首页> 外文期刊>Biological trace element research >Decreased Expression of CHST-12, CHST-13, and UST in the Proximal Interphalangeal Joint Cartilage of School-Age Children with Kashin-Beck Disease: an Endemic Osteoarthritis in China Caused by Selenium Deficiency
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Decreased Expression of CHST-12, CHST-13, and UST in the Proximal Interphalangeal Joint Cartilage of School-Age Children with Kashin-Beck Disease: an Endemic Osteoarthritis in China Caused by Selenium Deficiency

机译:CHST-12,CHST-13和UST表达下降在学龄前儿童近端间患有KASHIN-BECK疾病的临床间关节软骨中:由硒缺乏引起的中国人群骨关节炎

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The objective of this study is to investigate changes in the expression of enzymes involved in chondroitin sulfate (CS) sulfation in distal articular surface of proximal interphalangeal joint isolated from school-age children patients with Kashin-Beck disease (KBD), using normal children as controls. Articular cartilage samples were collected from four normal and four KBD children (7-12 years old), and these children were assigned to control and KBD groups. Hematoxylin and eosin (H&E), toluidine blue (TB), and immunohistochemical (IHC) stainings were utilized to evaluate changes in joint pathology and expression of enzymes involved in CS sulfation, including carbohydrate sulfotransferase 12 (CHST-12), carbohydrate sulfotransferase 13 (CHST-13), and uronyl 2-O-sulfotransferase (UST). The correspondence results were examined by semi-quantitative analysis. Compared with the control group, the KBD group showed the following: a significant decrease of total chondrocytes in superficial, middle, and deep layers and deposition of sulfated glycosaminoglycans in extracellular matrix of KBD cartilage were observed; positive staining chondrocytes of CHST-12, CHST-13, and UST were significantly less in superficial zone of KBD cartilage; and CHST-13 positive staining chondrocytes was reduced in deep zone of KBD cartilage. In contrast, the positive staining rates of CHST-12, CHST-13, and UST in KBD were significantly higher than those in the control group. The decreased expression of these enzymes and the physiologic compensatory reaction may be the signs of early-stage KBD. The alterations of CS structure modifying sulfotransferases in finger articular cartilage might play an important role in the onset and pathogenesis of school-age KBD children.
机译:本研究的目的是探讨从学龄儿童患者(KBD)的近端间间关节的远端关节表面中所涉及的硫酸软骨素(CS)硫酸盐硫化的酶表达的变化(KBD),使用正常的儿童控制。关节软骨样品从四个正常和四个KBD儿童(7-12岁)收集,这些儿童被分配到控制和KBD组。利用血杂环素和曙红(H&E),甲苯胺蓝(TB)和免疫组织化学(IHC)染色,评价CS硫化的关节病理学和表达的变化,包括碳水化合物磺旋转转移酶12(CHST-12),碳水化合物磺基转移酶13( CHST-13)和核心2-O-磺膦转移酶(UST)。通过半定量分析检查了对应结果。与对照组相比,KBD组显示以下:浅表,中间层,中层,深层,硫化糖蛋白聚糖的沉积中的总软骨细胞的总体细胞内,观察到以下内容下降的显着降低; CHST-12,CHST-13和UST的阳性染色软骨细胞在KBD软骨的浅表区内显着较低;和CHST-13阳性染色软骨细胞在KBD软骨深处降低。相反,KBD中CHST-12,CHST-13和UST的阳性染色率显着高于对照组中的染色率。这些酶的表达和生理学补偿反应的表达降低可能是早期KBD的迹象。在手指关节软骨中改变Cs结构改变磺基转移酶的变化可能在学龄儿童发病和发病机制中发挥着重要作用。

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