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J. Exp. Med.,
Volume 188, Number 8, October 19, 1998 1473-1484
By


From the * Laboratoire d'Immunologie Cellulaire, Centre National de la Recherche Scientifique UMR
7627, CERVI, 75013 Paris, France; the Dendritic cells (DCs) are much more potent antigen (Ag)-presenting cells than resting B cells
for the activation of naive T cells. The mechanisms underlying this difference have been analyzed under conditions where ex vivo DCs or B cells presented known numbers of specific
Ag-major histocompatibility complex (MHC) complexes to naive CD4+ T cells from T cell
antigen receptor (TCR) transgenic mice. Several hundred Ag-MHC complexes presented by
B cells were necessary to elicit the formation of a few T-B conjugates with small contact zones,
and the resulting individual T cell Ca2+ responses were all-or-none. In contrast, Ag-specific T
cell Ca2+ responses can be triggered by DCs bearing an average of 30 Ag-MHC complexes per
cell. Formation of T-DC conjugates is Ag-independent, but in the presence of the Ag, the surface of the contact zone increases and so does the amplitude of the T cell Ca2+ responses.
These results suggest that Ag is better recognized by T cells on DCs essentially because T-DC
adhesion precedes Ag recognition, whereas T-B adhesion requires Ag recognition. Surprisingly, we also recorded small Ca2+ responses in T cells interacting with unpulsed DCs. Using
DCs purified from MHC class II knockout mice, we provide evidence that this signal is mostly
due to MHC-TCR interactions. Such an Ag-independent, MHC-triggered calcium response
could be a survival signal that DCs but not B cells are able to deliver to naive T cells.
INSERM CJF 96-08, Hôpital de la Pitié-Salpêtrière,
75013 Paris, France; and the § Laboratoire de Microscopie Électronique des Compartiments Cellulaires,
Institut Curie, Section de Recherche, Centre National de la Recherche Scientifique UMR 144, 75005 Paris, France
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