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Dual Mechanisms for Shedding of the Cellular Prion Protein.

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Dual Mechanisms for Shedding of the Cellular Prion Protein. / Parkin, Edward T.; Watt, Nicole T.; Turner, Anthony J. et al.
In: Journal of Biological Chemistry, Vol. 279, No. 12, 19.03.2004, p. 11170-11178.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Parkin, ET, Watt, NT, Turner, AJ & Hooper, NM 2004, 'Dual Mechanisms for Shedding of the Cellular Prion Protein.', Journal of Biological Chemistry, vol. 279, no. 12, pp. 11170-11178. https://doi.org/10.1074/jbc.M312105200

APA

Parkin, E. T., Watt, N. T., Turner, A. J., & Hooper, N. M. (2004). Dual Mechanisms for Shedding of the Cellular Prion Protein. Journal of Biological Chemistry, 279(12), 11170-11178. https://doi.org/10.1074/jbc.M312105200

Vancouver

Parkin ET, Watt NT, Turner AJ, Hooper NM. Dual Mechanisms for Shedding of the Cellular Prion Protein. Journal of Biological Chemistry. 2004 Mar 19;279(12):11170-11178. doi: 10.1074/jbc.M312105200

Author

Parkin, Edward T. ; Watt, Nicole T. ; Turner, Anthony J. et al. / Dual Mechanisms for Shedding of the Cellular Prion Protein. In: Journal of Biological Chemistry. 2004 ; Vol. 279, No. 12. pp. 11170-11178.

Bibtex

@article{6c02bf6c5767470baaf0958ce895f2d2,
title = "Dual Mechanisms for Shedding of the Cellular Prion Protein.",
abstract = "The cellular prion protein (PrPC) is essential for the pathogenesis and transmission of prion diseases. Whereas the majority of PrPC is bound to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor, a secreted form of the protein has been identified. Here we show that PrPC can be shed into the medium of human neuroblastoma SH-SY5Y cells by both protease- and phospholipase-mediated mechanisms. The constitutive shedding of PrPC was inhibited by a range of hydroxamate-based zinc metalloprotease inhibitors in a manner identical to the -secretase-mediated shedding of the amyloid precursor protein, indicating a proteolytic shedding mechanism. Like amyloid precursor protein, this zinc metalloprotease-mediated shedding of PrPC could be stimulated by phorbol myristate acetate and by copper ions. The lipid raft-disrupting agents filipin and methyl--cyclodextrin promoted the shedding of PrPC via a distinct mechanism that was not inhibited by hydroxamate-based inhibitors. Filipin-mediated shedding of PrPC is likely to occur via phospholipase cleavage of the GPI anchor, since a transmembrane polypeptide-anchored PrP construct was not shed in response to filipin treatment. Collectively, our data indicate that shedding of PrPC can occur via both secretase-like proteolytic cleavage of the protein and phospholipase cleavage of the GPI anchor moiety.",
author = "Parkin, {Edward T.} and Watt, {Nicole T.} and Turner, {Anthony J.} and Hooper, {Nigel M.}",
year = "2004",
month = mar,
day = "19",
doi = "10.1074/jbc.M312105200",
language = "English",
volume = "279",
pages = "11170--11178",
journal = "Journal of Biological Chemistry",
issn = "1083-351X",
publisher = "American Society for Biochemistry and Molecular Biology Inc.",
number = "12",

}

RIS

TY - JOUR

T1 - Dual Mechanisms for Shedding of the Cellular Prion Protein.

AU - Parkin, Edward T.

AU - Watt, Nicole T.

AU - Turner, Anthony J.

AU - Hooper, Nigel M.

PY - 2004/3/19

Y1 - 2004/3/19

N2 - The cellular prion protein (PrPC) is essential for the pathogenesis and transmission of prion diseases. Whereas the majority of PrPC is bound to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor, a secreted form of the protein has been identified. Here we show that PrPC can be shed into the medium of human neuroblastoma SH-SY5Y cells by both protease- and phospholipase-mediated mechanisms. The constitutive shedding of PrPC was inhibited by a range of hydroxamate-based zinc metalloprotease inhibitors in a manner identical to the -secretase-mediated shedding of the amyloid precursor protein, indicating a proteolytic shedding mechanism. Like amyloid precursor protein, this zinc metalloprotease-mediated shedding of PrPC could be stimulated by phorbol myristate acetate and by copper ions. The lipid raft-disrupting agents filipin and methyl--cyclodextrin promoted the shedding of PrPC via a distinct mechanism that was not inhibited by hydroxamate-based inhibitors. Filipin-mediated shedding of PrPC is likely to occur via phospholipase cleavage of the GPI anchor, since a transmembrane polypeptide-anchored PrP construct was not shed in response to filipin treatment. Collectively, our data indicate that shedding of PrPC can occur via both secretase-like proteolytic cleavage of the protein and phospholipase cleavage of the GPI anchor moiety.

AB - The cellular prion protein (PrPC) is essential for the pathogenesis and transmission of prion diseases. Whereas the majority of PrPC is bound to the cell membrane via a glycosylphosphatidylinositol (GPI) anchor, a secreted form of the protein has been identified. Here we show that PrPC can be shed into the medium of human neuroblastoma SH-SY5Y cells by both protease- and phospholipase-mediated mechanisms. The constitutive shedding of PrPC was inhibited by a range of hydroxamate-based zinc metalloprotease inhibitors in a manner identical to the -secretase-mediated shedding of the amyloid precursor protein, indicating a proteolytic shedding mechanism. Like amyloid precursor protein, this zinc metalloprotease-mediated shedding of PrPC could be stimulated by phorbol myristate acetate and by copper ions. The lipid raft-disrupting agents filipin and methyl--cyclodextrin promoted the shedding of PrPC via a distinct mechanism that was not inhibited by hydroxamate-based inhibitors. Filipin-mediated shedding of PrPC is likely to occur via phospholipase cleavage of the GPI anchor, since a transmembrane polypeptide-anchored PrP construct was not shed in response to filipin treatment. Collectively, our data indicate that shedding of PrPC can occur via both secretase-like proteolytic cleavage of the protein and phospholipase cleavage of the GPI anchor moiety.

U2 - 10.1074/jbc.M312105200

DO - 10.1074/jbc.M312105200

M3 - Journal article

VL - 279

SP - 11170

EP - 11178

JO - Journal of Biological Chemistry

JF - Journal of Biological Chemistry

SN - 1083-351X

IS - 12

ER -