Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathies

Annals of Neurology

Volumn 40, Issue 6, 1996, Pages 864-872

  Mirabella, Massimiliano ^a   Alvarez, Renate B ^a   Engel, W King ^a   Weisgraber, Karl H ^b   Askanas, Valerie ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN E; CONGO RED; MESSENGER RNA;

ARTICLE; CELL VACUOLE; CLINICAL ARTICLE; CONTROLLED STUDY; HUMAN; HUMAN TISSUE; IMMUNOCYTOCHEMISTRY; IN SITU HYBRIDIZATION; INCLUSION BODY MYOSITIS; MUSCLE BIOPSY; MUSCLE REGENERATION; MYOFILAMENT; MYOPATHY; NEUROMUSCULAR SYNAPSE; PRIORITY JOURNAL; PROTEIN DOMAIN; ULTRASTRUCTURE;

AMYOTROPHIC LATERAL SCLEROSIS; APOLIPOPROTEINS E; HUMANS; MUSCLE FIBERS; MYOSITIS; MYOSITIS, INCLUSION BODY; RNA, MESSENGER;

EID: 0030483060     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410400608     Document Type: Article

References (42)

1. Askanas V, Engel WK. New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies. Curr Opin Rheumatol 1995;7:486-496
2. Griggs RC, Askanas V, DiMauro S, et al. Inclusion body myositis and myopathies. Ann Neurol 1995;38:705-713
3. Mendell JR, Sahenk Z, Gales T, Paul L. Amyloid filaments in inclusion body myositis. Arch Neurol 1991;48:1229-1234
4. Askanas V, Engel WK, Alvarez RB. Light- and electronmicroscopic localization of β-amyloid protein in muscle biopsies of patients with inclusion-body myositis. Am J Pathol 1992;141: 31-36
5. Askanas V, Engel WK, Bilak M, et al. Twisted tubulofilaments of inclusion-body myositis muscle resemble paired helical filaments of Alzheimer brain contain hyper-phosphorylated tau. Am J Pathol 1994;144:177-187
6. Askanas V, Alvarez RB, Engel WK. β-Amyloid precursor epitopes in muscle fibers of inclusion-body myositis. Ann Neurol 1993;34:551-560
7. Sarkozi E, Askanas V, Johnson SA, et al. β-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle. NeuroReport 1993;4:815-818
8. Askanas V, Bilak M, Engel WK, et al. Prion protein is abnormally accumulated in inclusion-body myositis. NeuroReport 1993;5:25-28
9. Sarkozi E, Askanas V, Engel WK. Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy. Am J Pathol 1994;145:1280-1284
10. Mitrani-Rosenbaum S, Argov Z, Blumenfeld A, et al. Hereditary inclusion body myopathy maps to chromosome 9p1-q1. Hum Mol Genet 1996;5:159-163
11. Mirabella M, Alvarez RB, Bilak M, et al. Difference in expression of phosphorylated tau epitopes between sporadic inclusion-body myositis and hereditary inclusion-body myopathies. J Neuropathol Exp Neurol 1996;55:761-773
12. Askanas V, Mirabella M, Engel WK, et al. Apolipoprotein E immunoreactive deposits in inclusion-body muscle diseases. Lancet 1994;343:364-365
13. Alvarez RB, Mirabella M, Sarkozi E, et al. Partial expression of cellular phenotype of sporadic inclusion-body myositis in autosomal dominant inclusion-body myopathy. Neurology 1996;46:487
14. Engel WK. Muscle biopsies in neuromuscular diseases. Pediatr Clin North Am 1967;14:963-995
15. Askanas V, Engel WK, Alvarez RB. Enhanced detection of Congo-red positive amyloid deposits in muscle fibers of inclusion-body myositis and brain of Alzheimer disease using fluorescence technique. Neurology 1993;43:1265-1267
16. Weisgraber KH, Shinto LH. Identification of the disulfide-linked homodimer of apolipoprotein E3 in plasma. Impact on receptor binding activity. J Biol Chem 1991;226:12029-12034
17. Wong CW, Quaranta V, Glenner GG. Neuritic plaques and cerebrovascular amyloid in Alzheimer's disease are antigenically related. Proc Natl Acad Sci USA 1985;82:8729-8732
18. Askanas V, Engel WK, Alvarez RB. Strong immunoreactivity of β-amyloid precursor protein, including the β-amyloid protein sequence, at human neuromuscular junctions. Neurosci Lett 1992;143:96-100
19. Gorycki M, Askanas V. Improved technique for electron microscopy of cultured cells. Stain Technol 1977;52:249-254
