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Published in: Acta Neuropathologica 5/2007

Open Access 01-11-2007 | Original Paper

NOGO is increased and binds to BACE1 in sporadic inclusion-body myositis and in AβPP-overexpressing cultured human muscle fibers

Authors: Slawomir Wojcik, W. King Engel, Riqiang Yan, Janis McFerrin, Valerie Askanas

Published in: Acta Neuropathologica | Issue 5/2007

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Abstract

Increased amyloid-β precursor protein (AβPP) and amyloid-β (Aβ) accumulation appear to be upstream steps in the pathogenesis of sporadic inclusion-body myositis (s-IBM). BACE1, participating in Aβ production is also increased in s-IBM muscle fibers. Nogo-B and Nogo-A belong to a family of integral membrane reticulons, and Nogo-B binding to BACE1 blocks BACE1 access to AβPP, decreasing Aβ production. We studied Nogo-B and Nogo-A in s-IBM muscle and in our IBM muscle culture models, based on AβPP-overexpression or ER-stress-induction in cultured human muscle fibers (CHMFs). We report that: (1) in biopsied s-IBM fibers, Nogo-B is increased, accumulates in aggregates, is immuno-co-localized with BACE1, and binds to BACE1; Nogo-A is undetectable. (2) In CHMFs, (a) AβPP overexpression increases Nogo-B, Nogo-A, and BACE1, (b) ER stress increases BACE1 but decreases Nogo-B and Nogo-A, (c) Nogo-B and Nogo-A associate with BACE1. Accordingly, two novel mechanisms, AβPP overexpression and ER stress, are involved in Nogo-B and Nogo-A expression in human muscle. We propose that in s-IBM muscle the Nogo-B increase may represent an attempt by muscle fiber to decrease Aβ production. However, the increase of Nogo-B seems insufficient because Aβ continues to accumulate and the disease progresses. We propose that manipulations, which increase Nogo-B in s-IBM muscle might offer a new therapeutic opportunity.
Literature
1.
go back to reference Acevedo L, Yu J, Erdjument-Bromage H, Miao RQ, Kim JE, Fulton D, Tempst P, Strittmatter SM, Sessa WC (2004) A new role for Nogo as a regulator of vascular remodeling. Nat Med 10:382–388PubMedCrossRef Acevedo L, Yu J, Erdjument-Bromage H, Miao RQ, Kim JE, Fulton D, Tempst P, Strittmatter SM, Sessa WC (2004) A new role for Nogo as a regulator of vascular remodeling. Nat Med 10:382–388PubMedCrossRef
2.
go back to reference Askanas V, Engel WK (1992) Cultured normal and genetically abnormal human muscle, in the handbook of clinical neurology. In: Rowland LP, Di Mauro S (eds) Myopathies, vol 18. North Holland, Amsterdam, pp 85–116 Askanas V, Engel WK (1992) Cultured normal and genetically abnormal human muscle, in the handbook of clinical neurology. In: Rowland LP, Di Mauro S (eds) Myopathies, vol 18. North Holland, Amsterdam, pp 85–116
3.
go back to reference Askanas V, Alvarez RB, Engel WK (1993) β-amyloid precursor epitopes in muscle fibers of inclusion body myositis. Ann Neurol 34:551–560PubMedCrossRef Askanas V, Alvarez RB, Engel WK (1993) β-amyloid precursor epitopes in muscle fibers of inclusion body myositis. Ann Neurol 34:551–560PubMedCrossRef
4.
go back to reference Askanas V, Sarkozi E, Bilak M, Engel WK (1994) Expression of β-amyloid precursor protein, prion and acetylcholine receptor and their mRNAs in human muscle fibers regenerating in vivo. Brain Pathol 4:322 Askanas V, Sarkozi E, Bilak M, Engel WK (1994) Expression of β-amyloid precursor protein, prion and acetylcholine receptor and their mRNAs in human muscle fibers regenerating in vivo. Brain Pathol 4:322
5.
go back to reference Askanas V, McFerrin J, Baque S, Alvarez RB, Sarkozi E, Engel WK (1996) Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle. Proc Natl Acad Sci USA 93:1314–1319PubMedCrossRef Askanas V, McFerrin J, Baque S, Alvarez RB, Sarkozi E, Engel WK (1996) Transfer of beta-amyloid precursor protein gene using adenovirus vector causes mitochondrial abnormalities in cultured normal human muscle. Proc Natl Acad Sci USA 93:1314–1319PubMedCrossRef
6.
