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Open AccessJournal ArticleDOI

T-cell priming by dendritic cells in lymph nodes occurs in three distinct phases

Thorsten R. Mempel, +2 more
- 08 Jan 2004 - 
- Vol. 427, Iss: 6970, pp 154-159
TLDR
T-cell priming by DCs occurs in three successive stages: transient serial encounters during the first activation phase are followed by a second phase of stable contacts culminating in cytokine production, which makes a transition into a third phase of high motility and rapid proliferation.
Abstract
Primary T-cell responses in lymph nodes (LNs) require contact-dependent information exchange between T cells and dendritic cells (DCs). Because lymphocytes continually enter and leave normal LNs, the resident lymphocyte pool is composed of non-synchronized cells with different dwell times that display heterogeneous behaviour in mouse LNs in vitro. Here we employ two-photon microscopy in vivo to study antigen-presenting DCs and naive T cells whose dwell time in LNs was synchronized. During the first 8 h after entering from the blood, T cells underwent multiple short encounters with DCs, progressively decreased their motility, and upregulated activation markers. During the subsequent 12 h T cells formed long-lasting stable conjugates with DCs and began to secrete interleukin-2 and interferon-gamma. On the second day, coinciding with the onset of proliferation, T cells resumed their rapid migration and short DC contacts. Thus, T-cell priming by DCs occurs in three successive stages: transient serial encounters during the first activation phase are followed by a second phase of stable contacts culminating in cytokine production, which makes a transition into a third phase of high motility and rapid proliferation.

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Follicular Helper CD4 T Cells (TFH)

TL;DR: This review discusses recent progress and areas of uncertainty or disagreement in the literature, and debates the developmental relationship between T(FH) cells and other CD4 T cell subsets (Th1, Th2, Th17, iTreg).
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EVOLUTION: Of Mice . . .

S. J. Simpson
- 24 Dec 2004 - 
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mTOR regulates memory CD8 T-cell differentiation

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Rapid leukocyte migration by integrin-independent flowing and squeezing

TL;DR: It is shown here that functional integrins do not contribute to migration in three-dimensional environments, and these cells migrate by the sole force of actin-network expansion, which promotes protrusive flowing of the leading edge.
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Lymphangiogenesis: Molecular Mechanisms and Future Promise

TL;DR: The growth of lymphatic vessels is actively involved in a number of pathological processes including tissue inflammation and tumor dissemination but is insufficient in patients suffering from lymphedema, a debilitating condition characterized by chronic tissue edema and impaired immunity.
References
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Journal ArticleDOI

The Immunological Synapse: A Molecular Machine Controlling T Cell Activation

TL;DR: Immunological synapse formation is now shown to be an active and dynamic mechanism that allows T cells to distinguish potential antigenic ligands and was a determinative event for T cell proliferation.
Journal ArticleDOI

Three-dimensional segregation of supramolecular activation clusters in T cells

TL;DR: The three-dimensional distribution of receptors and intracellular proteins that cluster at the contacts between T cells and APCs during antigen-specific interactions, Surprisingly, instead of showing uniform oligomerization, these proteins clustered into segregated three- dimensional domains within the cell contacts.
Journal ArticleDOI

EVOLUTION: Of Mice . . .

S. J. Simpson
- 24 Dec 2004 - 
Journal ArticleDOI

Induction by antigen of intrathymic apoptosis of CD4+CD8+TCRlo thymocytes in vivo

TL;DR: Results provide direct evidence for the in vivo role of apoptosis in the development of antigen-induced tolerance in mice transgenic for a T cell receptor that reacts to this peptide.
Journal ArticleDOI

SINGLE-PARTICLE TRACKING: Applications to Membrane Dynamics

TL;DR: Measurements of trajectories of individual proteins or lipids in the plasma membrane of cells show a variety of types of motion, including directed motion, confined motion, and anomalous diffusion, which requires a revision of existing views of membrane structure and dynamics.
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