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Volumn 23, Issue 17, 2014, Pages 4543-4558

Overexpression of LARGE suppresses muscle regeneration via down-regulation of insulin-like growth factor 1 and aggravates muscular dystrophy in mice

Author keywords

[No Author keywords available]

Indexed keywords

FUKUTIN; LAMININ ALPHA2; LIKE ACETYLGLUCOSAMINYLTRANSFERASE; SOMATOMEDIN C; TRANSFERASE; UNCLASSIFIED DRUG; DYSTROGLYCAN; FCMD PROTEIN, MOUSE; LARGE PROTEIN, MOUSE; N ACETYLGLUCOSAMINYLTRANSFERASE; PROTEIN;

EID: 84905668632     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu168     Document Type: Article
Times cited : (24)

References (66)
  • 4
    • 0027275643 scopus 로고
    • A role for the dystrophin- glycoprotein complex as a transmembrane linker between laminin and actin
    • Ervasti, J.M. and Campbell, K.P. (1993) A role for the dystrophin- glycoprotein complex as a transmembrane linker between laminin and actin. J. Cell. Biol., 122, 809-823.
    • (1993) J. Cell. Biol. , vol.122 , pp. 809-823
    • Ervasti, J.M.1    Campbell, K.P.2
  • 5
    • 0028805790 scopus 로고
    • Identification and characterization of the dystrophin anchoring site on β-dystroglycan
    • Jung, D., Yang, B., Meyer, J., Chamberlain, J.S. and Campbell, K.P. (1995) Identification and characterization of the dystrophin anchoring site on β-dystroglycan. J. Biol. Chem., 270, 27305-27310.
    • (1995) J. Biol. Chem. , vol.270 , pp. 27305-27310
    • Jung, D.1    Yang, B.2    Meyer, J.3    Chamberlain, J.S.4    Campbell, K.P.5
  • 7
    • 38649099374 scopus 로고    scopus 로고
    • Processing and secretion of the N-terminal domain of α-dystroglycan in cell culture media
    • Saito, F., Saito-Arai, Y., Nakamura, A., Shimizu, T. and Matsumura, K. (2008) Processing and secretion of the N-terminal domain of α-dystroglycan in cell culture media. FEBS Lett., 582, 439-444.
    • (2008) FEBS Lett. , vol.582 , pp. 439-444
    • Saito, F.1    Saito-Arai, Y.2    Nakamura, A.3    Shimizu, T.4    Matsumura, K.5
  • 10
    • 84855515852 scopus 로고    scopus 로고
    • Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE
    • Inamori, K., Yoshida-Moriguchi, T., Hara, Y., Anderson, M.E., Yu, L. and Campbell, K.P. (2012) Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE. Science, 335, 93-96.
    • (2012) Science , vol.335 , pp. 93-96
    • Inamori, K.1    Yoshida-Moriguchi, T.2    Hara, Y.3    Anderson, M.E.4    Yu, L.5    Campbell, K.P.6
  • 13
    • 84862226445 scopus 로고    scopus 로고
    • Dystroglycan and dystroglycanopathies: report of the 187th ENMC Workshop 11-13 November 2011, Naarden, The Netherlands
    • Brown, S.C. and Winder, S.J. (2011)Dystroglycan and dystroglycanopathies: report of the 187th ENMC Workshop 11-13 November 2011, Naarden, The Netherlands. Neuromuscul. Disord., 22, 659-668.
    • (2011) Neuromuscul. Disord , vol.22 , pp. 659-668
    • Brown, S.C.1    Winder, S.J.2
  • 17
    • 0347635516 scopus 로고    scopus 로고
    • Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity
    • Manya, H., Chiba, A., Yoshida, A., Wang, X., Chiba, Y., Jigami, Y., Margolis, R.U. and Endo, T. (2004) Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity. Proc. Natl. Acad. Sci. USA, 101, 500-505.
