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Volumn 71, Issue 10, 2012, Pages 894-906

Muscle fiber atrophy and regeneration coexist in collagen VI-deficient human muscle: Role of calpain-3 and nuclear factor-κB signaling

Author keywords

Calpain 3; Collagen type VI; Extracellular matrix; Muscle atrophy; Muscle regeneration; NF B; Ullrich congenital muscular dystrophy

Indexed keywords

ATROGIN 1; CALPAIN 3; COLLAGEN TYPE 6; I KAPPA B; MESSENGER RNA; MUSCLE RING FINGER 1 PROTEIN; PROTEASOME; RNA; UBIQUITIN;

EID: 84866728930     PISSN: 00223069     EISSN: 15546578     Source Type: Journal    
DOI: 10.1097/NEN.0b013e31826c6f7b     Document Type: Article
Times cited : (22)

References (35)
  • 1
    • 79954517898 scopus 로고    scopus 로고
    • The collagen viyrelated myopathies ullrich congenital muscular dystrophy and bethlem myopathy
    • Bonnemann CG. The collagen VIYrelated myopathies Ullrich congenital muscular dystrophy and Bethlem myopathy. Handb Clin Neurol 2011; 101:81-96
    • (2011) Handb Clin Neurol , vol.101 , pp. 81-89
    • Bonnemann, C.G.1
  • 2
    • 68249154901 scopus 로고    scopus 로고
    • Natural history of ullrich congenital muscular dystrophy
    • Nadeau A, Kinali M, Main M, et al. Natural history of Ullrich congenital muscular dystrophy. Neurology 2009;73:25-31
    • (2009) Neurology , vol.73 , pp. 25-23
    • Nadeau, A.1    Kinali, M.2    Main, M.3
  • 3
    • 18544371603 scopus 로고    scopus 로고
    • Congenital muscular dystrophy: Molecular and cellular aspects
    • Jimenez-Mallebrera C, Brown SC, Sewry CA, et al. Congenital muscular dystrophy: Molecular and cellular aspects. Cell Mol Life Sci 2005;62: 809-23
    • (2005) Cell Mol Life Sci , vol.62 , pp. 809-802
    • Jimenez-Mallebrera, C.1    Brown, S.C.2    Sewry, C.A.3
  • 4
    • 51349161707 scopus 로고    scopus 로고
    • Predominant fiber atrophy and fiber type disproportion in early ullrich disease
    • Schessl J, Goemans NM, Magold AI, et al. Predominant fiber atrophy and fiber type disproportion in early Ullrich disease. Muscle Nerve 2008;38: 1184-91
    • (2008) Muscle Nerve , vol.38 , pp. 1184-1189
    • Schessl, J.1    Goemans, N.M.2    Magold, A.I.3
  • 5
    • 10744233522 scopus 로고    scopus 로고
    • Mitochondrial dysfunction and apoptosis in myopathic mice with collagen vi deficiency
    • Irwin WA, Bergamin N, Sabatelli P, et al. Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency. Nat Genet 2003;35:367-71
    • (2003) Nat Genet , vol.35 , pp. 367-367
    • Irwin, W.A.1    Bergamin, N.2    Sabatelli, P.3
  • 7
    • 24944559356 scopus 로고    scopus 로고
    • Collagen vi related muscle disorders
    • Lampe AK, Bushby KM. Collagen VI related muscle disorders. J Med Genet 2005;42:673-85
    • (2005) J Med Genet , vol.42 , pp. 673-678
    • Lampe, A.K.1    Bushby, K.M.2
  • 8
    • 0030296598 scopus 로고    scopus 로고
    • Collagen vi regulates normal and transformed mesenchymal cell proliferation in vitro
    • Atkinson JC, Ruhl M, Becker J, et al. Collagen VI regulates normal and transformed mesenchymal cell proliferation in vitro. Exp Cell Res 1996; 228:283-91
    • (1996) Exp Cell Res , vol.228 , pp. 283-289
    • Atkinson, J.C.1    Ruhl, M.2    Becker, J.3
  • 9
    • 0041023717 scopus 로고    scopus 로고
