Heterogeneous PrPC metabolism in skeletal muscle cells

FEBS Letters

Volumn 580, Issue 3, 2006, Pages 878-884

  Massimino, Maria Lina ^a,b   Ferrari, Jessica ^a   Sorgato, Maria Catia ^a   Bertoli, Alessandro ^a  

^a UNIVERSITY OF PADOVA   (Italy)

^b CNR   (Italy)

Author keywords

Fast fibres; Muscle differentiation; Myocyte; Prion protein; Skeletal muscle; Slow fibres

Indexed keywords

PRION PROTEIN;

ANIMAL CELL; ARTICLE; CELL FUNCTION; CELLULAR DISTRIBUTION; CONTROLLED STUDY; MOUSE; MUSCLE CELL; MUSCLE CONTRACTILITY; MUSCLE DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN GLYCOSYLATION; PROTEIN METABOLISM; SKELETAL MUSCLE; ANIMAL; ANTIBODY SPECIFICITY; HUMAN; METABOLISM; NEWBORN; PATHOLOGY; PRION DISEASE;

ANIMALIA; MURINAE;

ANIMALS; ANIMALS, NEWBORN; HUMANS; MICE; MUSCLE DEVELOPMENT; MUSCLE FIBERS; MUSCLE, SKELETAL; ORGAN SPECIFICITY; PRION DISEASES; PRPC PROTEINS;

EID: 31444435798     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2006.01.008     Document Type: Article

References (32)

