SorLA modulates atheroprotective properties of CLA by regulating monocyte migration

Atherosclerosis. 2010 Dec;213(2):400-7. doi: 10.1016/j.atherosclerosis.2010.09.025. Epub 2010 Oct 20.

Abstract

Objective: We have previously shown that CLA induces regression of pre-established atherosclerotic lesions in apoE(-/-) mice. CLA is a known ligand of peroxisome proliferator activated receptors (PPARs) and it is postulated that CLA mediates its atheroprotective effects through activation of PPARs. Earlier work in our group identified the monocyte/macrophage cell as the primary cellular target of CLA. In this study we identified novel genes regulated by CLA during the regression of atherosclerosis and characterised a role for one of these, SorLA. SorLA is a member of the vacuolar protein sorting 10 protein (Vps10p) domain receptor family, which has structural homology with the LDLR family.

Methods and results: Expression of SorLA was identified with its Vps10p family member Sort1 by transcriptomic analysis of murine aorta following CLA-induced regression of atherosclerosis. Decreased expression of both receptors was confirmed by real-time PCR in the aorta of CLA-supplemented mice. SorLA protein expression was predominantly localised to monocyte/macrophage cells in the vasculature by immunohistochemistry. CLA and the PPAR-γ agonists, troglitazone, and 15-deoxy-prostaglandin (PG) J(2), decreased protein and RNA expression of SorLA in THP-1 monocytes; while pre-treatment with a PPAR-γ antagonist established a PPAR-γ dependent role for CLA regulation of SorLA. CLA inhibits monocyte migration. Consistent with a role for SorLA in mediating this response, overexpression of SorLA increased migration of THP-1 monocytes to monocyte chemoattractant protein-1 with a coincident increase in UPAR expression.

Conclusion: CLA may mediate its atheroprotective effects in part through reduced expression of SorLA and a resulting inhibition of monocyte migration in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / prevention & control
  • Cell Movement / drug effects
  • Chemokine CCL2 / pharmacology
  • Chromans / pharmacology
  • Humans
  • Linoleic Acids, Conjugated / pharmacology*
  • Membrane Transport Proteins / biosynthesis
  • Membrane Transport Proteins / physiology*
  • Mice
  • Monocytes / drug effects
  • Monocytes / physiology*
  • PPAR gamma / antagonists & inhibitors
  • PPAR gamma / metabolism
  • Receptors, LDL / biosynthesis
  • Receptors, LDL / physiology*
  • Receptors, Urokinase Plasminogen Activator / metabolism
  • Thiazolidinediones / pharmacology
  • Troglitazone

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Chromans
  • Linoleic Acids, Conjugated
  • Membrane Transport Proteins
  • PPAR gamma
  • Receptors, LDL
  • Receptors, Urokinase Plasminogen Activator
  • Sorl1 protein, mouse
  • Thiazolidinediones
  • 9,11-linoleic acid
  • Troglitazone