Published September 11, 2009 | Version v1
Journal article

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.2009.06.119

Additional 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.