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Volumn 25, Issue 12, 2014, Pages 2789-2799

Aberrant glycosylation and localization of polycystin-1 cause polycystic kidney in an AQP11 knockout model

Author keywords

[No Author keywords available]

Indexed keywords

AQUAPORIN; AQUAPORIN 11; MEMBRANE PROTEIN; POLYCYSTIN 1; POLYCYSTIN 2; UNCLASSIFIED DRUG; AQP11 PROTEIN, MOUSE; POLYCYSTIC KIDNEY DISEASE 1 PROTEIN; POLYCYSTIN;

EID: 84923872599     PISSN: 10466673     EISSN: 15333450     Source Type: Journal    
DOI: 10.1681/ASN.2013060614     Document Type: Article
Times cited : (40)

References (42)
  • 2
    • 79954424212 scopus 로고    scopus 로고
    • Water permeability and characterization of aquaporin-11
    • Yakata K, Tani K, Fujiyoshi Y: Water permeability and characterization of aquaporin-11. J Struct Biol 174: 315-320, 2011
    • (2011) J Struct Biol , vol.174 , pp. 315-320
    • Yakata, K.1    Tani, K.2    Fujiyoshi, Y.3
  • 6
    • 67649844614 scopus 로고    scopus 로고
    • Polycystins and primary cilia: Primers for cell cycle progression
    • Zhou J: Polycystins and primary cilia: Primers for cell cycle progression. Annu Rev Physiol 71: 83-113, 2009
    • (2009) Annu Rev Physiol , vol.71 , pp. 83-113
    • Zhou, J.1
  • 8
    • 0036785149 scopus 로고    scopus 로고
    • The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia
    • Yoder BK, Hou X, Guay-Woodford LM: The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. J Am Soc Nephrol 13: 2508-2516, 2002
    • (2002) J Am Soc Nephrol , vol.13 , pp. 2508-2516
    • Yoder, B.K.1    Hou, X.2    Guay-Woodford, L.M.3
  • 9
    • 77249128360 scopus 로고    scopus 로고
    • Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease
    • Janssen MJ, Waanders E, Woudenberg J, Lefeber DJ, Drenth JP: Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease. J Hepatol 52: 432-440, 2010
    • (2010) J Hepatol , vol.52 , pp. 432-440
    • Janssen, M.J.1    Waanders, E.2    Woudenberg, J.3    Lefeber, D.J.4    Drenth, J.P.5
  • 10
    • 0037168674 scopus 로고    scopus 로고
    • Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations
    • Qian F, Boletta A, Bhunia AK, Xu H, Liu L, Ahrabi AK, Watnick TJ, Zhou F, Germino GG: Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations. Proc Natl Acad Sci U S A 99: 16981-16986, 2002
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 16981-16986
    • Qian, F.1    Boletta, A.2    Bhunia, A.K.3    Xu, H.4    Liu, L.5    Ahrabi, A.K.6    Watnick, T.J.7    Zhou, F.8    Germino, G.G.9
  • 12
    • 77952491724 scopus 로고    scopus 로고
    • Pkd1 transgenic mice: Adult model of polycystic kidney disease with extrarenal and renal phenotypes
    • Kurbegovic A, CôtéO, Couillard M, Ward CJ, Harris PC, Trudel M: Pkd1 transgenic mice: Adult model of polycystic kidney disease with extrarenal and renal phenotypes. Hum Mol Genet 19: 1174-1189, 2010
    • (2010) Hum Mol Genet , vol.19 , pp. 1174-1189
    • Kurbegovic, A.1    Côté, O.2    Couillard, M.3    Ward, C.J.4    Harris, P.C.5    Trudel, M.6
  • 13
    • 0037036350 scopus 로고    scopus 로고
    • Identification, characterization, and localization of a novel kidney polycystin-1-polycystin-2 complex
    • Newby LJ, Streets AJ, Zhao Y, Harris PC, Ward CJ, Ong AC: Identification, characterization, and localization of a novel kidney polycystin-1-polycystin-2 complex. J Biol Chem 277: 20763-20773, 2002
    • (2002) J Biol Chem , vol.277 , pp. 20763-20773
    • Newby, L.J.1    Streets, A.J.2    Zhao, Y.3    Harris, P.C.4    Ward, C.J.5    Ong, A.C.6
  • 14
    • 78650482131 scopus 로고    scopus 로고
