Fractalkine in the nervous system: neuroprotective or neurotoxic molecule?

被引:90
作者
Lauro, Clotilde [1 ]
Catalano, Myriam [1 ,2 ]
Trettel, Flavia [1 ]
Limatola, Cristina [1 ,2 ]
机构
[1] Univ Roma La Sapienza, Ist Pasteur Fdn Cenci Bolognetti, Dept Physiol & Pharmacol, I-00185 Rome, Italy
[2] IRCCS NeuroMed, Pozzilli, Italy
来源
NEUROIMMUNOMODULATION IN HEALTH AND DISEASE | 2015年 / 1351卷
关键词
fractalkine; neuroprotection; inflammation; brain disease; microglia; FOCAL CEREBRAL-ISCHEMIA; MICROGLIAL ACTIVATION; MOUSE MODEL; SOLUBLE FRACTALKINE; INFLAMMATORY RESPONSE; COGNITIVE IMPAIRMENT; LUPUS-ERYTHEMATOSUS; HIPPOCAMPAL-NEURONS; AMYLOID DEPOSITION; PLASMA FRACTALKINE;
D O I
10.1111/nyas.12805
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fractalkine (CX3CL1) is an intriguing chemokine that plays a central role in the nervous system. The expression of CX3CL1 on neurons and of its receptor CX3CR1 on microglia facilitates a privileged interaction, playing important roles in regulating the function and maturation of these cells. CX3CL1 is reported to have neuroprotective and anti-inflammatory activities in several experimental systems and animal models of disease, and its expression correlates with positive outcomes in human neuropathologies. However, a comparable amount of evidence shows that CX3CL1 sustains neuroinflammatory conditions and contributes to neurotoxicity. This review discusses the evidence in favor of the CX3CL1/CX3CR1 pair being neuroprotective and other evidence that it is neurotoxic. Our aim is to stimulate future research examining the molecular and cellular determinants responsible for this unique functional switch, which could be important for several neuropathologies.
引用
收藏
页码:141 / 148
页数:8
相关论文
共 76 条
[1]   Role of fractalkine-CX3CR1 pathway in seizure-induced microglial activation, neurodegeneration, and neuroblast production in the adult rat brain [J].
Ali, Idrish ;
Chugh, Deepti ;
Ekdahl, Christine T. .
NEUROBIOLOGY OF DISEASE, 2015, 74 :194-203
[2]   Fractalkine and CX3CR1 regulate hippocampal neurogenesis in adult and aged rats [J].
Bachstetter, Adam D. ;
Morganti, Josh M. ;
Jernberg, Jennifer ;
Schlunk, Andrea ;
Mitchell, Staten H. ;
Brewster, Kaelin W. ;
Hudson, Charles E. ;
Cole, Michael J. ;
Harrison, Jeffrey K. ;
Bickford, Paula C. ;
Gemma, Carmelina .
NEUROBIOLOGY OF AGING, 2011, 32 (11) :2030-2044
[3]   A new class of membrane-bound chemokine with a CX(3)C motif [J].
Bazan, JF ;
Bacon, KB ;
Hardiman, G ;
Wang, W ;
Soo, K ;
Rossi, D ;
Greaves, DR ;
Zlotnik, A ;
Schall, TJ .
NATURE, 1997, 385 (6617) :640-644
[4]   Fractalkine/CX3CL1 depresses central synaptic transmission in mouse hippocampal slices [J].
Bertollini, Cristina ;
Ragozzino, Davide ;
Gross, Cornelius ;
Limatola, Cristina ;
Eusebi, Fabrizio .
NEUROPHARMACOLOGY, 2006, 51 (04) :816-821
[5]   Neuronal 'On' and 'Off' signals control microglia [J].
Biber, Knut ;
Neumann, Harald ;
Inoue, Kazuhide ;
Boddeke, Hendrikus W. G. M. .
TRENDS IN NEUROSCIENCES, 2007, 30 (11) :596-602
[6]   RETRACTED: Chronic neuroinflammation and cognitive impairment following transient global cerebral ischemia: role of fractalkine/CX3CR1 signaling (Retracted article. See vol. 12, 220, 2015) [J].
Briones, Teresita L. ;
Woods, Julie ;
Wadowska, Magdalena .
JOURNAL OF NEUROINFLAMMATION, 2014, 11
[7]   Control of microglial neurotoxicity by the fractalkine receptor [J].
Cardona, Astrid E. ;
Pioro, Erik P. ;
Sasse, Margaret E. ;
Kostenko, Volodymyr ;
Cardona, Sandra M. ;
Dijkstra, Ineke M. ;
Huang, DeRen ;
Kidd, Grahame ;
Dombrowski, Stephen ;
Dutta, RanJan ;
Lee, Jar-Chi ;
Cook, Donald N. ;
Jung, Steffen ;
Lira, Sergio A. ;
Littman, Dan R. ;
Ransohoff, Richard M. .
NATURE NEUROSCIENCE, 2006, 9 (07) :917-924
[8]   CX3CL1 protects neurons against excitotoxicity enhancing GLT-1 activity on astrocytes [J].
Catalano, Myriam ;
Lauro, Clotilde ;
Cipriani, Raffaela ;
Chece, Giuseppina ;
Ponzetta, Andrea ;
Di Angelantonio, Silvia ;
Ragozzino, Davide ;
Limatola, Cristina .
JOURNAL OF NEUROIMMUNOLOGY, 2013, 263 (1-2) :75-82
[9]   Fractalkine cleavage from neuronal membranes represents an acute event in the inflammatory response to excitotoxic brain damage [J].
Chapman, GA ;
Moores, K ;
Harrison, D ;
Campbell, CA ;
Stewart, BR ;
Strijbos, PJLM .
JOURNAL OF NEUROSCIENCE, 2000, 20 (15)
[10]   Neuroinflammation and M2 microglia: the good, the bad, and the inflamed [J].
Cherry, Jonathan D. ;
Olschowka, John A. ;
O'Banion, M. Kerry .
JOURNAL OF NEUROINFLAMMATION, 2014, 11