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BOR - Papers in Press, published online ahead of print June 18, 2008.
Biol Reprod 2008, 10.1095/biolreprod.107.067041
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BIOLOGY OF REPRODUCTION 79, 624–632 (2008)
DOI: 10.1095/biolreprod.107.067041
© 2008 by the Society for the Study of Reproduction, Inc.

Identification of ITGA4/ITGB7 and ITGAE/ITGB7 Expressing Subsets of Decidual Dendritic-Like Cells Within Distinct Microdomains of the Pregnant Mouse Uterus1

Jochen Behrends , Christian M. Karsten , Sonja Wilke , Astrid Röbke , and Andrea Kruse 2

Institut für Systemische Entzündungsforschung, University of Lübeck, 23538 Lübeck, Germany

ABSTRACT

Several leukocyte populations have been described within the pregnant mouse uterus, some of which express the integrin beta 7 (ITGB7). Here we demonstrate that the majority of the ITGB7+ decidual leukocytes belong to the dendritic cell (DC) lineage. By multiparameter flow cytometric analysis we demonstrated the existence of three distinct DC subsets, characterized by differential expression of ITGA4/ITGB7 (formerly alpha4beta7-integrin) and ITGAE/ITGB7 (formerly alphaEbeta7-integrin). Importantly, the predominant DC subsets reside in distinct microdomains of the Day 9 pregnant mouse uterus. ITGAX+ ITGAMmed ITGA4/ITGB7+ ITGAE (formerly CD11c+ CD11bmed alpha4beta7+ alphaE) cells represent the majority of DCs in the vascular zone (VZ), whereas ITGAX+ ITGAM ITGAE/ITGB7+ (formerly CD11c+ CD11b alphaEbeta7+) DCs are mainly located in the lower central decidua basalis (cDB) and the underlying myometrium. A population of ITGAX+ ITGAMlow DCs lacking ITGB7 are restricted to the cDB. Confocal microscopy studies show direct contact of VZ DCs with uterine natural killer (uNK) cells, suggesting a functional relationship between both cell populations. Collectively, our data identify three phenotypically distinct DC subsets residing in distinct microdomains of the uterus. The differential expression of ITGA4/ITGB7 and ITGAE/ITGB7 suggests distinct functional roles of the different DC subsets during early pregnancy.

decidua, dendritic cells, integrins, mouse, pregnancy, reproductive immunology, uterine NK cells


FOOTNOTES

1Supported in part by Deutsche Forschungsgemeinschaft grants GRK288C5 and Kr 1515/3-1.

Correspondence: 2Andrea Kruse, Institut für Systemische Entzündungsforschung, Universität zu Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany. FAX: 49 451 5003069; e-mail: kruse{at}immu.mu-luebeck.de







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Copyright © 2008 by the Society for the Study of Reproduction.