DCC is specifically required for the survival of retinal ganglion and displaced amacrine cells in the developing mouse retina

Developmental Biology

Volumn 348, Issue 1, 2010, Pages 87-96

  Shi, Ming ^a,b   Zheng, Min Hua ^c   Liu, Zhi Rong ^b   Hu, Ze Lan ^a   Huang, Ying ^a   Chen, Jia Yin ^a   Zhao, Gang ^b   Han, Hua ^c   Ding, Yu Qiang ^a  

^a TONGJI UNIVERSITY SCHOOL OF MEDICINE   (China)

^b FOURTH MILITARY MEDICAL UNIVERSITY   (China)

^c FOURTH MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

Apoptosis; DCC; Development; Displaced amacrine cells; Neurogenesis; Retina; Retinal ganglion cells

Indexed keywords

CASPASE 3; MEMBRANE PROTEIN; NETRIN 1; PROTEIN DCC; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL PROLIFERATION; CELL SURVIVAL; CONTROLLED STUDY; FEMALE; GENE MUTATION; GENOTYPE; IMMUNOREACTIVITY; MOUSE; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN FUNCTION; RETINA AMACRINE CELL; RETINA DEVELOPMENT; RETINA GANGLION CELL; SIGNAL TRANSDUCTION;

MUS;

EID: 78149407528     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2010.09.013     Document Type: Article

References (52)

