메뉴 건너뛰기




Volumn 28, Issue 12, 2013, Pages 2993-3003

Podocyte expression of nonmuscle myosin heavy chain-IIA decreases in idiopathic nephrotic syndrome, especially in focal segmental glomerulosclerosis

Author keywords

Focal segmental glomerulosclerosis; Myh9; Nonmuscle myosin heavy chain IIA; Podocyte; Primary process

Indexed keywords

ANTIBODY; MYOSIN IIA; MYOSIN IIB; NONMUSCULAR MYOSIN HEAVY CHAIN IIA ANTIBODY; PODOCALYXIN; PROTEIN ZO1; PUROMYCIN AMINONUCLEOSIDE; UNCLASSIFIED DRUG;

EID: 84890040995     PISSN: 09310509     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gft350     Document Type: Article
Times cited : (20)

References (43)
  • 1
    • 0042466540 scopus 로고    scopus 로고
    • Nephrotic syndrome in childhood
    • Eddy AA, Symons JM. Nephrotic syndrome in childhood. Lancet 2003; 362: 629-639
    • (2003) Lancet , vol.362 , pp. 629-639
    • Eddy, A.A.1    Symons, J.M.2
  • 2
    • 0034034757 scopus 로고    scopus 로고
    • NPHS2, Encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
    • Erratum in Nat Genet. 2000;25:125
    • Boute N, Gribouval O, Roselli S et al. NPHS2, Encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nat Genet 2000; 24: 349-354. Erratum in Nat Genet. 2000;25:125
    • (2000) Nat Genet , vol.24 , pp. 349-354
    • Boute, N.1    Gribouval, O.2    Roselli, S.3
  • 3
    • 0034051681 scopus 로고    scopus 로고
    • Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
    • Kaplan JM, Kim SH, North KN et al. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nat Genet 2000; 24: 251-256
    • (2000) Nat Genet , vol.24 , pp. 251-256
    • Kaplan, J.M.1    Kim, S.H.2    North, K.N.3
  • 4
    • 20844461826 scopus 로고    scopus 로고
    • A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
    • Winn MP, Conlon PJ, Lynn KL et al. A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. Science 2005; 308: 1801-1804
    • (2005) Science , vol.308 , pp. 1801-1804
    • Winn, M.P.1    Conlon, P.J.2    Lynn, K.L.3
  • 5
    • 33751531864 scopus 로고    scopus 로고
    • Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
    • Hinkes B,Wiggins RC, Gbadegesin R et al. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nat Genet 2006; 38: 1397-1405
    • (2006) Nat Genet , vol.38 , pp. 1397-1405
    • Hinkes, B.1    Wiggins, R.C.2    Gbadegesin, R.3
  • 6
    • 52949110955 scopus 로고    scopus 로고
    • MYH9 Is a major-effect risk gene for focal segmental glomerulosclerosis
    • Kopp JB, Smith MW, Nelson GW et al. MYH9 Is a major-effect risk gene for focal segmental glomerulosclerosis. Nat Genet 2008; 40: 1175-1184
    • (2008) Nat Genet , vol.40 , pp. 1175-1184
    • Kopp, J.B.1    Smith, M.W.2    Nelson, G.W.3
  • 7
    • 52949092735 scopus 로고    scopus 로고
    • Family investigation of nephropathy and diabetes research group: MYH9 is associated with nondiabetic end-stage renal disease in African Americans
    • Kao WH, Klag MJ, Meoni LA et al. Family investigation of nephropathy and diabetes research group: MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet 2008; 40: 1185-1192
    • (2008) Nat Genet , vol.40 , pp. 1185-1192
    • Kao, W.H.1    Klag, M.J.2    Meoni, L.A.3
  • 8
    • 77955646179 scopus 로고    scopus 로고
    • Association of trypanolytic ApoL1 variants with kidney disease in African Americans
    • Genovese G, Friedman DJ, Ross MD et al. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science 2010; 329: 841-845
    • (2010) Science , vol.329 , pp. 841-845
    • Genovese, G.1    Friedman, D.J.2    Ross, M.D.3
  • 9
    • 80555148891 scopus 로고    scopus 로고
    • Population-based risk assessment of APOL1 on renal disease
    • Friedman DJ, Kozlitina J, Genovese G et al. Population-based risk assessment of APOL1 on renal disease. J Am Soc Nephrol 2011; 22: 2098-2105
    • (2011) J Am Soc Nephrol , vol.22 , pp. 2098-2105
    • Friedman, D.J.1    Kozlitina, J.2    Genovese, G.3
  • 10
    • 80555148890 scopus 로고    scopus 로고
    • Genetic variation in APOL1 associates with younger age at hemodialysis initiation
    • Kanji Z, Powe CE, Wenger JB et al. Genetic variation in APOL1 associates with younger age at hemodialysis initiation. J Am Soc Nephrol 2011; 22: 2091-2097
