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Gut. Published Online First: 20 October 2009. doi:10.1136/gut.2009.183772
Copyright © 2009 BMJ Publishing Group Ltd & British Society of Gastroenterology.

Paper

The lymphatic system controls intestinal inflammation and inflammation-associated colon cancer through the chemokine decoy receptor D6

Stefania Vetrano1, Elena M Borroni2, Adelaida Sarukhan2, Benedetta Savino2, Raffaella Bonecchi2, Carmen Correale1, Vincenzo Arena3, Massimo Fantini4, Massimo Roncalli1, Alberto Malesci1, Alberto Mantovani2, Massimo Locati2, Silvio Danese5,*

1 Division of Gastroenterology, Istituto Clinico Humanitas IRCCS, Rozzano, Italy;
2 Department of Translational Medicine, University of Milan, Istituto Clinico Humanitas IRCCS, Rozzano, Italy;
3 Department of Internal Medicine, Catholic University of Rome, Italy;
4 Division of Gastroenterology, University of Tor Vergata, Rome, Italy;
5 Istituto Clinico Humanitas, Italy

Correspondence to: Silvio Danese, Istituto Clinico Humanitas, Viale Manzoni 56, Rozzano, Milan, 20089, Italy; sdanese{at}hotmail.com

Accepted 14 August 2009

ABSTRACT

Inflammatory CC chemokines have been associated with cancer, but unequivocal genetic evidence that they play a role in clinically relevant models of carcinogenesis is lacking. D6 is a promiscuous decoy receptor and scavenger for CC chemokines and plays a non-redundant role in taming of inflammatory response in various organs. As inflammation is a key player in the development of inflammatory bowel disease (IBD) and IBD-associated colorectal cancer, we investigated D6 expression in human colitis and colon cancer, and its role in experimental colitis and inflammation-associated colon cancer. In humans, D6 was mainly expressed by lymphatic vessels and leukocytes in the mucosa of individuals with IBD and colon cancer, as well as control individuals. Mice lacking expression of D6 were significantly more susceptible to experimental colitis than WT mice and upon repeated irritant administration failed to resolve colitis, and showed significantly higher levels of several pro-inflammatory chemokines. Using bone marrow chimeras the regulatory function of D6 on colitis was tracked to the stromal/lymphatic compartment, with no contribution of hemopoietic cells. Finally, D6-/- mice showed increased susceptibility to colitis-associated cancer in the distal segment of the colon compared with WT mice. The decoy receptor D6 expressed on lymphatic vessels plays a key role in the control of intestinal inflammation and in the development of inflammation-associated colon cancer. Our results unveil the lymphatic system as a new cellular compartment with an unexpected role in the pathogenesis of IBD and intestinal cancer, and candidate chemokines as novel players in tumor promotion and progression.


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