    • Soluble collagen vi induces tyrosine phosphorylation of paxillin and focal adhesion kinase and activates the map kinase erk2 in fibroblasts
    • Ruhl M, Johannsen M, Atkinson J, et al. Soluble collagen VI induces tyrosine phosphorylation of paxillin and focal adhesion kinase and activates the MAP kinase erk2 in fibroblasts. Exp Cell Res 1999;250:548-57
    • (1999) Exp Cell Res , vol.250 , pp. 548-545
    • Ruhl, M.1    Johannsen, M.2    Atkinson, J.3
  • 10
    • 0036022140 scopus 로고    scopus 로고
    • Ng2 proteoglycan mediates beta1 integrinyindependent cell adhesion and spreading on collagen vi
    • Tillet E, Gential B, Garrone R, et al. NG2 proteoglycan mediates beta1 integrinYindependent cell adhesion and spreading on collagen VI. J Cell Biochem 2002;86:726-36
    • (2002) J Cell Biochem , vol.86 , pp. 726-723
    • Tillet, E.1    Gential, B.2    Garrone, R.3
  • 11
    • 42949160078 scopus 로고    scopus 로고
    • Muscle interstitial fibroblasts are the main source of collagen vi synthesis in skeletal muscle: Implications for congenital muscular dystrophy types ullrich and bethlem
    • Zou Y, Zhang RZ, Sabatelli P, et al. Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: Implications for congenital muscular dystrophy types Ullrich and Bethlem. J Neuropathol Exp Neurol 2008;67:144-54
    • (2008) J Neuropathol Exp Neurol , vol.67 , pp. 144-145
    • Zou, Y.1    Zhang, R.Z.2    Sabatelli, P.3
  • 12
    • 0037167523 scopus 로고    scopus 로고
    • Ullrich disease: Collagen vi deficiency: Em suggests a new basis for muscular weakness
    • Ishikawa H, Sugie K, Murayama K, et al. Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness. Neurology 2002;59:920-3
    • (2002) Neurology , vol.59 , pp. 920-923
    • Ishikawa, H.1    Sugie, K.2    Murayama, K.3
  • 13
    • 78149319082 scopus 로고    scopus 로고
    • Autophagy is defective in collagen vi muscular dystrophies, and its reactivation rescues myofiber degeneration
    • Grumati P, Coletto L, Sabatelli P, et al. Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration. Nat Med 2010;16:1313-20
    • (2010) Nat Med , vol.16 , pp. 1313-1312
    • Grumati, P.1    Coletto, L.2    Sabatelli, P.3
  • 15
    • 54849438119 scopus 로고    scopus 로고
    • Collagen vi glycine mutations: Perturbed assembly and a spectrum of clinical severity
    • Pace RA, Peat RA, Baker NL, et al. Collagen VI glycine mutations: Perturbed assembly and a spectrum of clinical severity. Ann Neurol 2008; 64:294-303
    • (2008) Ann Neurol , vol.64 , pp. 294-293
    • Pace, R.A.1    Peat, R.A.2    Baker, N.L.3
  • 16
    • 0032160138 scopus 로고    scopus 로고
    • The essentially of histo- and cytochemical studies muscle in the investigation of neuromuscular disease
    • Engel WK. The essentiality of histo-And cytochemical studies of skeletal muscle in the investigation of neuromuscular disease. 1962. Neurology 1998;51:655 (Pubitemid 28449235)
    • (1998) Neurology , vol.51 , Issue.3 , pp. 655
    • Engel, W.K.1
  • 17
    • 79953738995 scopus 로고    scopus 로고
    • The role and regulation of mafbx/atrogin-1 and murf1 in skeletal muscle atrophy
    • Foletta VC, White LJ, Larsen AE, et al. The role and regulation of MAFbx/atrogin-1 and MuRF1 in skeletal muscle atrophy. Pflugers Arch 2011;461:325-35
    • (2011) Pflugers Arch , vol.461 , pp. 325-323
    • Foletta, V.C.1    White, L.J.2    Larsen, A.E.3
