Antigen-specific IL-23/17 pathway activation by murine semi-mature DC-like cells
- 1. Department of Biological Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda-shi, Chiba 278-8510 (Japan)
Description
We analyzed the phenotype and function of bone marrow-derived dendritic cells (DCs) induced in vitro without using any serum during the late stage of cultivation. These 'serum-free' DCs (SF-DCs) possessed the ability to induce T cell proliferation as well as antibody responses, indicating that they were functional DCs. Surprisingly, the SF-DCs akin to semi-mature DCs in terms of both phenotypic and functional characteristics. The SF-DCs did not produce IL-12 but produced large amounts of IL-23 following lipopolysaccharide stimulation. The antigen-specific production of IL-17 by CD4+ T cells co-cultured with OVA-loaded SF-DCs was significantly higher than that with OVA-loaded conventional DCs. These results suggest that SF-DCs tend to produce IL-23 and can consequently induce the IL-17 producing CD4+ T cells. The semi-mature DC-like cells reported here will be useful vehicles for DC immunization and might contribute to studies on the possible involvement of semi-mature DCs in Th17 cell differentiation.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2009.06.119Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2009.06.119;
- PII
- S0006-291X(09)01265-0;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 387
- Journal Issue
- 1
- Journal Page Range
- p. 52-57
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45020611
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANTIBODIES; ANTIGENS; BONE MARROW; CELL DIFFERENTIATION; CELL PROLIFERATION; CULTIVATION; DENDRITES; IN VITRO; OVA; PHENOTYPE; VEHICLES
- Descriptors DEC
- ANIMAL TISSUES; BODY; CRYSTALS; GAMETES; GERM CELLS; HEMATOPOIETIC SYSTEM; ORGANS
Optional Information
- Copyright
- Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.