Fibrinogen in neurological diseases: mechanisms, imaging and therapeutics

被引:457
作者
Petersen, Mark A. [1 ,2 ]
Ryu, Jae Kyu [1 ]
Akassoglou, Katerina [1 ,3 ]
机构
[1] Gladstone Inst, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Pediat, Div Neonatol, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
BLOOD-BRAIN-BARRIER; TISSUE-PLASMINOGEN-ACTIVATOR; MULTIPLE-SCLEROSIS LESIONS; COAGULATION-FACTOR-XII; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; AMYOTROPHIC-LATERAL-SCLEROSIS; PROMOTES THROMBIN GENERATION; ENDOTHELIAL-CELL RECEPTOR; AMYLOID-BETA DEPOSITION; SCIATIC-NERVE INJURY;
D O I
10.1038/nrn.2018.13
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
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.
引用
收藏
页码:283 / 301
页数:19
相关论文
共 213 条
[1]
Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[2]
Fibrinogen signal transduction as a mediator and therapeutic target in inflammation: Lessons from multiple sclerosis [J].
Adams, R. A. ;
Schachtrup, C. ;
Davalos, D. ;
Tsigelny, I. ;
Akassoglou, K. .
CURRENT MEDICINAL CHEMISTRY, 2007, 14 (27) :2925-2936
[3]
Adams RA, 2004, MOL INTERV, V4, P163
[4]
THE MORBID ANATOMY OF THE DEMYELINATIVE DISEASES [J].
ADAMS, RD ;
KUBIK, CS .
AMERICAN JOURNAL OF MEDICINE, 1952, 12 (05) :510-546
[5]
The fibrin-derived γ377-395 peptide inhibits microglia activation and suppresses relapsing paralysis in central nervous system autoimmune disease [J].
Adams, Ryan A. ;
Bauer, Jan ;
Flick, Matthew J. ;
Sikorski, Shoana L. ;
Nuriel, Tal ;
Lassmann, Hans ;
Degen, Jay L. ;
Akassoglou, Katerina .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (03) :571-582
[6]
A novel Aβ-fibrinogen interaction inhibitor rescues altered thrombosis and cognitive decline in Alzheimer's disease mice [J].
Ahn, Hyung Jin ;
Glickman, J. Fraser ;
Poon, Ka Lai ;
Zamolodchikov, Daria ;
Jno-Charles, Odella C. ;
Norris, Erin H. ;
Strickland, Sidney .
JOURNAL OF EXPERIMENTAL MEDICINE, 2014, 211 (06) :1049-1062
[7]
Alzheimer's disease peptide β-amyloid interacts with fibrinogen and induces its oligomerization [J].
Ahn, Hyung Jin ;
Zamolodchikov, Daria ;
Cortes-Canteli, Marta ;
Norris, Erin H. ;
Glickman, J. Fraser ;
Strickland, Sidney .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (50) :21812-21817
[8]
Tissue plasminogen activator-mediated fibrinolysis protects against axonal degeneration and demyelination after sciatic nerve injury [J].
Akassoglou, K ;
Kombrinck, KW ;
Degen, JL ;
Strickland, S .
JOURNAL OF CELL BIOLOGY, 2000, 149 (05) :1157-1166
[9]
Fibrin depletion decreases inflammation and delays the onset of demyelination in a tumor necrosis factor transgenic mouse model for multiple sclerosis [J].
Akassoglou, K ;
Adams, RA ;
Bauer, J ;
Mercado, P ;
Tseveleki, V ;
Lassmann, H ;
Probert, L ;
Strickland, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6698-6703
[10]
Fibrin is a regulator of Schwann cell migration after sciatic nerve injury in mice [J].
Akassoglou, K ;
Akpinar, P ;
Murray, S ;
Strickland, S .
NEUROSCIENCE LETTERS, 2003, 338 (03) :185-188