Abstract:Salmonellosis is a gastrointestinal disease caused by non-typhoidal Salmonella serovars such as Salmonella Typhimurium. This pathology is a zoonosis, and food animals with subclinical infection constitute a vast reservoir for disease. After intestinal colonization, Salmonella Typhimurium reaches mesenteric lymph nodes (MLN), where infection is controlled avoiding systemic spread. Although the molecular basis of this infection has been extensively studied, little is known about how microRNA (miRNA) regulate the… Show more
“…The ceRNA network of GAS5 has been reported (Liu et al, 2019;Fang et al, 2020). After literature search, we found that there were many abnormal expression of miR in mesenteric lymph nodes after ST infection (Herrera-Uribe et al, 2018). Additionally, biological website prediction, RNA pull-down and dual luciferase reporter gene assays confirmed that miR-23a has binding relation to GAS5.…”
Section: The Cerna Network Of Gas5/mir-23a/ Ptenmentioning
confidence: 72%
“…GAS5 can play a role in regulating diseases through the ceRNA mechanism. Through literature search, we found that there were many abnormal expression of miR in mesenteric lymph nodes after ST infection ( Herrera-Uribe et al, 2018 ). Therefore, we screened these miRs in the biological websites, and found miR-23a has binding relation to GAS5 ( Figure 6E ).…”
Background: Salmonella typhimurium (ST) causes several intestinal diseases. Polyphenols including chlorogenic acid (CGA) inhibit pathogenesis. Objective: This study aimed to investigate the mechanisms of CGA in ST infection. Methods: The intestinal pathological changes and survival rate of ST-infected mice were measured to verify the protection of CGA on ST infection. The antibacterial effects of CGA in vitro on the invasion to intestinal epithelial cells and autophagy was evaluated. The relationships among GAS5, miR-23a, and PTEN were verified. Expression of inflammation-and autophagy-related proteins was detected. Results: CGA treatment alleviated pathological damage, improved the secretion disturbance of intestinal cytokines caused by ST infection, and reduced the mortality of mice. Intestinal GAS5 was upregulated after CGA treatment. LncRNA GAS5 competitively bound to miR-23a to upregulate PTEN and inhibit the p38 MAPK pathway. CGA regulated the p38 MAPK pathway through lncRNA GAS5/miR-23a/PTEN axis to promote autophagy in ST infection. The functional rescue experiments of miR-23a and PTEN further identified these effects. Conclusion: CGA promotes autophagy and inhibits ST infection through the GAS5/miR-23a/PTEN axis and the p38 MAPK pathway.
“…The ceRNA network of GAS5 has been reported (Liu et al, 2019;Fang et al, 2020). After literature search, we found that there were many abnormal expression of miR in mesenteric lymph nodes after ST infection (Herrera-Uribe et al, 2018). Additionally, biological website prediction, RNA pull-down and dual luciferase reporter gene assays confirmed that miR-23a has binding relation to GAS5.…”
Section: The Cerna Network Of Gas5/mir-23a/ Ptenmentioning
confidence: 72%
“…GAS5 can play a role in regulating diseases through the ceRNA mechanism. Through literature search, we found that there were many abnormal expression of miR in mesenteric lymph nodes after ST infection ( Herrera-Uribe et al, 2018 ). Therefore, we screened these miRs in the biological websites, and found miR-23a has binding relation to GAS5 ( Figure 6E ).…”
Background: Salmonella typhimurium (ST) causes several intestinal diseases. Polyphenols including chlorogenic acid (CGA) inhibit pathogenesis. Objective: This study aimed to investigate the mechanisms of CGA in ST infection. Methods: The intestinal pathological changes and survival rate of ST-infected mice were measured to verify the protection of CGA on ST infection. The antibacterial effects of CGA in vitro on the invasion to intestinal epithelial cells and autophagy was evaluated. The relationships among GAS5, miR-23a, and PTEN were verified. Expression of inflammation-and autophagy-related proteins was detected. Results: CGA treatment alleviated pathological damage, improved the secretion disturbance of intestinal cytokines caused by ST infection, and reduced the mortality of mice. Intestinal GAS5 was upregulated after CGA treatment. LncRNA GAS5 competitively bound to miR-23a to upregulate PTEN and inhibit the p38 MAPK pathway. CGA regulated the p38 MAPK pathway through lncRNA GAS5/miR-23a/PTEN axis to promote autophagy in ST infection. The functional rescue experiments of miR-23a and PTEN further identified these effects. Conclusion: CGA promotes autophagy and inhibits ST infection through the GAS5/miR-23a/PTEN axis and the p38 MAPK pathway.
