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J Neuroimmunol. 2009 Apr 30;209(1-2):16-25. doi: 10.1016/j.jneuroim.2009.01.013. Epub 2009 Feb 20.

Human misfolded truncated tau protein promotes activation of microglia and leukocyte infiltration in the transgenic rat model of tauopathy.

Author information

1
Institute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovak Republic.

Abstract

It has been hypothesized that misfolded tau protein could be a mediator of the inflammatory response in human tauopathies. Here we show that neurodegenerative lesions caused by human truncated tau promote inflammatory response manifested by upregulation of immune-molecules (CD11a,b, CD18, CD4, CD45 and CD68) and morphological activation of microglial cells in a rat model of tauopathy. In parallel, the innate immune brain response promotes activation of MHC class II positive blood-borne leukocytes and their influx into the brain parenchyma. These findings have important consequences for the rationale drug development of effective inflammation-based therapeutic strategies for human tauopathies.

PMID:
19232747
DOI:
10.1016/j.jneuroim.2009.01.013
[Indexed for MEDLINE]

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