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Strain-Dependent Augmentation of Tight-Junction Barrier Function in Human Primary Epidermal Keratinocytes by Lactobacillus and Bifidobacterium Lysates
Author(s) -
Reshma Sultana,
Andrew J. McBain,
Catherine O’Neill
Publication year - 2013
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.00982-13
Subject(s) - lactobacillus rhamnosus , tight junction , bifidobacterium longum , microbiology and biotechnology , lactobacillus fermentum , probiotic , barrier function , lactobacillus reuteri , bifidobacterium breve , biology , lactobacillus plantarum , strain (injury) , lactobacillus , bifidobacterium , chemistry , bacteria , biochemistry , fermentation , genetics , anatomy , lactic acid
In this study, we investigated whether probiotic lysates can modify the tight-junction function of human primary keratinocytes. The keratinocytes were grown on cell culture inserts and treated with lysates fromBifidobacterium longum ,Lactobacillus plantarum ,Lactobacillus reuteri ,Lactobacillus fermentum , orLactobacillus rhamnosus GG. With the exception ofL. fermentum (which decreased cell viability), all strains markedly enhanced tight-junction barrier function within 24 h, as assessed by measurements of transepithelial electrical resistance (TEER). However,B. longum andL. rhamnosus GG were the most efficacious, producing dose-dependent increases in resistance that were maintained for 4 days. These increases in TEER correlated with elevated expression of tight-junction protein components. Neutralization of Toll-like receptor 2 abolished both the increase in TEER and expression of tight-junction proteins induced byB. longum , but notL. rhamnosus GG. These data suggest that some bacterial strains increase tight-junction function via modulation of protein components but the different pathways involved may vary depending on the bacterial strain.

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