“…3b, Table S2). These mRNAs included 5 validated miR-1-3p targets ( CDC42 [30], FN1 [31], PDIA3 [32], SARS [33], and SOD1 [34]) and 27 predicted targets (based on results from the miRNA target prediction tool Targetscan 7.2) (Table S2) (35). Interestingly, we also identified CORIN itself as one of the enriched miR-1/AGO2-associated mRNAs.…”
Atrial natriuretic peptide (ANP) represents an attractive therapeutic target in hypertension and heart failure. The biologically active form of ANP is produced by the cardiac serine protease corin, and modulation of its activity might therefore represent a novel approach for ANP augmentation. MicroRNAs (miRNAs) are pervasive regulators of gene expression, but their potential role in regulating corin activity has not been elucidated.
“…This molecule is referred to as the master regulator of inflammation (Mahesh, Biswas, 2019). The high expression of miRNA-155 was reported in monocytes, macrophages, T and B lymphocytes, NK cells and DC (Dickey et al, 2017;Herrera-Uribe et al, 2018;King et al, 2016). In the above-mentioned cells, miRNA-155 is responsible for regulating the secretion of chemokines, cytokines and transcription factors in such a way that the immune response is optimal (Dickey et al, 2017).…”
Section: Key Mirnas Involved In Immune Regulationmentioning
confidence: 99%
“…Its presence in the body may lead to the development of typhoid fever or gastroenteritis (Naveed et al, 2017;Zhou et al, 2018). It is usually transmitted through food (mainly on products of animal origin contaminated with faeces) (Herrera-Uribe et al, 2018;Szewczyk et al, 2013). There are three main serotypes of Salmonella: Typhi, Typhimurium and Enteritidis (Zhou et al, 2018).…”
MicroRNAs (miRNAs)-small, conserved RNA molecules, containing 22 to 25 nucleotides and occurring in the cells of living organisms. As regulatory molecules, they have enormous biological potential and can influence a number of cellular processes. In the context of immunology, the role of miRNAs as novel immunity regulators is invaluable. The miRNAs regulate immune phenomena at many levels-starting from the impact on the processes of maturation, proliferation and differentiation of the immune system cells, through the regulation of the secretion of their products, to the regulation of intracellular signalling pathways. In all these areas, the miRNAs can play the role of both an inducer and an inhibitor by appropriately increasing the intensity of or suppressing the immune processes they regulate. In the future, it will be possible to regulate the host's immune response to the pathogen thanks to the properly controlled expression of miRNAs in the immune system cells. Cząsteczki mikroRNA jako nowe regulatory odporności w infekcjach wirusowych i bakteryjnych Słowa kluczowe mikroRNA, odporność, wirusy, bakterie Streszczenie MikroRNA (miRNA), małe, konserwatywne 22-25 nukleotydowe cząsteczki RNA występujące powszechnie w komórkach żywych organizmów. Jako cząsteczki regulatorowe mają ogromny potencjał biologiczny i mogą wypływać na wiele procesów komórkowych. W kontekście immunologii nieoceniona jest rola miRNA jako nowych regulatorów odporności. MiRNA regulują zjawiska odpornościowe na wielu poziomach. Począwszy od wpływu na procesy dojrzewania, proliferacji oraz różnicowania komórek układu odpornościowego, przez regulację wydzielania ich produktów, po regulację wewnątrzkomórkowych szlaków sygnalizacyjnych. Na wszystkich tych polach miRNA może odgrywać rolę zarówno induktora, jak i inhibitora, odpowiednio zwiększając nasilenie lub wygaszając regulowane przez siebie procesy odpornościowe. W przyszłości dzięki właściwie pokierowanej ekspresji miRNA w komórkach układu odpornościowego możliwe będzie regulowanie przebiegu odpowiedzi immunologicznej gospodarza w odpowiedzi na patogen.
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