Gladstone Institutes, San Francisco, CA USA.
Division of Neonatology, Department of Pediatrics, University of California, San Francisco, CA, USA.
Nat Rev Neurosci. 2018 May;19(5):283-301. doi: 10.1038/nrn.2018.13. Epub 2018 Apr 5.
The blood coagulation protein fibrinogen is deposited in the brain in a wide range of neurological diseases and traumatic injuries with blood-brain barrier (BBB) disruption. Recent research has uncovered pleiotropic roles for fibrinogen in the activation of CNS inflammation, induction of scar formation in the brain, promotion of cognitive decline and inhibition of repair. Such diverse roles are possible in part because of the unique structure of fibrinogen, which contains multiple binding sites for cellular receptors and proteins expressed in the nervous system. The cellular and molecular mechanisms underlying the actions of fibrinogen are beginning to be elucidated, providing insight into its involvement in neurological diseases, such as multiple sclerosis, Alzheimer disease and traumatic CNS injury. Selective drug targeting to suppress the damaging functions of fibrinogen in the nervous system without affecting its beneficial effects in haemostasis opens a new fibrinogen therapeutics pipeline for neurological disease.
纤维蛋白原是凝血蛋白,在广泛的伴有血脑屏障(BBB)破坏的神经疾病和创伤性损伤中在大脑中沉积。最近的研究揭示了纤维蛋白原在中枢神经系统炎症激活、脑内瘢痕形成、认知能力下降促进和修复抑制中的多种作用。纤维蛋白原的这种多样作用在一定程度上是可能的,因为纤维蛋白原具有独特的结构,它包含多个细胞受体和神经系统中表达的蛋白质的结合位点。纤维蛋白原作用的细胞和分子机制开始被阐明,这为其在多发性硬化症、阿尔茨海默病和创伤性中枢神经系统损伤等神经疾病中的作用提供了深入了解。选择性药物靶向以抑制纤维蛋白原在神经系统中的破坏性作用,而不影响其在止血中的有益作用,为神经疾病的纤维蛋白原治疗开辟了新途径。