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 500-505
    • Manya, H.1    Chiba, A.2    Yoshida, A.3    Wang, X.4    Chiba, Y.5    Jigami, Y.6    Margolis, R.U.7    Endo, T.8
  • 20
    • 10744226857 scopus 로고    scopus 로고
    • Mutations in the humanLARGEgene causeMDC1D,a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan
    • Longman, C., Brockington, M., Torelli, S., Jimenez-Mallebrera, C., Kennedy, C., Khalil, N., Feng, L., Saran, R.K., Voit, T., Merlini, L. et al. (2003) Mutations in the humanLARGEgene causeMDC1D,a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan. Hum. Mol. Genet., 12, 2853-2861.
    • (2003) Hum. Mol. Genet. , vol.12 , pp. 2853-2861
    • Longman, C.1    Brockington, M.2    Torelli, S.3    Jimenez-Mallebrera, C.4    Kennedy, C.5    Khalil, N.6    Feng, L.7    Saran, R.K.8    Voit, T.9    Merlini, L.10
  • 25
    • 84880285119 scopus 로고    scopus 로고
    • Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan
    • Carss, K.J., Stevens, E., Foley, A.R., Cirak, S., Riemersma, M., Torelli, S., Hoischen, A., Willer, T., van, S.M., Moore, S.A. et al. (2013) Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan. Am. J. Hum. Genet., 93, 29-41.
    • (2013) Am. J. Hum. Genet. , vol.93 , pp. 29-41
    • Carss, K.J.1    Stevens, E.2    Foley, A.R.3    Cirak, S.4    Riemersma, M.5    Torelli, S.6    Hoischen, A.7    Willer, T.8    van, S.M.9    Moore, S.A.10
  • 29
    • 0035212037 scopus 로고    scopus 로고
    • Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin a2 deficiency and abnormal glycosylation of α-dystroglycan
    • Brockington, M., Blake, D.J., Prandini, P., Brown, S.C., Torelli, S., Benson, M.A., Ponting, C.P., Estournet, B., Romero, N.B., Mercuri, E. et al. (2001) Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin a2 deficiency and abnormal glycosylation of α-dystroglycan. Am. J. Hum. Genet., 69, 1198-1209.
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 1198-1209
    • Brockington, M.1    Blake, D.J.2    Prandini, P.3    Brown, S.C.4    Torelli, S.5    Benson, M.A.6    Ponting, C.P.7    Estournet, B.8    Romero, N.B.9    Mercuri, E.10
  • 35
    • 4444234437 scopus 로고    scopus 로고
    • The congenital muscular dystrophies in 2004: a century of exciting progress
    • Muntoni, F. and Voit, T. (2004) The congenital muscular dystrophies in 2004: a century of exciting progress. Neuromuscul. Disord., 14, 635-649.
    • (2004) Neuromuscul. Disord. , vol.14 , pp. 635-649
    • Muntoni, F.1    Voit, T.2
  • 39
    • 0029024847 scopus 로고
    • Identification of a novel mutant transcript of laminin a2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice
    • Sunada, Y., Bernier, S.M., Utani, A., Yamada, Y. and Campbell, K.P. (1995) Identification of a novel mutant transcript of laminin a2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice. Hum. Mol. Genet., 4, 1055-1061.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 1055-1061
    • Sunada, Y.1    Bernier, S.M.2    Utani, A.3    Yamada, Y.4    Campbell, K.P.5
  • 40
    • 84880256175 scopus 로고    scopus 로고
    • Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression
    • Kanagawa, M., Yu, C.C., Ito, C., Fukada, S., Hozoji-Inada, M., Chiyo, T., Kuga, A., Matsuo, M., Sato, K., Yamaguchi, M. et al. (2013) Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression. Hum. Mol. Genet., 22, 3003-3015.
