Factors determining the spontaneous activation of splenic dendritic cells in culture.


Autoria(s): Vremec D.; O'Keeffe M.; Wilson A.; Ferrero I.; Koch U.; Radtke F.; Scott B.; Hertzog P.; Villadangos J.; Shortman K.
Data(s)

2011

Resumo

Dendritic cells (DCs) serve as a link between the innate and adaptive immune systems. The activation state of DCs is crucial in this role. However, when DCs are isolated from lymphoid tissues, purified and placed in culture they undergo 'spontaneous' activation. The basis of this was explored, using up-regulation of DC surface MHC II, CD40, CD80 and CD86 as indicators of DC activation. No evidence was found for DC damage during isolation or for microbial products causing the activation. The culture activation of spleen DCs differed from that of Langerhans cells when released from E-cadherin-mediated adhesions, since E-cadherin was not detected and activation still occurred with β-catenin null DCs. Much of the activation could be attributed to DC-DC interactions. Although increases in surface MHC II levels occurred under all culture conditions tested, the increase in expression of CD40, CD80 and CD86 was much less under culture conditions where such interactions were minimised. DC-to-DC contact under the artificial conditions of high DC concentration in culture induced the production of soluble factors and these, in turn, induced the up-regulation of co-stimulatory molecules on the DC surface.

Identificador

http://serval.unil.ch/?id=serval:BIB_1D6EB452855C

isbn:1753-4267 (Electronic)

pmid:20501515

doi:10.1177/1753425910371396

isiid:000291243800010

Idioma(s)

en

Fonte

Innate Immunity, vol. 17, no. 3, pp. 338-352

Palavras-Chave #Animals; Antigens, CD/genetics; Antigens, CD/metabolism; Cadherins/metabolism; Cell Adhesion; Cell Communication/immunology; Cell Differentiation; Cells, Cultured; Chimera; Cytokines/genetics; Cytokines/metabolism; Dendritic Cells/immunology; Dendritic Cells/metabolism; Histocompatibility Antigens Class II/genetics; Histocompatibility Antigens Class II/metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Spleen; Up-Regulation/immunology; beta Catenin/genetics
Tipo

info:eu-repo/semantics/article

article