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叉头框蛋白 A1 在急性肺损伤中的作用。

A role for forkhead box A1 in acute lung injury.

机构信息

Laboratory of Shock, Department of Pathophysiology, Xiangya School of Medicine, Central South University, Hunan, People's Republic of China.

出版信息

Inflammation. 2009 Oct;32(5):322-32. doi: 10.1007/s10753-009-9139-x.

Abstract

Forkhead box protein A1 (FoxA1) is an evolutionarily conserved winged helix transcription factor with diverse regulatory functions. However, little is known about the role of FoxA1 in acute lung injury (ALI) and pulmonary cell injury. In this study, an in vivo model was employed whereby rats were administered an intravenous injection of oleic acid (OA, 0.1 ml/kg), and alveolar type II epithelial cells (AT-2 cells) injury was induced by hydrogen peroxide (H(2)O(2)) in vitro. OA injection resulted in lung injury and AT-2 cells apoptosis in vivo. OA injection and H(2)O(2) upregulated FoxA1 mRNA and protein in lung tissue of the in vivo ALI model and in H(2)O(2) challenged AT-2 cells. Overexpression of FoxA1 promoted apoptosis, whereas FoxA1 deficiency, induced by antisense oligonucleotides, decreased AT-2 cells apoptosis induced by H(2)O(2), as shown by flow cytometry. These results suggest that FoxA1 may play an important role in ALI by promoting apoptosis of pulmonary epithelial cells.

摘要

叉头框蛋白 A1(FoxA1)是一种进化上保守的翼状螺旋转录因子,具有多种调节功能。然而,FoxA1 在急性肺损伤(ALI)和肺细胞损伤中的作用知之甚少。在本研究中,采用体内模型,通过静脉注射油酸(OA,0.1ml/kg)诱导大鼠急性肺损伤,并在体外通过过氧化氢(H₂O₂)诱导肺泡 II 型上皮细胞(AT-2 细胞)损伤。OA 注射导致体内 ALI 模型的肺损伤和 AT-2 细胞凋亡。OA 注射和 H₂O₂上调体内 ALI 模型肺组织和 H₂O₂刺激的 AT-2 细胞中的 FoxA1 mRNA 和蛋白。FoxA1 的过表达促进细胞凋亡,而反义寡核苷酸诱导的 FoxA1 缺失减少了 H₂O₂诱导的 AT-2 细胞凋亡,流式细胞术结果显示。这些结果表明,FoxA1 可能通过促进肺上皮细胞凋亡在 ALI 中发挥重要作用。

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