    • (2013) Hum. Mol. Genet. , vol.22 , pp. 3003-3015
    • Kanagawa, M.1    Yu, C.C.2    Ito, C.3    Fukada, S.4    Hozoji-Inada, M.5    Chiyo, T.6    Kuga, A.7    Matsuo, M.8    Sato, K.9    Yamaguchi, M.10
  • 42
    • 0033581703 scopus 로고    scopus 로고
    • The laminin a2 expressed by dystrophic dy(2J) mice is defective in its ability to form polymers
    • Colognato, H. and Yurchenco, P.D. (1999) The laminin a2 expressed by dystrophic dy(2J) mice is defective in its ability to form polymers. Curr. Biol., 9, 1327-1330.
    • (1999) Curr. Biol. , vol.9 , pp. 1327-1330
    • Colognato, H.1    Yurchenco, P.D.2
  • 43
    • 0030783172 scopus 로고    scopus 로고
    • Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
    • Straub, V., Rafael, J.A., Chamberlain, J.S. and Campbell, K.P. (1997) Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J. Cell. Biol., 139, 375-385.
    • (1997) J. Cell. Biol. , vol.139 , pp. 375-385
    • Straub, V.1    Rafael, J.A.2    Chamberlain, J.S.3    Campbell, K.P.4
  • 44
    • 0028212874 scopus 로고
    • Expression pattern of M-cadherin in normal, denervated, and regenerating mouse muscles
    • Irintchev, A., Zeschnigk, M., Starzinski-Powitz, A. and Wernig, A. (1994) Expression pattern of M-cadherin in normal, denervated, and regenerating mouse muscles. Dev. Dyn., 199, 326-337.
    • (1994) Dev. Dyn. , vol.199 , pp. 326-337
    • Irintchev, A.1    Zeschnigk, M.2    Starzinski-Powitz, A.3    Wernig, A.4
  • 45
    • 77955173286 scopus 로고    scopus 로고
    • Elevated satellite cell number in Duchenne muscular dystrophy
    • Kottlors, M. and Kirschner, J. (2010) Elevated satellite cell number in Duchenne muscular dystrophy. Cell Tissue Res., 340, 541-548.
    • (2010) Cell Tissue Res. , vol.340 , pp. 541-548
    • Kottlors, M.1    Kirschner, J.2
  • 47
    • 69949091564 scopus 로고    scopus 로고
    • Role of IGF-I in skeletal muscle mass maintenance
    • Clemmons, D.R. (2009) Role of IGF-I in skeletal muscle mass maintenance. Trends Endocrinol. Metab., 20, 349-356.
    • (2009) Trends Endocrinol. Metab. , vol.20 , pp. 349-356
    • Clemmons, D.R.1
  • 48
    • 78650845413 scopus 로고    scopus 로고
    • Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscle
    • Brockington, M., Torelli, S., Sharp, P.S., Liu, K., Cirak, S., Brown, S.C., Wells, D.J. and Muntoni, F. (2010) Transgenic overexpression of LARGE induces α-dystroglycan hyperglycosylation in skeletal and cardiac muscle. PLoS One, 5, e14434.
    • (2010) PLoS One , vol.5
    • Brockington, M.1    Torelli, S.2    Sharp, P.S.3    Liu, K.4    Cirak, S.5    Brown, S.C.6    Wells, D.J.7    Muntoni, F.8
  • 49
    • 84873036427 scopus 로고    scopus 로고
    • Muscle-specific expression of LARGE restores neuromuscular transmission deficits in dystrophic LARGEmyd mice
    • Gumerson, J.D., Davis, C.S., Kabaeva, Z.T., Hayes, J.M., Brooks, S.V. and Michele, D.E. (2013) Muscle-specific expression of LARGE restores neuromuscular transmission deficits in dystrophic LARGEmyd mice. Hum. Mol. Genet., 22, 757-768.
