University of Tasmania
Browse

File(s) under permanent embargo

Role of cystatin C in amyloid precursor protein-induced proliferation of neural stem/progenitor cells

journal contribution
posted on 2023-05-17, 18:29 authored by Hu, Y, Hung, AC, Cui, H, Dawkins, E, Bolos, M, Lisa FoaLisa Foa, Kaylene YoungKaylene Young, David SmallDavid Small
The amyloid precursor protein (APP) is well studied for its role in Alzheimer's disease. However, little is known about its normal function. In this study, we examined the role of APP in neural stem/progenitor cell (NSPC) proliferation. NSPCs derived from APP-overexpressing Tg2576 transgenic mice proliferated more rapidly than NSPCs from the corresponding background strain (C57Bl/6xSJL) wild-type mice. In contrast, NSPCs from APP knockout (APP-KO) mice had reduced proliferation rates compared to NSPCs from the corresponding background strain (C57Bl/6). A secreted factor, identified as cystatin C, was found to be responsible for this effect. Levels of cystatin C were higher in the Tg2576 conditioned medium and lower in the APP-KO conditioned medium. Furthermore, immunodepletion of cystatin C from the conditioned medium completely removed the ability of the conditioned medium to increase NSPC proliferation. The results demonstrate that APP expression stimulates NSPC proliferation, and that this effect is mediated via an increase in cystatin C secretion.

Funding

National Health & Medical Research Council

History

Publication title

Journal of Biological Chemistry

Volume

288

Issue

26

Pagination

18853-18862

ISSN

0021-9258

Department/School

Menzies Institute for Medical Research

Publisher

Amer Soc Biochemistry Molecular Biology Inc

Place of publication

9650 Rockville Pike, Bethesda, USA, Md, 20814-3996

Rights statement

Copyright 2013 The American Society for Biochemistry and Molecular Biology, Inc.

Repository Status

  • Restricted

Socio-economic Objectives

Expanding knowledge in the biological sciences

Usage metrics

    University Of Tasmania

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC