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Taurine Protects Blood-Milk Barrier Integrity Via Limiting Inflammatory Response in Streptococcus Uberis Infections

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inferredcites →https://doi.org/10.1002/jcb.27160openalex-extracted
IL‐1β induces increased tight junction permeability in bovine mammary epithelial cells via the IL‐1β‐ERK1/2‐MLCK axis upon blood‐milk barrier damage
inferredcites →https://doi.org/10.1002/pmic.200300723openalex-extracted
Differential protein composition of bovine whey: A comparison of whey from healthy animals and from those with clinical mastitis
inferredcites →https://doi.org/10.1007/s00441-018-2789-yopenalex-extracted
Bovine neutrophils in health and disease
inferredcites →https://doi.org/10.1007/s00726-009-0448-zopenalex-extracted
Taurine restores Axl/Gas6 expression in vascular smooth muscle cell calcification model
inferredcites →https://doi.org/10.1007/s00726-011-1047-3openalex-extracted
Taurine attenuates Streptococcus uberis-induced mastitis in rats by increasing T regulatory cells
inferredcites →https://doi.org/10.1007/s10911-011-9231-3openalex-extracted
Mastitis and its Impact on Structure and Function in the Ruminant Mammary Gland
inferredcites →https://doi.org/10.1007/s10911-013-9309-1openalex-extracted
The Role of Tight Junctions in Mammary Gland Function
inferredcites →https://doi.org/10.1007/s11250-014-0689-zopenalex-extracted
The prevalence of heifer mastitis and its associated risk factors in Huanggang, Central China
inferredcites →https://doi.org/10.1007/s12223-021-00879-9openalex-extracted
Potential factors involved in the early pathogenesis of Streptococcus uberis mastitis: a review
inferredcites →https://doi.org/10.1016/j.abb.2018.01.004openalex-extracted
Myeloperoxidase: Its role for host defense, inflammation, and neutrophil function
inferredcites →https://doi.org/10.1016/j.bbamem.2007.08.018openalex-extracted
Crosstalk of tight junction components with signaling pathways
inferredcites →https://doi.org/10.1016/j.cardiores.2006.06.028openalex-extracted
MAPK activation and apoptotic alterations in hearts subjected to calcium paradox are attenuated by taurine
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2016.04.022openalex-extracted
Variant innate immune responses of mammary epithelial cells to challenge by Staphylococcus aureus, Escherichia coli and the regulating effect of taurine on these bioprocesses
inferredcites →https://doi.org/10.1016/j.intimp.2011.06.008openalex-extracted
The effect of taurine on the toll-like receptors/nuclear factor kappa B (TLRs/NF-κB) signaling pathway in Streptococcus uberis-induced mastitis in rats
inferredcites →https://doi.org/10.1016/j.intimp.2013.05.007openalex-extracted
The role of NADPH oxidase in taurine attenuation of Streptococcus uberis-induced mastitis in rats
inferredcites →https://doi.org/10.1016/j.intimp.2019.106142openalex-extracted
Role of Toll-like receptor 2 against Streptococcus uberis infection in primary mouse mammary epithelial cells
inferredcites →https://doi.org/10.1016/j.intimp.2020.107076openalex-extracted
Resveratrol alleviates oxidative stress caused by Streptococcus uberis infection via activating the Nrf2 signaling pathway
inferredcites →https://doi.org/10.1016/j.jinf.2006.06.010openalex-extracted
Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis
inferredcites →https://doi.org/10.1016/j.semcdb.2014.09.002openalex-extracted
Tight junction, selective permeability, and related diseases
inferredcites →https://doi.org/10.1016/j.tibs.2018.09.008openalex-extracted
The Claudins: From Tight Junctions to Biological Systems
