Prions: Protein Aggregation and Infectious Diseases - Physiological ...
Prions: Protein Aggregation and Infectious Diseases - Physiological ...
Prions: Protein Aggregation and Infectious Diseases - Physiological ...
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1148 ADRIANO AGUZZI AND ANNA MARIA CALELLA<br />
volves autonomic fibers of the splanchnic <strong>and</strong> vagus nerves. J Virol<br />
75: 9320–9327, 2001.<br />
337. McKinley MP, Bolton DC, Prusiner SB. A protease-resistant<br />
protein is a structural component of the scrapie prion. Cell 35:<br />
57–62, 1983.<br />
338. McKinley MP, Meyer RK, Kenaga L, Rahbar F, Cotter R,<br />
Serban A, Prusiner SB. Scrapie prion rod formation in vitro<br />
requires both detergent extraction <strong>and</strong> limited proteolysis. J Virol<br />
65: 1340–1351, 1991.<br />
339. Mead S. Prion disease genetics. Eur J Hum Genet 14: 273–281,<br />
2006.<br />
340. Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE,<br />
Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich<br />
H, Verzilli C, Alpers MP, Whittaker JC, Collinge J. Genetic risk<br />
factors for variant Creutzfeldt-Jakob disease: a genome-wide association<br />
study. Lancet Neurol 8: 57–66, 2009.<br />
341. Mead S, Stumpf MP, Whitfield J, Beck JA, Poulter M, Campbell<br />
T, Uphill JB, Goldstein D, Alpers M, Fisher EM, Collinge<br />
J. Balancing selection at the prion protein gene consistent with<br />
prehistoric kurulike epidemics. Science 300: 640–643, 2003.<br />
342. Meggendorfer F. Klinische und genealogische Beobachtungen bei<br />
einem Fall von spastischer Pseudosklerose Jakobs. Z Ges Neurol<br />
Psychiatr 128: 337–341, 1930.<br />
343. Meier P, Genoud N, Prinz M, Maissen M, Rulicke T, Zurbriggen<br />
A, Raeber AJ, Aguzzi A. Soluble dimeric prion protein binds<br />
PrP(Sc) in vivo <strong>and</strong> antagonizes prion disease. Cell 113: 49–60,<br />
2003.<br />
344. Merz PA, Somerville RA, Wisniewski HM, Manuelidis L, Manuelidis<br />
EE. Scrapie-associated fibrils in Creutzfeldt-Jakob disease.<br />
Nature 306: 474–476, 1983.<br />
345. Meyer-Luehmann M, Coomaraswamy J, Bolmont T, Kaeser S,<br />
Schaefer C, Kilger E, Neuenschw<strong>and</strong>er A, Abramowski D,<br />
Frey P, Jaton AL, Vigouret JM, Paganetti P, Walsh DM,<br />
Mathews PM, Ghiso J, Staufenbiel M, Walker LC, Jucker M.<br />
Exogenous induction of cerebral beta-amyloidogenesis is governed<br />
by agent <strong>and</strong> host. Science 313: 1781–1784, 2006.<br />
346. Meyer RK, McKinley MP, Bowman KA, Braunfeld MB, Barry<br />
RA, Prusiner SB. Separation <strong>and</strong> properties of cellular <strong>and</strong><br />
scrapie prion proteins. Proc Natl Acad Sci USA 83: 2310–2314,<br />
1986.<br />
347. Miele G, Seeger H, Marino D, Eberhard R, Heikenwalder M,<br />
Stoeck K, Basagni M, Knight R, Green A, Chianini F, Wuthrich<br />
RP, Hock C, Zerr I, Aguzzi A. Urinary alpha1-antichymotrypsin:<br />
a biomarker of prion infection. PLoS ONE 3: e3870, 2008.<br />
348. Miller MW, Williams ES. Prion disease: horizontal prion transmission<br />
