Original Articles
Copyright ©The Author(s) 2001. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 15, 2001; 7(2): 193-197
Published online Apr 15, 2001. doi: 10.3748/wjg.v7.i2.193
Transepithelial transport of putrescine across monolayers of the human intestinal epithelial cell line, Caco-2
Vladan Milovic, Lyudmila Turchanowa, Jürgen Stein, Wolfgang F. Caspary
Vladan Milovic, Lyudmila Turchanowa, Jürgen Stein, Wolfgang F. Caspary, 2nd Department of Medicine, Johann Wolfgang Goethe University, Frankfurt, Germany
Vladan Milovic, graduate of the Belgrade University School of Medicine (Yugoslavia), is a former recipient of Alexander von Humboldt and Knut & Alice Wallenberg Postdoctoral Research Fellowships, and is at present approaching his Senior Lectureship in Experimental Medicine at the Johann Wolfgang University in Frankfurt.
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. med. Vladan Milovic, Medizinische Klinik II, J.W.Goethe Universität, Theodor Stern Kai 7, D-60590 Frankfurt, Germany. Milovic@em.uni-frankfurt.de
Telephone: +49-69 6301-5326 Fax: +49-69 6301-6246
Received: February 6, 2001
Revised: February 23, 2001
Accepted: March 1, 2001
Published online: April 15, 2001
Abstract

AIM: To study the transepithelial transport characteristics of the polyamine putrescine in human intestinal Caco-2 cell monolayers to elucidate the mechanisms of the putrescine intestinal absorption.

METHODS: The transepithelial transport and the cellular accumulation of putrescine was measured using Caco-2 cell monolayers grown on permeable filters.

RESULTS: Transepithelial transport of putrescine in physiological concentrations ( > 0.5 mM) from the apical to basolateral side was linear. Intracellular accumulation of putrescine was higher in confluent than in fully differentiated Caco-2 cells, but still negligible (less than 0.5%) of the overall transport across the monolayers in apical to basolateral direction.EGF enhanced putrescine accumulation in Caco-2 cells by four fold, as well as putrescine conversion to spermidine and spermine by enhancing the activity of S adenosylmethionine decarboxylase. However, EGF did not have any significant influence on putrescine flux across the Caco- 2 cell monolayers. Excretion of putrescine from Caco-2 cells into the basolateral medium did not exceed 50 picomoles, while putrescine passive flux from the apical to the basolateral chamber, contributed hundreds of micromoles polyamines to the basolateral chamber.

CONCLUSION: Transepithelial transport of putrescine across Caco-2 cell monolayers occurs in passive diffusion, and is not influenced when epithelial cells are stimulated to proliferate by a potent mitogen such as EGF.

Keywords: putrescine/metabolism; Caco 2 cells/ metabolism; polyamines/metabolism; biological transport