Fyn knock-down increases Aβ, decreases phospho-tau, and worsens spatial learning in 3 x Tg-AD mice

NEUROBIOLOGY OF AGING

卷:33

Article

Minami, S. Sakura¹  Clifford, Thomas G.¹  Hoe, Hyang-Sook^1,2  Matsuoka, Yasuji²  Rebeck, G. William¹ 

[1] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20057 USA

[2] Georgetown Univ, Med Ctr, Dept Neurol, Washington, DC 20057 USA

关键词: Fyn;    APP;    A beta;    Tau;    Phosphorylation;   

DOI  :  10.1016/j.neurobiolaging.2011.05.014

来源: Elsevier

【 摘 要 】

Fyn kinase phosphorylates tau and exacerbates amyloid beta (A beta)-mediated synaptic dysfunction. However, Fyn also increases the nonpathological cleavage of amyloid precursor protein (APP), suggesting opposing roles for Fyn in the pathogenesis of Alzheimer's disease (AD). To determine the effect of Fyn on both A beta and tau pathologies, we crossed homozygous Alzheimer's disease triple transgenic (3 x Tg) mice harboring mutations in amyloid precursor protein, presenilin-1, and tau with wild-type or Fyn knockout mice to generate Fyn(+/+) 3 x Tg(+/-) or Fyn(+/-) 3 x Tg(+/-) mice. We found that Fyn(+/-) 3 x Tg(+/-) mice had increased soluble and intracellular A beta, and these changes were accompanied by impaired performance on the Morris water maze at 18 months. Fyn(+/-)3 x Tg(+/-) mice had decreased phosphorylated tau at 15-18 months (as did Fyn knockout mice), but Fyn(+/-)3 x Tg(+/-) mice had increased phosphorylated tau by 24 months. In addition, we observed that Fyn(+/-)3 x Tg(+/-) males were delayed in developing A beta pathology compared with females, and displayed better spatial learning performance at 18 months. Overall, these findings suggest that loss of Fyn at early stages of disease increases soluble A beta accumulation and worsens spatial learning in the absence of changes in tau phosphorylation. (C) 2012 Elsevier Inc. All rights reserved.

【 授权许可】

Free