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Publication : Abnormalities of plasma cytokines and spleen in senile APP/PS1/Tau transgenic mouse model.

First Author  Yang SH Year  2015
Journal  Sci Rep Volume  5
Pages  15703 PubMed ID  26503550
Mgi Jnum  J:269053 Mgi Id  MGI:6215720
Doi  10.1038/srep15703 Citation  Yang SH, et al. (2015) Abnormalities of plasma cytokines and spleen in senile APP/PS1/Tau transgenic mouse model. Sci Rep 5:15703
abstractText  The blood-based diagnosis has a potential to provide an alternative approach for easy diagnosis of Alzheimer's disease (AD) with less invasiveness and low-cost. However, present blood-based AD diagnosis mainly focuses on measuring the plasma Abeta level because no other biomarkers are found to possess evident transport mechanisms to pass the blood-brain barrier. In order to avoid diagnosing non-demented individuals with Abeta abnormality, finding additional biomarkers to supplement plasma Abeta is essential. In this study, we introduce potential neurodegenerative biomarkers for blood-based diagnosis. We observed severe splenomegaly and structural destruction in the spleen with significantly decreased B lymphocytes in senile APPswe, PS1M146V and TauP301L transgenic mice. We also found that inflammatory cytokines associated with splenic dysfunction were altered in the plasma of these mice. These findings suggest potential involvement of the splenic dysfunction in AD and the importance of biomarker level alterations in the plasma as putative diagnostic targets for AD.
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