  • 18
    • 6944226810 scopus 로고    scopus 로고
    • Disuse atrophy and exercise rehabilitation in humans profoundly affects the expression of genes associated with the regulation of skeletal muscle mass
    • DOI 10.1096/fj.03-1228fje
    • Jones SW, Hill RJ, Krasney PA, et al. Disuse atrophy and exercise rehabilitation in humans profoundly affects the expression of genes associated with the regulation of skeletal muscle mass. FASEB J 2004; 18:1025-7 (Pubitemid 39561513)
    • (2004) FASEB Journal , vol.18 , Issue.9 , pp. 1025-1027
    • Jones, S.W.1    Hill, R.J.2    Krasney, P.A.3    O'Conner, B.4    Peirce, N.5    Greenhaff, P.L.6
  • 19
    • 0034937370 scopus 로고    scopus 로고
    • Pathophysiology of limb girdle muscular dystrophy type 2a: Hypothesis and new insights into the ikappabalpha/nf-kappab survival pathway in skeletal muscle
    • Baghdiguian S, Richard I, Martin M, et al. Pathophysiology of limb girdle muscular dystrophy type 2A: Hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle. J Mol Med (Berl) 2001;79:254-61
    • (2001) J Mol Med (Berl , vol.79 , pp. 254-256
    • Baghdiguian, S.1    Richard, I.2    Martin, M.3
  • 20
    • 0032941594 scopus 로고    scopus 로고
    • Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the ikappab alpha/nf-kappab pathway in limb-girdle muscular dystrophy type 2a
    • Baghdiguian S, Martin M, Richard I, et al. Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A. Nat Med 1999;5:503-11
    • (1999) Nat Med , vol.5 , pp. 503-501
    • Baghdiguian, S.1    Martin, M.2    Richard, I.3
  • 21
    • 33750320417 scopus 로고    scopus 로고
    • The skeletal muscle satellite cell: The stem cell that came in from the cold
    • Zammit PS, Partridge TA, Yablonka-Reuveni Z. The skeletal muscle satellite cell: The stem cell that came in from the cold. J Histochem Cytochem 2006;54:1177-91
    • (2006) J Histochem Cytochem , vol.54 , pp. 1177-1179
    • Zammit, P.S.1    Partridge, T.A.2    Yablonka-Reuveni, Z.3
  • 22
    • 33744518925 scopus 로고    scopus 로고
    • Pax7 and myogenic progression in skeletal muscle satellite cells
    • Zammit PS, Relaix F, Nagata Y, et al. Pax7 and myogenic progression in skeletal muscle satellite cells. J Cell Sci 2006;119:1824-32
    • (2006) J Cell Sci , vol.119 , pp. 1824-1823
    • Zammit, P.S.1    Relaix, F.2    Nagata, Y.3
  • 23
    • 0031474106 scopus 로고    scopus 로고
    • Expression of myogenic regulatory factors (mrfs) in human neuromuscular disorders
    • Olive M, Martinez-Matos JA, Pirretas P, et al. Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders. Neuropathol Appl Neurobiol 1997;23:475-82
    • (1997) Neuropathol Appl Neurobiol , vol.23 , pp. 475-478
    • Olive, M.1    Martinez-Matos, J.A.2    Pirretas, P.3
  • 24
    • 0018424046 scopus 로고
    • Quantitative ultrastructural study of muscle satellite cells in Duchenne dystrophy
    • Wakayama Y, Schotland DL, Bonilla E, et al. Quantitative ultrastructural study of muscle satellite cells in Duchenne dystrophy. Neurology 1979; 29:401-7 (Pubitemid 9111029)
    • (1979) Neurology , vol.29 , Issue.3 , pp. 401-407
    • Wakayama, Y.1    Schotland, D.L.2    Bonilla, E.3    Orecchio, E.4
  • 25
    • 70449724660 scopus 로고    scopus 로고
    • Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1
