In neuroscience, Ephs and ephrins are perhaps best known for their role in axon guidance. It was first shown in the visual system that graded expression of these proteins is instrumental in providing molecular coordinates that define topographic maps, particularly in the visual system, but also in the auditory, vomeronasal and somatosensory systems as well as in the hippocampus, cerebellum and other structures. Perhaps unsurprisingly, the role of these proteins in regulating cell-cell interactions also has an impact on cell mobility, with evidence that Eph-ephrin interactions segregate cell populations based on contact-mediated attraction or repulsion. Consistent with these studies, evidence has accumulated that Ephs and ephrins play important roles in the migration of specific cell populations in the developing and adult brain. This review focusses on two examples of neuronal migration that require Eph/ephrin signalling – radial and tangential migration of neurons in cortical development and the migration of newly generated neurons along the rostral migratory stream to the olfactory bulb in the adult brain. We discuss the challenge involved in understanding how cells determine whether they respond to signals by migration or axon guidance.

1.
Marin O, Valiente M, Ge X, Tsai LH: Guiding neuronal cell migrations. Cold Spring Harb Perspect Biol 2010;2:a001834.
2.
Drescher U: Axon guidance: push and pull with ephrins and GDNF. Curr Biol 2011;21:R30–R32.
3.
Saeger BM, Suhm M, Neubuser A: Ephrin/ephrin receptor expression during early stages of mouse inner ear development. Dev Dyn 2011;240:1578–1585.
4.
Zhou N, Zhao WD, Liu DX, Liang Y, Fang WG, Li B, Chen YH: Inactivation of EphA2 promotes tight junction formation and impairs angiogenesis in brain endothelial cells. Microvasc Res 2011;82:113–121.
5.
Wilby MJ, Muir EM, Fok-Seang J, Gour BJ, Blaschuk OW, Fawcett JW: N-cadherin inhibits Schwann cell migration on astrocytes. Mol Cell Neurosci 1999;14:66–84.
6.
Prestoz L, Chatzopoulou E, Lemkine G, Spassky N, Lebras B, Kagawa T, Ikenaka K, Zalc B, Thomas JL: Control of axonophilic migration of oligodendrocyte precursor cells by Eph-ephrin interaction. Neuron Glia Biol 2004;1:73–83.
7.
Zimmer G, Kastner B, Weth F, Bolz J: Multiple effects of ephrin-A5 on cortical neurons are mediated by SRC family kinases. J Neurosci 2007;27:5643–5653.
8.
Zimmer G, Garcez P, Rudolph J, Niehage R, Weth F, Lent R, Bolz J: Ephrin-A5 acts as a repulsive cue for migrating cortical interneurons. Eur J Neurosci 2008;28:62–73.
9.
Torii M, Hashimoto-Torii K, Levitt P, Rakic P: Integration of neuronal clones in the radial cortical columns by EphA and ephrin-A signalling. Nature 2009;461:524–528.
10.
Rudolph J, Zimmer G, Steinecke A, Barchmann S, Bolz J: Ephrins guide migrating cortical interneurons in the basal telencephalon. Cell Adh Migr 2010;4:400–408.
11.
Senturk A, Pfennig S, Weiss A, Burk K, Acker-Palmer A: Ephrin Bs are essential components of the Reelin pathway to regulate neuronal migration. Nature 2011;472:356–360.
12.
Conover JC, Doetsch F, Garcia-Verdugo J-M, Gale NW, Yancopoulos GD, Alvarez-Buylla A: Disruption of Eph/ephrin signaling affects migration and proliferation in the adult subventricular zone. Nat Neurosci 2000;3:1091–1097.
13.
Ricard J, Salinas J, Garcia L, Liebl DJ: EphrinB3 regulates cell proliferation and survival in adult neurogenesis. Mol Cell Neurosci 2006;31:713–722.
14.
Coulthard M, Duffy S, Down M, Evans B, Power M, Smith F, Stylianou C, Kleikamp S, Oates A, Lackmann M, Burns G, Boyd A: The role of the Eph-ephrin signalling system in the regulation of developmental patterning. Int J Dev Biol 2002;46:375–384.
15.
Palmer A, Klein R: Multiple roles of ephrins in morphogenesis, neuronal networking, and brain function. Genes Dev 2003;17:1429–1450.
