Inhibition of prion propagation in scrapie-infected mouse neuroblastoma cell lines using mouse monoclonal antibodies against prion protein

被引:22
|
作者
Miyamoto, K
Nakamura, N
Aosasa, M
Nishida, N
Yokoyama, T
Horiuchi, H
Furusawa, S
Matsuda, H
机构
[1] Hiroshima Univ, Lab Immunobiol, Dept Mol & Appl Biosci, Grad Sch Biosphere Sci, Hiroshima 7398528, Japan
[2] Nagasaki Univ, Grad Sch Med Sci, Dept Mol Microbiol & Immunol, Nagasaki 8528523, Japan
[3] Natl Inst Anim Hlth, Pr Dis Res Ctr, Tsukuba, Ibaraki 3050856, Japan
[4] Hiroshima Prefectural Inst Ind Sci & Technol, Hiroshima 7390046, Japan
关键词
PrP-specific antibody; inhibition of prion accumulation; helix 1 of PrP; 154th tyrosine of PrP; prion strain;
D O I
10.1016/j.bbrc.2005.07.063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We screened six mouse monoclonal antibodies (mAbs) against prion protein (PrP), which were previously established in our laboratory, for inhibitory activity against PrPSc-accumulation in scrapie-infected cell lines and identified two mAbs, 3S9 and 2H9, as possessing this inhibitory activity. mAb 3S9 recognized an epitope including 154th tyrosine in the helix I region of PrP, while mAb 2H9 recognized a discontinuous region that included helix 1. In three scrapie-infected cell lines infected with different mouse-adapted scrapie strains, mAb 3S9 strongly inhibited accumulation of PrPSc, while mAb 2H9 moderately inhibited accumulation of PrPSc, indicating that inhibition of prion propagation by mAbs may be dependent on PrPSc characteristics. Furthermore, mAb 3S9 completely excluded PrPSc from these cell lines. These results suggest that mAbs 3S9 and 2H9 might be useful for clarifying the mechanisms of prion propagation and prevention by PrP-specific antibodies, and for tracing the conversion of PrPC to other PrPSc isoforms. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:197 / 204
页数:8
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