inferredcites →https://doi.org/10.1016/j.vetmic.2011.07.031openalex-extracted
Development of an experimentally induced Streptococcus uberis subclinical mastitis in goats
inferredcites →https://doi.org/10.1016/j.vetmic.2016.06.008openalex-extracted
The role of Ca 2+ mediated signaling pathways on the effect of taurine against Streptococcus uberis infection
inferredcites →https://doi.org/10.1016/s0749-0720(02)00073-7openalex-extracted
Immunity and mastitis Some new ideas for an old disease
inferredcites →https://doi.org/10.1023/b:jomg.0000017431.45314.07openalex-extracted
The Organization of Tight Junctions in Epithelia: Implications for Mammary Gland Biology and Breast Tumorigenesis
inferredcites →https://doi.org/10.1038/nri.2017.142openalex-extracted
NF-κB, inflammation, immunity and cancer: coming of age
inferredcites →https://doi.org/10.1038/nri3495openalex-extracted
Mitogen-activated protein kinases in innate immunity
inferredcites →https://doi.org/10.1038/s41396-020-0651-1openalex-extracted
The gut microbiota contributes to the development of Staphylococcus aureus -induced mastitis in mice
inferredcites →https://doi.org/10.1053/jcpa.2002.0620openalex-extracted
Early Pathogenesis and Inflammatory Response in Experimental Bovine Mastitis Due to Streptococcus uberis
inferredcites →https://doi.org/10.1128/iai.00788-20openalex-extracted
Taurine-Mediated IDOL Contributes to Resolution of Streptococcus uberis Infection
inferredcites →https://doi.org/10.1371/journal.pone.0062187openalex-extracted
Lipopolysaccharide Disrupts the Milk-Blood Barrier by Modulating Claudins in Mammary Alveolar Tight Junctions
inferredcites →https://doi.org/10.2527/jas.2007-0302openalex-extracted
Mammary tissue damage during bovine mastitis: Causes and control1
inferredcites →https://doi.org/10.2527/jas2017.1845openalex-extracted
TRIENNIAL LACTATION SYMPOSIUM/BOLFA: Pathogen-specific immune response and changes in the blood–milk barrier of the bovine mammary gland1
inferredcites →https://doi.org/10.3168/jds.2012-6150openalex-extracted
Short communication: Differential immunoglobulin transfer during mastitis challenge by pathogen-specific components
inferredcites →https://doi.org/10.3168/jds.2016-10927openalex-extracted
Short communication: Differential loss of bovine mammary epithelial barrier integrity in response to lipopolysaccharide and lipoteichoic acid
inferredcites →https://doi.org/10.3389/fimmu.2017.01108openalex-extracted
Propionate Protects against Lipopolysaccharide-Induced Mastitis in Mice by Restoring Blood–Milk Barrier Disruption and Suppressing Inflammatory Response
inferredcites →https://doi.org/10.3389/fimmu.2019.01825openalex-extracted
Taurine Attenuates Streptococcus uberis-Induced Bovine Mammary Epithelial Cells Inflammation via Phosphoinositides/Ca2+ Signaling
inferredcites →https://doi.org/10.3389/fimmu.2021.631113openalex-extracted
Taurine Alleviates Streptococcus uberis-Induced Inflammation by Activating Autophagy in Mammary Epithelial Cells
inferredcites →https://doi.org/10.3389/fimmu.2021.696101openalex-extracted
Taurine Reprograms Mammary-Gland Metabolism and Alleviates Inflammation Induced by Streptococcus uberis in Mice
inferredcites →https://doi.org/10.3389/fphys.2018.01942openalex-extracted
Tight Junction Proteins and Signaling Pathways in Cancer and Inflammation: A Functional Crosstalk
inferredcites →https://doi.org/10.3390/cells9020494openalex-extracted
TLR2 Signaling Pathway Combats Streptococcus uberis Infection by Inducing Mitochondrial Reactive Oxygen Species Production
inferredcites →https://doi.org/10.4062/biomolther.2017.251openalex-extracted
Effects and Mechanisms of Taurine as a Therapeutic Agent
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