1. S.B. Prusiner Prions Proc. Natl. Acad. Sci. USA 95 1998 13363 13383
2. P.J. Bosque, C. Ryou, G. Telling, D. Peretz, G. Legname, S.J. DeArmond, and S.B. Prusiner Prions in skeletal muscle Proc. Natl. Acad. Sci. USA 99 2002 3812 3817
3. M. Glatzel, E. Abela, M. Maissen, and A. Aguzzi Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease N. Engl. J. Med. 349 2003 1812 1820
4. Sc accumulation in myocytes from sheep incubating natural scrapie Nat. Med. 10 2004 591 593
5. Sc in muscles of hamsters orally exposed to scrapie J. Clin. Invest. 113 2004 1465 1472
6. C. Casalone, C. Corona, M.I. Crescio, F. Martucci, M. Mazza, G. Ru, E. Bozzetta, P.L. Acutis, and M. Caramelli Pathological prion protein in the tongues of sheep infected with naturally occurring scrapie J. Virol. 79 2005 5847 5849
7. K. Hsiao, H.F. Baker, T.J. Crow, M. Poulter, F. Owen, J.D. Terwilliger, D. Westaway, J. Ott, and S.B. Prusiner Linkage of a prion protein missense variant to Gerstmann-Straussler syndrome Nature 338 1989 342 345
8. H.A. Kretzschmar, P. Kufer, G. Riethmuller, S. DeArmond, S.B. Prusiner, and D. Schiffer Prion protein mutation at codon 102 in an Italian family with Gerstmann-Straussler-Scheinker syndrome Neurology 42 1992 809 810
9. G.C. Telling, T. Haga, M. Torchia, P. Tremblay, S.J. DeArmond, and S.B. Prusiner Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice Genes Dev. 10 1996 1736 1750
10. Sc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation Neurobiol. Dis. 8 2001 279 288
11. D. Westaway, S.J. DeArmond, J. Cayetano-Canlas, D. Groth, D. Foster, S.L. Yang, M. Torchia, G.A. Carlson, and S.B. Prusiner Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins Cell 76 1994 117 129
12. V. Askanas, M. Bilak, W.K. Engel, R.B. Alvarez, F. Tome, and A. Leclerc Prion protein is abnormally accumulated in inclusion-body myositis Neuroreport 5 1993 25 28
13. E. Sarkozi, V. Askanas, and W.K. Engel Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy Am. J. Pathol. 145 1994 1280 1284
14. G. Zanusso, G. Vattemi, S. Ferrari, M. Tabaton, E. Pedini, T. Cavallaio, G. Tomelleri, M. Filosto, P. Tonin, E. Nardelli, N. Rizzato, and S. Monaco Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy Brain Pathol. 11 2001 182 189
15. G.G. Kovacs, E. Lindeck-Pozza, L. Chimelli, A.Q. Araujo, A.A. Gabbai, T. Strobel, M. Glatzel, A. Aguzzi, and H. Budka Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle Ann. Neurol. 55 2004 121 125
16. D.R. Brown, B. Schmidt, M.H. Groschup, and H.A. Kretzschmar Prion protein expression in muscle cells and toxicity of a prion protein fragment Eur. J. Cell. Biol. 75 1998 29 37
17. D.R. Brown Prion and prejudice: normal protein and the synapse Trends Neurosci. 24 2001 85 90
18. A. Negro, C. Ballarin, A. Bertoli, M.L. Massimino, and M.C. Sorgato The metabolism and imaging in live cells of the bovine prion protein in its native form or carrying single amino acid substitutions Mol. Cell. Neurosci. 17 2001 521 538
19. M.L. Massimino, C. Ballarin, A. Bertoli, S. Casonato, S. Genovesi, A. Negro, and M.C. Sorgato Human Doppel and prion protein share common membrane microdomains and internalization pathways Int. J. Biochem. Cell. Biol. 36 2004 2016 2031
20. U.K. Laemmli Cleavage of structural proteins during the assembly of the head of bacteriophage T4 Nature 227 1970 680 685
21. A. Negro, F. Meggio, A. Bertoli, R. Battistutta, M.C. Sorgato, and L.A. Pinna Susceptibility of the prion protein to enzymic phosphorylation Biochem. Biophys. Res. Commun. 271 2000 337 341
22. A. Karsai, S. Muller, S. Platz, and M.T. Hauser Evaluation of a homemade SYBR green I reaction mixture for real-time PCR quantification of gene expression Biotechniques 32 2002 790 792 pp. 794-796
23. M.W. Pfaffl A new mathematical model for relative quantification in real-time RT-PCR Nucleic Acids Res. 29 2001 e45
24. M.L. Massimino, E. Rapizzi, M. Cantini, L.D. Libera, F. Mazzoleni, P. Arslan, and U. Carraro ED2+ macrophages increase selectively myoblast proliferation in muscle cultures Biochem. Biophys. Res. Commun. 235 1997 754 759
25. S.G. Chen, D.B. Teplow, P. Parchi, J.K. Teller, P. Gambetti, and L. Autilio-Gambetti Truncated forms of the human prion protein in normal brain and in prion diseases J. Biol. Chem. 270 1995 19173 19180
26. A. Jimenez-Huete, P.M. Lievens, R. Vidal, P. Piccardo, B. Ghetti, F. Tagliavini, B. Frangione, and F. Prelli Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues Am. J. Pathol. 153 1998 1561 1572
27. H. Weintraub The MyoD family and myogenesis: redundancy, networks, and thresholds Cell 75 1993 1241 1244
28. S. Schiaffino, and C. Reggiani Molecular diversity of myofibrillar proteins: gene regulation and functional significance Physiol. Rev. 76 1996 371 423
29. P.E. Bendheim, H.R. Brown, R.D. Rudelli, L.J. Scala, N.L. Goller, G.Y. Wen, R.J. Kascsak, N.R. Cashman, and D.C. Bolton Nearly ubiquitous tissue distribution of the scrapie agent precursor protein Neurology 42 1992 149 156
30. M. Moudjou, Y. Frobert, J. Grassi, and C. Bonnardiere La Cellular prion protein status in sheep: tissue-specific biochemical signatures J. Gen. Virol. 82 2001 2017 2024
31. G. Miele, A.R. Alejo Blanco, H. Baybutt, S. Horvat, J. Manson, and M. Clinton Embryonic activation and developmental expression of the murine prion protein gene Gene Expr. 11 2003 1 12
32. G.G. Kovacs, O. Kalev, E. Gelpi, C. Haberler, J. Wanschitz, M. Strohschneider, M.J. Molnar, L. Laszlo, and H. Budka The prion protein in human neuromuscular diseases J. Pathol. 204 2004 241 247