16.
Jiao JW, Feldheim DA, Chen DF: Ephrins as negative regulators of adult neurogenesis in diverse regions of the central nervous system. Proc Natl Acad Sci USA 2008;105:8778–8783.
17.
Hansen MJ, Dallal GE, Flanagan JG: Retinal axon response to ephrin-As shows a graded, concentration-dependent transition from growth promotion to inhibition. Neuron 2004;42:717–730.
18.
Yates PA, Roskies AL, McLaughlin T, O’Leary DDM: Topographic-specific axon branching controlled by ephrin-As is the critical event in retinotectal map development. J Neurosci 2001;21:8548–8563.
19.
Rodger J, Vitale PN, Tee LB, King CE, Bartlett CA, Fall A, Brennan C, O’Shea JE, Dunlop SA, Beazley LD: EphA/ephrin-A interactions during optic nerve regeneration: restoration of topography and regulation of ephrin-A2 expression. Mol Cell Neurosci 2004;25:56–68.
20.
Goldshmit Y, McLenachan S, Turnley A: Roles of Eph receptors and ephrins in the normal and damaged adult CNS. Brain Res Rev 2006;52:327–345.
21.
Depaepe V, Suarez-Gonzalez N, Dufour A, Passante L, Gorski JA, Jones KR, Ledent C, Vanderhaeghen P: Ephrin signalling controls brain size by regulating apoptosis of neural progenitors. Nature 2005;435:1244–1250.
22.
Daniel TO, Stein E, Cerretti DP, St John PL, Robert B, Abrahamson DR: ELK and LERK-2 in developing kidney and microvascular endothelial assembly. Kidney Int Suppl 1996;57:S73–S81.
23.
Wang HU, Chen ZF, Anderson DJ: Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4. Cell 1998;93:741–753.
24.
Goldshmit Y, Galea MP, Bartlett PF, Turnley AM: EphA4 regulates central nervous system vascular formation. J Comp Neurol 2006;497:864–875.
25.
Fujii H, Fujiwara H, Horie A, Sato Y, Konishi I: Ephrin A1 induces intercellular dissociation in Ishikawa cells: possible implication of the Eph-ephrin A system in human embryo implantation. Hum Reprod 2011;26:299–306.
26.
Herath NI, Boyd AW: The role of Eph receptors and ephrin ligands in colorectal cancer. Int J Cancer 2010;126:2003–2011.
27.
Mitra S, Duggineni S, Koolpe M, Zhu X, Huang Z, Pasquale EB: Structure-activity relationship analysis of peptides targeting the EphA2 receptor. Biochemistry 2010;49:6687–6695.
28.
Mellitzer G, Xu G, Wilkinson D: Control of cell behaviour by signalling through Eph receptors and ephrins. Curr Opin Cell Biol 2000;10:400–408.
29.
Lackmann M, Boyd AW: Eph, a protein family coming of age: more confusion, insight, or complexity? Sci Signal 2008;1:re2.
30.
Pitulescu ME, Adams RH: Eph/ephrin molecules – a hub for signaling and endocytosis. Genes Dev 2010;24:2480–2492.
31.
Committee EN: Unified nomenclature for Eph family receptors and their ligands, the ephrins. Eph Nomenclature Committee. Cell 1997;90:403–404.
32.
Lemke G: A coherent nomenclature for Eph receptors and their ligands. Mol Cell Neurosci 1997;9:331–332.
33.
Wilkinson DG: Multiple roles of Eph receptors and ephrins in neural development. Nat Rev Neurosci 2001;2:155–164.
34.
Himanen JP, Chumley MJ, Lackmann M, Li C, Barton WA, Jeffrey PD, Vearing C, Geleick D, Feldheim DA, Boyd AW, Henkemeyer M, Nikolov DB: Repelling class discrimination: ephrin-A5 binds to and activates EphB2 receptor signaling. Nat Neurosci 2004;7:501–509.
35.
Pasquale EB: Eph-ephrin promiscuity is now crystal clear. Nat Neurosci 2004;7:417–418.
36.