    • (2011) J Am Soc Nephrol , vol.22 , pp. 2091-2097
    • Kanji, Z.1    Powe, C.E.2    Wenger, J.B.3
  • 11
    • 79955529193 scopus 로고    scopus 로고
    • The APOL1 gene and allograft survival after kidney transplantation
    • Reeves-Daniel AM, DePalma JA, Bleyer AJ et al. The APOL1 gene and allograft survival after kidney transplantation. Am J Transplant 2011; 11: 1025-1030
    • (2011) Am J Transplant , vol.11 , pp. 1025-1030
    • Reeves-Daniel, A.M.1    Depalma, J.A.2    Bleyer, A.J.3
  • 12
    • 79957491313 scopus 로고    scopus 로고
    • The MYH9/APOL1 region and chronic kidney disease in European-Americans
    • O'Seaghdha CM, Parekh RS, Hwang SJ et al. The MYH9/APOL1 region and chronic kidney disease in European-Americans. Hum Mol Genet 2011; 20: 2450-2456
    • (2011) Hum Mol Genet , vol.20 , pp. 2450-2456
    • O'seaghdha, C.M.1    Parekh, R.S.2    Hwang, S.J.3
  • 13
    • 84859314693 scopus 로고    scopus 로고
    • Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
    • Cooke JN, Bostrom MA, Hicks PJ et al. Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans. Nephrol Dial Transplant 2012; 27: 1505-1511
    • (2012) Nephrol Dial Transplant , vol.27 , pp. 1505-1511
    • Cooke, J.N.1    Bostrom, M.A.2    Hicks, P.J.3
  • 14
    • 0034755959 scopus 로고    scopus 로고
    • Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes
    • Heath KE, Campos-Barros A, Toren A et al. Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes. Am J Hum Genet 2001; 69: 1033-1045
    • (2001) Am J Hum Genet , vol.69 , pp. 1033-1045
    • Heath, K.E.1    Campos-Barros, A.2    Toren, A.3
  • 15
    • 0037910378 scopus 로고    scopus 로고
    • MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
    • SeriM, Pecci A, Di Bari F et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003; 82: 203-215
    • (2003) Medicine (Baltimore) , vol.82 , pp. 203-215
    • Seri, M.1    Pecci, A.2    Di Bari, F.3
  • 16
    • 18244406592 scopus 로고    scopus 로고
    • Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions
    • Kunishima S, Matsushita T, Kojima T et al. Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions. J Hum Genet 2001; 46: 722-729
    • (2001) J Hum Genet , vol.46 , pp. 722-729
    • Kunishima, S.1    Matsushita, T.2    Kojima, T.3
  • 17
    • 77954224966 scopus 로고    scopus 로고
    • Glomerular pathology in autosomal dominant MYH9 spectrum disorders: What are the clues telling us about disease mechanism?
    • Kopp JB. Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism? Kidney Int 2010; 78: 130-133
    • (2010) Kidney Int , vol.78 , pp. 130-133
    • Kopp, J.B.1
  • 18
    • 9844267961 scopus 로고    scopus 로고
    • Normal distribution of collagen IV in renal basement membranes in Epstein's syndrome
    • Naito I, Nomura S, Inoue S et al. Normal distribution of collagen IV in renal basement membranes in Epstein's syndrome. J Clin Pathol 1997; 50: 919-922
    • (1997) J Clin Pathol , vol.50 , pp. 919-922
    • Naito, I.1    Nomura, S.2    Inoue, S.3
  • 19
    • 77954242769 scopus 로고    scopus 로고
    • Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease
    • Sekine T, Konno M, Sasaki S et al. Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease. Kidney Int 2010; 78: 207-214
    • (2010) Kidney Int , vol.78 , pp. 207-214
    • Sekine, T.1    Konno, M.2    Sasaki, S.3
  • 20
    • 84862908887 scopus 로고    scopus 로고
    • Mouse models of MYH9-related disease: Mutations in nonmuscle myosin II-A
    • Zhang Y, Conti MA, Malide D et al. Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A. Blood 2012; 119: 238-250
    • (2012) Blood , vol.119 , pp. 238-250
    • Zhang, Y.1    Conti, M.A.2    Malide, D.3
  • 21
    • 79956071512 scopus 로고    scopus 로고
    • Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy
    • Johnstone DB, Zhang J, George B et al. Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy. Mol Cell Biol 2011; 31: 2162-2170
    • (2011) Mol Cell Biol , vol.31 , pp. 2162-2170
    • Johnstone, D.B.1    Zhang, J.2    George, B.3
  • 22
    • 0026557199 scopus 로고
