Affiliation:
1. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO
Abstract
We examined the transcriptional profiles of macrophages that reside in the islets of Langerhans of 3-wk-old non-obese diabetic (NOD), NOD.Rag1−/−, and B6.g7 mice. Islet macrophages expressed an activation signature with high expression of Tnf, Il1b, and MHC-II at both the transcript and protein levels. These features are common with barrier macrophages of the lung and gastrointestinal tract. Moreover, injection of lipopolysaccharide induced rapid inflammatory gene expression, indicating that blood stimulants are accessible to the macrophages and that these macrophages can sense them. In NOD mice, the autoimmune process imparted an increased inflammatory signature, including elevated expression of chemokines and chemokine receptors and an oxidative response. The elevated inflammatory signature indicates that the autoimmune program was active at the time of weaning. Thus, the macrophages of the islets of Langerhans are poised to mount an immune response even at steady state, while the presence of the adaptive immune system elevates their activation state.
Funder
National Institutes of Health
Janssen Pharmaceuticals
Washington University
National Cancer Institute
Institute for Clinical and Translational Science
National Center for Research Resources
NIH
Publisher
Rockefeller University Press
Subject
Immunology,Immunology and Allergy
Cited by
87 articles.
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