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1 Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark
2 The Finsen Laboratory, Rigshospitalet, Denmark
3 Department of International Health, immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark
4 Panum, United States
5 Department of Medical Biochemistry & Genetics, University of Copenhagen, Copenhagen, Denmark
* To whom correspondence should be addressed. E-mail: jolsen{at}imbg.ku.dk.
During the early postnatal period lymphocytes migrate into the mouse small intestine. Migrating infiltrative lymphocytes have the potential to affect the epithelial cells via secreted cytokines. Such cross-talk can result in the elicitation of an epithelial transcriptional response. Knowledge about such physiological cross-talk between the immune system and the epithelium in the postnatal small intestinal mucosa is lacking. We have investigated the transcriptome changes occurring in the postnatal mouse small intestine using DNA microarray technology, immunocytochemistry and quantitative real-time RT-PCR analysis. The DNA microarray data were analyzed bioinformatically using a combination of projections to latent structures (PLS) analysis and functional annotation analysis. The results show that infiltrating lymphocytes appear in the mouse small intestine in the late post-weaning period and give rise to distinct changes in the epithelial transcriptome. Of particular interest is the expression of three genes encoding a mucin (Muc4), a mucin-like protein (16000D21Rik) and ATP citrate lyase (Acly). All three genes were shown to be expressed by the epithelium and to be up-regulated in response to lymphocytic migration into the small intestinal mucosa.
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