The chemokine receptors ACKR 2 and CCR 2 reciprocally regulate lymphatic vessel density

KM Lee, R Danuser, JV Stein, D Graham… - The EMBO …, 2014 - embopress.org
KM Lee, R Danuser, JV Stein, D Graham, RJB Nibbs, GJ Graham
The EMBO journal, 2014embopress.org
Macrophages regulate lymphatic vasculature development; however, the molecular
mechanisms regulating their recruitment to developing, and adult, lymphatic vascular sites
are not known. Here, we report that resting mice deficient for the inflammatory chemokine‐
scavenging receptor, ACKR 2, display increased lymphatic vessel density in a range of
tissues under resting and regenerating conditions. This appears not to alter dendritic cell
migration to draining lymph nodes but is associated with enhanced fluid drainage from …
Abstract
Macrophages regulate lymphatic vasculature development; however, the molecular mechanisms regulating their recruitment to developing, and adult, lymphatic vascular sites are not known. Here, we report that resting mice deficient for the inflammatory chemokine‐scavenging receptor, ACKR2, display increased lymphatic vessel density in a range of tissues under resting and regenerating conditions. This appears not to alter dendritic cell migration to draining lymph nodes but is associated with enhanced fluid drainage from peripheral tissues and thus with a hypotensive phenotype. Examination of embryonic skin revealed that this lymphatic vessel density phenotype is developmentally established. Further studies indicated that macrophages and the inflammatory CC‐chemokine CCL2, which is scavenged by ACKR2, are associated with this phenotype. Accordingly, mice deficient for the CCL2 signalling receptor, CCR2, displayed a reciprocal phenotype of reduced lymphatic vessel density. Further examination revealed that proximity of pro‐lymphangiogenic macrophages to developing lymphatic vessel surfaces is increased in ACKR2‐deficient mice and reduced in CCR2‐deficient mice. Therefore, these receptors regulate vessel density by reciprocally modulating pro‐lymphangiogenic macrophage recruitment, and proximity, to developing, resting and regenerating lymphatic vessels.
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