20. Vogel T, Weisgraber KH, Zeevi MI, et al. Human apolipoprotein E expression in Escherichia coli: structural and functional identity of the bacterially produced protein with plasma apolipoprotein E. Proc Natl Acad Sci USA 1985;82:8686-8700
21. Mahley RW. Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. Science 1988;240:622-630
22. Weisgraber KH. Apolipoprotein E: structure-function relationships. Adv Protein Chem 1994;45:249-302
23. Ignatius MJ, Gebicke-Harter PJ, Skene JHP, et al. Expression of apolipoprotein E during nerve degeneration and regeneration. Proc Natl Acad Sci USA 1986;83:1125-1129
24. Namba Y, Tomonaga M, Kawasaki H, et al. Apolipoprotein E immunoreactivity in cerebral amyloid deposits and neurofibrillary tangles in Alzheimer's disease and kuru plaque amyloid in Creutzfeld-Jakob disease. Brain Res 1991;541:163-166
25. Hans S-H, Einstein G, Weisgraber KH, et al. Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic study. J Neuropathol Exp Neurol 1994;53:535-544
26. Saunders AM, Strittmatter WJ, Schmechel DE, et al. Association of apolipoprotein E allele ε4 with late-onset familial and sporadic Alzheimer's disease. Neurology 1993;43:1467-1472
27. Roses AD. Perspective: on the metabolism of apolipoprotein E and the Alzheimer diseases. Exp Neurol 1995;132:149-156
28. Wisniewski T, Golabek AA, Matsubara E, et al. Apolipoprotein E: binding to soluble Alzheimer's β-amyloid. Biochem Biophys Res Commun 1993;192:359-365
29. Strittmatter WJ, Saunders AM, Schmechel DE, et al. Apolipoprotein E: high-avidity binding to β-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA 1993;90:1977-1981
30. Richey PL, Siedlak SL, Smith MA, Perry G. Apolipoprotein E interaction with the neurofibrillary tangles and senile plaques in Alzheimer disease: implications for disease pathogenesis. Biochem Biophys Res Commun 1995;208:657-663
31. Benzing WC, Mufson EJ. Apolipoprotein E immunoreactivity within neurofibrillary tangles: relationship to tau and PHF in Alzheimer's disease. Exp Neurol 1995;132:162-171
32. Wisniewski T, Frangione B. Apolipoprotein E: a pathological chaperone protein in patients with cerebral and systemic amyloid. Neurosci Lett 1992;135:235-238
33. Gallo G, Wisniewski T, Choi-Miura N-H, et al. Potential role of apolipoprotein-E in fibrillogenesis. Am J Pathol 1994;145: 526-530
34. Askanas V, Serdaroglu P, Engel WK, Alvarez RB. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy. Neurosci Lett 1991;130:73-76
35. Diedrich JF, Minnigan H, Carp RI, et al. Neurological changes in scrapie and Alzheimer's disease are associated with increased expression of apolipoprotein E and cathepsin D in astrocytes. J Virol 1991;65:4759-4768
36. Garlepp MJ, Tabarias H, van Bockxmeer FM, et al. Apolipoprotein E ε4 in inclusion body myosiris. Ann Neurol 1995; 38:957-959.
37. Harrington CR, Anderson JR, Chan KK. Apolipoprotein E type ε4 allele frequency is not increased in patients with sporadic inclusion-body myositis. Neurosci Lett 1995;183:35-38
38. Askanas V, Engel WK, Mirabella M, et al. Apolipoprotein E alleles in sporadic inclusion-body myositis and hereditary inclusion-body myopathy. Ann Neurol 1996;40:264
39. Mirabella M, Askanas V, Engel WK, Weisgraber KH. Immunocytochemical localization of apolipoprotein E (apoE) in inclusion body myositis (IBM). Neurology 1994;44:347
40. Akaaboune M, Villanova M, Festoff BW, et al. Apolipoprotein E expression at neuromuscular junctions in mouse, rat and human skeletal muscle. FEBS Lett 1994;351:246-248
41. Askanas V, McFerrin J, Baqué S, et al. Transfer of β-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle. Proc Natl Acad Sci USA 1996;93:1314-1319
42. Alvarez RB, Fardeau M, Askanas V, et al. Characteristic filamentous inclusions reproduced in cultured innervated muscle fibers from patients with familial "inclusion body myositis." J Neurol Sci 1990;98:178