Oncomodulin is a macrophage-derived signal for axon regeneration in retinal ganglion cells

被引:395
作者
Yin, Yuqin
Henzl, Michael T.
Lorber, Barbara
Nakazawa, Toru
Thomas, Tommy T.
Jiang, Fan
Langer, Robert
Benowitz, Larry I.
机构
[1] Childrens Hosp, Dept Neurosurg, Boston, MA 02115 USA
[2] Childrens Hosp, Neurobiol Program, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Surg, Boston, MA 02115 USA
[4] Univ Missouri, Dept Biochem, Columbia, MO 65211 USA
[5] Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA 02115 USA
[6] MIT, Dept Chem & Biomed Engn, Cambridge, MA 02139 USA
[7] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
关键词
D O I
10.1038/nn1701
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The optic nerve, like most mature CNS pathways, does not regenerate after injury. Through unknown mechanisms, however, macrophage activation in the eye stimulates retinal ganglion cells (RGCs) to regenerate long axons beyond the site of optic nerve injury. Here we identify the calcium (Ca2+)-binding protein oncomodulin as a potent macrophage-derived growth factor for RGCs and other neurons. Oncomodulin binds to rat RGCs with high affinity in a cyclic AMP (cAMP)-dependent manner and stimulates more extensive outgrowth than other known trophic agents. Depletion of oncomodulin from macrophage-conditioned media (MCM) eliminates the axon-promoting activity of MCM. The effects of oncomodulin involve downstream signaling via Ca2+/calmodulin kinase and gene transcription. In vivo, oncomodulin released from microspheres promotes regeneration in the mature rat optic nerve. Oncomodulin also stimulates outgrowth from peripheral sensory neurons. Thus, oncomodulin is a new growth factor for neurons of the mature central and peripheral nervous systems.
引用
收藏
页码:843 / 852
页数:10
相关论文
共 50 条
[1]   DEGENERATIVE AND REGENERATIVE RESPONSES OF INJURED NEURONS IN THE CENTRAL-NERVOUS-SYSTEM OF ADULT MAMMALS [J].
AGUAYO, AJ ;
RASMINSKY, M ;
BRAY, GM ;
CARBONETTO, S ;
MCKERRACHER, L ;
VILLEGASPEREZ, MP ;
VIDALSANZ, M ;
CARTER, DA .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1991, 331 (1261) :337-343
[2]   IMMUNOLOGICAL, MORPHOLOGICAL, AND ELECTROPHYSIOLOGICAL VARIATION AMONG RETINAL GANGLION-CELLS PURIFIED BY PANNING [J].
BARRES, BA ;
SILVERSTEIN, BE ;
COREY, DP ;
CHUN, LLY .
NEURON, 1988, 1 (09) :791-803
[3]   Peripheral nerve explants grafted into the vitreous body of the eye promote the regeneration of retinal ganglion cell axons severed in the optic nerve [J].
Berry, M ;
Carlile, J ;
Hunter, A .
JOURNAL OF NEUROCYTOLOGY, 1996, 25 (02) :147-170
[4]  
BUXSER S, 1990, J BIOL CHEM, V265, P12701
[5]   Prior exposure to neurotrophins blocks inhibition of axonal regeneration by MAG and myelin via a cAMP-dependent mechanism [J].
Cai, DM ;
Shen, YJ ;
De Bellard, M ;
Tang, S ;
Filbin, MT .
NEURON, 1999, 22 (01) :89-101
[6]   TrkB gene transfer protects retinal ganglion cells from axotomy-induced death in vivo [J].
Cheng, L ;
Sapieha, P ;
Kittlerová, P ;
Hauswirth, WW ;
Di Polo, A .
JOURNAL OF NEUROSCIENCE, 2002, 22 (10) :3977-3986
[7]  
Chierzi S, 1999, J NEUROSCI, V19, P8367
[8]   EFFECTS OF BRAIN-DERIVED NEUROTROPHIC FACTOR ON OPTIC AXON BRANCHING AND REMODELING IN-VIVO [J].
COHENCORY, S ;
FRASER, SE .
NATURE, 1995, 378 (6553) :192-196
[9]   Intraocular elevation of cyclic AMP potentiates ciliary neurotrophic factor-induced regeneration of adult rat retinal ganglion cell axons [J].
Cui, Q ;
Yip, HK ;
Zhao, RCH ;
So, KF ;
Harvey, AR .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 22 (01) :49-61
[10]   Counteracting the Nogo receptor enhances optic nerve regeneration if retinal ganglion cells are in an active growth state [J].
Fischer, D ;
He, ZG ;
Benowitz, LI .
JOURNAL OF NEUROSCIENCE, 2004, 24 (07) :1646-1651