Stein E, Lane AA, Cerretti DP, Schoecklmann HO, Schroff AD, Van Etten RL, Daniel TO: Eph receptors discriminate specific ligand oligomers to determine alternative signaling complexes, attachment, and assembly responses. Genes Dev 1998;12:667–678.
37.
Poopalasundaram S, Marler KJ, Drescher U: EphrinA6 on chick retinal axons is a key component for p75(NTR)-dependent axon repulsion and TrkB-dependent axon branching. Mol Cell Neurosci 2011;47:131–136.
38.
Davy A, Soriano P: Ephrin signaling in vivo: look both ways. Dev Dyn 2005;232:1–10.
39.
Poliakov A, Cotrina M, Wilkinson DG: Diverse roles of Eph receptors and ephrins in the regulation of cell migration and tissue assembly. Dev Cell 2004;7:465–480.
40.
Himanen JP, Saha N, Nikolov DB: Cell-cell signaling via Eph receptors and ephrins. Curr Opin Cell Biol 2007;19:534–542.
41.
Santiago A, Erickson CA: Ephrin-B ligands play a dual role in the control of neural crest cell migration. Development 2002;129:3621–3632.
42.
McLaughlin T, O’Leary DD: Molecular gradients and development of retinotopic maps. Annu Rev Neurosci 2005;28:327–355.
43.
Lin D, Gish GD, Songyang Z, Pawson T: The carboxyl terminus of B class ephrins constitutes a PDZ domain binding motif. J Biol Chem 1999;274:3726–3733.
44.
Cowan CA, Henkemeyer M: The SH2/SH3 adaptor Grb4 transduces B-ephrin reverse signals. Nature 2001;413:174–179.
45.
Murai KK, Pasquale EB: ‘Eph’ective signaling: forward, reverse and crosstalk. J Cell Sci 2003;116:2823–2832.
46.
Pasquale EB: Eph-ephrin bidirectional signaling in physiology and disease. Cell 2008;133:38–52.
47.
Davy A, Gale NW, Murray EW, Klinghoffer RA, Soriano P, Feuerstein C, Robbins SM: Compartmentalised signaling by GPI-anchored ephrin-A5 requires the Fyn tyrosine kinase to regulate cellular adhesion. Genes Dev 1999;13:3125–3135.
48.
Hornberger M, Dutting D, Ciossek T, Yamada T, Handwerker C, Lang S, Weth F, Huf J, Wessel R, Logan C, Tanaka H, Drescher U: Modulation of EphA receptor function by coexpressed ephrinA ligands on retinal ganglion cell axons. Neuron 1999;22:731–742.
49.
Sobieszczuk DF, Wilkinson DG: Masking of Eph receptors and ephrins. Curr Biol 1999;9:R469–R470.
50.
Marquardt T, Shirasaki R, Ghosh S, Andrews SE, Carter N, Hunter T, Pfaff SL: Coexpressed EphA receptors and ephrin-A ligands mediate opposing actions on growth cone navigation from distinct membrane domains. Cell 2005;121:127–139.
51.
Marler KJ, Becker-Barroso E, Martinez A, Llovera M, Wentzel C, Poopalasundaram S, Hindges R, Soriano E, Comella J, Drescher U: A TrkB/EphrinA interaction controls retinal axon branching and synaptogenesis. J Neurosci 2008;28:12700–12712.
52.
Kao TJ, Kania A: Ephrin-mediated cis-attenuation of Eph receptor signaling is essential for spinal motor axon guidance. Neuron 2011;71:76–91.
53.
Fitzgerald M, Buckley A, Lukehurst SS, Dunlop SA, Beazley LD, Rodger J: Neurite responses to ephrin-A5 modulated by BDNF: evidence for TrkB-EphA interactions. Biochem Biophys Res Commun 2008;374:625–630.
54.
Rodger J, Goto H, Cui Q, Chen PB, Harvey AR: cAMP regulates axon outgrowth and guidance during optic nerve regeneration in goldfish. Mol Cell Neurosci 2005;30:452–464.
55.
Nicol X, Muzerelle A, Rio J, Metin C, Gaspar P: Requirement of Adenylate Cyclase 1 for the ephrin-A5-dependent retraction of exuberant retinal axons. J Neurosci 2006;26:862–872.
56.
