The FASEB journal, 2016-02, Vol.30 (2), p.933-947
2016
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- Autor(en) / Beteiligte
- Titel
- Leukotriene B4 receptor type 2 (BLT2) enhances skin barrier function by regulating tight junction proteins
- Ist Teil von
- The FASEB journal, 2016-02, Vol.30 (2), p.933-947
- Ort / Verlag
- Bethesda, MD, USA: Federation of American Societies for Experimental Biology
- Erscheinungsjahr
- 2016
- Quelle
- Access via Wiley Online Library
- Beschreibungen/Notizen
- GPCRs are involved in numerous physiologic functions and are important drug targets. Although the epithelial barrier is important for protection from invading pathogens, the correlation between GPCRs and epithelial barrier function remains unknown. Leukotriene B4 (LTB4) receptor type 2 (BLT2), mainly expressed in epithelial cells, is a GPCR for 12(S)‐hydroxyheptadeca‐5Z,8E,10E‐trienoic acid (12‐HHT) and LTB4. In our study, BLT2 localized at the lateral membrane in BLT2‐overexpressing Madin‐Darby canine kidney (MDCK) II cells and in the small intestine of BLT2‐transgenic mice. BLT2‐deficient mice exhibited higher transepidermal water loss and were more sensitive to epicutaneous sensitization. MDCK‐BLT2 cells recovered transepithelial electrical resistance (TER) after a calcium switch faster than did MDCK‐Mock cells, and 12‐HHT stimulation accelerated TER recovery only in MDCK‐BLT2 cells. Quantitative PCR and immunoblot analyses revealed that the 12‐HHT/BLT2 axis up‐regulated claudin‐4 (CLDN4) expression in MDCK‐BLT2 cells and human primary keratinocytes, and CLDN4 knockdown abolished 12‐HHT‐dependent TER recovery. Acceleration of TER recovery and induction of CLDN4 expression by 12‐HHT stimulation were abolished by inhibition of Gαi protein or p38 MAPK. These results show that 12‐HHT/BLT2 enhances epithelial barrier function by increasing CLDN4 expression via the Gαi protein‐p38 MAPK pathway.—Ishii, Y., Saeki, K., Liu, M., Sasaki, F., Koga, T., Kitajima, K., Meno, C., Okuno, T., Yokomizo, T. Leukotriene B4 receptor type 2 (BLT2) enhances skin barrier function by regulating tight junction proteins. FASEB J. 30, 933–947 (2016). www.fasebj.org
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0892-6638eISSN: 1530-6860DOI: 10.1096/fj.15-279653Titel-ID: cdi_proquest_miscellaneous_1762343994
- Format
- –
- Schlagworte
- Animals, Claudin-4 - biosynthesis, Claudin-4 - genetics, claudin‐4, Dogs, Fatty Acids, Unsaturated - pharmacology, G protein, Gene Expression Regulation - drug effects, Gene Expression Regulation - physiology, GPCR, Humans, Madin Darby Canine Kidney Cells, MAP Kinase Signaling System - drug effects, MAP Kinase Signaling System - physiology, Mice, Mice, Knockout, p38 MAPK, p38 Mitogen-Activated Protein Kinases - genetics, p38 Mitogen-Activated Protein Kinases - metabolism, Receptors, Leukotriene B4 - genetics, Receptors, Leukotriene B4 - metabolism, Skin - cytology, Skin - metabolism, Tight Junctions - genetics, Tight Junctions - metabolism