Essential role for ICSBP in the in vivo development of murine CD8α+dendritic cells

• Published in: Blood Vol. 101; no. 1; pp. 305 - 310
• Main Authors: Aliberti, Julio, Schulz, Oliver, Pennington, Daniel J., Tsujimura, Hideki, Reis e Sousa, Caetano, Ozato, Keiko, Sher, Alan
• Format: Journal Article
• Language: English
• Published: Washington, DC Elsevier Inc 01.01.2003; The Americain Society of Hematology
• Subjects: Biological and medical sciences; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Immunobiology; Monocytes, macrophages; Myeloid cells: ontogeny, maturation, markers, receptors; Dendritic cell; Stem cell; Cytokine; Rodentia; Interferon consensus sequence binding protein; Hematopoietic cell; Inflammation; Cell differentiation; Signal transduction; Vertebrata; Mammalia; Mouse; Antigen presenting cell; Animal; Interferon; Transcription factor; Phagocyte
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood-2002-04-1088

Interferon (IFN) consensus sequence-binding protein (ICSBP) is an important transcription factor regulating proinflammatory cytokine production and the development of mononuclear phagocytes in vitro. Here we analyzed the role of ICSBP in the in vivo differentiation of 3 major subsets of murine dendritic cells (DCs). We found that ICSBP is predominantly expressed by the CD8α+subset, and more important, that ICSBP−/−mice have a profound and selective deficiency in CD8α+DEC205+DCs in lymphoid tissues. Studies using wild-type/ICSBP−/−chimeras revealed that this defect in CD8α+DC development is intrinsic to bone marrow–derived progenitors and not dependent on ICSBP expression in the nonhemopoietic compartment. Because DC precursor frequencies are unaltered in the bone marrow of ICSBP−/−mice, ICSBP appears to function by regulating CD8α+DC differentiation downstream from the generation of common DC progenitors. Although CD8α−DCs are present in normal numbers in ICSBP−/−animals, up-regulation of CD40, CD80, and major histocompatibility complex (MHC) class II expression was found to be impaired in this subset after in vivo microbial stimulation. Together these results demonstrate that ICSBP is critically required for the in vivo differentiation of CD8α+DCs and may also influence the functional maturation of the CD8α−subsets.