Human prion diseases and the prion protein - what is the current state of knowledge?

被引:5
|
作者
Nafe, Reinhold [1 ]
Arendt, Christophe T. [1 ]
Hattingen, Elke [1 ]
机构
[1] Clin Johann Wolfgang Goethe Univ, Dept Neuroradiol, Schleusenweg 2-16, D-60528 Frankfurt, Germany
关键词
Creutzfeldt-Jakob disease; variably protease-sensitive prionopathy; fatal familial insomnia; Gerstmann-Straussler-Scheinker disease; Kuru; CREUTZFELDT-JAKOB-DISEASE; FATAL FAMILIAL INSOMNIA; SENSITIVE PRIONOPATHY; HUNTINGTON-DISEASE; A-BETA; SPONGIFORM ENCEPHALOPATHY; CYCLIC AMPLIFICATION; VARIANT; PRPC; EXPRESSION;
D O I
10.1515/tnsci-2022-0315
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Prion diseases and the prion protein are only partially understood so far in many aspects. This explains the continued research on this topic, calling for an overview on the current state of knowledge. The main objective of the present review article is to provide a comprehensive up-to-date presentation of all major features of human prion diseases bridging the gap between basic research and clinical aspects. Starting with the prion protein, current insights concerning its physiological functions and the process of pathological conversion will be highlighted. Diagnostic, molecular, and clinical aspects of all human prion diseases will be discussed, including information concerning rare diseases like prion-associated amyloidoses and Huntington disease-like 1, as well as the question about a potential human threat due to the transmission of prions from prion diseases of other species such as chronic wasting disease. Finally, recent attempts to develop future therapeutic strategies will be addressed.
引用
收藏
页数:23
相关论文
共 50 条
  • [1] HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN
    KITAMOTO, T
    TATEISHI, J
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1994, 343 (1306) : 391 - 398
  • [2] Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type
    Pan, T
    Li, RL
    Kang, SC
    Pastore, M
    Wong, BS
    Ironside, J
    Gambetti, P
    Sy, MS
    JOURNAL OF NEUROCHEMISTRY, 2005, 92 (01) : 132 - 142
  • [3] Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseases
    Kovacs, GG
    Voigtländer, T
    Hainfellner, JA
    Budka, H
    ACTA NEUROPATHOLOGICA, 2002, 104 (03) : 320 - 326
  • [4] Prion protein aggregation assays in the diagnosis of human prion diseases
    Green, Alison J. E.
    FUTURE NEUROLOGY, 2015, 10 (03) : 217 - 228
  • [5] Distribution of intraneuronal immunoreactivity for the prion protein in human prion diseases
    Gabor G. Kovacs
    Till Voigtländer
    Johannes A. Hainfellner
    Herbert Budka
    Acta Neuropathologica, 2002, 104 : 320 - 326
  • [6] The prion protein in human neuromuscular diseases
    Kovács, GG
    Kalev, O
    Gelpi, E
    Haberler, C
    Wanschitz, J
    Strohschneider, M
    Molnár, MJ
    László, L
    Budka, H
    JOURNAL OF PATHOLOGY, 2004, 204 (03): : 241 - 247
  • [7] The prion hypothesis and the human prion diseases
    Aguzzi, AA
    BERLINER UND MUNCHENER TIERARZTLICHE WOCHENSCHRIFT, 2002, 115 (3-4): : 91 - 98
  • [8] TRUNCATED FORMS OF THE HUMAN PRION PROTEIN IN NORMAL BRAIN AND IN PRION DISEASES
    CHEN, SG
    TEPLOW, DB
    PARCHI, P
    TELLER, JK
    GAMBETTI, P
    AUTILIOGAMBETTI, L
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) : 19173 - 19180
  • [9] Accumulation of prion protein in the peripheral nervous system in human prion diseases
    Lee, CCM
    Kuo, LT
    Wang, CH
    Scaravilli, F
    An, SF
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2005, 64 (08): : 716 - 721
  • [10] Conformational conversion of prion protein in prion diseases
    Zhou, Zheng
    Xiao, Gengfu
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2013, 45 (06) : 465 - 476