Glucose and calcium ions may modulate the efficiency of bovine β-casomorphin-7 permeability through a monolayer of Caco-2 cells

被引:10
作者
Jarmolowska, Beata [1 ]
Teodorowicz, Malgorzata [2 ]
Fiedorowicz, Ewa [1 ]
Sienkiewicz-Szlapka, Edyta [1 ]
Matysiewicz, Michal [1 ]
Kostyra, Elzbieta [1 ]
机构
[1] Univ Warmia & Mazury, Fac Biol & Biotechnol, Dept Biochem, PL-10719 Olsztyn, Poland
[2] Univ Wageningen & Res Ctr, Cell Biol & Immunol Grp, NL-6708 WD Wageningen, Netherlands
关键词
beta-Casomorphin-7; Caco-2 cells monolayer; Food allergy; Infant formula; Permeability coefficient; BETA-CASOMORPHIN; OPIOID-PEPTIDES; TIGHT JUNCTIONS; INTESTINAL PERMEABILITY; GENE-EXPRESSION; TRANSPORT; MILK; ABSORPTION; IV; CASEIN;
D O I
10.1016/j.peptides.2013.08.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Milk and dairy products provide a lot of valuable nutritive elements. They are also sources of biologically active peptides, including beta-casomorphins that manifest the properties of morphine. An activity of DPPIV seems to be most crucial factor decreasing the efficiency of the beta-casomorphin-7 (BCM7) transport. The increase of BCM7 concentration in blood may intensify symptoms of apparent life threatening events (ALTE), autism, schizophrenia, and allergy. This study aimed at identifying the influence of several selected substances on a transport efficiency of bovine BCM7 through an intestinal monolayer in a Caco-2 cell model system. Applying the ELISA method, the permeability coefficient of BCM7 through the Caco-2 monolayer was calculated. TEER values were used to evaluate the integrity of Caco-2 cell monolayers. An increase of glucose and Ca2+ concentrations in the culture medium was accompanied by an increase of the BCM7 transport efficiency. The lowest permeability coefficients of BCM7 were observed for the membranes with high electrical resistances. The transport was enhanced in the presence of milk infant formulas, whereas no changes were observed when using mu-opioid receptor antagonist (casoxin-6). The results may be useful in understanding the pathogenesis of inflammation and food allergy in infants. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:59 / 67
页数:9
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