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Natural and synthetic pathogen associated molecular patterns modulategalectin expression in cow blood

机译:天然和合成病原体相关分子模式调节牛血中半乳糖凝集素的表达

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摘要

Pathogen-associated Molecular Patterns (PAMPs) are highly conserved structural motifs that are recognized by Pathogen Recognition receptors (PRRs) to initiate immune responses. Infection by these pathogens and the immune response to PAMPS such as lipopolysaccharide (LPS), Peptidoglycan (PGN), bacterial oligodeoxynucleotides [CpG oligodeoxynucleotides 2006 (CpG ODN2006) and CpG oligodeoxynucleotides 2216 (CpG ODN2216)], and viral RNA Polyinosinic-Polycytidylic Acid (Poly I:C), are associated with infectious and metabolic diseases in animals impacting health and production. It is established that PAMPs mediate the production of cytokines by binding to PRRs such as Toll-like receptors (TLR) on immune cells. Galectins (Gal) are carbohydrate-binding proteins that when expressed play essential roles in the resolution of infectious and metabolic diseases. Thus it is important to determine if the expression of galectin gene (LGALS) and Gal secretion in blood are affected by exposure to LPS and PGN, PolyI:C and bacterial CpG ODNs. LPS increased transcription of LGALS4 and 12 (2.5 and 2.02 folds respectively) and decreased secretion of Gal 4 (p < 0.05). PGN increased transcription of LGALS-1, -2, -3, -4, -7, and -12 (3.0, 2.3, 2.0, 4.1, 3.3, and2.4 folds respectively) and secretion of Gal-8 and Gal-9 (p< 0.05). Poly I:C tended to increase the transcription of LGALS1, LGALS4,and LGALS8 (1.78, 1.88, and 1.73 folds respectively). Secretion of Gal-1, -3, -8and nine were significantly increased in treated samples compared to control(p < 0.05). CpG ODN2006 did not cause anysignificant fold changes in LGALS transcription (FC < 2) but increasedsecretion of Gal-1, and-3 (p < 0.05) in plasma comparedto control. Gal-4 was however reduced in plasma (p <0.05). CpG ODN2216 increased transcription of LGALS1 and LGALS3 (3.8 and 1.6folds respectively), but reduced LGALS2, LGALS4, LGALS7, and LGALS12(–1.9, –2.0, –2.0 and; –2.7 folds respectively).Secretion of Gal-2 and -3 in plasma was increased compared to control(p < 0.05). Gal-4 secretion was reduced in plasma(p < 0.05). The results demonstrate that PAMPsdifferentially modulate galectin transcription and translation of galectins incow blood.
机译:病原相关分子模式(PAMP)是高度保守的结构基序,可被病原识别受体(PRR)识别以启动免疫反应。这些病原体的感染以及对PAMPS的免疫应答,例如脂多糖(LPS),肽聚糖(PGN),细菌寡脱氧核苷酸[CpG寡脱氧核苷酸2006(CpG ODN2006)和CpG寡脱氧核苷酸2216(CpG ODN2216)]和病毒RNA聚肌苷酸Poly I:C)与动物的传染性和代谢性疾病有关,影响健康和生产。已经确定PAMP通过与免疫细胞上的Torr样受体(TLR)之类的PRR结合而介导细胞因子的产生。 Galectins(Gal)是碳水化合物结合蛋白,表达后在解决传染性和代谢性疾病中起重要作用。因此,确定暴露于LPS和PGN,PolyI:C和细菌CpG ODN是否会影响血液中半乳糖凝集素基因(LGALS)的表达和Gal分泌是否重要。 LPS增加了LGALS4和12的转录(分别为2.5和2.02倍),并减少了Gal 4的分泌(p <0.05)。 PGN增加LGALS-1,-2,-3,-4,-7和-12(3.0、2.3、2.0、4.1、3.3和分别是2.4倍)和Gal-8和Gal-9的分泌(p<0.05)。 Poly I:C倾向于增加LGALS1,LGALS4,和LGALS8(分别为1.78、1.88和1.73倍)。 Gal-1,-3,-8的分泌与对照组相比,处理过的样品中有9个显着增加(p <0.05)。 CpG ODN2006没有造成任何LGALS转录的显着倍数变化(FC <2),但增加了比较血浆中Gal-1和3的分泌(p <0.05)控制。但是,Gal-4的血浆浓度降低(p <0.05)。 CpG ODN2216增加了LGALS1和LGALS3的转录(3.8和1.6分别折叠),但减少了LGALS2,LGALS4,LGALS7和LGALS12(分别为–1.9,–2.0,–2.0和; –2.7倍)。与对照组相比,血浆中Gal-2和-3的分泌增加(p <0.05)。血浆中Gal-4分泌减少(p <0.05)。结果表明,PAMPs差异调节半乳糖凝集素的转录和翻译牛血。

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