1. Belecky-Adams T., Tomarev S., Li H.S., Ploder L., McInnes R.R., Sundin O., Adler R. Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells. Invest. Ophthalmol. Vis. Sci. 1997, 38:1293-1303.
2. Brown N.L., Patel S., Brzezinski J., Glaser T. Math5 is required for retinal ganglion cell and optic nerve formation. Development 2001, 128:2497-2508.
3. Cepko C.L. The roles of intrinsic and extrinsic cues and bHLH genes in the determination of retinal cell fates. Curr. Opin. Neurobiol. 1999, 9:37-46.
4. Cepko C.L., Austin C.P., Yang X., Alexiades M., Ezzeddine D. Cell fate determination in the vertebrate retina. Proc. Natl. Acad. Sci. U. S. A. 1996, 93:589-595.
5. Chan S.S., Zheng H., Su M.W., Wilk R., Killeen M.T., Hedgecock E.M., Culotti J.G. UNC-40, a C. elegans homolog of DCC (Deleted in Colorectal Cancer), is required in motile cells responding to UNC-6 netrin cues. Cell 1996, 87:187-195.
6. Chen H., Weber A.J. Expression of glial fibrillary acidic protein and glutamine synthetase by Muller cells after optic nerve damage and intravitreal application of brain-derived neurotrophic factor. Glia 2002, 38:115-125.
7. Chen Y.Q., Hsieh J.T., Yao F., Fang B., Pong R.C., Cipriano S.C., Krepulat F. Induction of apoptosis and G2/M cell cycle arrest by DCC. Oncogene 1999, 18:2747-2754.
8. Chen J., Rattner A., Nathans J. The rod photoreceptor-specific nuclear receptor Nr2e3 represses transcription of multiple cone-specific genes. J. Neurosci. 2005, 25:118-129.
9. Davidson F.F., Loewen P.C., Khorana H.G. Structure and function in rhodopsin: replacement by alanine of cysteine residues 110 and 187, components of a conserved disulfide bond in rhodopsin, affects the light-activated metarhodopsin II state. Proc. Natl. Acad. Sci. U. S. A. 1994, 91:4029-4033.
10. de Melo J., Du G., Fonseca M., Gillespie L.A., Turk W.J., Rubenstein J.L., Eisenstat D.D. Dlx1 and Dlx2 function is necessary for terminal differentiation and survival of late-born retinal ganglion cells in the developing mouse retina. Development 2005, 132:311-322.
11. Deiner M.S., Kennedy T.E., Fazeli A., Serafini T., Tessier-Lavigne M., Sretavan D.W. Netrin-1 and DCC mediate axon guidance locally at the optic disc: loss of function leads to optic nerve hypoplasia. Neuron 1997, 19:575-589.
12. Dickson B.J. Molecular mechanisms of axon guidance. Science 2002, 298:1959-1964.
13. Ding Y.Q., Kim J.Y., Xu Y.S., Rao Y., Chen Z.F. Ventral migration of early-born neurons requires DCC and is essential for the projections of primary afferents in the spinal cord. Development 2005, 132:2047-2056.
14. Elshatory Y., Deng M., Xie X., Gan L. Expression of the LIM-homeodomain protein Isl1 in the developing and mature mouse retina. J. Comp. Neurol. 2007, 503:182-197.
15. Fazeli A., Dickinson S.L., Hermiston M.L., Tighe R.V., Steen R.G., Small C.G., Stoeckli E.T., Keino-Masu K., Masu M., Rayburn H., Simons J., Bronson R.T., Gordon J.I., Tessier-Lavigne M., Weinberg R.A. Phenotype of mice lacking functional Deleted in Colorectal Cancer (Dcc) gene. Nature 1997, 386:796-804.
16. Feng L., Xie X., Joshi P.S., Yang Z., Shibasaki K., Chow R.L., Gan L. Requirement for Bhlhb5 in the specification of amacrine and cone bipolar subtypes in mouse retina. Development 2006, 133:4815-4825.
17. Finger J.H., Bronson R.T., Harris B., Johnson K., Przyborski S.A., Ackerman S.L. The Netrin 1 receptors Unc5h3 and Dcc are necessary at multiple choice points for the guidance of corticospinal tract axons. J. Neurosci. 2002, 22:10346-10356.
18. Forcet C., Ye X., Granger L., Corset V., Shin H., Bredesen D.E., Mehlen P. The dependence receptor DCC (Deleted in Colorectal Cancer) defines an alternative mechanism for caspase activation. Proc. Natl. Acad. Sci. U. S. A. 2001, 98:3416-3421.
19. Fujitani Y., Fujitani S., Luo H., Qiu F., Burlison J., Long Q., Kawaguchi Y., Edlund H., MacDonald R.J., Furukawa T., Fujikado T., Magnuson M.A., Xiang M., Wright C.V. Ptf1a determines horizontal and amacrine cell fates during mouse retinal development. Development 2006, 133:4439-4450.
20. Furne C., Corset V., Herincs Z., Cahuzac N., Hueber A.O., Mehlen P. The dependence receptor DCC requires lipid raft localization for cell death signaling. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:4128-4133.
21. Furne C., Rama N., Corset V., Chedotal A., Mehlen P. Netrin-1 is a survival factor during commissural neuron navigation. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:14465-14470.
22. Gad J.M., Keeling S.L., Shu T., Richards L.J., Cooper H.M. The spatial and temporal expression patterns of netrin receptors, DCC and neogenin, in the developing mouse retina. Exp. Eye Res. 2000, 70:711-722.
23. Harris W.A. Cellular diversification in the vertebrate retina. Curr. Opin. Genet. Dev. 1997, 7:651-658.
24. Haverkamp S., Wassle H. Immunocytochemical analysis of the mouse retina. J. Comp. Neurol. 2000, 424:1-23.
25. Haverkamp S., Ghosh K.K., Hirano A.A., Wassle H. Immunocytochemical description of five bipolar cell types of the mouse retina. J. Comp. Neurol. 2003, 455:463-476.
