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奶牛亚临床型乳腺炎中嗜中性粒细胞凋亡延迟

Delayed neutrophil apoptosis in bovine subclinical mastitis.

作者信息

Boutet P, Boulanger D, Gillet L, Vanderplasschen A, Closset R, Bureau F, Lekeux P

机构信息

Department of Physiology, University of Liége, Belgium.

出版信息

J Dairy Sci. 2004 Dec;87(12):4104-14. doi: 10.3168/jds.S0022-0302(04)73553-5.

Abstract

Bovine subclinical mastitis can be defined as a moderated inflammatory disease characterized by a persistent accumulation of neutrophils in milk. As GMCSF-mediated delay of neutrophil apoptosis contributes to the accumulation of inflammatory cells at the site of inflammation in many human diseases, we sought to determine whether subclinical mastitis in cows is also associated with a GMCSF-dependent increase in milk-neutrophil survival. We first addressed the hypothesis that GMCSF delays bovine neutrophil apoptosis by activation of the signal transducer and activator of transcription (STAT) family members STAT3 and STAT5, which are critical regulators of the expression of various Bcl-2 family proteins. Granulocyte-macrophage colony-stimulating factor significantly delayed apoptosis of blood neutrophils obtained from healthy cows. In these cells, GMCSF activated STAT5, but not STAT3, and induced an increase in the mRNA of the antiapoptotic Bcl-2 member, Bcl-xL. Granulocyte-macrophage colony-stimulating factor-dependent STAT5 activation and up-regulation of Bcl-xL mRNA were blocked by the Jak inhibitor, AG-490. This inhibition was associated with abrogation of the prosurvival effect of GMCSF, demonstrating a key role for STAT5 in delayed neutrophil apoptosis. We further found that GMCSF expression was increased in milk cells from cows affected with subclinical mastitis. Neutrophils from these cows demonstrated a significant delay of apoptosis as compared with neutrophils obtained from healthy cows and were unresponsive to GMCSF. Active STAT5 complexes were detected in these neutrophils. Finally, in the presence of AG-490, apoptosis was induced and a time-dependent down-regulation of Bcl-xL mRNA was observed in milk neutrophils from mastitis-affected cows. These results indicate that neutrophil survival is enhanced in milk of subclinical mastitis-affected cows and suggest a role for a GMCSF-activated STAT5 signaling pathway in this phenomenon. This pathway could thus represent a target for the control of persistent accumulation of neutrophils in the bovine mammary gland.

摘要

牛亚临床型乳腺炎可被定义为一种中度炎症性疾病,其特征是乳汁中持续存在中性粒细胞积聚。由于在许多人类疾病中,GMCSF介导的中性粒细胞凋亡延迟导致炎症部位炎症细胞的积聚,我们试图确定奶牛亚临床型乳腺炎是否也与乳汁中性粒细胞存活的GMCSF依赖性增加有关。我们首先探讨了GMCSF通过激活信号转导和转录激活因子(STAT)家族成员STAT3和STAT5来延迟牛中性粒细胞凋亡的假说,STAT3和STAT5是各种Bcl-2家族蛋白表达的关键调节因子。粒细胞-巨噬细胞集落刺激因子显著延迟了从健康奶牛获得的血液中性粒细胞的凋亡。在这些细胞中,GMCSF激活了STAT5,但未激活STAT3,并诱导抗凋亡Bcl-2成员Bcl-xL的mRNA增加。Jak抑制剂AG-490阻断了粒细胞-巨噬细胞集落刺激因子依赖性的STAT5激活和Bcl-xL mRNA的上调。这种抑制与GMCSF促存活作用的消除有关,表明STAT5在延迟中性粒细胞凋亡中起关键作用。我们进一步发现,GMCSF在受亚临床型乳腺炎影响的奶牛的乳汁细胞中表达增加。与从健康奶牛获得的中性粒细胞相比,这些奶牛的中性粒细胞凋亡显著延迟,并且对GMCSF无反应。在这些中性粒细胞中检测到活性STAT5复合物。最后,在AG-490存在的情况下,诱导了受乳腺炎影响的奶牛乳汁中性粒细胞凋亡,并观察到Bcl-xL mRNA的时间依赖性下调。这些结果表明,受亚临床型乳腺炎影响的奶牛乳汁中的中性粒细胞存活增强,并提示GMCSF激活的STAT5信号通路在这一现象中起作用。因此,该通路可能代表控制牛乳腺中中性粒细胞持续积聚的一个靶点。

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