LT beta R expression on hematopoietic cells regulates acute inflammation and influences maturation of myeloid subpopulations

Wege, Anja K. and Huber, Barbara and Wimmer, Nadin and Maennel, Daniela N. and Hehlgans, Thomas (2014) LT beta R expression on hematopoietic cells regulates acute inflammation and influences maturation of myeloid subpopulations. INNATE IMMUNITY, 20 (5). pp. 461-470. ISSN 1753-4259, 1753-4267

Full text not available from this repository. (Request a copy)

Abstract

Lymphotoxin beta-receptor (LT beta R) is involved in the formation and maintenance of secondary lymphoid structures, as well as in the regulation of inflammatory responses. Because LT beta R lymphoid structure formation continues to develop in infants, we compared two different chimera models: one using adult mice and the other using a transplantation model of neonatal mice. To elucidate the function of LT beta R on lymphoid and non-lymphoid cells, we generated bone marrow chimeras on the wild type C57Bl/6 and the LT beta R-deficient (LT beta R- /-) background, and reconstituted the mice with bone marrow cells reciprocally. These chimeric mice were analyzed in the experimental model of acute dextran sulfate sodium-induced colitis. Interestingly, both models revealed not only equal reconstitution levels but also similar immunological responses: LT beta R expression on stromal cells is essential for lymph node formation, whereas LT beta R on hematopoietic cells is crucial for a decrease in inflammation. In addition, mice lacking LT beta R on hematopoietic cells revealed (a) an increase of immature granulocytic cells in the spleen and (b) a reduced proportion of myeloid cells in peripheral blood and spleen expressing CD11b(+)Ly6C(+)Ly6G(-) (myeloid-derived suppressor cells expression profile). In conclusion, LT beta R expression on hematopoietic cells seems to be involved in the down-regulation of acute inflammatory reactions paralleled by the appearance of immature myeloid cells.

Item Type: Article
Uncontrolled Keywords: INDUCED INTESTINAL INFLAMMATION; LYMPHOTOXIN-BETA; SUPPRESSOR-CELLS; RECEPTOR ACTIVATION; B-LYMPHOCYTES; IMMUNE SUPPRESSION; LYMPHOID ORGANS; DENDRITIC CELLS; T-LYMPHOCYTES; NITRIC-OXIDE; Bone marrow chimera; dampening inflammation; DSS-induced colitis; LT beta R; MDSC
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Frauenheilkunde und Geburtshilfe (Schwerpunkt Frauenheilkunde)
Medicine > Lehrstuhl für Immunologie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 17 Oct 2019 12:05
Last Modified: 17 Oct 2019 12:05
URI: https://pred.uni-regensburg.de/id/eprint/9985

Actions (login required)

View Item View Item