z-logo
Premium
Ascorbic acid stimulates barrier function of cultured endothelial cell monolayer
Author(s) -
Utoguchi Naoki,
Ikeda Kenji,
Saeki Kazuhiko,
Oka Naomi,
Mizuguchi Hiroyuki,
Kubo Kazuyosi,
Nakagawa Shinsaku,
Mayumi Tadanori
Publication year - 1995
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.1041630219
Subject(s) - ascorbic acid , umbilical vein , endothelial stem cell , dithiothreitol , permeability (electromagnetism) , human umbilical vein endothelial cell , biochemistry , chemistry , monolayer , in vitro , biophysics , biology , enzyme , food science , membrane
The macromolecular permeability of cultured bovine aortic, bovine venous, and human umbilical vein endothelial cell monolayers was decreased significantly in culture medium containing L‐ascorbic acid (Asc Acid; 0.01–0.1 mM) and L‐ascorbic acid 2‐phosphate (Asc 2‐P). Dithiothreitol, which shows reducing activity equivalent to that of Asc Acid, did not affect endothelial permeability. Asc Acid induced a sixfold increase in collagen synthesis by the endothelial cells. The coexistence of L‐azetidine 2‐carboxylic acid, an inhibitor of collagen synthesis, attenuated the effect of Asc 2‐P in a dose‐dependent manner. Another collagen synthesis inhibitor, ethyl‐3,4‐dihydroxybenzoate, also inhibited collagen synthesis and increased endothelial permeability. The decrease in permeability of the endothelial monolayer was dependent on a reduction of the permeability coefficient of the endothelial monolayer. These findings indicate that endothelial barrier function is stimulated by Asc Acid via an increase in collagen synthesis. © 1995 Wiley‐Liss, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom