Thymus-homing peripheral dendritic cells constitute two of the three major subsets of dendritic cells in the steady-state thymus

Author:

Li JiChu1,Park JooHung2,Foss Deborah3,Goldschneider Irving3

Affiliation:

1. Department of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Boston, MA 02215

2. Department of Biology, Changwon National University, Changwon, Kyongnam, 641-773, Korea

3. Department of Immunology, School of Medicine, University of Connecticut Health Center, Farmington, CT 06030

Abstract

Many dendritic cells (DCs) in the normal mouse thymus are generated intrathymically from common T cell/DC progenitors. However, our previous work suggested that at least 50% of thymic DCs originate independently of these progenitors. We now formally demonstrate by parabiotic, adoptive transfer, and developmental studies that two of the three major subsets of thymic DCs originate extrathymically and continually migrate to the thymus, where they occupy a finite number of microenvironmental niches. The thymus-homing DCs consisted of immature plasmacytoid DCs (pDCs) and the signal regulatory protein α–positive (Sirpα+) CD11b+ CD8α− subset of conventional DCs (cDCs), both of which could take up and transport circulating antigen to the thymus. The cDCs of intrathymic origin were mostly Sirpα− CD11b− CD8αhi cells. Upon arrival in the thymus, the migrant pDCs enlarged and up-regulated CD11c, major histocompatibility complex II (MHC II), and CD8α, but maintained their plasmacytoid morphology. In contrast, the migrant cDCs proliferated extensively, up-regulated CD11c, MHC II, and CD86, and expressed dendritic processes. The possible functional implications of these findings are discussed.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference67 articles.

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