메뉴 건너뛰기




Volumn 46, Issue 1, 2012, Pages 125-129

Did giant mitochondria delay muscle maturation? An uncommon congenital myopathy

Author keywords

Abnormal fission fusion machinery; Congenital myopathy; Giant mitochondria; Muscle cell immaturity; Primary myotube like cells

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; CREATINE KINASE; FRUCTOSE BISPHOSPHATE ALDOLASE;

EID: 84862314079     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.23365     Document Type: Article
Times cited : (2)

References (24)
  • 1
    • 0018854073 scopus 로고
    • Human ontogenesis. Part 1. Ultrastructural characteristics of developing human muscle
    • Fidziańska A. Human ontogenesis. Part 1. Ultrastructural characteristics of developing human muscle. J Neuropathol Exp Neurol 1980; 39: 476-486.
    • (1980) J Neuropathol Exp Neurol , vol.39 , pp. 476-486
    • Fidziańska, A.1
  • 2
    • 33745274726 scopus 로고    scopus 로고
    • Mitochondria: dynamic organelles in disease, aging and development
    • Chan DEC. Mitochondria: dynamic organelles in disease, aging and development. Cell 2006; 125: 1241-1251.
    • (2006) Cell , vol.125 , pp. 1241-1251
    • Chan, D.E.C.1
  • 3
    • 0033231549 scopus 로고    scopus 로고
    • C elegans dynamin-related protein DRP1 controls severing of the mitochondrial outer membrane
    • Labrousse AM, Zapaterra MD, Rube DA, vander Bliek AM. C elegans dynamin-related protein DRP1 controls severing of the mitochondrial outer membrane. Mol Cell 1999; 4: 815-826.
    • (1999) Mol Cell , vol.4 , pp. 815-826
    • Labrousse, A.M.1    Zapaterra, M.D.2    Rube, D.A.3    vander Bliek, A.M.4
  • 4
    • 27744491193 scopus 로고    scopus 로고
    • Emerging functions of mammalian mitochondrial fusion and fission
    • Chen H, Chan DC. Emerging functions of mammalian mitochondrial fusion and fission. Hum Mol Genet 2005; 14: 283-289.
    • (2005) Hum Mol Genet , vol.14 , pp. 283-289
    • Chen, H.1    Chan, D.C.2
  • 5
    • 0035166814 scopus 로고    scopus 로고
    • Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells
    • Smirnova E, Griparic L, Shurland DL, van der Blick AM. Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells. Mol Biol Cell 2001; 12: 2245-2256.
    • (2001) Mol Biol Cell , vol.12 , pp. 2245-2256
    • Smirnova, E.1    Griparic, L.2    Shurland, D.L.3    van der Blick, A.M.4
  • 6
  • 8
    • 77957829340 scopus 로고    scopus 로고
    • Nitric oxide inhibition of Drp1-mediated mitochondrial fission is critical for myogenic differentation
    • De Palma C, Falcone S, Pisoni S, Cipolat S, Panzeri C, Pambianco S, et al. Nitric oxide inhibition of Drp1-mediated mitochondrial fission is critical for myogenic differentation. Cell Death Differ 2010; 17: 1684-1696.
    • (2010) Cell Death Differ , vol.17 , pp. 1684-1696
    • De Palma, C.1    Falcone, S.2    Pisoni, S.3    Cipolat, S.4    Panzeri, C.5    Pambianco, S.6
  • 9
    • 77955298543 scopus 로고    scopus 로고
    • Dynamic regulation of mitochondrial fission through modification of the dynamin-related protein Drp1
    • Chang CR, Blackstone C. Dynamic regulation of mitochondrial fission through modification of the dynamin-related protein Drp1. Ann NY Acad Sci 2010; 1201: 34-39.
    • (2010) Ann NY Acad Sci , vol.1201 , pp. 34-39
    • Chang, C.R.1    Blackstone, C.2
  • 11
    • 0037455575 scopus 로고    scopus 로고
    • Mitofusins Mfn1 and Mfn2 cordinately regulate mitochondrial fusion and are essential for embryonic development
    • Chen H, Detmer SA, Ewald AJ, Griffin EE, Faser SE, Chan DC. Mitofusins Mfn1 and Mfn2 cordinately regulate mitochondrial fusion and are essential for embryonic development. J Cell Biol 2003; 160: 189-200.
    • (2003) J Cell Biol , vol.160 , pp. 189-200
    • Chen, H.1    Detmer, S.A.2    Ewald, A.J.3    Griffin, E.E.4    Faser, S.E.5    Chan, D.C.6
  • 12
    • 22544451586 scopus 로고    scopus 로고
    • Disruption of fusion results in mitochondrial heterogeneity and dysfunction
