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首页> 外文期刊>American Journal of Pathology: Official Publication of the American Association of Pathologists >Human articular chondrocytes express multiple gap junction proteins: Differential expression of connexins in normal and osteoarthritic cartilage
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Human articular chondrocytes express multiple gap junction proteins: Differential expression of connexins in normal and osteoarthritic cartilage

机译:人关节软骨细胞表达多种间隙连接蛋白:正常和骨关节炎软骨中连接蛋白的差异表达

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摘要

Osteoarthritis (OA) is the most common joint disease and involves progressive degeneration of articular cartilage. The aim of this study was to investigate if chondrocytes from human articular cartilage express gap junction proteins called connexins (Cxs). We show that human chondrocytes in tissue express Cx43, Cx45, Cx32, and Cx46. We also find that primary chondrocytes from adults retain the capacity to form functional voltage-dependent gap junctions. Immunohistochemistry experiments in cartilage from OA patients revealed significantly elevated levels of Cx43 and Cx45 in the superficial zone and down through the next approximately 1000 μm of tissue. These zones corresponded with regions damaged in OA that also had high levels of proliferative cell nuclear antigen. An increased number of Cxs may help explain the increased proliferation of cells in clusters that finally lead to tissue homeostasis loss. Conversely, high levels of Cxs in OA cartilage reflect the increased number of adjacent cells in clusters that are able to interact directly by gap junctions as compared with hemichannels on single cells in normal cartilage. Our data provide strong evidence that OA patients have a loss of the usual ordered distribution of Cxs in the damaged zones and that the reductions in Cx43 levels are accompanied by the loss of correct Cx localization in the nondamaged areas.
机译:骨关节炎(OA)是最常见的关节疾病,涉及关节软骨的进行性变性。这项研究的目的是调查人类关节软骨的软骨细胞是否表达间隙连接蛋白,称为连接蛋白(Cxs)。我们显示,人类软骨细胞在组织中表达Cx43,Cx45,Cx32和Cx46。我们还发现成人的原代软骨细胞保留了形成功能性电压依赖性间隙连接的能力。在OA患者的软骨中进行的免疫组织化学实验显示,表层区域Cx43和Cx45的水平显着升高,并在接下来的约1000μm组织中下降。这些区域对应于OA中受损的区域,该区域也具有高水平的增殖细胞核抗原。 Cx数量的增加可能有助于解释簇中细胞增殖的增加,最终导致组织稳态的丧失。相反,与正常软骨中单个细胞的半通道相比,OA软骨中高水平的Cxs反映了能够通过间隙连接直接相互作用的簇中相邻细胞的数量增加。我们的数据提供了有力的证据,表明OA患者在受损区域中Cx的正常有序分布丢失,并且Cx43水平的降低伴随着在未受损区域中正确的Cx定位丢失。

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