Differential Regulation of Responsiveness to fMLP and C5a Upon Dendritic Cell Maturation: Correlation with Receptor Expression

• Published in: The Journal of immunology (1950) 2000-09, Vol.165 (5), p.2694-2702
• Main Authors: Yang, De, Chen, Qian, Stoll, Sabine, Chen, Xin, Howard, O. M. Zack, Oppenheim, Joost J
• Format: Article
• Language: English
• Subjects: Animals; Antigens, CD - biosynthesis; CD40 Antigens - immunology; CD40 Antigens - metabolism; CD40 Ligand; Cell Differentiation - immunology; Chemotaxis, Leukocyte - immunology; Complement C5a - immunology; Complement C5a - metabolism; complement component C5a; Dendritic Cells - cytology; Dendritic Cells - immunology; Dendritic Cells - metabolism; Down-Regulation - immunology; Female; fMLP protein; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - immunology; Humans; Ligands; Membrane Glycoproteins - immunology; Membrane Glycoproteins - metabolism; Mice; Mice, Inbred C57BL; Monocytes - cytology; Monocytes - immunology; Monocytes - metabolism; N-Formylmethionine Leucyl-Phenylalanine - immunology; N-Formylmethionine Leucyl-Phenylalanine - metabolism; Receptor, Anaphylatoxin C5a; Receptors, Complement - biosynthesis; Receptors, Formyl Peptide; Receptors, Immunologic - biosynthesis; Receptors, Peptide - biosynthesis; Time Factors
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.165.5.2694

The trafficking of immature and mature dendritic cells (DCs) to different anatomical sites in vivo is critical for fulfilling their roles in the induction of Ag-specific immune responses. Although this process is complex and regulated by many mediators, the capacity of DCs to migrate is predominantly dependent on the expression of particular chemotactic receptors on the surface of DCs that enable them to move along chemotactic gradients formed by the corresponding chemokines and/or classical chemoattractants. Here we show that immature DCs (iDCs) respond to both fMLP and C5a as determined by chemotaxis and Ca2+ mobilization, whereas mature DCs (mDCs) respond to C5a, but not fMLP. Additionally, iDCs express the receptors for both fMLP and C5a at mRNA and protein levels. Upon maturation of DCs, fMLP receptor expression is almost completely absent, whereas C5a receptor mRNA and protein expression is maintained. Concomitantly, mDCs migrate chemotactically and mobilize intracellular Ca2+ in response to C5a, but not fMLP. Thus the interaction between C5a and its receptor is likely involved in the regulation of trafficking of both iDCs and mDCs, whereas fMLP mobilizes only iDCs. The differential responsiveness to fMLP and C5a of iDCs and mDCs suggests that they play different roles in the initiation of immune responses.