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Heat-killed Lactobacillus rhamnosus GG Modulates Urocortin and Cytokine Release in Primary Trophoblast Cells

Abstract A number of studies are showing that probiotic treatment induces an anti-inflammatory state. Intrauterine infection can lead to preterm delivery by modulating immune function and efforts to prevent this condition are ongoing nowadays. Lactobacillus rhamnosus GG (LGG) is a probiotic known to...

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Published in:Placenta (Eastbourne) 2010-10, Vol.31 (10), p.867-872
Main Authors: Bloise, E, Torricelli, M, Novembri, R, Borges, L.E, Carrarelli, P, Reis, F.M, Petraglia, F
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description Abstract A number of studies are showing that probiotic treatment induces an anti-inflammatory state. Intrauterine infection can lead to preterm delivery by modulating immune function and efforts to prevent this condition are ongoing nowadays. Lactobacillus rhamnosus GG (LGG) is a probiotic known to ameliorate inflammation by increasing local anti-inflammatory mediators in urinary and gastrointestinal tracts. The present study then analyzed the effect of heat-killed LGG over β-hCG, progesterone, interleukins (IL) 4 and 10, tumor necrosis factor-α (TNF-α), corticotropin releasing hormone (CRH) and urocortin (Ucn) release by primary trophoblast cells. Normal human term placentas (n = 6) were collected and purified trophoblast cells were incubated in the presence of LGG, lipopolysaccharide (LPS) or either LGG + LPS during 3 h, after which the target substances were quantified by ELISA and real-time PCR. LGG did not affect β-hCG, progesterone, or CRH secretion. Conversely, LGG increased IL-4 protein and mRNA expression ( P  
doi_str_mv 10.1016/j.placenta.2010.04.007
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Intrauterine infection can lead to preterm delivery by modulating immune function and efforts to prevent this condition are ongoing nowadays. Lactobacillus rhamnosus GG (LGG) is a probiotic known to ameliorate inflammation by increasing local anti-inflammatory mediators in urinary and gastrointestinal tracts. The present study then analyzed the effect of heat-killed LGG over β-hCG, progesterone, interleukins (IL) 4 and 10, tumor necrosis factor-α (TNF-α), corticotropin releasing hormone (CRH) and urocortin (Ucn) release by primary trophoblast cells. Normal human term placentas (n = 6) were collected and purified trophoblast cells were incubated in the presence of LGG, lipopolysaccharide (LPS) or either LGG + LPS during 3 h, after which the target substances were quantified by ELISA and real-time PCR. LGG did not affect β-hCG, progesterone, or CRH secretion. Conversely, LGG increased IL-4 protein and mRNA expression ( P  < 0.05) while IL-10 and Ucn secretion were increased in a dose dependent manner and the highest dose of LGG increased significantly IL-10 mRNA ( P  < 0.05). LGG did not alter TNF-α, while LPS exposure increased TNF-α protein ( P  < 0.001) and mRNA expression ( P  < 0.01). Conversely, LGG treatment reversed LPS-induced TNF-α release at both protein ( P  < 0.01) and mRNA levels ( P  < 0.05) in a dose dependent fashion. In conclusion, LGG stimulates IL-4, IL-10 and Ucn expression and reverses LPS-induced TNF-α release from trophoblast cells, with no change in β-hCG or progesterone release, suggesting that this probiotic may play a role as an immunomodulatory agent in human placenta without altering basic trophoblast functions.]]