The Detergent Effect of Mesalazine Interferes with Phosphatidylcholine Binding to Mucin 2.

CaCo2 cells Mesalazine Mucin 2 Phosphatidylcholine Ulcerative colitis

Journal

Inflammatory intestinal diseases
ISSN: 2296-9365
Titre abrégé: Inflamm Intest Dis
Pays: Switzerland
ID NLM: 101677990

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 15 05 2018
accepted: 29 08 2018
entrez: 2 3 2019
pubmed: 2 3 2019
medline: 2 3 2019
Statut: ppublish

Résumé

Therapeutically applied delayed-release phosphatidylcholine (PC) revealed mucosa protection and clinical improvement of ulcerative colitis. However, a recent trial with simultaneous application of delayed-release PC and mesalazine showed lack of efficacy. It is hypothesized that mesalazine acts as detergent to prohibit PC integration into mucus as target compartment, thus preventing topical mucus protection. In vitro PC-binding studies with mucin 2 and intestinally differentiated CaCo2 cells as well as outcome analysis of a therapeutic trial with delayed-release PC and additional mesalazine. Choline-containing phospholipids, in particular PC, bind to mucin 2 as main scaffold protein of intestinal mucus to establish a hydrophobic barrier towards microbiota in the intestinal lumen. PC also binds to the apical surface of polarized CaCo2 cells with membrane-anchored mucin 3. Mesalazine removes mucin-bound PC and, thus, reduces transepithelial resistance. A post hoc analysis of patients from a previous multicenter phase IIB trial with delayed-release PC revealed that those without mesalazine showed a PC dose-dependent outcome with regard to achievement of partial and complete remission ( Mesalazine solubilizes PC and, thus, prevents the protective action of therapeutically applied delayed-release PC within mucus.

Identifiants

pubmed: 30820432
doi: 10.1159/000493347
pii: iid-0003-0107
pmc: PMC6390417
doi:

Types de publication

Journal Article

Langues

eng

Pagination

107-115

Références

Biochim Biophys Acta. 2004 Jun 1;1682(1-3):63-71
pubmed: 15158757
Scand J Gastroenterol. 2004 Aug;39(8):737-42
pubmed: 15513358
Gut. 2005 Jul;54(7):966-71
pubmed: 15951544
Ann Intern Med. 2007 Nov 6;147(9):603-10
pubmed: 17975182
Mucosal Immunol. 2008 May;1(3):183-97
pubmed: 19079178
Inflamm Bowel Dis. 2009 Nov;15(11):1705-20
pubmed: 19504612
Int J Colorectal Dis. 2011 Aug;26(8):989-98
pubmed: 21455745
Aliment Pharmacol Ther. 2012 Aug;36(3):248-56
pubmed: 22690748
Dig Dis. 2012;30 Suppl 3:85-91
pubmed: 23295697
FASEB J. 2014 Jul;28(7):3159-70
pubmed: 24719358
Am J Gastroenterol. 2014 Jul;109(7):1041-51
pubmed: 24796768
BMJ Case Rep. 2015 May 02;2015:null
pubmed: 25935912
J Crohns Colitis. 2016 Feb;10(2):149-58
pubmed: 26619893
Cochrane Database Syst Rev. 2016 May 09;(5):CD000544
pubmed: 27158764
Biochim Biophys Acta. 2016 Sep;1861(9 Pt A):1161-1169
pubmed: 27365309
Immunopharmacol Immunotoxicol. 2017 Feb;39(1):45-53
pubmed: 28071183
Eur J Rheumatol. 2017 Mar;4(1):1-10
pubmed: 28293446
J Crohns Colitis. 2017 Oct 1;11(10):1247-1257
pubmed: 28575164
Inflamm Intest Dis. 2018 Mar;2(3):180-187
pubmed: 29922677

Auteurs

Wolfgang Stremmel (W)

Department of Gastroenterology and Infectious Diseases, University Hospital of Heidelberg, Heidelberg, Germany.

Simone Staffer (S)

Department of Gastroenterology and Infectious Diseases, University Hospital of Heidelberg, Heidelberg, Germany.

Sven Gehrke (S)

Medical Center Baden-Baden, Baden-Baden, Germany.

Classifications MeSH