首页> 美国卫生研究院文献>other >A SINGLE BLUNT IMPACT ON CARTILAGE PROMOTES FIBRONECTIN FRAGMENTATION AND UPREGULATES CARTILAGE DEGRADING STROMELYSIN-1/MATRIX METALLOPROTEINASE-3 IN A BOVINE EX-VIVO MODEL
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A SINGLE BLUNT IMPACT ON CARTILAGE PROMOTES FIBRONECTIN FRAGMENTATION AND UPREGULATES CARTILAGE DEGRADING STROMELYSIN-1/MATRIX METALLOPROTEINASE-3 IN A BOVINE EX-VIVO MODEL

机译:牛的单一钝化作用促进牛纤连蛋白模型中纤维蛋白的裂解并使上皮降解STROMELYSIN-1 /基质金属蛋白酶-3。

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摘要

Post-traumatic osteoarthritis (PTOA) is characterized by progressive cartilage degeneration in injured joints. Since fibronectin fragments (Fn-fs) degrade cartilage mainly through up-regulating matrix metalloproteinases (MMPs) and pro-inflammatory cytokines, we hypothesized that Fn-fs play a key role in PTOA by promoting chondrolysis in and around injured cartilage. To test this hypothesis, we profiled the catabolic events focusing on fibronectin fragmentation and proteinase expression in bovine osteochondral explants following a single blunt impact on cartilage with a drop tower device which created partial-thickness tissue damage. Injured and control explants were cultured for up to 14 days. The presence of Fn-fs, MMPs (-1, -3, -13), ADAMTS-5 in culture media and in cartilage was determined with immunoblotting. The daily proteoglycan (PG) depletion of cartilage matrix was assessed with DMMB assay. The effect of explant-conditioned media on chondrocytes was also examined with immunoblotting. Impacted cartilage released significantly higher amount of native Fn, three chondrolytic Fn-fs and PG than non-impacted controls did. Those increases coincided with up-regulation of MMP-3 both in conditioned media and in impacted cartilage. These findings support our hypothesis that PTOA may be propelled by Fn-fs which act as catabolic mediators through up-regulating cartilage-damaging proteinases.
机译:创伤后骨关节炎(PTOA)的特征是受伤关节的进行性软骨变性。由于纤连蛋白片段(Fn-fs)主要通过上调基质金属蛋白酶(MMPs)和促炎性细胞因子来降解软骨,因此我们假设Fn-fs通过促进受损软骨及其周围软骨的软骨溶解在PTOA中起关键作用。为了检验这个假设,我们对落石代谢事件进行了研究,重点研究了用落塔装置对软骨进行的钝性撞击后,牛骨软骨外植体中纤连蛋白的片段化和蛋白酶表达,这造成了部分厚度的组织损伤。将受伤的和对照的外植体培养长达14天。用免疫印迹法测定培养基和软骨中Fn-fs,MMPs(-1,-3,-13),ADAMTS-5的存在。用DMMB测定法评估软骨基质的每日蛋白聚糖(PG)消耗。还用免疫印迹检查了外植条件培养基对软骨细胞的作用。受影响的软骨释放的天然Fn,三种软骨溶解性Fn-fs和PG的含量明显高于未受影响的对照。这些增加与条件培养基和受影响的软骨中MMP-3的上调相吻合。这些发现支持了我们的假设,即PTOA可能受Fn-fs的推动,而Fn-fs通过上调软骨破坏性蛋白酶而充当分解代谢介质。

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