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PMID: 2423882 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mechanism of membrane damage mediated by human eosinophil cationic protein.

Nature ·Vol. 321 ·No. 6070 ·1986-00-00 ·Pages 613-6

Young JD, Peterson CG, Venge P, Cohn ZA

Abstract

Recent evidence suggests a role for eosinophil granule proteins in contact-dependent antibody-mediated cytotoxicity. Cytolysis may involve a secretory phenomenon whereby granule proteins are released at the site of contact between eosinophil and target cells. Several basic proteins have been isolated from eosinophil granules, including the major basic protein, eosinophil cationic protein, eosinophil protein-X and eosinophil peroxidase. One of the major granule proteins of human eosinophils is the eosinophil cationic protein (ECP) which has been shown to damage schistosomula of Schistosoma mansoni at concentrations as low as 10(-7). Here, we describe the formation of functional channels by purified human ECP. The transmembrane pores formed by ECP are relatively voltage-insensitive and non-ion-selective, suggesting a role for channel formation by ECP in target cell damage mediated by eosinophils. Channel formation by granule proteins of immune effector cells may represent a general and effective mechanism of target cell killing.

MeSH Terms
Animals Anions/metabolism Blood Proteins/pharmacology Cations/metabolism Cell Line Cell Membrane/drug effects,metabolism Cell Membrane Permeability/drug effects Electric Conductivity Eosinophil Granule Proteins Eosinophils Humans Ion Channels/metabolism Lipid Bilayers Liposomes/metabolism Membrane Potentials Ribonucleases
Chemicals
Anions Blood Proteins Cations Eosinophil Granule Proteins Ion Channels Lipid Bilayers Liposomes Ribonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Young J D
Peterson C G
Venge P
Cohn Z A
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1986-00-00
Pages
613-6
Language
English
Region
England
NLM ID
0410462
Subset
IM
Grants
NIAID NIH HHS · AI 070122 · United States
NCI NIH HHS · CA 30198 · United States
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