Ong Evan, Gao Xiao-Pei, Predescu Dan, Broman Michael, Malik Asrar B
Dept. of Pharmacology, College of Medicine, The University of Illinois, 835 South Wolcott Avenue, Chicago, IL 60612-7343, USA.
Am J Physiol Lung Cell Mol Physiol. 2005 Dec;289(6):L1094-103. doi: 10.1152/ajplung.00179.2005. Epub 2005 Sep 23.
We addressed the in vivo role of phosphatidylinositol 3-kinase-gamma (PI3K-gamma) in signaling the sequestration of polymorphonuclear leukocytes (PMNs) in lungs and in the mechanism of inflammatory lung vascular injury. We studied mice with deletion of the p110 catalytic subunit of PI3K-gamma (PI3K-gamma(-/-) mice). We measured lung tissue PMN sequestration, microvascular permeability, and edema formation after bacteremia induced by intraperitoneal Escherichia coli challenge. PMN infiltration into the lung interstitium in PI3K-gamma(-/-) mice as assessed morphometrically was increased 100% over that in control mice within 1 h after bacterial challenge. PI3K-gamma(-/-) mice also developed a greater increase in lung microvascular permeability after E. coli challenge, resulting in edema formation. The augmented lung tissue PMN sequestration in PI3K-gamma(-/-) mice was associated with increased expression of the PMN adhesive proteins CD47 and beta(3)-integrins. We observed increased association of CD47 and beta(3)-integrins with the extracellular matrix protein vitronectin in lungs of PI3K-gamma(-/-) mice after E. coli challenge. PMNs from these mice also showed increased beta(3)-integrin expression and augmented beta(3)-integrin-dependent PMN adhesion to vitronectin. These results point to a key role of PMN PI3K-gamma in negatively regulating CD47 and beta(3)-integrin expression in gram-negative sepsis. PI3K-gamma activation in PMNs induced by E. coli may modulate the extent of lung tissue PMN sequestration secondary to CD47 and beta(3)-integrin expression. Therefore, the level of PI3K-gamma activation may be an important determinant of PMN-dependent lung vascular injury.
我们探讨了磷脂酰肌醇3激酶γ(PI3K-γ)在介导多形核白细胞(PMN)在肺内滞留的信号传导以及炎症性肺血管损伤机制中的体内作用。我们研究了缺失PI3K-γ的p110催化亚基的小鼠(PI3K-γ(-/-)小鼠)。我们测量了腹腔注射大肠杆菌激发引起菌血症后肺组织中PMN的滞留、微血管通透性和水肿形成情况。在细菌攻击后1小时内,通过形态计量学评估,PI3K-γ(-/-)小鼠肺间质中PMN的浸润比对照小鼠增加了100%。在大肠杆菌攻击后,PI3K-γ(-/-)小鼠的肺微血管通透性也有更大程度的增加,导致水肿形成。PI3K-γ(-/-)小鼠肺组织中PMN滞留增加与PMN黏附蛋白CD47和β3整合素的表达增加有关。我们观察到在大肠杆菌攻击后,PI3K-γ(-/-)小鼠肺中CD47和β3整合素与细胞外基质蛋白玻连蛋白的结合增加。这些小鼠的PMN也显示出β3整合素表达增加以及β3整合素依赖性PMN与玻连蛋白的黏附增强。这些结果表明PMN的PI3K-γ在革兰氏阴性脓毒症中对CD47和β3整合素表达的负调节中起关键作用。大肠杆菌诱导的PMN中PI3K-γ激活可能调节继发于CD47和β3整合素表达的肺组织PMN滞留程度。因此,PI3K-γ激活水平可能是PMN依赖性肺血管损伤的一个重要决定因素。