go back to reference Askanas V, McFerrin J, Alvarez RB, Baque S, Engel WK (1997) βAPP gene transfer into cultured human muscle induces inclusion-body myositis aspects. Neuroreport 8:2155–2158PubMedCrossRef Askanas V, McFerrin J, Alvarez RB, Baque S, Engel WK (1997) βAPP gene transfer into cultured human muscle induces inclusion-body myositis aspects. Neuroreport 8:2155–2158PubMedCrossRef
7.
go back to reference Askanas V, Engel WK, Yang CC, Alvarez RB, Lee VM, Wisniewski T (1998) Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy. Am J Pathol 152:889–895PubMed Askanas V, Engel WK, Yang CC, Alvarez RB, Lee VM, Wisniewski T (1998) Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy. Am J Pathol 152:889–895PubMed
8.
go back to reference Askanas V, Engel WK (2001) Inclusion-body myositis: newest concepts of pathogenesis and relation to aging and Alzheimer disease. J Neuropathol Exp Neurol 60:1–14PubMed Askanas V, Engel WK (2001) Inclusion-body myositis: newest concepts of pathogenesis and relation to aging and Alzheimer disease. J Neuropathol Exp Neurol 60:1–14PubMed
9.
go back to reference Askanas V, Engel WK (2006) Inclusion-body myositis: a myodegenerative conformational disorder associated with Aβ, protein misfolding, and proteasome inhibition. Neurology 66:S39–S48PubMedCrossRef Askanas V, Engel WK (2006) Inclusion-body myositis: a myodegenerative conformational disorder associated with Aβ, protein misfolding, and proteasome inhibition. Neurology 66:S39–S48PubMedCrossRef
10.
go back to reference Back SH, Schroder M, Lee K, Zhang K, Kaufman RJ (2005) ER stress signaling by regulated splicing: IRE1/HAC1/XBP1. Methods 35:395–416PubMedCrossRef Back SH, Schroder M, Lee K, Zhang K, Kaufman RJ (2005) ER stress signaling by regulated splicing: IRE1/HAC1/XBP1. Methods 35:395–416PubMedCrossRef
11.
go back to reference Buss A, Sellhaus B, Wolmsley A, Noth J, Schwab ME, Brook GA (2005) Expression pattern of NOGO-A protein in the human nervous system. Acta Neuropathol (Berl) 110:113–119CrossRef Buss A, Sellhaus B, Wolmsley A, Noth J, Schwab ME, Brook GA (2005) Expression pattern of NOGO-A protein in the human nervous system. Acta Neuropathol (Berl) 110:113–119CrossRef
12.
go back to reference Cordy JM, Hooper NM, Turner AJ (2006) The involvement of lipid rafts in Alzheimer’s disease. Mol Membr Biol 23:111–122PubMedCrossRef Cordy JM, Hooper NM, Turner AJ (2006) The involvement of lipid rafts in Alzheimer’s disease. Mol Membr Biol 23:111–122PubMedCrossRef
13.
go back to reference Dalakas MC (2006) Inflammatory, immune, and viral aspects of inclusion-body myositis. Neurology 66:S33–S38PubMedCrossRef Dalakas MC (2006) Inflammatory, immune, and viral aspects of inclusion-body myositis. Neurology 66:S33–S38PubMedCrossRef
14.
go back to reference Engel WK, Askanas V (2006) Inclusion-body myositis: clinical, diagnostic, and pathologic aspects. Neurology 66:S20–S29PubMedCrossRef Engel WK, Askanas V (2006) Inclusion-body myositis: clinical, diagnostic, and pathologic aspects. Neurology 66:S20–S29PubMedCrossRef
15.
go back to reference Fratta P, Engel WK, McFerrin J, Davies KJ, Lin SW, Askanas V (2005) Proteasome inhibition and aggresome formation in sporadic inclusion-body myositis and in amyloid-beta precursor protein-overexpressing cultured human muscle fibers. Am J Pathol 167:517–526PubMed Fratta P, Engel WK, McFerrin J, Davies KJ, Lin SW, Askanas V (2005) Proteasome inhibition and aggresome formation in sporadic inclusion-body myositis and in amyloid-beta precursor protein-overexpressing cultured human muscle fibers. Am J Pathol 167:517–526PubMed
16.
go back to reference Fukuchi K, Pham D, Hart M, Li L, Lindsey JR (1998) Amyloid-beta deposition in skeletal muscle of transgenic mice: possible model of inclusion body myopathy. Am J Pathol 153:1687–1693PubMed Fukuchi K, Pham D, Hart M, Li L, Lindsey JR (1998) Amyloid-beta deposition in skeletal muscle of transgenic mice: possible model of inclusion body myopathy. Am J Pathol 153:1687–1693PubMed
17.
