Literature DB >> 33428128

Tau in Alzheimer's Disease: Pathological Alterations and an Attractive Therapeutic Target.

Jian-Lan Gu1,2, Fei Liu3.   

Abstract

Alzheimer's disease (AD) is an age-related neurodegenerative disease with two major hallmarks: extracellular amyloid plaques made of amyloid-β (Aβ) and intracellular neurofibrillary tangles (NFTs) of abnormally hyperphosphorylated tau. The number of NFTs correlates positively with the severity of dementia in AD patients. However, there is still no efficient therapy available for AD treatment and prevention so far. A deeper understanding of AD pathogenesis has identified novel strategies for the generation of specific therapies over the past few decades. Several studies have suggested that the prion-like seeding and spreading of tau pathology in the brain may be a key driver of AD. Tau protein is considered as a promising candidate target for the development of therapeutic interventions due to its considerable pathological role in a variety of neurodegenerative disorders. Abnormal tau hyperphosphorylation plays a detrimental pathological role, eventually leading to neurodegeneration. In the present review, we describe the recent research progresses in the pathological mechanisms of tau protein in AD and briefly discuss tau-based therapeutic strategies.

Entities:  

Keywords:  Alzheimer’s disease; hyperphosphorylation; propagation of tau pathology; tau protein

Year:  2021        PMID: 33428128     DOI: 10.1007/s11596-020-2282-1

Source DB:  PubMed          Journal:  Curr Med Sci        ISSN: 2523-899X


  130 in total

1.  The pathological process underlying Alzheimer's disease in individuals under thirty.

Authors:  Heiko Braak; Kelly Del Tredici
Journal:  Acta Neuropathol       Date:  2010-12-15       Impact factor: 17.088

2.  Microtubule-associated protein tau. A component of Alzheimer paired helical filaments.

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Journal:  J Biol Chem       Date:  1986-05-05       Impact factor: 5.157

3.  Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.

Authors:  I Grundke-Iqbal; K Iqbal; Y C Tung; M Quinlan; H M Wisniewski; L I Binder
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

Review 4.  Staging of Alzheimer's disease-related neurofibrillary changes.

Authors:  H Braak; E Braak
Journal:  Neurobiol Aging       Date:  1995 May-Jun       Impact factor: 4.673

5.  Memory and mental status correlates of modified Braak staging.

Authors:  E Grober; D Dickson; M J Sliwinski; H Buschke; M Katz; H Crystal; R B Lipton
Journal:  Neurobiol Aging       Date:  1999 Nov-Dec       Impact factor: 4.673

6.  Hyperphosphorylation induces self-assembly of tau into tangles of paired helical filaments/straight filaments.

Authors:  A Alonso ; T Zaidi; M Novak; I Grundke-Iqbal; K Iqbal
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-29       Impact factor: 11.205

7.  Neurofibrillary tangles but not senile plaques parallel duration and severity of Alzheimer's disease.

Authors:  P V Arriagada; J H Growdon; E T Hedley-Whyte; B T Hyman
Journal:  Neurology       Date:  1992-03       Impact factor: 9.910

8.  Role of abnormally phosphorylated tau in the breakdown of microtubules in Alzheimer disease.

Authors:  A C Alonso; T Zaidi; I Grundke-Iqbal; K Iqbal
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-07       Impact factor: 11.205

Review 9.  Neuropathological stageing of Alzheimer-related changes.

Authors:  H Braak; E Braak
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

10.  Alzheimer's neurofibrillary pathology and the spectrum of cognitive function: findings from the Nun Study.

Authors:  Kathryn P Riley; David A Snowdon; William R Markesbery
Journal:  Ann Neurol       Date:  2002-05       Impact factor: 10.422

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  2 in total

Review 1.  The regulatory role of Pin1 in neuronal death.

Authors:  Shu-Chao Wang; Xi-Min Hu; Kun Xiong
Journal:  Neural Regen Res       Date:  2023-01       Impact factor: 6.058

2.  Inhibition of heat shock proteins increases autophagosome formation, and reduces the expression of APP, Tau, SOD1 G93A and TDP-43.

Authors:  Paul Dent; Laurence Booth; Jane L Roberts; Andrew Poklepovic; Derek Cridebring; Eric M Reiman
Journal:  Aging (Albany NY)       Date:  2021-07-12       Impact factor: 5.682

  2 in total

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