    • Myosin II distribution in neurons is consistent with a role in growth cone motility but not synaptic vesicle mobilization
    • Miller M, Bower E, Levitt P et al. Myosin II distribution in neurons is consistent with a role in growth cone motility but not synaptic vesicle mobilization. Neuron 1992; 8: 25-44
    • (1992) Neuron , vol.8 , pp. 25-44
    • Miller, M.1    Bower, E.2    Levitt, P.3
  • 23
    • 0035865524 scopus 로고    scopus 로고
    • Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
    • Kunishima S, Kojima T, Matsushita T et al. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). Blood 2001; 97: 1147-1149
    • (2001) Blood , vol.97 , pp. 1147-1149
    • Kunishima, S.1    Kojima, T.2    Matsushita, T.3
  • 24
    • 8844261172 scopus 로고    scopus 로고
    • Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: Hematological, nephrological, and otological studies of heterozygous KO mice
    • Matsushita T, Hayashi H, Kunishima S et al. Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice. Biochem Biophys Res Com 2004; 325: 1163-1171
    • (2004) Biochem Biophys Res Com , vol.325 , pp. 1163-1171
    • Matsushita, T.1    Hayashi, H.2    Kunishima, S.3
  • 25
    • 0033983608 scopus 로고    scopus 로고
    • Non-muscle myosin IIB-like immunoreactivity is present at the drebrin-binding cytoskeleton in neurons
    • Cheng XT, Hayashi K, Shirao T. Non-muscle myosin IIB-like immunoreactivity is present at the drebrin-binding cytoskeleton in neurons. Neurosci Res 2000; 36: 167-173
    • (2000) Neurosci Res , vol.36 , pp. 167-173
    • Cheng, X.T.1    Hayashi, K.2    Shirao, T.3
  • 26
    • 67649778673 scopus 로고    scopus 로고
    • Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-gamma
    • Harita Y, Kurihara H, Kosako H et al. Phosphorylation of nephrin triggers Ca2+ signaling by recruitment and activation of phospholipase C-gamma. J Biol Chem 2009; 284: 8951-8962
    • (2009) J Biol Chem , vol.284 , pp. 8951-8962
    • Harita, Y.1    Kurihara, H.2    Kosako, H.3
  • 27
    • 44049087922 scopus 로고    scopus 로고
    • Neph1, a component of the kidney slit diaphragm, is tyrosine- phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2
    • Harita Y, Kurihara H, Kosako H et al. Neph1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2. J Biol Chem 2008; 283: 9177-9186
    • (2008) J Biol Chem , vol.283 , pp. 9177-9186
    • Harita, Y.1    Kurihara, H.2    Kosako, H.3
  • 28
    • 84865216663 scopus 로고    scopus 로고
    • SIRPα interacts with nephrin at the podocyte slit diaphragm
    • Kajiho Y, Harita Y, Kurihara H et al. SIRPα interacts with nephrin at the podocyte slit diaphragm. FEBS J 2012; 279: 3010-3021
    • (2012) FEBS J , vol.279 , pp. 3010-3021
    • Kajiho, Y.1    Harita, Y.2    Kurihara, H.3
  • 29
    • 0031830798 scopus 로고    scopus 로고
    • Monoclonal antibody P-31 recognizes a novel intermediate filament-associated protein (p250) in rat podocytes
    • Kurihara H, Sunagawa N, Kobayashi T et al. Monoclonal antibody P-31 recognizes a novel intermediate filament-associated protein (p250) in rat podocytes. Am J Physiol 1998; 274: F986-F997
    • (1998) Am J Physiol , vol.274
    • Kurihara, H.1    Sunagawa, N.2    Kobayashi, T.3
  • 30
    • 0037377624 scopus 로고    scopus 로고
    • Intussusceptive capillary growth is required for glomerular repair in rat Thy-1. 1 nephritis
    • Notoya M, Shinosaki T, Kobayashi T et al. Intussusceptive capillary growth is required for glomerular repair in rat Thy-1.1 nephritis. Kidney Int 2003; 63: 1365-1373
    • (2003) Kidney Int , vol.63 , pp. 1365-1373
    • Notoya, M.1    Shinosaki, T.2    Kobayashi, T.3
  • 31
    • 0024318954 scopus 로고
    • Use of poly(vinylpyrrolidone) and poly(vinyl alcohol) for cryoultramicrotomy
    • Tokuyasu KT. Use of poly(vinylpyrrolidone) and poly(vinyl alcohol) for cryoultramicrotomy. Histochem J 1989; 21: 163-171
    • (1989) Histochem J , vol.21 , pp. 163-171
    • Tokuyasu, K.T.1
  • 32
    • 33645577952 scopus 로고    scopus 로고
    • Upregulation of nestin, vimentin, and desmin in rat podocytes in response to injury