Nicol X, Voyatzis S, Muzerelle A, Narboux-Neme N, Sudhof T, Miles R, Gaspar P: cAMP oscillations and retinal activity are permissive for ephrin signalling during the establishment of the retinotopic map. Nat Neurosci 2007;10:340–347.
57.
Truitt L, Freywald A: Dancing with the dead: Eph receptors and their kinase-null partners. Biochem Cell Biol 2011;89:115–129.
58.
Peuckert C, Wacker E, Rapus J, Levitt P, Bolz J: Adaptive changes in gene expression patterns in the somatosensory cortex after deletion of ephrinA5. Mol Cell Neurosci 2008;39:21–31.
59.
Hattori M, Osterfield M, Flanagan JG: Regulated cleavage of a contact-mediated axon repellent. Science 2000;289:1360–1364.
60.
Janes PW, Saha N, Barton WA, Kolev MV, Wimmer-Kleikamp SH, Nievergall E, Blobel CP, Himanen JP, Lackmann M, Nikolov DB: Adam meets Eph: an ADAM substrate recognition module acts as a molecular switch for ephrin cleavage in trans. Cell 2005;123:291–304.
61.
Marston D, Dickinson S, Nobes C: Rac-dependent trans-endocytosis of ephrinBs regulates Eph-ephrin contact repulsion. Nat Cell Biol 2003;5:879–888.
62.
Zimmer M, Palmer A, Kohler J, Klein R: EphB-ephrinB bi-directional endocytosis terminates adhesion allowing contact mediated repulsion. Nat Cell Biol 2003;5:869–878.
63.
Mellitzer G, Xu Q, Wilkinson DG: Eph receptors and ephrins restrict cell intermingling and communication. Nature 1999;400:77–80.
64.
Honda H, Mochizuki A: Formation and maintenance of distinctive cell patterns by coexpression of membrane-bound ligands and their receptors. Dev Dyn 2002;223:180–192.
65.
Feldheim DA, Kim Y-I, Bergemann AD, Frisen J, Barbacid M, Flanagan JG: Genetic analysis of ephrin-A2 and ephrin-A5 shows their requirement in multiple aspects of retinocollicular mapping. Neuron 2000;25:563–574.
66.
Haustead D, Lukehurst S, Clutton GB, Bartlett CA, Dunlop S, Arrese CA, Sherrard RM, Rodger J: Functional topography and integration of the contralateral and ipsilateral retinocollicular projections in ephrin-A–/– mice. J Neurosci 2008;28:7376–7386.
67.
Rakic P, Caviness VS Jr: Cortical development: view from neurological mutants two decades later. Neuron 1995;14:1101–1104.
68.
Bielle F, Griveau A, Narboux-Neme N, Vigneau S, Sigrist M, Arber S, Wassef M, Pierani A: Multiple origins of Cajal-Retzius cells at the borders of the developing pallium. Nat Neurosci 2005;8:1002–1012.
69.
Angevine JB Jr, Sidman RL: Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature 1961;192:766–768.
70.
Bielas S, Higginbotham H, Koizumi H, Tanaka T, Gleeson JG: Cortical neuronal migration mutants suggest separate but intersecting pathways. Annu Rev Cell Dev Biol 2004;20:593–618.
71.
Ang ES Jr, Haydar TF, Gluncic V, Rakic P: Four-dimensional migratory coordinates of GABAergic interneurons in the developing mouse cortex. J Neurosci 2003;23:5805–5815.
72.
Tanaka D, Nakaya Y, Yanagawa Y, Obata K, Murakami F: Multimodal tangential migration of neocortical GABAergic neurons independent of GPI-anchored proteins. Development 2003;130:5803–5813.
73.
Mountcastle VB: The columnar organization of the neocortex. Brain 1997;120:701–722.
74.
Yu YC, Bultje RS, Wang X, Shi SH: Specific synapses develop preferentially among sister excitatory neurons in the neocortex. Nature 2009;458:501–504.
75.
Buxhoeveden DP, Casanova MF: The minicolumn hypothesis in neuroscience. Brain 2002;125:935–951.
76.
Yun ME, Johnson RR, Antic A, Donoghue MJ: EphA family gene expression in the developing mouse neocortex: regional patterns reveal intrinsic programs and extrinsic influence. J Comp Neurol 2003;456:203–216.
