Estrogen hormones are important for cartilage homeostasis, but nothing is known regarding the expression and role of the membrane G protein-coupled estrogen receptor (GPER), G protein-coupled receptor 30 (GPR30), in adult articular chondrocytes. Using immunohistochemistry of cartilage sections, quantitative real-time polymerase chain reaction and Western blot of chondrocyte extracts, we found that these cells express GPR30. Nonetheless, the pattern of bands detected by two distinct antibodies does not overlap, suggesting that the proteins detected represent partially degraded forms of the receptor. Treatment with GPR30 agonists did not induce Akt or ERK1/2 phosphorylation, two known GPR30-activated signaling pathways, suggesting that GPR30 is not functional in human chondrocytes. Therefore, the protective anti-osteoarthritic role of estrogen hormones in cartilage homeostasis is likely independent of GPR30. This study was performed using human cartilage collected from the distal femoral condyles of multiorgan donors at the Bone and Tissue Bank of the University and Hospital Center of Coimbra.

译文

雌激素激素对软骨稳态很重要,但关于成年关节软骨细胞中膜g蛋白偶联雌激素受体 (GPER),g蛋白偶联受体30 (GPR30) 的表达和作用尚不清楚。使用软骨切片的免疫组织化学,实时定量聚合酶链反应和软骨细胞提取物的蛋白质印迹,我们发现这些细胞表达gpr30。尽管如此,两种不同抗体检测到的条带模式不会重叠,这表明检测到的蛋白质代表了受体的部分降解形式。用GPR30激动剂治疗不会诱导Akt或ERK1/2磷酸化,这是两种已知的GPR30-activated信号通路,表明GPR30在人软骨细胞中不起作用。因此,雌激素在软骨稳态中的保护性抗骨关节炎作用可能与gpr30无关。这项研究是使用从科英布拉大学和医院中心的骨骼和组织库的多器官供体的股骨远端con收集的人类软骨进行的。

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