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== Further reading ==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
* {{cite journal | vauthors = Führer D, Wonerow P, Willgerodt H, Paschke R | title = Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 82 | issue = 12 | pages = 4234–8 | date = Dec 1997 | doi = 10.1210/jcem.82.12.4405 | pmid = 9398746 }}
* {{cite journal | vauthors = Führer D, Wonerow P, Willgerodt H, Paschke R | title = Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidism | journal = The Journal of Clinical Endocrinology and Metabolism | volume = 82 | issue = 12 | pages = 4234–8 | date = Dec 1997 | doi = 10.1210/jcem.82.12.4405 | pmid = 9398746 | doi-access = free }}
* {{cite journal | vauthors = Farid NR, Kascur V, Balazs C | title = The human thyrotropin receptor is highly mutable: a review of gain-of-function mutations | journal = European Journal of Endocrinology| volume = 143 | issue = 1 | pages = 25–30 | date = Jul 2000 | pmid = 10870027 | doi = 10.1530/eje.0.1430025 | doi-access = free }}
* {{cite journal | vauthors = Farid NR, Kascur V, Balazs C | title = The human thyrotropin receptor is highly mutable: a review of gain-of-function mutations | journal = European Journal of Endocrinology| volume = 143 | issue = 1 | pages = 25–30 | date = Jul 2000 | pmid = 10870027 | doi = 10.1530/eje.0.1430025 | doi-access = free }}
* {{cite journal | vauthors = Szkudlinski MW, Fremont V, Ronin C, Weintraub BD | title = Thyroid-stimulating hormone and thyroid-stimulating hormone receptor structure-function relationships | journal = Physiological Reviews | volume = 82 | issue = 2 | pages = 473–502 | date = Apr 2002 | pmid = 11917095 | doi = 10.1152/physrev.00031.2001 | s2cid = 2919509 | url = https://semanticscholar.org/paper/14a5636e2788d63866670400d20a03ffb2bcb167 }}
* {{cite journal | vauthors = Szkudlinski MW, Fremont V, Ronin C, Weintraub BD | title = Thyroid-stimulating hormone and thyroid-stimulating hormone receptor structure-function relationships | journal = Physiological Reviews | volume = 82 | issue = 2 | pages = 473–502 | date = Apr 2002 | pmid = 11917095 | doi = 10.1152/physrev.00031.2001 | s2cid = 2919509 | url = https://semanticscholar.org/paper/14a5636e2788d63866670400d20a03ffb2bcb167 }}

Revision as of 02:44, 29 January 2023

TSHR
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTSHR, CHNG1, LGR3, hTSHR-I, thyroid stimulating hormone receptor, Thyrotropin receptor, thyrotropin (TSH) receptor
External IDsOMIM: 603372; MGI: 98849; HomoloGene: 315; GeneCards: TSHR; OMA:TSHR - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000369
NM_001018036
NM_001142626

NM_001113404
NM_011648

RefSeq (protein)

NP_000360
NP_001018046
NP_001136098

NP_001106875
NP_035778

Location (UCSC)Chr 14: 80.95 – 81.15 MbChr 12: 91.35 – 91.52 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The thyrotropin receptor (or TSH receptor) is a receptor (and associated protein) that responds to thyroid-stimulating hormone (also known as "thyrotropin") and stimulates the production of thyroxine (T4) and triiodothyronine (T3). The TSH receptor is a member of the G protein-coupled receptor superfamily of integral membrane proteins[5] and is coupled to the Gs protein.[6]

It is primarily found on the surface of the thyroid epithelial cells, but also found on adipose tissue and fibroblasts. The latter explains the reason of the myxedema finding during Graves disease. In addition, it has also been found to be expressed in the anterior pituitary gland, hypothalamus and kidneys. Its presence in the anterior pituitary gland may be involved in mediating the paracrine signaling feedback inhibition of thyrotropin along the hypothalamus-pituitary-thyroid axis.[7]

Function

Upon binding circulating TSH, a G-protein signal cascade activates adenylyl cyclase and intracellular levels of cAMP rise. cAMP activates all functional aspects of the thyroid cell, including iodine pumping; thyroglobulin synthesis, iodination, endocytosis, and proteolysis; thyroid peroxidase activity; and hormone release. TSHR is involved in regulating seasonal reproduction in vertebrates.[8]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000165409Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020963Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Farid NR, Szkudlinski MW (Sep 2004). "Minireview: structural and functional evolution of the thyrotropin receptor". Endocrinology. 145 (9): 4048–57. doi:10.1210/en.2004-0437. PMID 15231707.
  6. ^ Calebiro D, Nikolaev VO, Lohse MJ (Jul 2010). "Imaging of persistent cAMP signaling by internalized G protein-coupled receptors". Journal of Molecular Endocrinology. 45 (1): 1–8. doi:10.1677/JME-10-0014. PMID 20378719.
  7. ^ Williams GR (April 2011). "Extrathyroidal expression of TSH receptor". Annales d'Endocrinologie. 54es Journees internationales d'Endocrinologie clinique. 72 (2): 68–73. doi:10.1016/j.ando.2011.03.006. PMID 21511243.
  8. ^ Nakane Y, Yoshimura T (February 2019). "Photoperiodic Regulation of Reproduction in Vertebrates". Annual Review of Animal Biosciences. 7 (1): 173–194. doi:10.1146/annurev-animal-020518-115216. PMID 30332291. S2CID 52984435.

Further reading