77.
Migani P, Bartlett C, Dunlop S, Beazley L, Rodger J: Ephrin-B2 immunoreactivity distribution in adult mouse brain. Brain Res 2007;1182:60–72.
78.
Migani P, Bartlett C, Dunlop S, Beazley L, Rodger J: Regional and cellular distribution of ephrin-B1 in adult mouse brain. Brain Res 2009;1247:50–61.
79.
Tissir F, Goffinet AM: Reelin and brain development. Nat Rev Neurosci 2003;4:496–505.
80.
Gallagher E, Howell BW, Soriano P, Cooper JA, Hawkes R: Cerebellar abnormalities in the disabled (mdab1–1) mouse. J Comp Neurol 1998;402:238–251.
81.
Trommsdorff M, Gotthardt M, Hiesberger T, Shelton J, Stockinger W, Nimpf J, Hammer RE, Richardson JA, Herz J: Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2. Cell 1999;97:689–701.
82.
Arnaud L, Ballif BA, Forster E, Cooper JA: Fyn tyrosine kinase is a critical regulator of disabled-1 during brain development. Curr Biol 2003;13:9–17.
83.
Bock HH, Herz J: Reelin activates SRC family tyrosine kinases in neurons. Curr Biol 2003;13:18–26.
84.
Palmer A, Zimmer M, Erdmann KS, Eulenburg V, Porthin A, Heumann R, Deutsch U, Klein R: EphrinB phosphorylation and reverse signaling: regulation by Src kinases and PTP-BL phosphatase. Mol Cell 2002;9:725–737.
85.
Marin O, Yaron A, Bagri A, Tessier-Lavigne M, Rubenstein JL: Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions. Science 2001;293:872–875.
86.
Flames N, Long JE, Garratt AN, Fischer TM, Gassmann M, Birchmeier C, Lai C, Rubenstein JL, Marin O: Short- and long-range attraction of cortical GABAergic interneurons by neuregulin-1. Neuron 2004;44:251–261.
87.
Andrews W, Barber M, Hernadez-Miranda LR, Xian J, Rakic S, Sundaresan V, Rabbitts TH, Pannell R, Rabbitts P, Thompson H, Erskine L, Murakami F, Parnavelas JG: The role of Slit-Robo signaling in the generation, migration and morphological differentiation of cortical interneurons. Dev Biol 2008;313:648–658.
88.
Powell EM, Mars WM, Levitt P: Hepatocyte growth factor/scatter factor is a motogen for interneurons migrating from the ventral to dorsal telencephalon. Neuron 2001;30:79–89.
89.
Marin O, Rubenstein JL: A long, remarkable journey: tangential migration in the telencephalon. Nat Rev Neurosci 2001;2:780–790.
90.
Marin O, Rubenstein JL: Cell migration in the forebrain. Annu Rev Neurosci 2003;26:441–483.
91.
Rodger J, Bartlett CA, Beazley LD, Dunlop SA: Transient up-regulation of the rostro-caudal gradient of ephrin A2 in the tectum coincides with re-establishment of orderly projections during optic nerve regeneration in goldfish. Exp Neurol 2000;166:196–200.
92.
Rodger J, Lindsay KA, Leaver SG, King CE, Dunlop SA, Beazley LD: Expression of ephrin-A2 in the superior colliculus and EphA5 in the retina following optic nerve section in adult rat. Eur J Neurosci 2001; 14:1929–1936.
93.
Gerlai R, Shinsky N, Shih A, Williams P, Winer J, Armanini M, Cairns B, Winslow J, Gao W-Q, Philips HS: Regulation of learning by EphA receptors: a protein targeting study. J Neurosci 1999;19:9538–9549.
94.
Bahi A, Dreyer JL: Cocaine-induced expression changes of axon guidance molecules in the adult rat brain. Mol Cell Neurosci 2005;28:275–291.
95.
Tabata H, Nakajima K: Multipolar migration: the third mode of radial neuronal migration in the developing cerebral cortex. J Neurosci 2003;23:9996–10001.
96.
Britanova O, Alifragis P, Junek S, Jones K, Gruss P, Tarabykin V: A novel mode of tangential migration of cortical projection neurons. Dev Biol 2006;298:299–311.