    • Chen H, Chomyn A, Chan DC. Disruption of fusion results in mitochondrial heterogeneity and dysfunction. J Biol Chem 2005; 280: 26185-26192.
    • (2005) J Biol Chem , vol.280 , pp. 26185-26192
    • Chen, H.1    Chomyn, A.2    Chan, D.C.3
  • 13
    • 68249087424 scopus 로고    scopus 로고
    • Mitochondria fission factor Drp1 is essential for embryonic development and synapse formation in mice
    • Ishihara N, Nomura M, Jofuku A, Kato H, Suzuki SO, Masuda K, et al. Mitochondria fission factor Drp1 is essential for embryonic development and synapse formation in mice. Nat Cell Biol 2009; 11: 986-996.
    • (2009) Nat Cell Biol , vol.11 , pp. 986-996
    • Ishihara, N.1    Nomura, M.2    Jofuku, A.3    Kato, H.4    Suzuki, S.O.5    Masuda, K.6
  • 14
    • 0033772264 scopus 로고    scopus 로고
    • OPA1 encoding a dynamin-related GTPase is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
    • Alexander C, Votruba M, Pesch UE, Thiselton DL, Mayer S, Moore A, et al. OPA1 encoding a dynamin-related GTPase is mutated in autosomal dominant optic atrophy linked to chromosome 3q28. Nat Genet 2000; 26: 211-215.
    • (2000) Nat Genet , vol.26 , pp. 211-215
    • Alexander, C.1    Votruba, M.2    Pesch, U.E.3    Thiselton, D.L.4    Mayer, S.5    Moore, A.6
  • 17
    • 64649093169 scopus 로고    scopus 로고
    • Mitochondrial dynamics and neurodegeneration
    • Lu B. Mitochondrial dynamics and neurodegeneration. Curr Neurol Neurosci Rep 2009; 9: 212-219.
    • (2009) Curr Neurol Neurosci Rep , vol.9 , pp. 212-219
    • Lu, B.1
  • 18
    • 0015970903 scopus 로고
    • Ultrastructural changes in muscle in spinal muscular atrophy: Werdnig-Hoffman disease
    • Fidziańska A. Ultrastructural changes in muscle in spinal muscular atrophy: Werdnig-Hoffman disease. Acta Neuropathol (Berl) 1974; 27: 247-256.
    • (1974) Acta Neuropathol (Berl) , vol.27 , pp. 247-256
    • Fidziańska, A.1
  • 19
    • 0017195462 scopus 로고
    • Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathological study of four cases
    • Sarnat HB, Silbert SW. Maturational arrest of fetal muscle in neonatal myotonic dystrophy. A pathological study of four cases. Arch Neurol 1976; 33: 466-474.
    • (1976) Arch Neurol , vol.33 , pp. 466-474
    • Sarnat, H.B.1    Silbert, S.W.2
  • 21
    • 0023867379 scopus 로고
    • Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin
    • Farkas-Bargeton E, Barbet JP, Dances S, Wehrler R, Checouri A, Dulac O. Immaturity of muscle fibers in the congenital form of myotonic dystrophy: its consequences and its origin. J Neurol Sci 1988; 83: 145-159.
    • (1988) J Neurol Sci , vol.83 , pp. 145-159
    • Farkas-Bargeton, E.1    Barbet, J.P.2    Dances, S.3    Wehrler, R.4    Checouri, A.5    Dulac, O.6
  • 22
    • 0020684043 scopus 로고
    • Fetal muscle characteristic in nemaline myopathy
    • Nonaka J, Tojo M, Sugita H. Fetal muscle characteristic in nemaline myopathy. Neuropediatrics 1983; 14: 47-52.
    • (1983) Neuropediatrics , vol.14 , pp. 47-52
    • Nonaka, J.1    Tojo, M.2    Sugita, H.3
  • 23
    • 0025373021 scopus 로고
    • Neonatal form of nemaline myopathy, muscle immaturity and a microvascular injury
    • Fidzianska A, Goebel HH, Kleine M. Neonatal form of nemaline myopathy, muscle immaturity and a microvascular injury. J Child Neurol 1990; 5: 122-126.
    • (1990) J Child Neurol , vol.5 , pp. 122-126
    • Fidzianska, A.1    Goebel, H.H.2    Kleine, M.3
  • 24
    • 0029872233 scopus 로고    scopus 로고
    • Severe neonatal nemaline myopathy with delayed maturation of muscle
    • Wada H, Nishio H, Kugo M, Waku S, Ikeda K, Takada S, et al. Severe neonatal nemaline myopathy with delayed maturation of muscle. Brain Dev 1996; 18: 135-138.
    • (1996) Brain Dev , vol.18 , pp. 135-138
    • Wada, H.1    Nishio, H.2    Kugo, M.3    Waku, S.4    Ikeda, K.5    Takada, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.