Department of Pediatrics, Division of Neurology, Children's Memorial Hospital, 2300 Children's Plaza, Chicago, IL 60614, USA.
J Neuroinflammation. 2012 Apr 16;9:68. doi: 10.1186/1742-2094-9-68.
Astrocytes are an integral component of the blood-brain barrier (BBB) which may be compromised by ischemic or traumatic brain injury. In response to trauma, astrocytes increase expression of the endopeptidase matrix metalloproteinase (MMP)-9. Compromise of the BBB leads to the infiltration of fluid and blood-derived proteins including albumin into the brain parenchyma. Albumin has been previously shown to activate astrocytes and induce the production of inflammatory mediators. The effect of albumin on MMP-9 activation in astrocytes is not known. We investigated the molecular mechanisms underlying the production of MMP-9 by albumin in astrocytes.
Primary enriched astrocyte cultures were used to investigate the effects of exposure to albumin on the release of MMP-9. MMP-9 expression was analyzed by zymography. The involvement of mitogen-activated protein kinase (MAPK), reactive oxygen species (ROS) and the TGF-β receptor-dependent pathways were investigated using pharmacological inhibitors. The production of ROS was observed by dichlorodihydrofluorescein diacetate fluorescence. The level of the MMP-9 inhibitor tissue inhibitor of metalloproteinase (TIMP)-1 produced by astrocytes was measured by ELISA.
We found that albumin induces a time-dependent release of MMP-9 via the activation of p38 MAPK and extracellular signal regulated kinase, but not Jun kinase. Albumin-induced MMP-9 production also involves ROS production upstream of the MAPK pathways. However, albumin-induced increase in MMP-9 is independent of the TGF-β receptor, previously described as a receptor for albumin. Albumin also induces an increase in TIMP-1 via an undetermined mechanism.
These results link albumin (acting through ROS and the p38 MAPK) to the activation of MMP-9 in astrocytes. Numerous studies identify a role for MMP-9 in the mechanisms of compromise of the BBB, epileptogenesis, or synaptic remodeling after ischemia or traumatic brain injury. The increase in MMP-9 produced by albumin further implicates both astrocytes and albumin in the acute and long-term complications of acute CNS insults, including cerebral edema and epilepsy.
星形胶质细胞是血脑屏障(BBB)的一个组成部分,它可能因缺血性或创伤性脑损伤而受损。星形胶质细胞在创伤后会增加内肽酶基质金属蛋白酶(MMP)-9 的表达。BBB 的破坏会导致液体和血液来源的蛋白质(包括白蛋白)渗透到脑组织中。白蛋白以前被证明可以激活星形胶质细胞并诱导炎症介质的产生。白蛋白对星形胶质细胞中 MMP-9 激活的影响尚不清楚。我们研究了白蛋白在星形胶质细胞中产生 MMP-9 的分子机制。
使用原代富集的星形胶质细胞培养物来研究暴露于白蛋白对 MMP-9 释放的影响。通过酶谱分析来分析 MMP-9 的表达。使用药理学抑制剂研究丝裂原活化蛋白激酶(MAPK)、活性氧(ROS)和 TGF-β 受体依赖性途径的参与。通过二氯二氢荧光素二乙酸酯荧光观察 ROS 的产生。通过 ELISA 测量星形胶质细胞产生的 MMP-9 抑制剂组织金属蛋白酶抑制剂(TIMP)-1 的水平。
我们发现白蛋白通过激活 p38 MAPK 和细胞外信号调节激酶,但不激活 Jun 激酶,诱导 MMP-9 的时间依赖性释放。白蛋白诱导的 MMP-9 产生还涉及 MAPK 途径上游的 ROS 产生。然而,白蛋白诱导的 MMP-9 增加与 TGF-β 受体无关,该受体先前被描述为白蛋白的受体。白蛋白还通过未知机制诱导 TIMP-1 的增加。
这些结果将白蛋白(通过 ROS 和 p38 MAPK 起作用)与星形胶质细胞中 MMP-9 的激活联系起来。许多研究表明 MMP-9 在 BBB 破坏、癫痫发生或缺血或创伤性脑损伤后的突触重塑等机制中起作用。白蛋白产生的 MMP-9 增加进一步表明,无论是星形胶质细胞还是白蛋白,都与急性和长期的急性中枢神经系统损伤并发症有关,包括脑水肿和癫痫。