Literature DB >> 27921040

New Insights into the Molecular Mechanisms Targeting Tubular Channels/Transporters in PKD Development.

Ming Wu1, Shengqiang Yu1.   

Abstract

BACKGROUND: Autosomal dominant polycystic kidney disease (PKD) or autosomal recessive PKD is caused by a mutation in the PKD1, PKD2 or PKHD1 gene, which encodes polycystin-1, polycystin-2 or fibrocystin, respectively. Embryonic and postnatal mutation studies show that transport or channel function is dysregulated before the initiation of cystogenesis, suggesting that the abnormality of transport or channel function plays a critical role in the pathology of PKD.
SUMMARY: Polycystin-2 by itself is a calcium-permeable cation channel, and its channel function can be regulated by polycystin-1 or fibrocystin. In this paper, we reviewed the current knowledge about calcium transports and cyclic adenosine monophosphate (cAMP)-driven chloride transports in PKD. In addition, the function and the underlining mechanism of glucose transporters, phosphate transporters and water channels in PKD are also discussed. KEY MESSAGES: Abnormalities in calcium handling and exuberant cAMP-dependent cystic fibrosis transmembrane conductance regulator-mediated fluid secretion in the collecting duct are the most important issues in the pathogenesis of PKD.

Entities:  

Keywords:  Channels; Molecular mechanism; Polycystic kidney disease; Transporters

Year:  2016        PMID: 27921040      PMCID: PMC5123004          DOI: 10.1159/000444839

Source DB:  PubMed          Journal:  Kidney Dis (Basel)        ISSN: 2296-9357


  80 in total

1.  Collecting duct-specific knockout of adenylyl cyclase type VI causes a urinary concentration defect in mice.

Authors:  Karl P Roos; Kevin A Strait; Kalani L Raphael; Mitsi A Blount; Donald E Kohan
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Review 2.  Aquaporins in kidney pathophysiology.

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Journal:  Nat Rev Nephrol       Date:  2010-01-26       Impact factor: 28.314

3.  The expression of water channels AQP1 and AQP2 in a large series of ADPKD kidneys.

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Journal:  Nephron       Date:  1998       Impact factor: 2.847

4.  Renal epithelial cyst formation and enlargement in vitro: dependence on cAMP.

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Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

5.  Cystic fibrosis and the phenotypic expression of autosomal dominant polycystic kidney disease.

Authors:  D A O'Sullivan; V E Torres; P A Gabow; S N Thibodeau; B F King; E J Bergstralh
Journal:  Am J Kidney Dis       Date:  1998-12       Impact factor: 8.860

6.  EP2 receptor mediates PGE2-induced cystogenesis of human renal epithelial cells.

Authors:  Gerard Elberg; Dorit Elberg; Teresa V Lewis; Suresh Guruswamy; Lijuan Chen; Charlotte J Logan; Michael D Chan; Martin A Turman
Journal:  Am J Physiol Renal Physiol       Date:  2007-08-29

7.  Anion secretion drives fluid secretion by monolayers of cultured human polycystic cells.

Authors:  R Mangoo-Karim; M Ye; D P Wallace; J J Grantham; L P Sullivan
Journal:  Am J Physiol       Date:  1995-09

8.  PKHD1 gene silencing may cause cell abnormal proliferation through modulation of intracellular calcium in autosomal recessive polycystic kidney disease.

Authors:  Jiyun Yang; Sizhong Zhang; Qin Zhou; Hong Guo; Ke Zhang; Rong Zheng; Cuiying Xiao
Journal:  J Biochem Mol Biol       Date:  2007-07-31

Review 9.  CFTR: a hub for kinases and crosstalk of cAMP and Ca2+.

Authors:  Karl Kunzelmann; Anil Mehta
Journal:  FEBS J       Date:  2013-08-27       Impact factor: 5.542

10.  Adenylyl cyclase 6 enhances NKCC2 expression and mediates vasopressin-induced phosphorylation of NKCC2 and NCC.

Authors:  Timo Rieg; Tong Tang; Shinichi Uchida; H Kirk Hammond; Robert A Fenton; Volker Vallon
Journal:  Am J Pathol       Date:  2012-11-01       Impact factor: 4.307

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1.  Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.

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Review 2.  Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT).

Authors:  Asha N Talati; Carolyn M Webster; Neeta L Vora
Journal:  Prenat Diagn       Date:  2019-08-05       Impact factor: 3.050

Review 3.  The Biology of Vasopressin.

Authors:  Samantha Sparapani; Cassandra Millet-Boureima; Joshua Oliver; Kathy Mu; Pegah Hadavi; Tamar Kalostian; Nazifa Ali; Carla Maria Avelar; Marion Bardies; Brenton Barrow; Minky Benedikt; Giuliana Biancardi; Raminder Bindra; Lisa Bui; Zakaria Chihab; Ashley Cossitt; Jeffrey Costa; Tina Daigneault; Jocelyn Dault; Isa Davidson; Jonathan Dias; Emie Dufour; Sabine El-Khoury; Nargess Farhangdoost; Anika Forget; Alexa Fox; Myriam Gebrael; Maria Concetta Gentile; Olivia Geraci; Ansley Gnanapragasam; Elias Gomah; Elie Haber; Claudia Hamel; Thivya Iyanker; Christina Kalantzis; Sara Kamali; Elsa Kassardjian; Hryssi Krissy Kontos; Thi Bich Uyen Le; Daniella LoScerbo; Yan Fang Low; Danielle Mac Rae; Flore Maurer; Sana Mazhar; Alice Nguyen; Kathy Nguyen-Duong; Chelsea Osborne-Laroche; Hwi Wun Park; Emilie Parolin; Kahlila Paul-Cole; Leah Sarah Peer; Margaux Philippon; Charles-Alexandre Plaisir; Jessica Porras Marroquin; Simran Prasad; Rewaparsad Ramsarun; Saad Razzaq; Samantha Rhainds; Damien Robin; Ryan Scartozzi; Davindra Singh; Sajad Soleimani Fard; Maxim Soroko; Nastaran Soroori Motlagh; Kiri Stern; Laila Toro; M Wyatt Toure; Stephanie Tran-Huynh; Sarah Trépanier-Chicoine; Claudia Waddingham; Aaliyah Jasmine Weekes; Allison Wisniewski; Chiara Gamberi
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Review 4.  Recent advances in understanding ion transport mechanisms in polycystic kidney disease.

Authors:  Anastasia V Sudarikova; Valeriia Y Vasileva; Regina F Sultanova; Daria V Ilatovskaya
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  4 in total

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