26. Hitchcock P.F., Macdonald R.E., VanDeRyt J.T., Wilson S.W. Antibodies against Pax6 immunostain amacrine and ganglion cells and neuronal progenitors, but not rod precursors, in the normal and regenerating retina of the goldfish. J. Neurobiol. 1996, 29:399-413.
27. Hong K., Hinck L., Nishiyama M., Poo M.M., Tessier-Lavigne M., Stein E. A ligand-gated association between cytoplasmic domains of UNC5 and DCC family receptors converts netrin-induced growth cone attraction to repulsion. Cell 1999, 97:927-941.
28. Jiang Y., Liu M.T., Gershon M.D. Netrins and DCC in the guidance of migrating neural crest-derived cells in the developing bowel and pancreas. Dev. Biol. 2003, 258:364-384.
29. Kanadia R.N., Clark V.E., Punzo C., Trimarchi J.M., Cepko C.L. Temporal requirement of the alternative-splicing factor Sfrs1 for the survival of retinal neurons. Development 2008, 135:3923-3933.
30. Keino-Masu K., Masu M., Hinck L., Leonardo E.D., Chan S.S., Culotti J.G., Tessier-Lavigne M. Deleted in Colorectal Cancer (DCC) encodes a netrin receptor. Cell 1996, 87:175-185.
31. Kolodziej P.A., Timpe L.C., Mitchell K.J., Fried S.R., Goodman C.S., Jan L.Y., Jan Y.N. Frazzled encodes a Drosophila member of the DCC immunoglobulin subfamily and is required for CNS and motor axon guidance. Cell 1996, 87:197-204.
32. Liu W., Khare S.L., Liang X., Peters M.A., Liu X., Cepko C.L., Xiang M. All Brn3 genes can promote retinal ganglion cell differentiation in the chick. Development 2000, 127:3237-3247.
33. Livesey F.J., Cepko C.L. Vertebrate neural cell-fate determination: lessons from the retina. Nat. Rev. Neurosci. 2001, 2:109-118.
34. Llambi F., Causeret F., Bloch-Gallego E., Mehlen P. Netrin-1 acts as a survival factor via its receptors UNC5H and DCC. EMBO J. 2001, 20:2715-2722.
35. Marcos S., Backer S., Causeret F., Tessier-Lavigne M., Bloch-Gallego E. Differential roles of Netrin-1 and its receptor DCC in inferior olivary neuron migration. Mol. Cell. Neurosci. 2009, 41:429-439.
36. Masland R.H. The fundamental plan of the retina. Nat. Neurosci. 2001, 4:877-886.
37. Matsunaga E., Tauszig-Delamasure S., Monnier P.P., Mueller B.K., Strittmatter S.M., Mehlen P., Chedotal A. RGM and its receptor neogenin regulate neuronal survival. Nat. Cell Biol. 2004, 6:749-755.
38. Mehlen P., Mazelin L. The dependence receptors DCC and UNC5H as a link between neuronal guidance and survival. Biol. Cell 2003, 95:425-436.
39. Mehlen P., Thibert C. Dependence receptors: between life and death. Cell. Mol. Life Sci. 2004, 61:1854-1866.
40. Mehlen P., Rabizadeh S., Snipas S.J., Assa-Munt N., Salvesen G.S., Bredesen D.E. The DCC gene product induces apoptosis by a mechanism requiring receptor proteolysis. Nature 1998, 395:801-804.
41. Morrow E.M., Furukawa T., Lee J.E., Cepko C.L. NeuroD regulates multiple functions in the developing neural retina in rodent. Development 1999, 126:23-36.
42. Murase S., Horwitz A.F. 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.
43. Nakhai H., Sel S., Favor J., Mendoza-Torres L., Paulsen F., Duncker G.I., Schmid R.M. Ptf1a is essential for the differentiation of GABAergic and glycinergic amacrine cells and horizontal cells in the mouse retina. Development 2007, 134:1151-1160.
44. Nishida A., Furukawa A., Koike C., Tano Y., Aizawa S., Matsuo I., Furukawa T. Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development. Nat. Neurosci. 2003, 6:1255-1263.
45. Ohsawa R., Kageyama R. Regulation of retinal cell fate specification by multiple transcription factors. Brain Res. 2008, 1192:90-98.
46. Rapaport D.H., Wong L.L., Wood E.D., Yasumura D., LaVail M.M. Timing and topography of cell genesis in the rat retina. J. Comp. Neurol. 2004, 474:304-324.
47. Shi M., Guo C., Dai J.X., Ding Y.Q. DCC is required for the tangential migration of noradrenergic neurons in locus coeruleus of mouse brain. Mol. Cell. Neurosci. 2008, 39:529-538.
48. Shin S.K., Nagasaka T., Jung B.H., Matsubara N., Kim W.H., Carethers J.M., Boland C.R., Goel A. Epigenetic and genetic alterations in Netrin-1 receptors UNC5C and DCC in human colon cancer. Gastroenterology 2007, 133:1849-1857.
49. Stein E., Zou Y., Poo M., Tessier-Lavigne M. Binding of DCC by Netrin-1 to mediate axon guidance independent of adenosine A2B receptor activation. Science 2001, 291:1976-1982.
50. Turner D.L., Cepko C.L. A common progenitor for neurons and glia persists in rat retina late in development. Nature 1987, 328:131-136.
51. Xie Y., Ding Y.Q., Hong Y., Feng Z., Navarre S., Xi C.X., Zhu X.J., Wang C.L., Ackerman S.L., Kozlowski D., Mei L., Xiong W.C. Phosphatidylinositol transfer protein-alpha in Netrin-1-induced PLC signalling and neurite outgrowth. Nat. Cell Biol. 2005, 7:1124-1132.
52. Xie Y., Hong Y., Ma X.Y., Ren X.R., Ackerman S., Mei L., Xiong W.C. DCC-dependent phospholipase C signaling in Netrin-1-induced neurite elongation. J. Biol. Chem. 2006, 281:2605-2611.