Pink, Matthias and Ratsch, Boris A. and Mardahl, Maibritt and Durek, Pawel and Polansky, Julia K. and Karl, Martin and Baumgrass, Ria and Wallner, Stefan and Cadenas, Cristina and Gianmoena, Kathrin and Floess, Stefan and Chen, Wei and Nordstroem, Karl and Tierling, Sascha and Olek, Sven and Walter, Joern and Hamann, Alf and Syrbe, Uta (2016) Imprinting of Skin/Inflammation Homing in CD4(+) T Cells Is Controlled by DNA Methylation within the Fucosyltransferase 7 Gene. JOURNAL OF IMMUNOLOGY, 197 (8). pp. 3406-3414. ISSN 0022-1767, 1550-6606
Full text not available from this repository. (Request a copy)Abstract
E- and P-selectin ligands (E- and P-ligs) guide effector memory T cells into skin and inflamed regions, mediate the inflammatory recruitment of leukocytes, and contribute to the localization of hematopoietic precursor cells. A better understanding of their molecular regulation is therefore of significant interest with regard to therapeutic approaches targeting these pathways. In this study, we examined the transcriptional regulation of fucosyltransferase 7 (FUT7), an enzyme crucial for generation of the glycosylated E- and P-ligs. We found that high expression of the coding gene fut7 in murine CD4(+) T cells correlates with DNA demethylation within a minimal promoter in skin/inflammation-seeking effector memory T cells. Retinoic acid, a known inducer of the gut-homing phenotype, abrogated the activation-induced demethylation of this region, which contains a cAMP responsive element. Methylation of the promoter or mutation of the cAMP responsive element abolished promoter activity and the binding of CREB, confirming the importance of this region and of its demethylation for fut7 transcription in T cells. Furthermore, studies on human CD4(+) effector memory T cells confirmed demethylation within FUT7 corresponding to high FUT7 expression. Monocytes showed an even more extensive demethylation of the FUT7 gene whereas hepatocytes, which lack selectin ligand expression, exhibited extensive methylation. In conclusion, we show that DNA demethylation within the fut7 gene controls selectin ligand expression in mice and humans, including the inducible topographic commitment of T cells for skin and inflamed sites.
Item Type: | Article |
---|---|
Uncontrolled Keywords: | FACTOR-BINDING SITES; SELECTIN LIGAND; MEMORY CD4(+); P-SELECTIN; DIFFERENTIAL REQUIREMENTS; LEUKOCYTE RECRUITMENT; EPIGENETIC REGULATION; FOXP3 EXPRESSION; CPG METHYLATION; DENDRITIC CELLS; |
Subjects: | 600 Technology > 610 Medical sciences Medicine |
Divisions: | Medicine > Lehrstuhl für Klinische Chemie und Laboratoriumsmedizin |
Depositing User: | Dr. Gernot Deinzer |
Date Deposited: | 24 Apr 2019 09:33 |
Last Modified: | 24 Apr 2019 09:33 |
URI: | https://pred.uni-regensburg.de/id/eprint/4091 |
Actions (login required)
![]() |
View Item |