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Parathyroid hormone receptor 1 is a parathyroid hormone receptor It is encoded by the gene PTHR1. It is a receptor for parathyroid hormone (PTH) and for parathyroid hormone-like hormone (PTHLH).

Function[]

It is the classical PTH receptor, is expressed in high levels in bone and kidney and regulates calcium ion homeostasis through activation of adenylate cyclase and phospholipase C.[1][2]

Mechanism[]

It is a member of the secretin family of G protein-coupled receptors. The activity of this receptor is mediated by Gs G proteins which activate adenylyl cyclase. Besides, they also activate phosphatidylinositol-calcium second messenger system.

Pathology[]

Defects in this receptor are known to be the cause of Jansen's metaphyseal chondrodysplasia (JMC), chondrodysplasia Blomstrand type (BOCD), as well as enchodromatosis.[3]

See also[]

References[]

  1. Mannstadt M, Jüppner H, Gardella TJ (1999). Receptors for PTH and PTHrP: their biological importance and functional properties. Am. J. Physiol. 277 (5 Pt 2): F665–75.
  2. Offermanns S, Iida-Klein A, Segre GV, Simon MI (1996). G alpha q family members couple parathyroid hormone (PTH)/PTH-related peptide and calcitonin receptors to phospholipase C in COS-7 cells. Mol. Endocrinol. 10 (5): 566–74.
  3. Entrez Gene: PTHR1 parathyroid hormone receptor 1.

Further reading[]


  • Bonaventure J, Silve C (2006). [Hereditary skeletal dysplasias and FGFR3 and PTHR1 signaling pathways]. Med Sci (Paris) 21 (11): 954–61.
  • Dawson SJ, White LA (1992). Treatment of Haemophilus aphrophilus endocarditis with ciprofloxacin.. J. Infect. 24 (3): 317–20.
  • Schipani E, Kruse K, Jüppner H (1995). A constitutively active mutant PTH-PTHrP receptor in Jansen-type metaphyseal chondrodysplasia.. Science 268 (5207): 98–100.
  • Schipani E, Weinstein LS, Bergwitz C, et al. (1995). Pseudohypoparathyroidism type Ib is not caused by mutations in the coding exons of the human parathyroid hormone (PTH)/PTH-related peptide receptor gene.. J. Clin. Endocrinol. Metab. 80 (5): 1611–21.
  • Pausova Z, Bourdon J, Clayton D, et al. (1994). Cloning of a parathyroid hormone/parathyroid hormone-related peptide receptor (PTHR) cDNA from a rat osteosarcoma (UMR 106) cell line: chromosomal assignment of the gene in the human, mouse, and rat genomes.. Genomics 20 (1): 20–6.
  • McCuaig KA, Clarke JC, White JH (1994). Molecular cloning of the gene encoding the mouse parathyroid hormone/parathyroid hormone-related peptide receptor.. Proc. Natl. Acad. Sci. U.S.A. 91 (11): 5051–5.
  • Schipani E, Karga H, Karaplis AC, et al. (1993). Identical complementary deoxyribonucleic acids encode a human renal and bone parathyroid hormone (PTH)/PTH-related peptide receptor.. Endocrinology 132 (5): 2157–65.
  • Schneider H, Feyen JH, Seuwen K, Movva NR (1993). Cloning and functional expression of a human parathyroid hormone receptor.. Eur. J. Pharmacol. 246 (2): 149–55.
  • Schipani E, Langman CB, Parfitt AM, et al. (1996). Constitutively activated receptors for parathyroid hormone and parathyroid hormone-related peptide in Jansen's metaphyseal chondrodysplasia.. N. Engl. J. Med. 335 (10): 708–14.
  • Zhou AT, Bessalle R, Bisello A, et al. (1997). Direct mapping of an agonist-binding domain within the parathyroid hormone/parathyroid hormone-related protein receptor by photoaffinity crosslinking.. Proc. Natl. Acad. Sci. U.S.A. 94 (8): 3644–9.
  • Schipani E, Jensen GS, Pincus J, et al. (1997). Constitutive activation of the cyclic adenosine 3',5'-monophosphate signaling pathway by parathyroid hormone (PTH)/PTH-related peptide receptors mutated at the two loci for Jansen's metaphyseal chondrodysplasia.. Mol. Endocrinol. 11 (7): 851–8.
  • Jobert AS, Zhang P, Couvineau A, et al. (1998). Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia.. J. Clin. Invest. 102 (1): 34–40.
  • Pellegrini M, Bisello A, Rosenblatt M, et al. (1998). Binding domain of human parathyroid hormone receptor: from conformation to function.. Biochemistry 37 (37): 12737–43.
  • Zhang P, Jobert AS, Couvineau A, Silve C (1998). A homozygous inactivating mutation in the parathyroid hormone/parathyroid hormone-related peptide receptor causing Blomstrand chondrodysplasia.. J. Clin. Endocrinol. Metab. 83 (9): 3365–8.
  • Adams AE, Bisello A, Chorev M, et al. (1999). Arginine 186 in the extracellular N-terminal region of the human parathyroid hormone 1 receptor is essential for contact with position 13 of the hormone.. Mol. Endocrinol. 12 (11): 1673–83.
  • Matsuzaki K, Katayama K, Takahashi Y, et al. (1999). Human osteoclast-like cells are formed from peripheral blood mononuclear cells in a coculture with SaOS-2 cells transfected with the parathyroid hormone (PTH)/PTH-related protein receptor gene.. Endocrinology 140 (2): 925–32.
  • Schipani E, Langman C, Hunzelman J, et al. (1999). A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasia.. J. Clin. Endocrinol. Metab. 84 (9): 3052–7.
  • Karperien M, van der Harten HJ, van Schooten R, et al. (1999). A frame-shift mutation in the type I parathyroid hormone (PTH)/PTH-related peptide receptor causing Blomstrand lethal osteochondrodysplasia.. J. Clin. Endocrinol. Metab. 84 (10): 3713–20.
  • Watson PH, Fraher LJ, Natale BV, et al. (2000). Nuclear localization of the type 1 parathyroid hormone/parathyroid hormone-related peptide receptor in MC3T3-E1 cells: association with serum-induced cell proliferation.. Bone 26 (3): 221–5.
  • Truneh A, Sharma S, Silverman C, et al. (2000). Temperature-sensitive differential affinity of TRAIL for its receptors. DR5 is the highest affinity receptor.. J. Biol. Chem. 275 (30): 23319–25.




External links[]


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