首页> 外文期刊>Microbes and infection >Role of the mitogen-activated protein kinase pathway in the differential response of bovine monocytes to Mycobacterium avium subsp. paratuberculosis and Mycobacterium avium subsp. avium.
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Role of the mitogen-activated protein kinase pathway in the differential response of bovine monocytes to Mycobacterium avium subsp. paratuberculosis and Mycobacterium avium subsp. avium.

机译:丝裂原激活的蛋白激酶途径在牛单核细胞对鸟分枝杆菌亚种的差异反应中的作用。副结核病和鸟分枝杆菌亚种。阿维姆

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We compared the kinetics of activation and antimicrobial activities of MAPK-p38 and MAPK-ERK in bovine monocytes infected with Mycobacterium avium subsp. paratuberculosis (MAP) and Mycobacterium avium subsp. avium (Maa). Monocytes were incubated with MAP or Maa organisms with or without a specific inhibitor of the MAPK-p38 pathway (SB203580), and MAPK phosphorylation and antimicrobial functions of monocytes were evaluated. At early time points MAPK-p38 phosphorylation was greater in MAP-infected bovine monocytes than in Maa-infected monocytes. At later time points MAPK-p38 phosphorylation by both organisms was similar. MAPKp38 phosphorylation in MAP-infected monocytes was similar to negative control cells, whereas in Maa-infected this activation remained greater than negative control cells. Increase phosphorylation MAPK-ERK was similar at all time points for both organisms. Bovine monocytes had minimal capacity to kill MAP organisms, to acidify MAP-containing phagosomes, or to form phagolysosome. Alternatively, bovine monocytes were able to kill Maa organisms. Addition of SB203580 to monocyte cultures increased phagosome acidification, phagolysosome formation, and killing of MAP and Maa organisms. Taken together these data indicate that early transient activation of MAPK-p38 in bovine mononuclear phagocytes by MAP organisms may be a key mechanism involved in the capacity of MAP to survive in bovine monocytes.
机译:我们比较了感染鸟分枝杆菌亚种的牛单核细胞中MAPK-p38和MAPK-ERK激活和抗菌活性的动力学。副结核病(MAP)和鸟分枝杆菌亚种。 avium(Maa)。将单核细胞与具有或不具有MAPK-p38途径的特异性抑制剂(SB203580)的MAP或Maa生物一起孵育,并评估单核细胞的MAPK磷酸化和抗菌功能。在早期时间点,MAP感染的牛单核细胞中的MAPK-p38磷酸化程度高于Maa感染的单核细胞。在稍后的时间点,两种生物的MAPK-p38磷酸化相似。 MAP感染的单核细胞中的MAPKp38磷酸化与阴性对照细胞相似,而在Maa感染的中,这种活化仍大于阴性对照细胞。两种生物体在所有时间点的磷酸化增加MAPK-ERK都相似。牛单核细胞杀死MAP生物,酸化含MAP的吞噬体或形成吞噬溶酶体的能力最低。或者,牛单核细胞能够杀死Maa生物。向单核细胞培养物中添加SB203580可增加吞噬体酸化,吞噬溶酶体形成以及MAP和Maa生物的杀灭。这些数据加在一起表明,MAP生物体在牛单核吞噬细胞中早期瞬时激活MAPK-p38可能是参与MAP在牛单核细胞中存活的关键机制。

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