Tamm-horsfall protein/uromodulin deficiency elicits tubular compensatory responses leading to hypertension and hyperuricemia

Yan Liu, David S. Goldfarb, Tarek M. El-Achkar, John C Lieske, Xue Ru Wu

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Expression of Tamm-Horsfall protein (THP or uromodulin) is highly restricted to the kidney thick ascending limb (TAL) of loop of Henle. Despite the unique location and recent association of THP gene mutations with hereditary uromodulin-associated kidney disease and THP single nucleotide polymorphisms with chronic kidney disease and hypertension, the physiological function(s) of THP and its pathological involvement remain incompletely understood. By studying age-dependent changes of THP knockout (KO) mice, we show here that young KO mice had significant salt and water wasting but were partially responsive to furosemide, due to decreased luminal translocation of Na-K-Cl cotransporter 2 (NKCC2) in the TAL. Aged THP KO mice were, however, markedly oliguric and unresponsive to furosemide, and their NKCC2 was localized primarily in the cytoplasm as evidenced by lipid raft floatation assay, cell fractionation, and confocal and immunoelectron microscopy. These aged KO mice responded to metolazone and acetazolamide, known to target distal and proximal tubules, respectively. They also had marked upregulation of renin in juxtaglomerular apparatus and serum, and they were hypertensive. Finally, the aged THP KO mice had significant upregulation of Na-coupled urate transporters Slc5a8 and Slc22a12 as well as sodium-hydrogen exchanger 3 (NHE3) in the proximal tubule and elevated serum uric acid and allantoin. Collectively, our results suggest that THP deficiency can cause progressive disturbances in renal functions via initially NKCC2 dysfunction and later compensatory responses, resulting in prolonged activation of the renin-angiotensin-aldosterone axis and hyperuricemia.

Original languageEnglish (US)
Pages (from-to)F1062-F1076
JournalAmerican Journal of Physiology - Renal Physiology
Volume314
Issue number6
DOIs
StatePublished - Jun 1 2018

Fingerprint

Uromodulin
Protein Deficiency
Hyperuricemia
Knockout Mice
Sodium-Potassium-Chloride Symporters
Hypertension
Furosemide
Renin
Metolazone
Up-Regulation
Juxtaglomerular Apparatus
Allantoin
Cell Fractionation
Loop of Henle
Kidney
Acetazolamide
Immunoelectron Microscopy
Angiotensins
Uric Acid
Aldosterone

Keywords

  • Hyperuricemia
  • Lipid rafts
  • NKCC2
  • Tamm-Horsfall protein
  • Thick ascending limb
  • Uromodulin

ASJC Scopus subject areas

  • Physiology
  • Urology

Cite this

Tamm-horsfall protein/uromodulin deficiency elicits tubular compensatory responses leading to hypertension and hyperuricemia. / Liu, Yan; Goldfarb, David S.; El-Achkar, Tarek M.; Lieske, John C; Wu, Xue Ru.

In: American Journal of Physiology - Renal Physiology, Vol. 314, No. 6, 01.06.2018, p. F1062-F1076.

Research output: Contribution to journalArticle

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abstract = "Expression of Tamm-Horsfall protein (THP or uromodulin) is highly restricted to the kidney thick ascending limb (TAL) of loop of Henle. Despite the unique location and recent association of THP gene mutations with hereditary uromodulin-associated kidney disease and THP single nucleotide polymorphisms with chronic kidney disease and hypertension, the physiological function(s) of THP and its pathological involvement remain incompletely understood. By studying age-dependent changes of THP knockout (KO) mice, we show here that young KO mice had significant salt and water wasting but were partially responsive to furosemide, due to decreased luminal translocation of Na-K-Cl cotransporter 2 (NKCC2) in the TAL. Aged THP KO mice were, however, markedly oliguric and unresponsive to furosemide, and their NKCC2 was localized primarily in the cytoplasm as evidenced by lipid raft floatation assay, cell fractionation, and confocal and immunoelectron microscopy. These aged KO mice responded to metolazone and acetazolamide, known to target distal and proximal tubules, respectively. They also had marked upregulation of renin in juxtaglomerular apparatus and serum, and they were hypertensive. Finally, the aged THP KO mice had significant upregulation of Na-coupled urate transporters Slc5a8 and Slc22a12 as well as sodium-hydrogen exchanger 3 (NHE3) in the proximal tubule and elevated serum uric acid and allantoin. Collectively, our results suggest that THP deficiency can cause progressive disturbances in renal functions via initially NKCC2 dysfunction and later compensatory responses, resulting in prolonged activation of the renin-angiotensin-aldosterone axis and hyperuricemia.",
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AU - Lieske, John C

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