Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.

A series of ultrashort lipopeptides and lipopeptoids were tested for their ability to induce cytokine production in macrophages. Fourteen compounds were found to strongly induce production of chemokines Groα and IL-8, with a structural bias that was absent from previous antibacterial activity invest...

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Main Authors: Brandon Findlay, Neeloffer Mookherjee, Frank Schweizer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3563528?pdf=render
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spelling doaj-351da805aff645ffb161381418c10c682020-11-24T21:18:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5428010.1371/journal.pone.0054280Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.Brandon FindlayNeeloffer MookherjeeFrank SchweizerA series of ultrashort lipopeptides and lipopeptoids were tested for their ability to induce cytokine production in macrophages. Fourteen compounds were found to strongly induce production of chemokines Groα and IL-8, with a structural bias that was absent from previous antibacterial activity investigations. Compounds based on LysGlyLys and NLysGlyNLys sequences did not induce cytokine production, whereas those based on LysLysLys and NLysNLysNLys were active only when linked to a lipid tail at least sixteen carbons long. Three lipopeptides induced high levels of IL-8 production, above that of equivalent concentrations of cathelicidin LL-37, while no compound induced production of the pro-inflammatory cytokine TNF-α at or below 100 µM. Two compounds, peptoids C16OH-NLysNLysNLys and C16OH-NHarNHarNHar, were selective for IL-8 production and did not induce TNF-α or IL-1β. These compounds may prove beneficial for in vivo treatment of infectious disease, with improved bioavailability over LL-37 due to their protease-resistant scaffold.http://europepmc.org/articles/PMC3563528?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Brandon Findlay
Neeloffer Mookherjee
Frank Schweizer
spellingShingle Brandon Findlay
Neeloffer Mookherjee
Frank Schweizer
Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
PLoS ONE
author_facet Brandon Findlay
Neeloffer Mookherjee
Frank Schweizer
author_sort Brandon Findlay
title Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
title_short Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
title_full Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
title_fullStr Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
title_full_unstemmed Ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
title_sort ultrashort cationic lipopeptides and lipopeptoids selectively induce cytokine production in macrophages.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description A series of ultrashort lipopeptides and lipopeptoids were tested for their ability to induce cytokine production in macrophages. Fourteen compounds were found to strongly induce production of chemokines Groα and IL-8, with a structural bias that was absent from previous antibacterial activity investigations. Compounds based on LysGlyLys and NLysGlyNLys sequences did not induce cytokine production, whereas those based on LysLysLys and NLysNLysNLys were active only when linked to a lipid tail at least sixteen carbons long. Three lipopeptides induced high levels of IL-8 production, above that of equivalent concentrations of cathelicidin LL-37, while no compound induced production of the pro-inflammatory cytokine TNF-α at or below 100 µM. Two compounds, peptoids C16OH-NLysNLysNLys and C16OH-NHarNHarNHar, were selective for IL-8 production and did not induce TNF-α or IL-1β. These compounds may prove beneficial for in vivo treatment of infectious disease, with improved bioavailability over LL-37 due to their protease-resistant scaffold.
url http://europepmc.org/articles/PMC3563528?pdf=render
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AT neeloffermookherjee ultrashortcationiclipopeptidesandlipopeptoidsselectivelyinducecytokineproductioninmacrophages
AT frankschweizer ultrashortcationiclipopeptidesandlipopeptoidsselectivelyinducecytokineproductioninmacrophages
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