Tamm–Horsfall protein

UMOD
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases UMOD, ADMCKD2, FJHN, HNFJ, HNFJ1, MCKD2, THGP, THP, uromodulin
External IDs OMIM: 191845 MGI: 102674 HomoloGene: 2522 GeneCards: UMOD
Genetically Related Diseases
hypertension, kidney disease[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

7369

22242

Ensembl

ENSG00000169344

ENSMUSG00000030963

UniProt

P07911

Q91X17

RefSeq (mRNA)

NM_001008389
NM_001278614
NM_003361

NM_001278605
NM_009470

RefSeq (protein)

NP_001008390.1
NP_001265543.1
NP_003352.2

NP_001265534.1
NP_033496.1

Location (UCSC) Chr 16: 20.33 – 20.36 Mb Chr 7: 119.46 – 119.48 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

The Tamm–Horsfall glycoprotein (THP), also known as uromodulin, is a glycoprotein that in humans is encoded by the UMOD gene.[4][5] Uromodulin is the most abundant protein excreted in ordinary urine.[6]

Gene

The human UMOD gene is located on chromosome 16. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform.[5]

Protein

THP is a GPI-anchored glycoprotein. It is not derived from blood plasma but is produced by the thick ascending limb of the loop of Henle of the mammalian kidney. While the monomeric molecule has a MW of approximately 85 kDa, it is physiologically present in urine in large aggregates of up to several million Da.[6] When this protein is concentrated at low pH, it forms a gel. Uromodulin represents the most quantitative protein in normal human urine (results based on MSMS determinations).[7] It is the matrix of urinary casts derived from the secretion of renal tubular cells.

Function

Uromodulin excretion in urine follows proteolytic cleavage of the ectodomain of its glycophosphatidylinositol-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. Uromodulin may act as a constitutive inhibitor of calcium crystallization in renal fluids. The excretion of uromodulin in urine may provide defense against urinary tract infections caused by uropathogenic bacteria.[5]

The function of THP is not well understood. Studies using THP deficient mice revealed that THP may have a role in regulatory physiology and actually participates in transporter function.[8] A role in bacterial binding and sequestration is suggested by studies showing that Escherichia coli which express MS (mannose-sensitive) pili or fimbriae (also fimbria, from the Latin word for "fringe") can be trapped by Tamm–Horsfall protein via its mannose-containing side chains.[6] THP may also be important in protection from kidney injury by down-regulating inflammation.[9]

Clinical significance

Uropontin, nephrocalcin and uromodulin (this protein) are the three known urinary glycoproteins that affect the formation of calcium-containing kidney stones or calculus. Tamm–Horsfall protein is part of the matrix in renal calculi but a role in kidney stone formation remains debatable. However, decreased levels of Tamm–Horsfall in urine have been found to be a good indicator of kidney stones.[6]

Defects in this gene are associated with the autosomal dominant renal disorders medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure.[5]

Antibodies to Tamm–Horsfall protein have been seen in various forms of nephritis (e.g., Balkan nephropathy), however, it remains unclear whether there is any pathophysiologic relevance to these findings.[10]

In multiple myeloma, there is often protein cast in the distal convoluted tubule and collecting duct of the kidneys, mainly consisting of immunoglobulin light chain known as Bence Jones protein, but often also contain Tamm–Horsfall protein.[11][12]

History

The glycoprotein was first purified in 1952 by Igor Tamm and Frank Horsfall from the urine of healthy individuals.[13] It was later detected in the urine of all mammals studied.

In January 2016, its 3D structure was determined for the first time by researchers at Karolinska Institutet.[14]


References

  1. ↑ "Diseases that are genetically associated with UMOD view/edit references on wikidata".
  2. ↑ "Human PubMed Reference:".
  3. ↑ "Mouse PubMed Reference:".
  4. ↑ Jeanpierre C, Whitmore SA, Austruy E, Cohen-Salmon M, Callen DF, Junien C (Mar 1993). "Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11". Cytogenet Cell Genet. 62 (4): 185–7. doi:10.1159/000133470. PMID 8382593.
  5. 1 2 3 4 "Entrez Gene: UMOD uromodulin (uromucoid, Tamm–Horsfall glycoprotein)".
  6. 1 2 3 4 Lau WH, Leong WS, Ismail Z, Gam LH (2008). "Qualification and application of an ELISA for the determination of Tamm Horsfall protein (THP) in human urine and its use for screening of kidney stone disease". Int. J. Biol. Sci. 4 (4): 215–22. doi:10.7150/ijbs.4.215. PMC 2500153Freely accessible. PMID 18695745.
  7. ↑ Nagaraj N, Mann M (February 2011). "Quantitative analysis of the intra- and inter-individual variability of the normal urinary proteome". J. Proteome Res. 10 (2): 637–45. doi:10.1021/pr100835s. PMID 21126025.
  8. ↑ Bachmann S, Mutig K, Bates J, Welker P, Geist B, Gross V, Luft FC, Alenina N, Bader M, Thiele BJ, Prasadan K, Raffi HS, Kumar S (2005). "Renal effects of Tamm-Horsfall protein (uromodulin) deficiency in mice". Am. J. Physiol. Renal Physiol. 288 (3): F559–67. doi:10.1152/ajprenal.00143.2004. PMID 15522986.
  9. ↑ El-Achkar TM, Wu XR, Rauchman M, McCracken R, Kiefer S, Dagher PC. Tamm-Horsfall protein protects the kidney from ischemic injury by decreasing inflammation and altering TLR4 expression. Am J Physiol Renal Physiol. 2008 Aug;295(2):F534-44. doi: 10.1152/ajprenal.00083.2008. Epub 2008 May 21. PMID 18495803
  10. ↑ Vizjak A, Trnacević S, Ferluga D, Halilbasić A (November 1991). "Renal function, protein excretion, and pathology of Balkan endemic nephropathy. IV. Immunohistology". Kidney Int. Suppl. 34: S68–74. PMID 1762338.
  11. ↑ Abbas AK, Gerber R, Mitchell RS, Kumar V, Fausto N (2006). Pocket companion to Robbins and Cotran Pathologic Basis of Disease (7th ed.). Philadelphia, Pa: Saunders, Elsevier. p. 353. ISBN 0-7216-0265-7.
  12. ↑ Aster JC (2007). "The Hematopoietic and Lymphoid Systems". In Kumar V, Abbas AK, Fauso N, Mitchell R. Robbins Basic Patholog (8th ed.). Philadelphia, PA: Saunders/Elsevier. p. 455. ISBN 1-4160-2973-7.
  13. ↑ Tamm I, Horsfall FL (January 1952). "A mucoprotein derived from human urine which reacts with influenza, mumps, and Newcastle disease viruses". J. Exp. Med. 95 (1): 71–97. doi:10.1084/jem.95.1.71. PMC 2212053Freely accessible. PMID 14907962.
  14. ↑ Bokhove M, Nishimura K, Brunati M, Han L, de Sanctis D, Rampoldi L, Jovine L (2016). "A structured interdomain linker directs self-polymerization of human uromodulin". Proc. Natl. Acad. Sci. U.S.A. 113 (6): 1552–1557. doi:10.1073/pnas.1519803113. PMC 4760807Freely accessible. PMID 26811476.

Further reading

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