Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/75277
Title: Acute exposure to apolipoprotein A1 inhibits macrophage chemotaxis in vitro and monocyte recruitment in vivo
Authors: Iqbal, Asif J
Barrett, Tessa J
Taylor, Lewis
McNeill, Eileen
Manmadhan, Arun
Recio Cruz, Carlota Pilar 
Carmineri, Alfredo
Brodermann, Maximillian H
White, Gemma E
Cooper, Dianne
DiDonato, Joseph A
Zamanian-Daryoush, Maryam
Hazen, Stanley L
Channon, Keith M
Greaves, David R
Fisher, Edward A
UNESCO Clasification: 3207 Patología
Issue Date: 2016
Journal: eLife 
Abstract: Apolipoprotein A1 (apoA1) is the major protein component of high-density lipoprotein (HDL) and has well documented anti-inflammatory properties. To better understand the cellular and molecular basis of the anti-inflammatory actions of apoA1, we explored the effect of acute human apoA1 exposure on the migratory capacity of monocyte-derived cells in vitro and in vivo. Acute (20–60 min) apoA1 treatment induced a substantial (50–90%) reduction in macrophage chemotaxis to a range of chemoattractants. This acute treatment was anti-inflammatory in vivo as shown by pre-treatment of monocytes prior to adoptive transfer into an on-going murine peritonitis model.We find that apoA1 rapidly disrupts membrane lipid rafts, and as a consequence, dampens the PI3K/Akt signalling pathway that coordinates reorganization of the actin cytoskeleton and cell migration. Our data strengthen the evidence base for therapeutic apoA1 infusions in situations where reduced monocyte recruitment to sites of inflammation could have beneficial outcomes.
URI: http://hdl.handle.net/10553/75277
ISSN: 2050-084X
DOI: 10.7554/eLife.15190
Source: eLife [ISSN 2050-084X], n. 5, e15190
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