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Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity.

Publication ,  Journal Article
Madenspacher, JH; Azzam, KM; Gong, W; Gowdy, KM; Vitek, MP; Laskowitz, DT; Remaley, AT; Wang, JM; Fessler, MB
Published in: J Biol Chem
December 21, 2012

The plasma lipoprotein-associated apolipoproteins (apo) A-I and apoE have well described anti-inflammatory actions in the cardiovascular system, and mimetic peptides that retain these properties have been designed as therapeutics. The anti-inflammatory mechanisms of apolipoprotein mimetics, however, are incompletely defined. Whether circulating apolipoproteins and their mimetics regulate innate immune responses at mucosal surfaces, sites where transvascular emigration of leukocytes is required during inflammation, remains unclear. Herein, we report that Apoai(-/-) and Apoe(-/-) mice display enhanced recruitment of neutrophils to the airspace in response to both inhaled lipopolysaccharide and direct airway inoculation with CXCL1. Conversely, treatment with apoA-I (L-4F) or apoE (COG1410) mimetic peptides reduces airway neutrophilia. We identify suppression of CXCR2-directed chemotaxis as a mechanism underlying the apolipoprotein effect. Pursuing the possibility that L-4F might suppress chemotaxis through heterologous desensitization, we confirmed that L-4F itself induces chemotaxis of human PMNs and monocytes. L-4F, however, fails to induce a calcium flux. Further exploring structure-function relationships, we studied the alternate apoA-I mimetic L-37pA, a bihelical analog of L-4F with two Leu-Phe substitutions. We find that L-37pA induces calcium and chemotaxis through formyl peptide receptor (FPR)2/ALX, whereas its D-stereoisomer (i.e. D-37pA) blocks L-37pA signaling and induces chemotaxis but not calcium flux through an unidentified receptor. Taken together, apolipoprotein mimetic peptides are novel chemotactic agents that possess complex structure-activity relationships to multiple receptors, displaying anti-inflammatory efficacy against innate immune responses in the airway.

Duke Scholars

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

December 21, 2012

Volume

287

Issue

52

Start / End Page

43730 / 43740

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Receptors, Lipoxin
  • Receptors, Formyl Peptide
  • Peptides
  • Neutrophils
  • Neutrophil Infiltration
  • Mice, Knockout
  • Mice
  • Humans
  • HEK293 Cells
 

Citation

APA
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MLA
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Madenspacher, J. H., Azzam, K. M., Gong, W., Gowdy, K. M., Vitek, M. P., Laskowitz, D. T., … Fessler, M. B. (2012). Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity. J Biol Chem, 287(52), 43730–43740. https://doi.org/10.1074/jbc.M112.377192
Madenspacher, Jennifer H., Kathleen M. Azzam, Wanghua Gong, Kymberly M. Gowdy, Michael P. Vitek, Daniel T. Laskowitz, Alan T. Remaley, Ji Ming Wang, and Michael B. Fessler. “Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity.J Biol Chem 287, no. 52 (December 21, 2012): 43730–40. https://doi.org/10.1074/jbc.M112.377192.
Madenspacher JH, Azzam KM, Gong W, Gowdy KM, Vitek MP, Laskowitz DT, et al. Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity. J Biol Chem. 2012 Dec 21;287(52):43730–40.
Madenspacher, Jennifer H., et al. “Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity.J Biol Chem, vol. 287, no. 52, Dec. 2012, pp. 43730–40. Pubmed, doi:10.1074/jbc.M112.377192.
Madenspacher JH, Azzam KM, Gong W, Gowdy KM, Vitek MP, Laskowitz DT, Remaley AT, Wang JM, Fessler MB. Apolipoproteins and apolipoprotein mimetic peptides modulate phagocyte trafficking through chemotactic activity. J Biol Chem. 2012 Dec 21;287(52):43730–43740.

Published In

J Biol Chem

DOI

EISSN

1083-351X

Publication Date

December 21, 2012

Volume

287

Issue

52

Start / End Page

43730 / 43740

Location

United States

Related Subject Headings

  • Structure-Activity Relationship
  • Receptors, Lipoxin
  • Receptors, Formyl Peptide
  • Peptides
  • Neutrophils
  • Neutrophil Infiltration
  • Mice, Knockout
  • Mice
  • Humans
  • HEK293 Cells