Literature DB >> 26611599

Gene Therapy Models of Alzheimer's Disease and Other Dementias.

Benjamin Combs1, Andrew Kneynsberg1,2, Nicholas M Kanaan3,4.   

Abstract

Dementias are among the most common neurological disorders, and Alzheimer's disease (AD) is the most common cause of dementia worldwide. AD remains a looming health crisis despite great efforts to learn the mechanisms surrounding the neuron dysfunction and neurodegeneration that accompanies AD primarily in the medial temporal lobe. In addition to AD, a group of diseases known as frontotemporal dementias (FTDs) are degenerative diseases involving atrophy and degeneration in the frontal and temporal lobe regions. Importantly, AD and a number of FTDs are collectively known as tauopathies due to the abundant accumulation of pathological tau inclusions in the brain. The precise role tau plays in disease pathogenesis remains an area of strong research focus. A critical component to effectively study any human disease is the availability of models that recapitulate key features of the disease. Accordingly, a number of animal models are currently being pursued to fill the current gaps in our knowledge of the causes of dementias and to develop effective therapeutics. Recent developments in gene therapy-based approaches, particularly in recombinant adeno-associated viruses (rAAVs), have provided new tools to study AD and other related neurodegenerative disorders. Additionally, gene therapy approaches have emerged as an intriguing possibility for treating these diseases in humans. This chapter explores the current state of rAAV models of AD and other dementias, discuss recent efforts to improve these models, and describe current and future possibilities in the use of rAAVs and other viruses in treatments of disease.

Entities:  

Keywords:  Animal model; Entorhinal cortex; Hippocampus; Neurofibrillary tangle; Recombinant adeno-associated virus; Tau protein

Mesh:

Substances:

Year:  2016        PMID: 26611599      PMCID: PMC4734109          DOI: 10.1007/978-1-4939-3271-9_25

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  146 in total

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Journal:  J Neurosci       Date:  2011-07-06       Impact factor: 6.167

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5.  Parkin reverses TDP-43-induced cell death and failure of amino acid homeostasis.

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Journal:  J Neurochem       Date:  2013-12-19       Impact factor: 5.372

6.  Beta-amyloid1-42 gene transfer model exhibits intraneuronal amyloid, gliosis, tau phosphorylation, and neuronal loss.

Authors:  G William Rebeck; Hyang-Sook Hoe; Charbel E-H Moussa
Journal:  J Biol Chem       Date:  2010-01-13       Impact factor: 5.157

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Journal:  J Neurosci       Date:  2013-04-10       Impact factor: 6.167

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Authors:  D G Drubin; M W Kirschner
Journal:  J Cell Biol       Date:  1986-12       Impact factor: 10.539

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Authors:  David Goertsen; Nicholas C Flytzanis; Nick Goeden; Miguel R Chuapoco; Alexander Cummins; Yijing Chen; Yingying Fan; Qiangge Zhang; Jitendra Sharma; Yangyang Duan; Liping Wang; Guoping Feng; Yu Chen; Nancy Y Ip; James Pickel; Viviana Gradinaru
Journal:  Nat Neurosci       Date:  2021-12-09       Impact factor: 24.884

Review 2.  The Path to Progress Preclinical Studies of Age-Related Neurodegenerative Diseases: A Perspective on Rodent and hiPSC-Derived Models.

Authors:  Gabriella MacDougall; Logan Y Brown; Boris Kantor; Ornit Chiba-Falek
Journal:  Mol Ther       Date:  2021-01-09       Impact factor: 11.454

Review 3.  Genetic Insights into Alzheimer's Disease.

Authors:  Caitlin S Latimer; Katherine L Lucot; C Dirk Keene; Brenna Cholerton; Thomas J Montine
Journal:  Annu Rev Pathol       Date:  2021-01-24       Impact factor: 23.472

4.  Impact of age and vector construct on striatal and nigral transgene expression.

Authors:  Nicole K Polinski; Fredric P Manfredsson; Matthew J Benskey; D Luke Fischer; Christopher J Kemp; Kathy Steece-Collier; Ivette M Sandoval; Katrina L Paumier; Caryl E Sortwell
Journal:  Mol Ther Methods Clin Dev       Date:  2016-12-07       Impact factor: 6.698

Review 5.  Axonal Degeneration in Tauopathies: Disease Relevance and Underlying Mechanisms.

Authors:  Andrew Kneynsberg; Benjamin Combs; Kyle Christensen; Gerardo Morfini; Nicholas M Kanaan
Journal:  Front Neurosci       Date:  2017-10-17       Impact factor: 4.677

6.  Persistent repression of tau in the brain using engineered zinc finger protein transcription factors.

Authors:  Susanne Wegmann; Sarah L DeVos; Bryan Zeitler; Kimberly Marlen; Rachel E Bennett; Marta Perez-Rando; Danny MacKenzie; Qi Yu; Caitlin Commins; Riley N Bannon; Bianca T Corjuc; Alison Chase; Lisa Diez; Hoang-Oanh B Nguyen; Sarah Hinkley; Lei Zhang; Alicia Goodwin; Annemarie Ledeboer; Stephen Lam; Irina Ankoudinova; Hung Tran; Nicholas Scarlott; Rainier Amora; Richard Surosky; Jeffrey C Miller; Ashley B Robbins; Edward J Rebar; Fyodor D Urnov; Michael C Holmes; Amy M Pooler; Brigit Riley; H Steve Zhang; Bradley T Hyman
Journal:  Sci Adv       Date:  2021-03-19       Impact factor: 14.136

7.  Synapsin-caveolin-1 gene therapy preserves neuronal and synaptic morphology and prevents neurodegeneration in a mouse model of AD.

Authors:  Shanshan Wang; Joseph S Leem; Sonia Podvin; Vivian Hook; Natalia Kleschevnikov; Paul Savchenko; Mehul Dhanani; Kimberly Zhou; Isabella C Kelly; Tong Zhang; Atsushi Miyanohara; Phuong Nguyen; Alexander Kleschevnikov; Steve L Wagner; John Q Trojanowski; David M Roth; Hemal H Patel; Piyush M Patel; Brian P Head
Journal:  Mol Ther Methods Clin Dev       Date:  2021-03-29       Impact factor: 6.698

  7 in total

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