Chen Xiaodi, Patra Aparna, Sadowska Grazyna B, Stonestreet Barbara S
Dev Neurosci. 2018;40(3):234-245. doi: 10.1159/000489700. Epub 2018 Jul 26.
Hypoxic-ischemic brain injury is a leading cause of neurodevelopmental morbidities in preterm and full-term infants. Blood-brain barrier dysfunction represents an important component of perinatal hypoxic-ischemic brain injury. The extracellular matrix (ECM) is a vital component of the blood-brain barrier. Matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs) are important ECM components. They contribute to brain development, blood-brain barrier maintenance, and to regenerative and repair processes after hypoxic-ischemic brain injury. We hypothesized that ischemia at different durations of reperfusion affects the ECM protein composition of MMPs and TIMPs in the cerebral cortex of fetal sheep. Cerebral cortical samples were snap-frozen from sham control fetuses at 127 days of gestation and from fetuses after exposure to 30-min carotid occlusion and 4-, 24-, and 48-h of reperfusion. Protein expression of MMP-2, -8, -9, and -13 and TIMP-1, -2, -3, and -4 was measured by Western immunoblotting along with the gelatinolytic activity of MMP-2 and MMP-9 by zymography. The expression of MMP-8 was increased (Kruskal-Wallis, p = 0.04) in fetuses 48 h after ischemia. In contrast, changes were not observed in the protein expression of MMP-2, -9, or -13. The gelatinolytic activity of pro-MMP-2 was increased (ANOVA, p = 0.02, Tukey HSD, p = 0.05) 24 h after ischemia. TIMP-1 and -3 expression levels were also higher (TIMP-1, ANOVA, p = 0.003, Tukey HSD, p = 0.01; TIMP-3, ANOVA, p = 0.006, Tukey HSD, p = 0.01) 24 h after ischemia compared with both the sham controls and with fetuses exposed to 4 h of reperfusion. The changes in the expression of TIMP-1, -2, and -3 correlated with the changes in the MMP-8 and -13 protein expression. We speculate that regulation of MMP-8, MMP-13, and TIMPs contributes to ECM remodeling after is chemic-reperfusion injury in the fetal brain.
缺氧缺血性脑损伤是早产和足月婴儿神经发育疾病的主要原因。血脑屏障功能障碍是围产期缺氧缺血性脑损伤的一个重要组成部分。细胞外基质(ECM)是血脑屏障的重要组成部分。基质金属蛋白酶(MMPs)和基质金属蛋白酶组织抑制剂(TIMPs)是重要的ECM成分。它们有助于大脑发育、血脑屏障维持以及缺氧缺血性脑损伤后的再生和修复过程。我们假设,不同再灌注持续时间的缺血会影响胎羊大脑皮质中MMPs和TIMPs的ECM蛋白质组成。在妊娠127天时,从假手术对照胎儿以及暴露于30分钟颈动脉闭塞并再灌注4小时、24小时和48小时后的胎儿中快速冷冻大脑皮质样本。通过蛋白质免疫印迹法测量MMP-2、-8、-9和-13以及TIMP-1、-2、-3和-4的蛋白质表达,并通过酶谱法测量MMP-2和MMP-9的明胶酶活性。缺血后48小时的胎儿中MMP-8的表达增加(Kruskal-Wallis检验,p = 0.04)。相比之下,未观察到MMP-2、-9或-13的蛋白质表达变化。缺血后24小时,前MMP-2的明胶酶活性增加(方差分析,p = 0.02,Tukey HSD检验,p = 0.05)。与假手术对照胎儿以及再灌注4小时的胎儿相比,缺血后24小时TIMP-1和-3的表达水平也更高(TIMP-1,方差分析,p = 0.003,Tukey HSD检验,p = 0.01;TIMP-3,方差分析,p = 0.006,Tukey HSD检验,p = 0.01)。TIMP-1、-2和-3表达的变化与MMP-8和-13蛋白质表达的变化相关。我们推测,MMP-8、MMP-13和TIMPs的调节有助于胎儿大脑缺血再灌注损伤后的ECM重塑。