Journal Article

PP2 and piceatannol inhibit PrP<sub>106–126</sub>-induced iNOS activation mediated by CD36 in BV2 microglia

Siming Zhang, Lifeng Yang, Mohammed Kouadir, Rongrong Tan, Yun Lu, Jiaxin Chang, Binrui Xu, Xiaomin Yin, Xiangmei Zhou and Deming Zhao

in Acta Biochimica et Biophysica Sinica

Published on behalf of Institute of Biochemistry and Cell Biology, SIBS, CAS

Volume 45, issue 9, pages 763-772
Published in print September 2013 | ISSN: 1672-9145
Published online July 2013 | e-ISSN: 1745-7270 | DOI: https://dx.doi.org/10.1093/abbs/gmt074
PP2 and piceatannol inhibit PrP106–126-induced iNOS activation mediated by CD36 in BV2 microglia

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Prion diseases are a group of transmissible fatal neurodegenerative disorders of humans and animals, including bovine spongiform encephalopathy, scrapie, and Creutzfeldt–Jakob disease. Microglia, the resident macrophages of the central nervous system, are exquisitely sensitive to pathological tissue alterations, altering their morphology and phenotype to adopt a so-called activated state and perform immunological functions in response to pathophysiological brain insults. Although recent findings have provided valuable insights into the role microglia play in the proinflammatory events observed in prion, the intracellular signaling molecules responsible for the initiation of these responses remain to be elucidated. It seems that microglial activation involve PrP106–126 binding and the activation of cell surface immune and adhesion molecules such as CD36 and integrins, with the subsequent recruitment of Src family tyrosine kinases such as Fyn, Lyn, and Syk kinases. In the present study, we show that CD36 is involved in PrP106–126-induced microglial activation and that PP2 and piceatannol (Pic) can abrogate neurotoxic prion peptides-induced inducible nitric oxide synthase activation in microglia. These findings unveil a previously unrecognized role of PP2 and Pic as Src family kinase Fyn and the tyrosine kinase Syk inhibitor involved in neurotoxic prion peptides–microglia interactions, thus providing new insights into mechanisms underlying the activation of microglia by neurotoxic prion peptides.

Keywords: cd36; pp2; piceatannol (Pic); PrP106–126; bv2 microglia; iNOS

Journal Article.  5080 words.  Illustrated.

Subjects: Biochemistry

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