></description><identifier>ISSN: 0143-4004</identifier><identifier>EISSN: 1532-3102</identifier><identifier>DOI: 10.1016/j.placenta.2010.04.007</identifier><identifier>PMID: 20696472</identifier><identifier>CODEN: PLACDF</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Chorionic Gonadotropin - immunology ; Corticotropin-Releasing Hormone - immunology ; Cytokines ; Cytokines - genetics ; Cytokines - immunology ; Embryology: invertebrates and vertebrates. Teratology ; Enzyme-Linked Immunosorbent Assay ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Internal Medicine ; Lactobacilli ; Lactobacillus rhamnosus - immunology ; Obstetrics and Gynecology ; Placenta ; Placenta - cytology ; Placenta - immunology ; Placenta - microbiology ; Pregnancy ; Preterm delivery ; Probiotics - pharmacology ; Progesterone - immunology ; Reverse Transcriptase Polymerase Chain Reaction ; RNA - chemistry ; RNA - genetics ; Trophoblasts - cytology ; Trophoblasts - immunology ; Urocortin ; Urocortins - genetics ; Urocortins - immunology</subject><ispartof>Placenta (Eastbourne), 2010-10, Vol.31 (10), p.867-872</ispartof><rights>2010</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010. 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Intrauterine infection can lead to preterm delivery by modulating immune function and efforts to prevent this condition are ongoing nowadays. Lactobacillus rhamnosus GG (LGG) is a probiotic known to ameliorate inflammation by increasing local anti-inflammatory mediators in urinary and gastrointestinal tracts. The present study then analyzed the effect of heat-killed LGG over β-hCG, progesterone, interleukins (IL) 4 and 10, tumor necrosis factor-α (TNF-α), corticotropin releasing hormone (CRH) and urocortin (Ucn) release by primary trophoblast cells. Normal human term placentas (n = 6) were collected and purified trophoblast cells were incubated in the presence of LGG, lipopolysaccharide (LPS) or either LGG + LPS during 3 h, after which the target substances were quantified by ELISA and real-time PCR. LGG did not affect β-hCG, progesterone, or CRH secretion. Conversely, LGG increased IL-4 protein and mRNA expression ( P  < 0.05) while IL-10 and Ucn secretion were increased in a dose dependent manner and the highest dose of LGG increased significantly IL-10 mRNA ( P  < 0.05). LGG did not alter TNF-α, while LPS exposure increased TNF-α protein ( P  < 0.001) and mRNA expression ( P  < 0.01). Conversely, LGG treatment reversed LPS-induced TNF-α release at both protein ( P  < 0.01) and mRNA levels ( P  < 0.05) in a dose dependent fashion. 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Conversely, LGG increased IL-4 protein and mRNA expression ( P  < 0.05) while IL-10 and Ucn secretion were increased in a dose dependent manner and the highest dose of LGG increased significantly IL-10 mRNA ( P  < 0.05). LGG did not alter TNF-α, while LPS exposure increased TNF-α protein ( P  < 0.001) and mRNA expression ( P  < 0.01). Conversely, LGG treatment reversed LPS-induced TNF-α release at both protein ( P  < 0.01) and mRNA levels ( P  < 0.05) in a dose dependent fashion. In conclusion, LGG stimulates IL-4, IL-10 and Ucn expression and reverses LPS-induced TNF-α release from trophoblast cells, with no change in β-hCG or progesterone release, suggesting that this probiotic may play a role as an immunomodulatory agent in human placenta without altering basic trophoblast functions.]]></abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>20696472</pmid><doi>10.1016/j.placenta.2010.04.007</doi><tpages>6</tpages></addata></record>
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subjects Biological and medical sciences
Chorionic Gonadotropin - immunology
Corticotropin-Releasing Hormone - immunology
Cytokines
Cytokines - genetics
Cytokines - immunology
Embryology: invertebrates and vertebrates. Teratology
Enzyme-Linked Immunosorbent Assay
Female
Fundamental and applied biological sciences. Psychology
Humans
Internal Medicine
Lactobacilli
Lactobacillus rhamnosus - immunology
Obstetrics and Gynecology
Placenta
Placenta - cytology
Placenta - immunology
Placenta - microbiology
Pregnancy
Preterm delivery
Probiotics - pharmacology
Progesterone - immunology
Reverse Transcriptase Polymerase Chain Reaction
RNA - chemistry
RNA - genetics
Trophoblasts - cytology
Trophoblasts - immunology
Urocortin
Urocortins - genetics
Urocortins - immunology
title Heat-killed Lactobacillus rhamnosus GG Modulates Urocortin and Cytokine Release in Primary Trophoblast Cells
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