in mule deer. Nature 425: 35–36, 2003.<br />
349. Miller MW, Williams ES, Hobbs NT, Wolfe LL. Environmental<br />
sources of prion transmission in mule deer. Emerg Infect Dis 10:<br />
1003–1006, 2004.<br />
350. Millson GC, Hunter GD, Kimberlin RH. An experimental examination<br />
of the scrapie agent in cell membrane mixtures. II. The<br />
association of scrapie activity with membrane fractions. J Comp<br />
Pathol 81: 255–265, 1971.<br />
351. Mishra RS, Basu S, Gu Y, Luo X, Zou WQ, Mishra R, Li R, Chen<br />
SG, Gambetti P, Fujioka H, Singh N. Protease-resistant human<br />
prion protein <strong>and</strong> ferritin are cotransported across Caco-2 epithelial<br />
cells: implications for species barrier in prion uptake from the<br />
intestine. J Neurosci 24: 11280–11290, 2004.<br />
352. Moechars D, Dewachter I, Lorent K, Reverse D, Baekel<strong>and</strong>t V,<br />
Naidu A, Tesseur I, Spittaels K, Haute CV, Checler F, Godaux<br />
E, Cordell B, Van Leuven F. Early phenotypic changes in transgenic<br />
mice that overexpress different mutants of amyloid precursor<br />
protein in brain. J Biol Chem 274: 6483–6492, 1999.<br />
353. Mohan J, Brown KL, Farquhar CF, Bruce ME, Mabbott NA.<br />
Scrapie transmission following exposure through the skin is dependent<br />
on follicular dendritic cells in lymphoid tissues. J Dermatol<br />
Sci 35: 101–111, 2004.<br />
354. Montrasio F, Cozzio A, Flechsig E, Rossi D, Klein MA, Rulicke<br />
T, Raeber AJ, Vosshenrich CA, Proft J, Aguzzi A, Weissmann<br />
C. B lymphocyte-restricted expression of prion protein does not<br />
enable prion replication in prion protein knockout mice. Proc Natl<br />
Acad Sci USA 98: 4034–4037, 2001.<br />
Physiol Rev VOL 89 OCTOBER 2009 www.prv.org<br />
355. Montrasio F, Frigg R, Glatzel M, Klein MA, Mackay F, Aguzzi<br />
A, Weissmann C. Impaired prion replication in spleens of mice<br />
lacking functional follicular dendritic cells. Science 288: 1257–1259,<br />
2000.<br />
356. Moore RC, Lee IY, Silverman GL, Harrison PM, Strome R,<br />
Heinrich C, Karunaratne A, Pasternak SH, Chishti MA, Liang<br />
Y, Mastrangelo P, Wang K, Smit AF, Katamine S, Carlson GA,<br />
Cohen FE, Prusiner SB, Melton DW, Tremblay P, Hood LE,<br />
Westaway D. Ataxia in prion protein (PrP)-deficient mice is associated<br />
with upregulation of the novel PrP-like protein doppel. J Mol<br />
Biol 292: 797–817, 1999.<br />
357. Morel E, Andrieu T, Casagr<strong>and</strong>e F, Gauczynski S, Weiss S,<br />
Grassi J, Rousset M, Dormont D, Chambaz J. Bovine prion is<br />
endocytosed by human enterocytes via the 37 kDa/67 kDa laminin<br />
receptor. Am J Pathol 167: 1033–1042, 2005.<br />
358. Moroncini G, Mangieri M, Morbin M, Mazzoleni G, Ghetti B,<br />
Gabrielli A, Williamson RA, Giaccone G, Tagliavini F. Pathologic<br />
prion protein is specifically recognized in situ by a novel PrP<br />
conformational antibody. Neurobiol Dis 23: 717–724, 2006.<br />
359. Munson L, Terio KA, Worley M, Jago M, Bagot-Smith A,<br />
Marker L. Extrinsic factors significantly affect patterns of disease<br />
