.

Monday, April 1, 2019

Anti-inflammatory Function of Gut Macrophages

Anti-instigative Function of Gut MacrophagesColonic mucous membrane is a very peculiar immunological site daily unfastened to a huge amount of harmless antigens. It is key for the resistant scheme to be able to recognize this innocuous antigens from pathogens. Among all the insubordinate cells, CX3CR1+ macrophages tapdance this critical map. In this commentary on our recent publication on Immunobiology (Non-redundant role of the chemokine sensory sense organ CX3CR1 in the anti- seditious function of gut macrophages(1)we regard to highlight the crucial and unique role of these macrophages in order to entertain homeostasis and avoid the rise of deviant exhilaration and tissue damage.The intestine is an sole(a) tissue able to maintain balance between the immune organisation activation and the tolerance against the very huge amount of harmless antigens that atomic number 18 in contact with the intestinal lumen, including food antigens and microflora.It is fundamental for ou r health that our immune system is able to respond with a robust and appropriate repartee to potency life-threatening antigens but the same reaction against harmless antigens, standardized commensal bacteria or dietary proteins, could be very dangerous and could give rise to allergies or chronic inflammation that, in the end, crowd out lead to tissue damage or cancer development. Many immune cells participate to the maintenance of the homeostasis in gut, with the role of understanding how an antigen is a potential danger for the organism and being silenced in response to commensal bacteria and food antigens.This complex landscape includes T and B lymphocytes, immanent killer cells, innate lymphoid cells, eosinophils and mononuclear phagocytes dendritic cells and macrophages.Among the latter, monocyte-derived macrophages, expressing the CX3CR1 receptor, constitute the approximately abundant population (2).The manuscript by Marelli et al., is focused on the role of CX3CR1+ ma crophages in both steady state and acute colitis. In the live some years intensive research has been performed in order to light up the role of these immune cells in the maintenance of homeostasis, but still, contrasting results welcome been reported regarding their role in the control of inflammatory response in the intestine (3,4). Considering this confused landscape, our paper aimed to clarify the role of CX3CR1+ cells in the development of acute colitis. By using mice lacking the receptor (CX3CR1GFP/GFP mice) we demonstrated that the absence of CX3CR1 on gut macrophages leads to a more severe degree of DSS-induced colitis, higher(prenominal) colon infiltration of inflammatory macrophages and Th17 lymphocytes and higher conceptualisation of inflammatory cytokines.Macrophages in the intestinal mucosa are considered mononuclear phagocytes that originate from a parking area myeloid progenitor which can differentiate also into dendritic cells (5). In contrast to separates re sident macrophages, they are continuously replenished from blood stream Ly6C+ monocytes, one by one from the CX3CR1 receptor (6). This issue caused considerable misunderstanding in the past, generating the belief that these cells were dendritic cells (7,8). However, today it is recognized that Ly6Chi monocytes are recruited in the mucosa and there, in few days, they differentiate in mature macrophages, progressively loosing Ly6C and starting to express distinctive markers, such as F4/80, CD64, MHCII and CX3CR1 (6). As highlighted before, different authors investigated the role of CX3CR1+ gut macrophages with moot outcomes.CX3CR1+ macrophages are supposed to maintain homeostasis in the gut (9). In symmetry with this concept, our data revealed an exacerbated intestinal inflammation with a huge accumulation of macrophages in CX3CR1-KO mice. As reported also by different authors, (3,10) the natural way out of the accumulation of macrophages is an increased production of cytokines, a nd hence a higher enlisting of immune cells in the colon, in particular T lymphocytes of the Th17 subset. On the contrary, some other authors (4) suggested that the lack of the receptor impairs macrophages accumulation in the lamina propria. Moreover they suggested that the engagement of the receptor by its unique ligand (Fracktalkine/CX3CL1) resulted in an intensification of iNOS production, an inflammatory enzyme. Our data, instead, clearly demonstrate that the absence of the receptor increases the level of iNOS and of many other pro-inflammatory cytokines. This is a tissue-specific competence of the intestine, being colonic resident macrophages an exemption from the rules. Indeed, in other tissues, the expression of CX3CR1 receptor is associated with a pro-inflammatory phenotype (11,12). In support of our data it is important to underline that, in the gut, CX3CR1 macrophages are fundamental to bring antigens and present them to DC in order to establish oral tolerance. When this mechanism is missing referable to the lack of the receptor, the immune system is activated and this results in an acute inflammatory response (8).We have shown in Marelli et al. that if the CX3CR1 receptor is lacking, the ability of these cells to control inflammation is lost. Of note, CX3CR1-KO macrophages try counter-balance this aberrant situation by producing more IL-10, a major(ip) immune-suppressive and anti-inflammatory cytokine. In spite of this increase, IL-10 is not sufficient to control the inflammatory disease and mice have an exacerbated colitis.Overall, with our study we wanted to propose a expressed protective and anti-inflammatory role of CX3CR1+ macrophages during the processes of acute colitis this concept whitethorn shed light also on the role of these cells in other pathological conditions of the gut associated with persistent inflammation. Our study established that macrophages expressing the functional CX3CR1 receptor have a non-redundant role in the control of aberrant intestinal inflammation, a harmful condition that may lead to tissue injury.CX3CR1 receptor expressed on intestinal macrophages is able to control colitis, avoiding the rise of aberrant inflammation. When the receptor is missing, the balance in the gut is broken, leading these cells to produce a huge amount of cytokines. Feeling the higher level of inflammation, CX3CR1 macrophages attempt to detain it by producing more IL-10, however this is not sufficient and the result is a higher accumulation of inflammatory Th17 lymphocytes and increased tissue injury.

No comments:

Post a Comment