    • Zou J, Yaoita E,Watanabe Y et al. Upregulation of nestin, vimentin, and desmin in rat podocytes in response to injury. Virchows Arch 2006; 448: 485-492
    • (2006) Virchows Arch , vol.448 , pp. 485-492
    • Zou, J.1    Yaoita, E.2    Watanabe, Y.3
  • 33
    • 33745039299 scopus 로고    scopus 로고
    • Immunoexpression of podocyte-associated preteins in acquired human glomerulopathies with nephrotic syndrome
    • Wagrowska-Danilewicz M, Stasikowska O, Danilewicz M. Immunoexpression of podocyte-associated preteins in acquired human glomerulopathies with nephrotic syndrome. Pol J Pathol 2006; 57: 17-21
    • (2006) Pol J Pathol , vol.57 , pp. 17-21
    • Wagrowska-Danilewicz, M.1    Stasikowska, O.2    Danilewicz, M.3
  • 34
    • 0035143252 scopus 로고    scopus 로고
    • Expression of nephrin in pediatric kidney diseases
    • Patrakka J, Ruotsalainen V, Ketola I et al. Expression of nephrin in pediatric kidney diseases. J Am Soc Nephrol 2001; 12: 289-296
    • (2001) J Am Soc Nephrol , vol.12 , pp. 289-296
    • Patrakka, J.1    Ruotsalainen, V.2    Ketola, I.3
  • 35
    • 1542359928 scopus 로고    scopus 로고
    • Expression of nephrin in acquired forms of nephrotic syndrome in childhood
    • Hingorani SR, Finn LS, Kowalewska J et al. Expression of nephrin in acquired forms of nephrotic syndrome in childhood. Pediatr Nephrol 2004; 19: 300-305
    • (2004) Pediatr Nephrol , vol.19 , pp. 300-305
    • Hingorani, S.R.1    Finn, L.S.2    Kowalewska, J.3
  • 36
    • 12244254488 scopus 로고    scopus 로고
    • Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome
    • Wernerson A, Duner F, Pettersson E et al. Altered ultrastructural distribution of nephrin in minimal change nephrotic syndrome. Nephrol Dial Transplant 2003; 18: 70-76
    • (2003) Nephrol Dial Transplant , vol.18 , pp. 70-76
    • Wernerson, A.1    Duner, F.2    Pettersson, E.3
  • 37
    • 0242441925 scopus 로고    scopus 로고
    • Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome
    • Guan N, Ding J, Zhang J et al. Expression of nephrin, podocin, alpha-actinin, and WT1 in children with nephrotic syndrome. Pediatr Nephrol. 2003; 18: 1122-1127
    • (2003) Pediatr Nephrol. , vol.18 , pp. 1122-1127
    • Guan, N.1    Ding, J.2    Zhang, J.3
  • 38
    • 0041842626 scopus 로고    scopus 로고
    • Expression of podocyteassociated molecules in acquired human kidney diseases
    • Koop K, Eikmans M, Baelde HJ et al. Expression of podocyteassociated molecules in acquired human kidney diseases. J Am Soc Nephrol 2003; 14: 2063-2071
    • (2003) J Am Soc Nephrol , vol.14 , pp. 2063-2071
    • Koop, K.1    Eikmans, M.2    Baelde, H.J.3
  • 40
    • 0036138503 scopus 로고    scopus 로고
    • Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes
    • Arrondel C, Vodovar N, Knebelmann B et al. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. J Am Soc Nephrol 2002; 13: 65-74
    • (2002) J Am Soc Nephrol , vol.13 , pp. 65-74
    • Arrondel, C.1    Vodovar, N.2    Knebelmann, B.3
  • 41
    • 0037225967 scopus 로고    scopus 로고
    • Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
    • Ghiggeri GM, Caridi G, Magrini U et al. Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome). Am J Kidney Dis 2003; 41: 95-104
    • (2003) Am J Kidney Dis , vol.41 , pp. 95-104
    • Ghiggeri, G.M.1    Caridi, G.2    Magrini, U.3
  • 42
    • 66549123467 scopus 로고    scopus 로고
    • Of mice and men: Relevance of cellular and molecular characterizations of myosin IIA to MYH9-related human disease
    • Even-Ram S, Yamada KM.: Of mice and men: relevance of cellular and molecular characterizations of myosin IIA to MYH9-related human disease. Cell Adh Migr 2007; 1: 152-155
    • (2007) Cell Adh Migr , vol.1 , pp. 152-155
    • Even-Ram, S.1    Yamada, K.M.2
  • 43
    • 80052435507 scopus 로고    scopus 로고
    • Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes
    • Babayeva S, Miller M, Zilber Y et al. Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes. Pediatr Nephrol 2011; 26: 1071-1081
    • (2011) Pediatr Nephrol , vol.26 , pp. 1071-1081
    • Babayeva, S.1    Miller, M.2    Zilber, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.