    • (2013) Hum. Mol. Genet. , vol.22 , pp. 757-768
    • Gumerson, J.D.1    Davis, C.S.2    Kabaeva, Z.T.3    Hayes, J.M.4    Brooks, S.V.5    Michele, D.E.6
  • 51
    • 84864317860 scopus 로고    scopus 로고
    • Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage
    • Relaix, F. and Zammit, P.S. (2012) Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage. Development, 139, 2845-2856.
    • (2012) Development , vol.139 , pp. 2845-2856
    • Relaix, F.1    Zammit, P.S.2
  • 54
    • 0036544519 scopus 로고    scopus 로고
    • Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice
    • Barton, E.R., Morris, L., Musaro, A., Rosenthal, N. and Sweeney, H.L. (2002) Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice. J. Cell. Biol., 157, 137-148.
    • (2002) J. Cell. Biol. , vol.157 , pp. 137-148
    • Barton, E.R.1    Morris, L.2    Musaro, A.3    Rosenthal, N.4    Sweeney, H.L.5
  • 55
    • 79957521292 scopus 로고    scopus 로고
    • Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A
    • Kumar, A., Yamauchi, J., Girgenrath, T. and Girgenrath, M. (2011) Muscle-specific expression of insulin-like growth factor 1 improves outcome in Lama2Dy-w mice, a model for congenital muscular dystrophy type 1A. Hum. Mol. Genet., 20, 2333-2343.
    • (2011) Hum. Mol. Genet. , vol.20 , pp. 2333-2343
    • Kumar, A.1    Yamauchi, J.2    Girgenrath, T.3    Girgenrath, M.4
  • 56
    • 0030934472 scopus 로고    scopus 로고
    • The mitogenic and myogenic actions of insulin-like growth factors utilize distinct signaling pathways
    • Coolican, S.A., Samuel, D.S., Ewton, D.Z., McWade, F.J. and Florini, J.R. (1997) The mitogenic and myogenic actions of insulin-like growth factors utilize distinct signaling pathways. J. Biol. Chem., 272, 6653-6662.
    • (1997) J. Biol. Chem. , vol.272 , pp. 6653-6662
    • Coolican, S.A.1    Samuel, D.S.2    Ewton, D.Z.3    McWade, F.J.4    Florini, J.R.5
  • 57
    • 0035914338 scopus 로고    scopus 로고
    • Insulin-like growth factor-mediated muscle differentiation: collaboration between phosphatidylinositol 3-kinase-Akt-signaling pathways and myogenin
    • Tureckova, J., Wilson, E.M., Cappalonga, J.L. and Rotwein, P. (2001) Insulin-like growth factor-mediated muscle differentiation: collaboration between phosphatidylinositol 3-kinase-Akt-signaling pathways and myogenin. J. Biol. Chem., 276, 39264-39270.
    • (2001) J. Biol. Chem. , vol.276 , pp. 39264-39270
    • Tureckova, J.1    Wilson, E.M.2    Cappalonga, J.L.3    Rotwein, P.4
  • 58
    • 0034027602 scopus 로고    scopus 로고
    • Adhesion-dependent tyrosine phosphorylation of β-dystroglycan regulates its interaction with utrophin
    • James, M., Nuttall, A., Ilsley, J.L., Ottersbach, K., Tinsley, J.M., Sudol, M. and Winder, S.J. (2000) Adhesion-dependent tyrosine phosphorylation of β-dystroglycan regulates its interaction with utrophin. J. Cell. Sci., 113, 1717-1726.
    • (2000) J. Cell. Sci. , vol.113 , pp. 1717-1726
    • James, M.1    Nuttall, A.2    Ilsley, J.L.3    Ottersbach, K.4    Tinsley, J.M.5    Sudol, M.6    Winder, S.J.7
  • 59
    • 0034903234 scopus 로고    scopus 로고
    • The interaction of dystrophin with β-dystroglycan is regulated by tyrosine phosphorylation
    • Ilsley, J.L., Sudol, M. and Winder, S.J. (2001) The interaction of dystrophin with β-dystroglycan is regulated by tyrosine phosphorylation. Cell Signal., 13, 625-632.
