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Interleukin-1 alpha induces focal degradation of biglycan and tissue degeneration in an in-vitro ovine meniscal model

机译:白细胞介素-1α在体外绵羊半月板模型中诱导双链聚糖的局部降解和组织变性

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We have developed an ovine meniscal explant model where the focal degradative events leading to characteristic fragmentation patterns of biglycan in human OA of the knee and hip, and evident in animal models of knee OA and IVD degeneration are reproduced in culture. Lateral and medial menisci were dissected into outer, mid and inner zones and established in explant culture +/- IL-1(10 ng/ml). The biglycan species present in conditioned media samples and in GuHCl extracts of tissues were examined by Western blotting using two C-terminal antibodies PR-85 and EF-Bgn. Clear differences were evident in the biglycan species in each meniscal tissue zone with the medial outer meniscus having lower biglycan levels and major fragments of 20, 28, 33 and 36, 39 kDa. Similar fragmentation was detected in articular cartilage samples, 42-45 kDa core protein species were also detected. Biglycan fragmentation was not as extensive in the IL-1 stimulated meniscal cultures with 36, 39, 42 and 45 kDa biglycan species evident. Thus the medial meniscus outer zone displayed the highest levels of biglycan processing in this model and correlated with a major zone of meniscal remodelling in OA in man. Significantly, enzymatic digests of meniscal tissues with MMP-13, ADAMTS-4 and ADAMTS-5 have also generated similar biglycan species in-vitro. Zymography confirmed that the medial outer zone was the region of maximal MMP activity. This model represents a convenient system to recapitulate matrix remodelling events driven by IL-1 in pathological cartilages and in animal models of joint degeneration. (C) 2016 Elsevier Inc. All fights reserved.
机译:我们已经开发了一种绵羊半月板外植体模型,在该模型中,导致人膝和髋关节OA的双链聚糖特征性断裂模式的局灶性降解事件在文化中得以再现,在膝OA和IVD变性的动物模型中也很明显。将外侧和内侧半月板解剖成外侧,中部和内侧区域,并在外植体培养物中+/- IL-1(10 ng / ml)建立。使用两种C末端抗体PR-85和EF-Bgn,通过蛋白质印迹法检测条件培养基样品和组织的GuHCl提取物中存在的双糖链蛋白物种。在每个半月板组织区域中的双链聚糖物种中,明显的差异是明显的,其中内侧半月板具有较低的双链聚糖水平,并且主要片段为20、28、33和36、39 kDa。在关节软骨样品中检测到类似的片段,还检测到42-45 kDa核心蛋白种类。在由IL-1刺激的半月板培养物中,双链糖蛋白片段化程度不如36 kDa,39 kDa,42 kDa和45 kDa双链糖蛋白明显。因此,在该模型中,内侧半月板外区显示出最高水平的双链聚糖加工,并且与人OA中半月板重塑的主要区域相关。重要的是,用MMP-13,ADAMTS-4和ADAMTS-5进行的半月板组织的酶消化也已经在体外产生了类似的双链多糖。 Zymography证实内侧外侧区域是最大的MMP活性区域。该模型代表了一个方便的系统,可以概括由IL-1在病理性软骨和关节变性动物模型中驱动的基质重塑事件。 (C)2016 Elsevier Inc.版权所有。

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