Upon exposure to immune or inflammatory stimuli, dendritic cells (DC) migrate from peripheral tissues to lymphoid organs, where they present antigen. The molecular basis for the peculiar trafficking properties of DC is largely unknown. In this study, mouse DC were generated from CD34+ bone marrow precursors and cultured with granulocyte-macrophage-CSF and Flt3 ligand for 9 days. Chemokines active on immature DC include MIP1alpha, RANTES, MIP1beta, MCP-1, MCP-3, and the constitutively expressed SDF1, MDC, and ELC. TNF-alpha-induced DC maturation caused reduction of migration to inducible chemokines (MIP1alpha, RANTES, MIP1beta, MCP-1, and MCP-3) and increased migration to SDF1, MDC, and ELC. Similar results were obtained by CD40 ligation or culture in the presence of bacterial lipopolysaccharide. TNF-alpha down-regulated CC chemokine receptor (CCR)1, CCR2, and CCR5 and up-regulated CCR7 mRNA levels, in agreement with functional data. This study shows that selective responsiveness of mature and immature DC to inducible vs. constitutively produced chemokines can contribute to the regulated trafficking of DC.

Differential responsiveness to constitutive vs. inducible chemokines of immature and mature mouse dendritic cells

R. Bonecchi;
1999-01-01

Abstract

Upon exposure to immune or inflammatory stimuli, dendritic cells (DC) migrate from peripheral tissues to lymphoid organs, where they present antigen. The molecular basis for the peculiar trafficking properties of DC is largely unknown. In this study, mouse DC were generated from CD34+ bone marrow precursors and cultured with granulocyte-macrophage-CSF and Flt3 ligand for 9 days. Chemokines active on immature DC include MIP1alpha, RANTES, MIP1beta, MCP-1, MCP-3, and the constitutively expressed SDF1, MDC, and ELC. TNF-alpha-induced DC maturation caused reduction of migration to inducible chemokines (MIP1alpha, RANTES, MIP1beta, MCP-1, and MCP-3) and increased migration to SDF1, MDC, and ELC. Similar results were obtained by CD40 ligation or culture in the presence of bacterial lipopolysaccharide. TNF-alpha down-regulated CC chemokine receptor (CCR)1, CCR2, and CCR5 and up-regulated CCR7 mRNA levels, in agreement with functional data. This study shows that selective responsiveness of mature and immature DC to inducible vs. constitutively produced chemokines can contribute to the regulated trafficking of DC.
1999
Animals; Dendritic Cells; Chemokines; CXC; Membrane Glycoproteins; Granulocyte-Macrophage Colony-Stimulating Factor; Hematopoietic Stem Cells; Chemotaxis; Receptors; Chemokine; Chemokine CCL19; CD40 Ligand; Cytokine; Down-Regulation; Cytokines; Gene Expression Regulation; Macrophage Inflammatory Proteins; Tumor Necrosis Factor-alpha; Chemokine CCL2; CCR5; Chemokine CCL22; Mice; CCR1; CCR2; Membrane Proteins; Monocyte Chemoattractant Proteins; Inbred DBA; RNA; Messenger; Chemokine CXCL12; CCR7; CC; Chemokine CCL7; Up-Regulation; Chemokine CCL4; Chemokine CCL5
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11699/7032
Citazioni
  • ???jsp.display-item.citation.pmc??? 39
  • Scopus 134
  • ???jsp.display-item.citation.isi??? 130
social impact