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The Journal of Immunology, 2002, 168: 5079-5087.
Copyright © 2002 by The American Association of Immunologists

Visualization of Lymphotoxin-{beta} and Lymphotoxin-{beta} Receptor Expression in Mouse Embryos1

Jeffrey L. Browning2,* and Lars E. French{dagger}

* Department of Exploratory Biology, Biogen, Cambridge, MA 02142; and {dagger} Department of Dermatology, University of Geneva, Geneva, Switzerland

The heteromeric lymphotoxin {alpha}{beta} ligand (LT) binds to the LT{beta} receptor (LT{beta}R) and provides an essential trigger for lymph node (LN) development. LT{beta}R signaling is also critical for the emergence of pathological ectopic lymph node-like structures and the maintenance of an organized splenic white pulp. To better understand the role of LT in development, the expression patterns of LT{beta} and LT{beta}R mRNA were examined by in situ hybridization in the developing mouse embryo. Images of LT{beta} ligand expression in developing peripheral LN in the E18.5 embryo revealed a relatively early phase structure and allowed for comparative staging with LN development in rat and humans. The LT{beta}R is expressed from E16.5 onward in respiratory, salivary, bronchial, and gastric epithelium, which may be consistent with early communication events between lymphoid elements and epithelial specialization over emerging mucosal LN. Direct comparison of mouse fetal and adult tissues by FACS analysis confirmed the elevated expression of LTBR in some embryonic epithelial layers. Therefore, surface LTBR expression may be elevated during fetal development in some epithelial layers.




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