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Open AccessJournal ArticleDOI

Lymphatic Endothelial Cell Activation and Dendritic Cell Transmigration Is Modified by Genetic Deletion of Clever-1.

TLDR
In this article, the authors demonstrated that Clever-1 is immunosuppressive towards migrating dendritic cells and thus regulates the magnitude of immune responses created by incoming DCs in the draining lymph nodes.
Abstract
Clever-1 also known as Stabilin-1 and FEEL-1 is a scavenger molecule expressed on a subpopulation of anti-inflammatory macrophages and lymphatic endothelial cells (LECs). However, its role in regulating dendritic cell (DC) trafficking and subsequent effects on immunity have remained unexplored. In this study, we demonstrate that DC trafficking from the skin into the draining lymph nodes is compromised in the absence of Clever-1. By adoptive transfer approaches we further show that the poor trafficking is due to the impaired entrance of DCs into afferent lymphatics. Despite this, injections of ovalbumin-loaded DCs into the footpads induced a stronger proliferative response of OT II T cells in the draining lymph nodes. This could be explained by the increased MHC II expression on DCs and a less tolerogenic phenotype of LECs in lymph nodes of Clever-1 knockout mice. Thus, although fewer DCs reach the nodes, they are more active in creating antigen-specific immune responses. This suggests that the DCs migrating to the draining lymph node within Clever-1 positive lymphatics experience immunosuppressive interactions with LECs. In conclusion, besides being a trafficking molecule on lymphatic vasculature Clever-1 is immunosuppressive towards migrating DCs and thus, regulates the magnitude of immune responses created by incoming DCs in the draining lymph nodes.

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Myeloid cell-targeted therapies for solid tumours

TL;DR: Key features of monocyte and macrophage biology that are being explored as potential targets for cancer therapies are highlighted and what aspects of myeloid cells need a deeper understanding to identify rational combinatorial strategies to improve clinical outcomes of patients with cancer are highlighted.
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Tumor microenvironment and cellular senescence: Understanding therapeutic resistance and harnessing strategies

TL;DR: The tumor microenvironment (TME) is a major contributor to cancer malignancy including development of therapeutic resistance, a process mediated in part through intercellular crosstalk as discussed by the authors .
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Tumor microenvironment and cellular senescence: Understanding therapeutic resistance and harnessing strategies

TL;DR: The tumor microenvironment (TME) is a major contributor to cancer malignancy including development of therapeutic resistance, a process mediated in part through intercellular crosstalk.
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Structure and Immune Function of Afferent Lymphatics and Their Mechanistic Contribution to Dendritic Cell and T Cell Trafficking

TL;DR: In this article, the authors describe how the anatomy of the lymphatic network supports leukocyte trafficking and provide updated knowledge regarding the cellular and molecular mechanisms responsible for lymphatic migration of dendritic cells and T cells.
References
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Journal ArticleDOI

An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow.

TL;DR: This method allows by simple means the generation of high numbers of murine DC with very low B cell or granulocyte contaminations, which will be valuable to study DC biology notably at the molecular level.
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Rapid leukocyte migration by integrin-independent flowing and squeezing

TL;DR: It is shown here that functional integrins do not contribute to migration in three-dimensional environments, and these cells migrate by the sole force of actin-network expansion, which promotes protrusive flowing of the leading edge.
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HEVs, lymphatics and homeostatic immune cell trafficking in lymph nodes

TL;DR: The current understanding of the functions of high endothelial venules, stroma and lymphatics in the entry, positioning and exit of immune cells in lymph nodes during homeostasis are reviewed, and the unexpected role of dendritic cells is highlighted in the control of lymphocyte homing through HEVs.
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Lymph node–resident lymphatic endothelial cells mediate peripheral tolerance via Aire-independent direct antigen presentation

TL;DR: It is demonstrated that LN-resident lymphatic endothelial cells express multiple peripheral tissue antigens (PTAs) independent of the autoimmune regulator (Aire), and that other LN stromal subpopulations express distinct PTAs by mechanisms that vary in their Aire dependence.
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