go back to reference Gil V, Nicolas O, Mingorance A, Urena JM, Tang BL, Hirata T, Saez-Valero J, Ferrer I, Soriano E, del Rio JA (2006) Nogo-A expression in the human hippocampus in normal aging and in Alzheimer disease. J Neuropathol Exp Neurol 65:433–444PubMedCrossRef Gil V, Nicolas O, Mingorance A, Urena JM, Tang BL, Hirata T, Saez-Valero J, Ferrer I, Soriano E, del Rio JA (2006) Nogo-A expression in the human hippocampus in normal aging and in Alzheimer disease. J Neuropathol Exp Neurol 65:433–444PubMedCrossRef
18.
go back to reference He W, Lu Y, Qahwash I, Hu XY, Chang A, Yan R (2004) Reticulon family members modulate BACE1 activity and amyloid-beta peptide generation. Nat Med 10:959–965PubMedCrossRef He W, Lu Y, Qahwash I, Hu XY, Chang A, Yan R (2004) Reticulon family members modulate BACE1 activity and amyloid-beta peptide generation. Nat Med 10:959–965PubMedCrossRef
19.
go back to reference He W, Hu X, Shi Q, Zhou X, Lu Y, Fisher C, Yan R (2006) Mapping of interaction mediating binding between BACE1 and RTN/Nogo proteins. J Mol Biol 363:625–634PubMedCrossRef He W, Hu X, Shi Q, Zhou X, Lu Y, Fisher C, Yan R (2006) Mapping of interaction mediating binding between BACE1 and RTN/Nogo proteins. J Mol Biol 363:625–634PubMedCrossRef
20.
go back to reference Jin LW, Hearn MG, Ogburn CE, Dang N, Nochlin D, Ladiges WC, Martin GM (1998) Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositis. Am J Pathol 153:1679–1686PubMed Jin LW, Hearn MG, Ogburn CE, Dang N, Nochlin D, Ladiges WC, Martin GM (1998) Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositis. Am J Pathol 153:1679–1686PubMed
21.
go back to reference Kitazawa M, Green KN, Caccamo A, LaFerla FM (2006) Genetically augmenting Abeta42 levels in skeletal muscle exacerbates inclusion body myositis-like pathology and motor deficits in transgenic mice. Am J Pathol 168:1986–1997PubMedCrossRef Kitazawa M, Green KN, Caccamo A, LaFerla FM (2006) Genetically augmenting Abeta42 levels in skeletal muscle exacerbates inclusion body myositis-like pathology and motor deficits in transgenic mice. Am J Pathol 168:1986–1997PubMedCrossRef
22.
go back to reference Lee AS (2005) The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress. Methods 35:373–381PubMedCrossRef Lee AS (2005) The ER chaperone and signaling regulator GRP78/BiP as a monitor of endoplasmic reticulum stress. Methods 35:373–381PubMedCrossRef
23.
go back to reference Marlow L, Cain M, Pappolla MA, Sambamurti K (2003) Beta-secretase processing of the Alzheimer’s amyloid protein precursor (APP). J Mol Neurosci 20:233–239PubMedCrossRef Marlow L, Cain M, Pappolla MA, Sambamurti K (2003) Beta-secretase processing of the Alzheimer’s amyloid protein precursor (APP). J Mol Neurosci 20:233–239PubMedCrossRef
24.
go back to reference McFerrin J, Engel WK, Askanas V (1998) Impaired innervation of cultured human muscle overexpressing Amyloid-betaPP experimentally and genetically: relevance to inclusion-body myopathies. Neuroreport 9:3201–3205PubMedCrossRef McFerrin J, Engel WK, Askanas V (1998) Impaired innervation of cultured human muscle overexpressing Amyloid-betaPP experimentally and genetically: relevance to inclusion-body myopathies. Neuroreport 9:3201–3205PubMedCrossRef
25.
go back to reference Ng CE, Tang BL (2002) Nogos and the Nogo-66 receptor: factors inhibiting CNS neuron regeneration. J Neurosci Res 67:559–565PubMedCrossRef Ng CE, Tang BL (2002) Nogos and the Nogo-66 receptor: factors inhibiting CNS neuron regeneration. J Neurosci Res 67:559–565PubMedCrossRef
26.
go back to reference Nogalska A, Engel WK, McFerrin J, Kokame K, Komano H, Askanas V (2006) Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced cultured human muscle fibers. J Neurochem 96:1491–1499PubMedCrossRef Nogalska A, Engel WK, McFerrin J, Kokame K, Komano H, Askanas V (2006) Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced cultured human muscle fibers. J Neurochem 96:1491–1499PubMedCrossRef
27.