97.
Pfeiffenberger C, Yamada J, Feldheim DA: Ephrin-As and patterned retinal activity act together in the development of topographic maps in the primary visual system. J Neurosci 2006;26:12873–12884.
98.
Cang J, Niell C, Liu X, Pfeiffenberger C, Feldheim D, Stryker M: Selective disruption of one cartesian axis of cortical maps and receptive fields by deficiency in ephrin-As and structured activity. Neuron 2008;57:511–523.
99.
Wilks T, Rodger J, Harvey AR: A role for ephrin-As in maintaining topographic organisation in register across interconnected central visual pathways. Eur J Neurosci 2010;31:613–622.
100.
Dalva MB, Takasu MA, Lin MZ, Shamah SM, Hu L, Gale NW, Greenberg ME: EphB receptors interact with NMDA receptors and regulate excitatory synapse formation. Cell 2000;103:945–956.
101.
Lennington JB, Yang Z, Conover JC: Neural stem cells and the regulation of adult neurogenesis. Reprod Biol Endocrinol 2003;1:99.
102.
Alvarez-Buylla A, Garcia-Verdugo JM: Neurogenesis in adult subventricular zone. J Neurosci 2002;22:629–634.
103.
Conover JC, Notti RQ: The neural stem cell niche. Cell Tissue Res 2008;331:211–224.
104.
Riquelme PA, Drapeau E, Doetsch F: Brain micro-ecologies: neural stem cell niches in the adult mammalian brain. Philos Trans R Soc Lond B Biol Sci 2008;363:123–137.
105.
Altman J: Autoradiographic and histological studies of postnatal neurogenesis. IV. Cell proliferation and migration in the anterior forebrain, with special reference to persisting neurogenesis in the olfactory bulb. J Comp Neurol 1969;137:433–457.
106.
Doetsch F, Alvarez-Buylla A: Network of tangential pathways for neuronal migration in adult mammalian brain. Proc Natl Acad Sci USA 1996;93:14895–14900.
107.
Doetsch F, Garcia-Verdugo JM, Alvarez-Buylla A: Cellular composition and three-dimensional organization of the subventricular germinal zone in the adult mammalian brain. J Neurosci 1997;17:5046– 5061.
108.
Peretto P, Merighi A, Fasolo A, Bonfanti L: Glial tubes in the rostral migratory stream of the adult rat. Brain Res Bull 1997;42:9–21.
109.
Gritti A, Bonfanti L, Doetsch F, Caille I, Alvarez-Buylla A, Lim DA, Galli R, Verdugo JM, Herrera DG, Vescovi AL: Multipotent neural stem cells reside into the rostral extension and olfactory bulb of adult rodents. J Neurosci 2002;22:437–445.
110.
Luskin MB: Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone. Neuron 1993;11:173–189.
111.
Lois C, Alvarez-Buylla A: Long-distance neuronal migration in the adult mammalian brain. Science 1994;264:1145–1148.
112.
Bovetti S, Bovolin P, Perroteau I, Puche AC: Subventricular zone-derived neuroblast migration to the olfactory bulb is modulated by matrix remodelling. Eur J Neurosci 2007;25:2021–2033.
113.
Snapyan M, Lemasson M, Brill MS, Blais M, Massouh M, Ninkovic J, Gravel C, Berthod F, Gotz M, Barker PA, Parent A, Saghatelyan A: Vasculature guides migrating neuronal precursors in the adult mammalian forebrain via brain-derived neurotrophic factor signaling. J Neurosci 2009;29:4172–4188.
114.
Whitman MC, Fan W, Rela L, Rodriguez-Gil DJ, Greer CA: Blood vessels form a migratory scaffold in the rostral migratory stream. J Comp Neurol 2009;516:94–104.
115.
Wichterle H, Garcia-Verdugo JM, Alvarez-Buylla A: Direct evidence for homotypic, glia-independent neuronal migration. Neuron 1997;18:779–791.
116.
Jankovski A, Sotelo C: Subventricular zone-olfactory bulb migratory pathway in the adult mouse: cellular composition and specificity as determined by heterochronic and heterotopic transplantation. J Comp Neurol 1996;371:376–396.
117.
