Distinct functions of chemokine receptor axes in the atherogenic mobilization and recruitment of classical monocytes

作者:Soehnlein Oliver*; Drechsler Maik; Doering Yvonne; Lievens Dirk; Hartwig Helene; Kemmerich Klaus; Ortega Gomez Almudena; Mandl Manuela; Vijayan Santosh; Projahn Delia; Garlichs Christoph D; Koenen Rory R; Hristov Mihail; Lutgens Esther; Zernecke Alma; Weber Christian
来源:EMBO Molecular Medicine, 2013, 5(3): 471-481.
DOI:10.1002/emmm.201201717

摘要

We used a novel approach of cytostatically induced leucocyte depletion and subsequent reconstitution with leucocytes deprived of classical (inflammatory/Gr1hi) or non-classical (resident/Gr1lo) monocytes to dissect their differential role in atheroprogression under high-fat diet (HFD). Apolipoprotein E-deficient (Apoe/) mice lacking classical but not non-classical monocytes displayed reduced lesion size and macrophage and apoptotic cell content. Conversely, HFD induced a selective expansion of classical monocytes in blood and bone marrow. Increased CXCL1 levels accompanied by higher expression of its receptor CXCR2 on classical monocytes and inhibition of monocytosis by CXCL1-neutralization indicated a preferential role for the CXCL1/CXCR2 axis in mobilizing classical monocytes during hypercholesterolemia. Studies correlating circulating and lesional classical monocytes in gene-deficient Apoe/ mice, adoptive transfer of gene-deficient cells and pharmacological modulation during intravital microscopy of the carotid artery revealed a crucial function of CCR1 and CCR5 but not CCR2 or CX3CR1 in classical monocyte recruitment to atherosclerotic vessels. Collectively, these data establish the impact of classical monocytes on atheroprogression, identify a sequential role of CXCL1 in their mobilization and CCR1/CCR5 in their recruitment.

  • 出版日期2013-3