    • (2001) Cell Signal. , vol.13 , pp. 625-632
    • Ilsley, J.L.1    Sudol, M.2    Winder, S.J.3
  • 60
    • 0035807788 scopus 로고    scopus 로고
    • Tyrosine phosphorylation of β-dystroglycan at itsWWdomain bindingmotif, PPxY, recruits SH2 domain containing proteins
    • Sotgia, F., Lee, H., Bedford, M.T., Petrucci, T., Sudol, M. and Lisanti, M.P. (2001) Tyrosine phosphorylation of β-dystroglycan at itsWWdomain bindingmotif, PPxY, recruits SH2 domain containing proteins. Biochemistry, 40, 14585-14592.
    • (2001) Biochemistry , vol.40 , pp. 14585-14592
    • Sotgia, F.1    Lee, H.2    Bedford, M.T.3    Petrucci, T.4    Sudol, M.5    Lisanti, M.P.6
  • 61
    • 0036842214 scopus 로고    scopus 로고
    • Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells
    • Langenbach, K.J. and Rando, T.A. (2002) Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells. Muscle Nerve., 26, 644-653.
    • (2002) Muscle Nerve. , vol.26 , pp. 644-653
    • Langenbach, K.J.1    Rando, T.A.2
  • 62
    • 37349039361 scopus 로고    scopus 로고
    • Laminin-induced activation of Rac1 and JNKp46 is initiated by Src family kinases and mimics the effects of skeletal muscle contraction
    • Zhou, Y., Jiang, D., Thomason, D.B. and Jarrett, H.W. (2007) Laminin-induced activation of Rac1 and JNKp46 is initiated by Src family kinases and mimics the effects of skeletal muscle contraction. Biochemistry, 46, 14907-14916.
    • (2007) Biochemistry , vol.46 , pp. 14907-14916
    • Zhou, Y.1    Jiang, D.2    Thomason, D.B.3    Jarrett, H.W.4
  • 63
    • 84855889400 scopus 로고    scopus 로고
    • Differential glycosylation of α-dystroglycan and proteins other than α-dystroglycan by like-glycosyltransferase
    • Zhang, P. and Hu, H. (2012) Differential glycosylation of α-dystroglycan and proteins other than α-dystroglycan by like-glycosyltransferase. Glycobiology, 22, 235-247.
    • (2012) Glycobiology , vol.22 , pp. 235-247
    • Zhang, P.1    Hu, H.2
  • 65
    • 84875465831 scopus 로고    scopus 로고
    • Adeno-associated viral-mediated LARGE gene therapy rescues the muscular dystrophic phenotype in mouse models of dystroglycanopathy
    • Yu, M., He, Y., Wang, K., Zhang, P., Zhang, S. and Hu, H. (2013) Adeno-associated viral-mediated LARGE gene therapy rescues the muscular dystrophic phenotype in mouse models of dystroglycanopathy. Hum. Gene. Ther., 24, 317-330.
    • (2013) Hum. Gene. Ther. , vol.24 , pp. 317-330
    • Yu, M.1    He, Y.2    Wang, K.3    Zhang, P.4    Zhang, S.5    Hu, H.6
  • 66
    • 34249786552 scopus 로고    scopus 로고
    • Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice
    • Saito, F., Masaki, T., Saito, Y., Nakamura, A., Takeda, S., Shimizu, T., Toda, T. and Matsumura, K. (2007) Defective peripheral nerve myelination and neuromuscular junction formation in fukutin-deficient chimeric mice. J. Neurochem., 101, 1712-1722.
    • (2007) J. Neurochem. , vol.101 , pp. 1712-1722
    • Saito, F.1    Masaki, T.2    Saito, Y.3    Nakamura, A.4    Takeda, S.5    Shimizu, T.6    Toda, T.7    Matsumura, K.8


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