The Journal of Experimental Medicine
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Published online November 3, 2008
doi:10.1084/jem.20081430
The Journal of Experimental Medicine, Vol. 205, No. 12, 2839-2850
The Rockefeller University Press, 0022-1007 $30.00
© 2008 Jakubzick et al.
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ARTICLE

Lymph-migrating, tissue-derived dendritic cells are minor constituents within steady-state lymph nodes

Claudia Jakubzick, Milena Bogunovic, Anthony J. Bonito, Emma L. Kuan, Miriam Merad, and Gwendalyn J. Randolph

Department of Gene and Cell Medicine, Mount Sinai School of Medicine, New York, NY 10029

CORRESPONDENCE Gwendalyn J. Randolph: gwendalyn.randolph{at}mssm.edu

Observations that dendritic cells (DCs) constitutively enter afferent lymphatic vessels in many organs and that DCs in some tissues, such as the lung, turnover rapidly in the steady state have led to the concept that a major fraction of lymph node DCs are derived from migratory DCs that enter the lymph node through upstream afferent lymphatic vessels. We used the lysozyme M–Cre reporter mouse strain to assess the relationship of lymph node and nonlymphoid organ DCs. Our findings challenge the idea that a substantial proportion of lymph node DCs derive from the upstream tissue during homeostasis. Instead, our analysis suggests that nonlymphoid organ DCs comprise a major population of DCs within lymph nodes only after introduction of an inflammatory stimulus.


Abbreviations used: BAL, bronchoalveolar lavage; EGFP, enhanced GFP; LP, lamina propria; LysM, lysozyme M; MDP, macrophage DC progenitor; TRITC, tetramethylrhodoamine-5-(and-6)-isothiocyanate.

© 2008 Jakubzick et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jem.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).


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