Inhibition of the lytic activity of perforin by lipoproteins

Details

Serval ID
serval:BIB_B73C8F5DD558
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Inhibition of the lytic activity of perforin by lipoproteins
Journal
Journal of Immunology
Author(s)
Tschopp  J., Masson  D., Schafer  S.
ISSN
0022-1767 (Print)
Publication state
Published
Issued date
09/1986
Volume
137
Number
6
Pages
1950-3
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Sep 15
Abstract
Cytoplasmic granules isolated from cytolytic T lymphocytes (CTL) lyse red blood cells or tumor cell lines in a nonspecific manner. The activity of highly purified granules was inhibited by human or rabbit serum at dilutions as high as 1/10,000. The main inhibitory activity of human serum was isolated by chromatography and was determined to be high density lipoprotein (HDL). HDL not only inhibited at a concentration of 70 ng/ml the lytic activity of isolated granules, but also of the purified, pore-forming protein perforin present in the granules. Purified low density lipoprotein was equally active. Because the CTL granule activity was inhibited by pure egg lecithin vesicles at a concentration equivalent to the phospholipid content of lipoproteins, the lipid portion of lipoproteins is the likely candidate for granule inactivation. Lipoproteins also decreased in a dose-dependent manner the cytotoxic activity of intact cytolytic T cells. However, cytotoxicity was not completely suppressed, and only in the case of CTL exhibiting low efficiency in killing their targets. It is proposed that lipoproteins inactivate perforin and may thereby inhibit a possible lysis of innocent bystander cells.
Keywords
Animals Cell Survival/drug effects Cytotoxicity, Immunologic/drug effects Humans Ion Channels Lipoproteins, HDL/*pharmacology *Membrane Glycoproteins Membrane Proteins/*antagonists & inhibitors Mice Pore Forming Cytotoxic Proteins T-Lymphocytes, Cytotoxic/drug effects/*physiology
Pubmed
Web of science
Create date
24/01/2008 16:19
Last modification date
20/08/2019 16:25
Usage data