The peptidyl-prolyl isomerase Pin1 determines parathyroid hormone mRNA levels and stability in rat models of secondary hyperparathyroidism

• Published in: The Journal of clinical investigation Vol. 119; no. 10; pp. 3102 - 3114
• Main Authors: Nechama, Morris, Uchida, Takafumi, Mor Yosef-Levi, Irit, Silver, Justin, Naveh-Many, Tally
• Format: Journal Article
• Language: English
• Published: United States American Society for Clinical Investigation 01.10.2009
• Subjects: Adaptor Proteins, Signal Transducing - genetics; Adaptor Proteins, Signal Transducing - metabolism; Animals; Biomedical research; Care and treatment; Cell growth; Cell Line; Chronic kidney failure; Complications and side effects; Cytokines; Cytotoxins - pharmacology; Development and progression; Diet; Gene expression; Humans; Hyperparathyroidism; Hyperparathyroidism, Secondary - etiology; Hyperparathyroidism, Secondary - genetics; Kidney diseases; Kidney Failure, Chronic - complications; Kidney Failure, Chronic - genetics; Male; Messenger RNA; Mice; Mice, Knockout; Naphthoquinones - pharmacology; Parathyroid Glands - cytology; Parathyroid Glands - drug effects; Parathyroid Glands - metabolism; Parathyroid hormone; Parathyroid Hormone - genetics; Parathyroid Hormone - metabolism; Peptides; Phosphorus; Properties; Proteins; Rats; Receptors, Glucocorticoid - genetics; Receptors, Glucocorticoid - metabolism; RNA Stability; RNA, Messenger - genetics; RNA, Messenger - metabolism; RNA-Binding Proteins - genetics; RNA-Binding Proteins - metabolism; Trans-Activators - genetics; Trans-Activators - metabolism; United States
• ISSN: 0021-9738; 1558-8238
• DOI: 10.1172/jci39522

Secondary hyperparathyroidism is a major complication of chronic kidney disease (CKD). In experimental models of secondary hyperparathyroidism induced by hypocalcemia or CKD, parathyroid hormone (PTH) mRNA levels increase due to increased PTH mRNA stability. K-homology splicing regulator protein (KSRP) decreases the stability of PTH mRNA upon binding a cis-acting element in the PTH mRNA 3' UTR region. As the peptidyl-prolyl isomerase (PPIase) Pin1 has recently been shown to regulate the turnover of multiple cytokine mRNAs, we investigated the role of Pin1 in regulating PTH mRNA stability in rat parathyroids and transfected cells. The data generated were consistent with Pin1 being a PTH mRNA destabilizing protein. Initial analysis indicated that Pin1 activity was decreased in parathyroid protein extracts from both hypocalcemic and CKD rats and that pharmacologic inhibition of Pin1 increased PTH mRNA levels posttranscriptionally in rat parathyroid and in transfected cells. Pin1 mediated its effects via interaction with KSRP, which led to KSRP dephosphorylation and activation. In the rat parathyroid, Pin1 inhibition decreased KSRP-PTH mRNA interactions, increasing PTH mRNA levels. Furthermore, Pin1-/- mice displayed increased serum PTH and PTH mRNA levels, suggesting that Pin1 determines basal PTH expression in vivo. These results demonstrate that Pin1 is a key mediator of PTH mRNA stability and indicate a role for Pin1 in the pathogenesis of secondary hyperparathyroidism in individuals with CKD.