Murase S, Horwitz AF: Deleted in colorectal carcinoma and differentially expressed integrins mediate the directional migration of neural precursors in the rostral migratory stream. J Neurosci 2002;22:3568–3579.
118.
Wu W, Wong K, Chen J, Jiang Z, Dupuis S, Wu JY, Rao Y: Directional guidance of neuronal migration in the olfactory system by the protein Slit. Nature 1999;400:331–336.
119.
Ng KL, Li JD, Cheng MY, Leslie FM, Lee AG, Zhou QY: Dependence of olfactory bulb neurogenesis on prokineticin 2 signaling. Science 2005;308:1923–1927.
120.
Paratcha G, Ibanez CF, Ledda F: GDNF is a chemoattractant factor for neuronal precursor cells in the rostral migratory stream. Mol Cell Neurosci 2006;31:505–514.
121.
Chiaramello S, Dalmasso G, Bezin L, Marcel D, Jourdan F, Peretto P, Fasolo A, De Marchis S: BDNF/TrkB interaction regulates migration of SVZ precursor cells via PI3-K and MAP-K signalling pathways. Eur J Neurosci 2007;26:1780–1790.
122.
Katakowski M, Zhang Z, de Carvalho AC, Chopp M: EphB2 induces proliferation and promotes a neuronal fate in adult subventricular neural precursor cells. Neurosci Lett 2005;385:204–209.
123.
Bush JO, Soriano P: Ephrin-B1 regulates axon guidance by reverse signaling through a PDZ-dependent mechanism. Genes Dev 2009;23:1586–1599.
124.
Nam SC, Kim Y, Dryanovski D, Walker A, Goings G, Woolfrey K, Kang SS, Chu C, Chenn A, Erdelyi F, Szabo G, Hockberger P, Szele FG: Dynamic features of postnatal subventricular zone cell motility: a two-photon time-lapse study. J Comp Neurol 2007;505:190–208.
125.
Gale NW, Yancopoulos GD: Ephrins and their receptors: a repulsive topic? Cell Tissue Res 1997;290:227–241.
126.
Bruckner K, Pasquale EB, Klein R: Tyrosine phosphorylation of transmembrane ligands for Eph receptors. Science 1997;275:1640–1643.
127.
Garzotto D, Giacobini P, Crepaldi T, Fasolo A, De Marchis S: Hepatocyte growth factor regulates migration of olfactory interneuron precursors in the rostral migratory stream through Met-Grb2 coupling. J Neurosci 2008;28:5901–5909.
128.
Kong H, Boulter J, Weber JL, Lai C, Chao MV: An evolutionarily conserved transmembrane protein that is a novel downstream target of neurotrophin and ephrin receptors. J Neurosci 2001;21:176–185.
129.
Cang J, Kaneko M, Yamada J, Woods G, Stryker MP, Feldheim DA: Ephrin-As guide the formation of functional maps in the visual cortex. Neuron 2005;48:577–589.
130.
Cang J, Wang L, Stryker MP, Feldheim DA: Roles of ephrin-As and structured activity in the development of functional maps in the superior colliculus. J Neurosci 2008;28:11015–11023.
131.
Triplett JW, Owens MT, Yamada J, Lemke G, Cang J, Stryker MP, Feldheim DA: Retinal input instructs alignment of visual topographic maps. Cell 2009;139:175–185.
132.
Boyle M, Nighorn A, Thomas JB: Drosophila Eph receptor guides specific axon branches of mushroom body neurons. Development 2006;133:1845–1854.
133.
Kaneko M, Nighorn A: Interaxonal Eph-ephrin signaling may mediate sorting of olfactory sensory axons in Manduca sexta. J Neurosci 2003;23:11523–11538.
134.
Coate TM, Swanson TL, Proctor TM, Nighorn AJ, Copenhaver PF: Eph receptor expression defines midline boundaries for ephrin-positive migratory neurons in the enteric nervous system of Manduca sexta. J Comp Neurol 2007;502:175–191.
135.
Coate TM, Wirz JA, Copenhaver PF: Reverse signaling via a glycosyl-phosphatidylinositol-linked ephrin prevents midline crossing by migratory neurons during embryonic development in Manduca. J Neurosci 2008;28:3846–3860.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.