    • Thornell LE, Lindstom M, Renault V, et al. Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1. Neuropathol Appl Neurobiol 2009;35:603-13
    • (2009) Neuropathol Appl Neurobiol , vol.35 , pp. 603-601
    • Thornell, L.E.1    Lindstom, M.2    Renault, V.3
  • 26
    • 0033958440 scopus 로고    scopus 로고
    • Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
    • Decary S, Hamida CB, Mouly V, et al. Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children. Neuromuscul Disord 2000;10:113-20
    • (2000) Neuromuscul Disord , vol.10 , pp. 113-112
    • Decary, S.1    Hamida, C.B.2    Mouly, V.3
  • 28
    • 0347285363 scopus 로고    scopus 로고
    • Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression
    • Lecker SH, Jagoe RT, Gilbert A, et al. Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression. FASEB J 2004;18:39-51
    • (2004) FASEB J , vol.18 , pp. 39-35
    • Lecker, S.H.1    Jagoe, R.T.2    Gilbert, A.3
  • 29
    • 67650258512 scopus 로고    scopus 로고
    • Atrogin-1, murf1, and foxo, as well as phosphorylated gsk-3beta and 4e-bp1 are reduced in skeletal muscle of chronic spinal cord-injured patients
    • Leger B, Senese R, Al-Khodairy AW, et al. Atrogin-1, MuRF1, and FoXO, as well as phosphorylated GSK-3beta and 4E-BP1 are reduced in skeletal muscle of chronic spinal cord-injured patients. Muscle Nerve 2009;40:69-78
    • (2009) Muscle Nerve , vol.40 , pp. 69-67
    • Leger, B.1    Senese, R.2    Al-Khodairy, A.W.3
  • 30
    • 0037101928 scopus 로고    scopus 로고
    • Molecular adaptations of neuromuscular disease-Associated proteins in response to eccentric exercise in human skeletal muscle
    • Feasson L, Stockholm D, Freyssenet D, et al. Molecular adaptations of neuromuscular disease-Associated proteins in response to eccentric exercise in human skeletal muscle. J Physiol 2002;543:297-306
    • (2002) J Physiol , vol.543 , pp. 297-293
    • Feasson, L.1    Stockholm, D.2    Freyssenet, D.3
  • 31
    • 0035836751 scopus 로고    scopus 로고
    • Secondary calpain3 deficiency in 2q-linked muscular dystrophy: Titin is the candidate gene
    • Haravuori H, Vihola A, Straub V, et al. Secondary calpain3 deficiency in 2q-linked muscular dystrophy: Titin is the candidate gene. Neurology 2001;56:869-77
    • (2001) Neurology , vol.56 , pp. 869-867
    • Haravuori, H.1    Vihola, A.2    Straub, V.3
  • 34
    • 77952525170 scopus 로고    scopus 로고
    • Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: Col6a1-/-And mdx
    • Canato M, Dal Maschio M, Sbrana F, et al. Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: Col6a1-/-And mdx. J Biomed Biotechnol 2010;2010:981945
    • (2010) J Biomed Biotechnol , vol.2010 , pp. 981945
    • Canato, M.1    Dal Maschio, M.2    Sbrana, F.3
  • 35
    • 18744394342 scopus 로고    scopus 로고
    • Abortive myogenesis in denervated skeletal muscle: Differentiative properties of satellite cells, their migration, and block of terminal differentiation
    • Borisov AB, Dedkov EI, Carlson BM. Abortive myogenesis in denervated skeletal muscle: Differentiative properties of satellite cells, their migration, and block of terminal differentiation. Anat Embryol (Berl) 2005;209:269-79
    • (2005) Anat Embryol (Berl , vol.209 , pp. 269-267
    • Borisov, A.B.1    Dedkov, E.I.2    Carlson, B.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.