Division of Neurology, Department of Neurosciences, Medical University of South Carolina, Charleston, SC 29425, USA.
J Neurochem. 2013 Jan;124(1):133-46. doi: 10.1111/jnc.12064. Epub 2012 Nov 22.
Optic neuritis (ON), which is an acute inflammatory autoimmune demyelinating disease of the central nervous system (CNS), often occurs in multiple sclerosis (MS). ON is an early diagnostic sign in most MS patients caused by damage to the optic nerve leading to visual dysfunction. Various features of both MS and ON can be studied following induction of experimental autoimmune encephalomyelitis (EAE), an animal model of MS, in Lewis rats. Inflammation and cell death in the optic nerve, with subsequent damage to the retinal ganglion cells in the retina, are thought to correlate with visual dysfunction. Thus, characterizing the pathophysiological changes that lead to visual dysfunction in EAE animals may help develop novel targets for therapeutic intervention. We treated EAE animals with and without the calpain inhibitor calpeptin (CP). Our studies demonstrated that the Ca(2+)-activated neutral protease calpain was upregulated in the optic nerve following induction of EAE at the onset of clinical signs (OCS) of the disease, and these changes were attenuated following treatment with CP. These reductions correlated with decreases in inflammation (cytokines, iNOS, COX-2, and NF-κB), and microgliosis (i.e. activated microglia). We observed that calpain inhibition reduced astrogliosis (reactive astroglia) and expression of aquaporin 4 (AQP4). The balance of Th1/Th2 cytokine production and also expression of the Th1-related CCR5 and CXCR3 chemokine receptors influence many pathological processes and play both causative and protective roles in neuron damage. Our data indicated that CP suppressed cytokine imbalances. Also, Bax:Bcl-2 ratio, production of tBid, PARP-1, expression and activities of calpain and caspases, and internucleosomal DNA fragmentation were attenuated after treatment with CP. Our results demonstrated that CP decreased demyelination [loss of myelin basic protein (MBP)] and axonal damage [increase in dephosphorylated neurofilament protein (de-NFP)], and also promoted intracellular neuroprotective pathways in optic nerve in EAE rats. Thus, these data suggest that calpain is involved in inflammatory as well as in neurodegenerative aspects of the disease and may be a promising target for treating ON in EAE and MS.
视神经炎(ON)是一种中枢神经系统(CNS)的急性炎症性自身免疫脱髓鞘疾病,常发生在多发性硬化症(MS)中。ON 是大多数 MS 患者的早期诊断标志,由视神经损伤引起,导致视觉功能障碍。在诱导实验性自身免疫性脑脊髓炎(EAE)后,可以研究 MS 和 ON 的各种特征,EAE 是 MS 的动物模型。在 Lewis 大鼠中,视神经的炎症和细胞死亡,随后视网膜神经节细胞在视网膜中的损伤,被认为与视觉功能障碍相关。因此,描述导致 EAE 动物视觉功能障碍的病理生理变化可能有助于为治疗干预开发新的靶点。我们用和不用钙蛋白酶抑制剂 calpeptin(CP)治疗 EAE 动物。我们的研究表明,钙蛋白酶在疾病临床症状开始时(OCS)EAE 诱导后,视神经中的钙激活中性蛋白酶 calpain 上调,而用 CP 治疗后这些变化减弱。这些减少与炎症减少(细胞因子、iNOS、COX-2 和 NF-κB)和小胶质细胞增生(即活化的小胶质细胞)相关。我们观察到钙蛋白酶抑制减少了星形胶质细胞增生(反应性星形胶质细胞)和水通道蛋白 4(AQP4)的表达。Th1/Th2 细胞因子产生的平衡以及 Th1 相关的 CCR5 和 CXCR3 趋化因子受体的表达也影响许多病理过程,并在神经元损伤中发挥致病和保护作用。我们的数据表明 CP 抑制了细胞因子失衡。此外,CP 治疗后 Bax:Bcl-2 比值、tBid、PARP-1、钙蛋白酶和半胱天冬酶的表达和活性以及核小体间 DNA 片段化减少。我们的结果表明 CP 减少了脱髓鞘(髓鞘碱性蛋白丢失)和轴突损伤(去磷酸化神经丝蛋白增加),并在 EAE 大鼠视神经中促进了细胞内神经保护途径。因此,这些数据表明钙蛋白酶参与了疾病的炎症和神经退行性方面,可能是治疗 EAE 和 MS 中 ON 的有希望的靶点。