Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1999 Feb 15;189(4):611-4.
doi: 10.1084/jem.189.4.611.

Mobilizing dendritic cells for tolerance, priming, and chronic inflammation

Affiliations
Review

Mobilizing dendritic cells for tolerance, priming, and chronic inflammation

F Sallusto et al. J Exp Med. .
No abstract available

PubMed Disclaimer

Figures

Figure 1
Figure 1
Mobilization and activation of DCs control the induction of tolerance, priming, and chronic inflammation. (A) Under steady state conditions, the recruitment of DC precursors into tissues and the migration of mature DCs to lymph nodes occur at low rates. Tissue antigens carried by short-lived migratory DCs may be transferred to resident lymphoid DCs that induce T cell tolerance. (B) Activated endothelial cells recruit DCs at higher rates. Immature DCs are attracted by inflammatory chemokines towards the site of inflammation, where bacterial and viral products induce DC maturation and activation. In the lymph node, activated T cells can further enhance DC activation and survival via CD40L and TRANCE. Because many and highly activated DCs are present, a productive T cell response is induced. (C) Mature DCs that fail to migrate to lymph nodes may serve as nucleation sites for chronic inflammatory reaction. Chemokines produced by these DCs attract maturing DCs as well as recently activated T cells, that maintain the inflammatory reaction. Thick lines indicate activated cells. Mo, monocytes; iDC, immature DCs; mDC, mature DCs; LyDC, lymphoid DCs.

Comment on

References

    1. Springer TA. Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell. 1994;76:301–314. - PubMed
    1. Robert C, Fuhlbrigge RC, Kieffer JD, Ayehunie S, Hynes RO, Cheng G, Grabbe S, von Andrian UH, Kupper TS. Interaction of dendritic cells with skin endothelium: a new perspective on immunosurveillance. J Exp Med. 1999;189:627–635. - PMC - PubMed
    1. McEver RP, Beckstead JH, Moore KL, Marshall-Carlson L, Bainton DF. GMP-140, a platelet alpha-granule membrane protein, is also synthesized by vascular endothelial cells and is localized in Weibel-Palade bodies. J Clin Invest. 1989;84:92–99. - PMC - PubMed
    1. Bonfanti R, Furie BC, Furie B, Wagner DD. PADGEM (GMP140) is a component of Weibel-Palade bodies of human endothelial cells. Blood. 1989;73:1109–1112. - PubMed
    1. Wolff B, Burns AR, Middleton J, Rot A. Endothelial cell “memory” of inflammatory stimulation: human venular endothelial cells store interleukin 8 in Weibel-Palade bodies. J Exp Med. 1998;188:1757–1762. - PMC - PubMed