    • Polycystin-1 surface localization is stimulated by polycystin-2 and cleavage at the G protein-coupled receptor proteolytic site
    • Chapin HC, Rajendran V, Caplan MJ: Polycystin-1 surface localization is stimulated by polycystin-2 and cleavage at the G protein-coupled receptor proteolytic site. Mol Biol Cell 21: 4338-4348, 2010
    • (2010) Mol Biol Cell , vol.21 , pp. 4338-4348
    • Chapin, H.C.1    Rajendran, V.2    Caplan, M.J.3
  • 16
    • 0034735526 scopus 로고    scopus 로고
    • Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella
    • Pazour GJ, Dickert BL, Vucica Y, Seeley ES, Rosenbaum JL, Witman GB, Cole DG: Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 151: 709-718, 2000
    • (2000) J Cell Biol , vol.151 , pp. 709-718
    • Pazour, G.J.1    Dickert, B.L.2    Vucica, Y.3    Seeley, E.S.4    Rosenbaum, J.L.5    Witman, G.B.6    Cole, D.G.7
  • 17
    • 0037884961 scopus 로고    scopus 로고
    • Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease
    • Lin F, Hiesberger T, Cordes K, Sinclair AM, Goldstein LS, Somlo S, Igarashi P: Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease. Proc Natl Acad Sci U S A 100: 5286-5291, 2003
    • (2003) Proc Natl Acad Sci U S A , vol.100 , pp. 5286-5291
    • Lin, F.1    Hiesberger, T.2    Cordes, K.3    Sinclair, A.M.4    Goldstein, L.S.5    Somlo, S.6    Igarashi, P.7
  • 19
    • 33749235323 scopus 로고    scopus 로고
    • Development of polycystic kidney disease in juvenile cystic kidneymice: Insights into pathogenesis, ciliary abnormalities, and common features with human disease
    • Smith LA, Bukanov NO, Husson H, Russo RJ, Barry TC, Taylor AL, Beier DR, Ibraghimov-Beskrovnaya O: Development of polycystic kidney disease in juvenile cystic kidneymice: Insights into pathogenesis, ciliary abnormalities, and common features with human disease. J Am Soc Nephrol 17: 2821-2831, 2006
    • (2006) J Am Soc Nephrol , vol.17 , pp. 2821-2831
    • Smith, L.A.1    Bukanov, N.O.2    Husson, H.3    Russo, R.J.4    Barry, T.C.5    Taylor, A.L.6    Beier, D.R.7    Ibraghimov-Beskrovnaya, O.8
  • 21
    • 40449121293 scopus 로고    scopus 로고
    • Nek8 regulates the expression and localization of polycystin-1 and polycystin-2
    • Sohara E, Luo Y, Zhang J, Manning DK, Beier DR, Zhou J: Nek8 regulates the expression and localization of polycystin-1 and polycystin-2. J Am Soc Nephrol 19: 469-476, 2008
    • (2008) J Am Soc Nephrol , vol.19 , pp. 469-476
    • Sohara, E.1    Luo, Y.2    Zhang, J.3    Manning, D.K.4    Beier, D.R.5    Zhou, J.6
  • 22
    • 79959725455 scopus 로고    scopus 로고
    • A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation
    • Fedeles SV, Tian X, Gallagher AR, Mitobe M, Nishio S, Lee SH, Cai Y, Geng L, Crews CM, Somlo S: A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation. Nat Genet 43: 639-647, 2011
    • (2011) Nat Genet , vol.43 , pp. 639-647
    • Fedeles, S.V.1    Tian, X.2    Gallagher, A.R.3    Mitobe, M.4    Nishio, S.5    Lee, S.H.6    Cai, Y.7    Geng, L.8    Crews, C.M.9    Somlo, S.10
  • 23
    • 54049149970 scopus 로고    scopus 로고
    • Aquaporin-11 knockout mice and polycystic kidney disease animals share a common mechanism of cyst formation
    • Okada S, Misaka T, Tanaka Y, Matsumoto I, Ishibashi K, Sasaki S, Abe K: Aquaporin-11 knockout mice and polycystic kidney disease animals share a common mechanism of cyst formation. FASEB J 22: 3672-3684, 2008
    • (2008) FASEB J , vol.22 , pp. 3672-3684
    • Okada, S.1    Misaka, T.2    Tanaka, Y.3    Matsumoto, I.4    Ishibashi, K.5    Sasaki, S.6    Abe, K.7
  • 25
    • 84874628531 scopus 로고    scopus 로고
    • Liver-specific Aquaporin 11 knockout mice show rapid vacuolization of the rough endoplasmic reticulum in periportal hepatocytes after amino acid feeding
