Secretion of angiopoietin-like 4 protein from intestinal cells | Functional Foods in Health and Disease - Online ISSN: 2160-3855; Print ISSN: 2378-7007 Skip to main content Skip to main navigation menu Skip to site footer Open Menu Functional Foods in Health and Disease - Online ISSN: 2160-3855; Print ISSN: 2378-7007 Home Food Science Publisher Functional Food Center Current Archives About About the Journal Aims and Scope Contact Editing Services Editorial Team Express Peer Review Graphical Abstract Journal Insights Privacy Statement Submissions Announcements Search Search Register Login Home / Archives / Vol. 5 No. 2 (2015): February 2015 / Research Articles Secretion of angiopoietin-like 4 protein from intestinal cells Authors Soren Drud Nielsen Department of Food Science, Aarhus University, Denmark Randi Jessen Department of Food Science, Aarhus University, Denmark Trine Kastrup Dalsgaard Department of Food Science, Aarhus University, Denmark Jette Feveile Young Department of Food Science, Aarhus University, Denmark DOI: https://doi.org/10.31989/ffhd.v5i2.171 Abstract Background: Angiopoietin-like 4 (ANGPTL4) has been suggested to play a role in lipid metabolism as a regulatory protein of lipoprotein lipase activity. Intestinal secretion of ANGPTL4, which is regulated by fatty acids, may inhibit the activity of circulating lipoprotein lipase; but, recent studies suggest that it could also inhibit pancreatic lipase in the gut and thereby reduce intestinal uptake of lipids. Secretion of the ANGPTL4 protein to either the lumen or tissue/blood side of the intestinal epithelial layer would indicate possible modes of action. Methods: Caco-2 cells were grown on permeable membranes and cultured for 21 days to spontaneously differentiate into an intact monolayer of intestinal cells, mimicking the epithelial cell layer lining the intestinal wall. Cells were treated with 9 mM butyrate and the time dependent gene expression and protein secretion to the apical and basolateral side was analysed over a time-course of 24 hours. Possible feedback from ANGPTL4 protein was investigated by adding 0.25 ng/ml recombinant ANGPTL4 protein to culture media. Results: Butyrate-induced ANGPTL4 gene expression increased in Caco-2 cells after 2 hours, reaching a plateau of approximately 6 fold after 6-24 hours, while the ANGPTL4 protein secretion to both the apical and basolateral sides was increased 18-24 hours after stimulation. A negative feedback on apical and basolateral secretion was observed in the presence of recombinant ANGPTL4 on the apical and basolateral sides, respectively. Conclusion: The present study indicates that, upon exposure to butyrate, the monolayer of epithelial cells secretes the ANGPTL4 protein to both the tissue/blood (basolateral) side and the luminal (apical) side of the monolayer which, in an in vivo situation, may be interpreted as potential inhibition of both the circulating and pancreatic lipase. Keywords: Angiopoietin-like 4, Caco-2, Permeable membrane, Protein, Secretion, Intestine, Negative feedback Downloads [Abstract] [Full Article] Published 2015-02-15 Issue Vol. 5 No. 2 (2015): February 2015 Section Research Articles License Authors retain the copyright of their articles and grant the Functional Food Center (FFC) and its journals the right of first publication under the terms of the Creative Commons Attribution 4.0 International License. This license permits unrestricted use, distribution, and reproduction in any medium, including commercial use, provided the original author(s) and source are properly credited. Authors may post and share their published work freely, provided that the original publication in this journal is acknowledged. By submitting to this journal, authors confirm that their manuscripts are original, not under consideration elsewhere, and that they hold the necessary rights to grant this license. The Functional Food Center encourages open scientific exchange and allows derivative and extended works, provided attribution to the original publication is maintained. About the Journal      Editing Services      Graphical Abstract      Journal Insights        Submissions        Editorial Team       Privacy Statement        Contact        Current        Archives   Open Journal Systems Hosting and Support by: OpenJournalSystems.com