Multiple signaling factors and drugs alleviate neuronal death induced by expression of human and zebrafish tau proteins in vivo

Bo Kai Wu, Rey Yue Yuan, Huang Wei Lien, Chin Chun Hung, Pung Pung Hwang, Rita Pei Yeh Chen, Chun Che Chang, Yung Feng Liao, Chang Jen Huang

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Background: The axonal tau protein is a tubulin-binding protein, which plays important roles in the formation and stability of the microtubule. Mutations in the tau gene are associated with familial forms of frontotemporal dementia with Parkinsonism linked to chromosome-17 (FTDP-17). Paired helical filaments of tau and extracellular plaques containing beta-amyloid are found in the brain of Alzheimer's disease (AD) patients. Results: Transgenic models, including those of zebrafish, have been employed to elucidate the mechanisms by which tau protein causes neurodegeneration. In this study, a transient expression system was established to express GFP fusion proteins of zebrafish and human tau under the control of a neuron-specific HuC promoter. Approximately ten neuronal cells expressing tau-GFP in zebrafish embryos were directly imaged and traced by time-lapse recording, in order to evaluate the neurotoxicity induced by tau-GFP proteins. Expression of tau-GFP was observed to cause high levels of neuronal death. However, multiple signaling factors, such as Bcl2-L1, Nrf2, and GDNF, were found to effectively protect neuronal cells expressing tau-GFP from death. Treatment with chemical compounds that exert anti-oxidative or neurotrophic effects also resulted in a similar protective effect and maintained human tau-GFP protein in a phosphorylated state, as detected by antibodies pT212 and AT8. Conclusions: The novel finding of this study is that we established an expression system expressing tau-GFP in zebrafish embryos were directly imaged and traced by time-lapse recording to evaluate the neurotoxicity induced by tau-GFP proteins. This system may serve as an efficient in vivo imaging platform for the discovery of novel drugs against tauopathy.

Original languageEnglish
Article number25
JournalJournal of Biomedical Science
Volume23
Issue number1
DOIs
Publication statusPublished - Feb 6 2016

Fingerprint

tau Proteins
Zebrafish
Cells
Pharmaceutical Preparations
Glial Cell Line-Derived Neurotrophic Factor
Proteins
Chemical compounds
Embryonic Structures
Tauopathies
Tubulin
Chromosomes
Amyloid
Frontotemporal Dementia
Chromosomes, Human, Pair 17
Neurons
Brain
Carrier Proteins
Brain Diseases
Drug Discovery
Fusion reactions

Keywords

  • Bcl2-L1
  • GDNF
  • Neurotoxicity
  • Nrf2
  • Tauopathy
  • Zebrafish

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Molecular Biology
  • Cell Biology
  • Biochemistry, medical
  • Endocrinology, Diabetes and Metabolism
  • Pharmacology (medical)

Cite this

Multiple signaling factors and drugs alleviate neuronal death induced by expression of human and zebrafish tau proteins in vivo. / Wu, Bo Kai; Yuan, Rey Yue; Lien, Huang Wei; Hung, Chin Chun; Hwang, Pung Pung; Chen, Rita Pei Yeh; Chang, Chun Che; Liao, Yung Feng; Huang, Chang Jen.

In: Journal of Biomedical Science, Vol. 23, No. 1, 25, 06.02.2016.

Research output: Contribution to journalArticle

Wu, Bo Kai ; Yuan, Rey Yue ; Lien, Huang Wei ; Hung, Chin Chun ; Hwang, Pung Pung ; Chen, Rita Pei Yeh ; Chang, Chun Che ; Liao, Yung Feng ; Huang, Chang Jen. / Multiple signaling factors and drugs alleviate neuronal death induced by expression of human and zebrafish tau proteins in vivo. In: Journal of Biomedical Science. 2016 ; Vol. 23, No. 1.
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AU - Yuan, Rey Yue

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AB - Background: The axonal tau protein is a tubulin-binding protein, which plays important roles in the formation and stability of the microtubule. Mutations in the tau gene are associated with familial forms of frontotemporal dementia with Parkinsonism linked to chromosome-17 (FTDP-17). Paired helical filaments of tau and extracellular plaques containing beta-amyloid are found in the brain of Alzheimer's disease (AD) patients. Results: Transgenic models, including those of zebrafish, have been employed to elucidate the mechanisms by which tau protein causes neurodegeneration. In this study, a transient expression system was established to express GFP fusion proteins of zebrafish and human tau under the control of a neuron-specific HuC promoter. Approximately ten neuronal cells expressing tau-GFP in zebrafish embryos were directly imaged and traced by time-lapse recording, in order to evaluate the neurotoxicity induced by tau-GFP proteins. Expression of tau-GFP was observed to cause high levels of neuronal death. However, multiple signaling factors, such as Bcl2-L1, Nrf2, and GDNF, were found to effectively protect neuronal cells expressing tau-GFP from death. Treatment with chemical compounds that exert anti-oxidative or neurotrophic effects also resulted in a similar protective effect and maintained human tau-GFP protein in a phosphorylated state, as detected by antibodies pT212 and AT8. Conclusions: The novel finding of this study is that we established an expression system expressing tau-GFP in zebrafish embryos were directly imaged and traced by time-lapse recording to evaluate the neurotoxicity induced by tau-GFP proteins. This system may serve as an efficient in vivo imaging platform for the discovery of novel drugs against tauopathy.

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