    • Rojek A, Füchtbauer EM, Füchtbauer A, Jelen S, Malmendal A, Fenton RA, Nielsen S: Liver-specific Aquaporin 11 knockout mice show rapid vacuolization of the rough endoplasmic reticulum in periportal hepatocytes after amino acid feeding. Am J Physiol Gastrointest Liver Physiol 304: G501-G515, 2013
    • (2013) Am J Physiol Gastrointest Liver Physiol , vol.304 , pp. G501-G515
    • Rojek, A.1    Füchtbauer, E.M.2    Füchtbauer, A.3    Jelen, S.4    Malmendal, A.5    Fenton, R.A.6    Nielsen, S.7
  • 27
    • 0033033706 scopus 로고    scopus 로고
    • Somatic PKD2 mutations in individual kidney and liver cysts support a "two-hit " model of cystogenesis in type 2 autosomal dominant polycystic kidney disease
    • Pei Y, Watnick T, He N, Wang K, Liang Y, Parfrey P, Germino G, St George-Hyslop P: Somatic PKD2 mutations in individual kidney and liver cysts support a "two-hit " model of cystogenesis in type 2 autosomal dominant polycystic kidney disease. J Am Soc Nephrol 10: 1524-1529, 1999
    • (1999) J am Soc Nephrol , vol.10 , pp. 1524-1529
    • Pei, Y.1    Watnick, T.2    He, N.3    Wang, K.4    Liang, Y.5    Parfrey, P.6    Germino, G.7    St George-Hyslop, P.8
  • 28
    • 0033358598 scopus 로고    scopus 로고
    • A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2
    • Torra R, Badenas C, San Millán JL, Pérez-Oller L, Estivill X, Darnell A: A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2. Am J Hum Genet 65: 345-352, 1999
    • (1999) Am J Hum Genet , vol.65 , pp. 345-352
    • Torra, R.1    Badenas, C.2    San Millán, J.L.3    Pérez-Oller, L.4    Estivill, X.5    Darnell, A.6
  • 33
    • 29744470060 scopus 로고    scopus 로고
    • Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease
    • Low SH, Vasanth S, Larson CH, Mukherjee S, Sharma N, Kinter MT, Kane ME, Obara T, Weimbs T: Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease. Dev Cell 10: 57-69, 2006
    • (2006) Dev Cell , vol.10 , pp. 57-69
    • Low, S.H.1    Vasanth, S.2    Larson, C.H.3    Mukherjee, S.4    Sharma, N.5    Kinter, M.T.6    Kane, M.E.7    Obara, T.8    Weimbs, T.9
  • 37
    • 84866543932 scopus 로고    scopus 로고
    • Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice
    • Nishida H, Sohara E, Nomura N, Chiga M, Alessi DR, Rai T, Sasaki S, Uchida S: Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice. Hypertension 60: 981-990, 2012
    • (2012) Hypertension , vol.60 , pp. 981-990
    • Nishida, H.1    Sohara, E.2    Nomura, N.3    Chiga, M.4    Alessi, D.R.5    Rai, T.6    Sasaki, S.7    Uchida, S.8
  • 39
    • 23344432987 scopus 로고    scopus 로고
    • Impaired urea accumulation in the inner medulla of mice lacking the urea transporter UT-A2
    • Uchida S, Sohara E, Rai T, Ikawa M, Okabe M, Sasaki S: Impaired urea accumulation in the inner medulla of mice lacking the urea transporter UT-A2. Mol Cell Biol 25: 7357-7363, 2005
    • (2005) Mol Cell Biol , vol.25 , pp. 7357-7363
    • Uchida, S.1    Sohara, E.2    Rai, T.3    Ikawa, M.4    Okabe, M.5    Sasaki, S.6
  • 42
    • 18744399322 scopus 로고    scopus 로고
    • In vivo protein biotinylation for identification of organ-specific antigens accessible from the vasculature
    • Rybak JN, Ettorre A, Kaissling B, Giavazzi R, Neri D, Elia G: In vivo protein biotinylation for identification of organ-specific antigens accessible from the vasculature. Nat Methods 2: 291-298, 2005
    • (2005) Nat Methods , vol.2 , pp. 291-298
    • Rybak, J.N.1    Ettorre, A.2    Kaissling, B.3    Giavazzi, R.4    Neri, D.5    Elia, G.6


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