜因子后,软骨细胞含有高水平的胶原酶mRNA,而其条件培养基具有相当大的胶原olytic活性。用滑膜物质处理后3 - 5小时,胶原酶mRNA开始出现在软骨细胞中。12 - 24小时后达到最高水平。重组人白细胞介素 - 1也诱导了这种mRNA的出现。我们得出结论,软骨细胞胶原酶可能与滑膜胶原酶是相同的基因产物,并且兔关节软骨细胞对其的调节可能发生在翻译前水平。