Expression and function of the nonclassical estrogen receptor, GPR30, in human cartilage and chondrocytes. Issue 11 (23rd April 2020)

• Record Type: Journal Article
• Authors: Ribeiro, Madalena; Sousa, Cátia; Rufino, Ana T.; Judas, Fernando; Mendes, Alexandrina F.
• Is Part Of: Journal of cellular physiology. Volume 235:Issue 11(2020:Nov.)
• Page Start: 8486
• Page End: 8494
• Publication Date: 2020-04-23
• Subjects: cartilage -- chondrocyte -- estradiol -- estrogen receptors -- GPER -- GPR30; Physiology -- Periodicals; Cell physiology -- Periodicals; 571.6
• DOI: 10.1002/jcp.29691
• Languages: English
• ISSNs: 0021-9541

Abstract

Abstract: 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. Abstract : Human chondrocytes in situ express G protein‐coupled receptor 30 (GPR30). Nonetheless, the receptor is partially degraded and, therefore, nonfunctional.