in free-ranging <strong>and</strong> captive cheetah (Acinonyx jubatus) populations.<br />
J Wildl Dis 41: 542–548, 2005.<br />
360. Muramoto T, DeArmond SJ, Scott M, Telling GC, Cohen FE,<br />
Prusiner SB. Heritable disorder resembling neuronal storage disease<br />
in mice expressing prion protein with deletion of an alphahelix.<br />
Nat Med 3: 750–755, 1997.<br />
361. Muramoto T, Scott M, Cohen FE, Prusiner SB. Recombinant<br />
Scrapie-like prion protein of 106 amino acids is soluble. Proc Natl<br />
Acad Sci USA 93: 15457–15462, 1996.<br />
362. Naslavsky N, Stein R, Yanai A, Friedl<strong>and</strong>er G, Taraboulos A.<br />
Characterization of detergent-insoluble complexes containing the<br />
cellular prion protein <strong>and</strong> its scrapie isoform. J Biol Chem 272:<br />
6324–6331, 1997.<br />
363. Neutra MR, Frey A, Kraehenbuhl JP. Epithelial M cells: gateways<br />
for mucosal infection <strong>and</strong> immunization. Cell 86: 345–348,<br />
1996.<br />
364. Nilsberth C, Westlind-Danielsson A, Eckman CB, Condron<br />
MM, Axelman K, Forsell C, Stenh C, Luthman J, Teplow DB,<br />
Younkin SG, Naslund J, Lannfelt L. The “Arctic” APP mutation<br />
(E693G) causes Alzheimer’s disease by enhanced Abeta protofibril<br />
formation. Nat Neurosci 4: 887–893, 2001.<br />
365. Nilsson KP, Aslund A, Berg I, Nystrom S, Konradsson P,<br />
Herl<strong>and</strong> A, Inganas O, Stabo-Eeg F, Lindgren M, Westermark<br />
GT, Lannfelt L, Nilsson LN, Hammarstrom P. Imaging distinct<br />
conformational states of amyloid-beta fibrils in Alzheimer’s disease<br />
using novel luminescent probes. ACS Chem Biol 2: 553–560, 2007.<br />
366. Nilsson KPR, Hammarstrom P, Ahlgren F, Herl<strong>and</strong> A, Schnell<br />
EA, Lindgren M, Westermark GT, Inganas O. Conjugated polyelectrolytes-conformation-sensitive<br />
optical probes for staining <strong>and</strong><br />
characterization of amyloid deposits. Chembiochem 7: 1096–1104,<br />
2006.<br />
367. Nilsson KPR, Herl<strong>and</strong> A, Hammarstrom P, Inganas O. Conjugated<br />
polyelectrolytes: conformation-sensitive optical probes for<br />
detection of amyloid fibril formation. Biochemistry 44: 3718–3724,<br />
2005.<br />
368. Nishida N, Tremblay P, Sugimoto T, Shigematsu K, Shirabe S,<br />
Petromilli C, Erpel SP, Nakaoke R, Atarashi R, Houtani T,<br />
Torchia M, Sakaguchi S, DeArmond SJ, Prusiner SB, Katamine<br />
S. A mouse prion protein transgene rescues mice deficient<br />
for the prion protein gene from Purkinje cell degeneration <strong>and</strong><br />
demyelination. Lab Invest 79: 689–697, 1999.<br />
369. Nonno R, Bari MA, Cardone F, Vaccari G, Fazzi P, Dell’omo G,<br />
Cartoni C, Ingrosso L, Boyle A, Galeno R, Sbriccoli M, Lipp<br />
HP, Bruce M, Pocchiari M, Agrimi U. Efficient transmission <strong>and</strong><br />
characterization of Creutzfeldt-Jakob disease strains in bank voles.<br />
PLoS Pathog 2: e12, 2006.<br />
370. Oesch B, Westaway D, Walchli M, McKinley MP, Kent SB,<br />
Aebersold R, Barry RA, Tempst P, Teplow DB, Hood LE,<br />
Weissmann C. A cellular gene encodes scrapie PrP 27–30 protein.<br />
Cell 40: 735–746, 1985.