go back to reference Nogalska A, Wojcik S, King Engel W, McFerrin J, Askanas V (2007) Endoplasmic reticulum stress induces myostatin precursor protein and NF-kappaB in cultured human muscle fibers: Relevance to inclusion body myositis. Exp Neurol 204:610–618PubMedCrossRef Nogalska A, Wojcik S, King Engel W, McFerrin J, Askanas V (2007) Endoplasmic reticulum stress induces myostatin precursor protein and NF-kappaB in cultured human muscle fibers: Relevance to inclusion body myositis. Exp Neurol 204:610–618PubMedCrossRef
28.
go back to reference Sarkozi E, Askanas V, Johnson SA, Engel WK, Alvarez RB (1993) beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle. Neuroreport 4:815–818PubMedCrossRef Sarkozi E, Askanas V, Johnson SA, Engel WK, Alvarez RB (1993) beta-Amyloid precursor protein mRNA is increased in inclusion-body myositis muscle. Neuroreport 4:815–818PubMedCrossRef
29.
go back to reference Sarkozi E, Askanas V, Johnson SA, McFerrin J, Engel WK (1994) Expression of beta-amyloid precursor protein gene is developmentally regulated in human muscle fibers in vivo and in vitro. Exp Neurol 128:27–33PubMedCrossRef Sarkozi E, Askanas V, Johnson SA, McFerrin J, Engel WK (1994) Expression of beta-amyloid precursor protein gene is developmentally regulated in human muscle fibers in vivo and in vitro. Exp Neurol 128:27–33PubMedCrossRef
30.
go back to reference Satoh J, Onoue H, Arima K, Yamamura T (2005) Nogo-A and nogo receptor expression in demyelinating lesions of multiple sclerosis. J Neuropathol Exp Neurol 64:129–138PubMedCrossRef Satoh J, Onoue H, Arima K, Yamamura T (2005) Nogo-A and nogo receptor expression in demyelinating lesions of multiple sclerosis. J Neuropathol Exp Neurol 64:129–138PubMedCrossRef
31.
go back to reference Sugarman MC, Yamasaki TR, Oddo S, Echegoyen JC, Murphy MP, Golde TE, Jannatipour M, Leissring MA, LaFerla FM (2002) Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle. Proc Natl Acad Sci USA 99:6334–6339PubMedCrossRef Sugarman MC, Yamasaki TR, Oddo S, Echegoyen JC, Murphy MP, Golde TE, Jannatipour M, Leissring MA, LaFerla FM (2002) Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle. Proc Natl Acad Sci USA 99:6334–6339PubMedCrossRef
32.
go back to reference Teng FY, Ling BM, Tang BL (2004) Inter- and intracellular interactions of Nogo: new findings and hypothesis. J Neurochem 89:801–806PubMedCrossRef Teng FY, Ling BM, Tang BL (2004) Inter- and intracellular interactions of Nogo: new findings and hypothesis. J Neurochem 89:801–806PubMedCrossRef
33.
go back to reference Tun H, Marlow L, Pinnix I, Kinsey R, Sambamurti K (2002) Lipid rafts play an important role in A-beta biogenesis by regulating the beta-secretase pathway. J Mol Neurosci 19:31–35PubMedCrossRef Tun H, Marlow L, Pinnix I, Kinsey R, Sambamurti K (2002) Lipid rafts play an important role in A-beta biogenesis by regulating the beta-secretase pathway. J Mol Neurosci 19:31–35PubMedCrossRef
34.
go back to reference Vattemi G, Engel WK, McFerrin J, Buxbaum JD, Pastorino L, Askanas V (2001) Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis. Lancet 358:1962–1964PubMedCrossRef Vattemi G, Engel WK, McFerrin J, Buxbaum JD, Pastorino L, Askanas V (2001) Presence of BACE1 and BACE2 in muscle fibres of patients with sporadic inclusion-body myositis. Lancet 358:1962–1964PubMedCrossRef
35.
go back to reference Vattemi G, Kefi M, Engel WK, Askanas V (2003) Nicastrin, a novel protein participating in amyloid-beta production, is overexpressed in sporadic inclusion-body myositis muscle. Neurology 60:A315 Vattemi G, Kefi M, Engel WK, Askanas V (2003) Nicastrin, a novel protein participating in amyloid-beta production, is overexpressed in sporadic inclusion-body myositis muscle. Neurology 60:A315
36.
go back to reference Vattemi G, Engel WK, McFerrin J, Pastorino L, Buxbaum JD, Askanas V (2003) BACE1 and BACE2 in pathologic and normal human muscle. Exp Neurol 179:150–158PubMedCrossRef Vattemi G, Engel WK, McFerrin J, Pastorino L, Buxbaum JD, Askanas V (2003) BACE1 and BACE2 in pathologic and normal human muscle. Exp Neurol 179:150–158PubMedCrossRef
37.
go back to reference Vattemi G, Engel WK, McFerrin J, Askanas V (2004) Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle. Am J Pathol 164:1–7PubMed Vattemi G, Engel WK, McFerrin J, Askanas V (2004) Endoplasmic reticulum stress and unfolded protein response in inclusion body myositis muscle. Am J Pathol 164:1–7PubMed
38.
go back to reference Vetrivel KS, Thinakaran G (2006) Amyloidogenic processing of beta-amyloid precursor protein in intracellular compartments. Neurology 66:S69–73PubMedCrossRef Vetrivel KS, Thinakaran G (2006) Amyloidogenic processing of beta-amyloid precursor protein in intracellular compartments. Neurology 66:S69–73PubMedCrossRef
39.
go back to reference Wang X, Chun SJ, Treloar H, Vartanian T, Greer CA, Strittmatter SM (2002) Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact. J Neurosci 22:5505–5515PubMed Wang X, Chun SJ, Treloar H, Vartanian T, Greer CA, Strittmatter SM (2002) Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact. J Neurosci 22:5505–5515PubMed
40.
go back to reference Wojcik S, Engel WK, McFerrin J, Askanas V (2005) Myostatin is increased and complexes with amyloid-beta within sporadic inclusion-body myositis muscle fibers. Acta Neuropathol (Berl) 110:173–177CrossRef Wojcik S, Engel WK, McFerrin J, Askanas V (2005) Myostatin is increased and complexes with amyloid-beta within sporadic inclusion-body myositis muscle fibers. Acta Neuropathol (Berl) 110:173–177CrossRef
41.
go back to reference Wojcik S, Engel WK, McFerrin J, Paciello O, Askanas V (2006) AbetaPP-overexpression and proteasome inhibition increase alphaB-crystallin in cultured human muscle: relevance to inclusion-body myositis. Neuromuscul Disord 16:839–844PubMedCrossRef Wojcik S, Engel WK, McFerrin J, Paciello O, Askanas V (2006) AbetaPP-overexpression and proteasome inhibition increase alphaB-crystallin in cultured human muscle: relevance to inclusion-body myositis. Neuromuscul Disord 16:839–844PubMedCrossRef
42.
go back to reference Wojcik S, Engel WK, Askanas V (2006) Increased expression of Nogo-A in ALS muscle biopsies is not unique for this disease. Acta Myologica 25:116–118PubMed Wojcik S, Engel WK, Askanas V (2006) Increased expression of Nogo-A in ALS muscle biopsies is not unique for this disease. Acta Myologica 25:116–118PubMed
43.
go back to reference Wojcik S, Nogalska A, McFerrin J, Engel WK, Oledzka G, Askanas V (2007) Myostatin precursor protein is increased and associates with amyloid-β precursor protein in inclusion-body myositis culture model. Neuropathol Appl Neurobiol 33:238–242PubMedCrossRef Wojcik S, Nogalska A, McFerrin J, Engel WK, Oledzka G, Askanas V (2007) Myostatin precursor protein is increased and associates with amyloid-β precursor protein in inclusion-body myositis culture model. Neuropathol Appl Neurobiol 33:238–242PubMedCrossRef
44.
go back to reference Yan R, Shi Q, Hu X, Zhou X (2006) Reticulon proteins: emerging players in neurodegenerative diseases. Cell Mol Life Sci 63:877–889PubMedCrossRef Yan R, Shi Q, Hu X, Zhou X (2006) Reticulon proteins: emerging players in neurodegenerative diseases. Cell Mol Life Sci 63:877–889PubMedCrossRef
Metadata
Title
NOGO is increased and binds to BACE1 in sporadic inclusion-body myositis and in AβPP-overexpressing cultured human muscle fibers
Authors
Slawomir Wojcik
W. King Engel
Riqiang Yan
Janis McFerrin
Valerie Askanas
Publication date
01-11-2007
Publisher
Springer-Verlag
Published in
Acta Neuropathologica / Issue 5/2007
Print ISSN: 0001-6322
Electronic ISSN: 1432-0533
DOI
https://doi.org/10.1007/s00401-007-0281-y

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