Gamma protocadherins are required for survival of spinal interneurons

Neuron

Volumn 36, Issue 5, 2002, Pages 843-854

  Wang, Xiaozhong ^a   Weiner, Joshua A ^b   Levi, Sabine ^b   Craig, Ann Marie ^b   Bradley, Allan ^a,c   Sanes, Joshua R ^b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CADHERIN; ISOPROTEIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL CULTURE; CELL DEATH; CELL DIFFERENTIATION; CELL MIGRATION; CELL SURVIVAL; CELL TYPE; CONTROLLED STUDY; INTERNEURON; MOTONEURON; MOUSE; NERVE DEGENERATION; NERVE FIBER GROWTH; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SENSORY NERVE CELL; SPINAL CORD NERVE CELL; SYNAPTOGENESIS;

EID: 18744410937     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0896-6273(02)01090-5     Document Type: Article

References (48)

1. Alagramam K.N., Yuan H., Kuehn M.H., Murcia C.L., Wayne S., Srisailpathy C.R., Lowry R.B., Knaus R., Van Laer L., Bernier F.P.et al. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum. Mol. Genet. 10:2001;1709-1718.
2. Angst B.D., Marcozzi C., Magee A.I. The cadherin superfamily. diversity in form and function J. Cell Sci. 114:2001;629-641.
3. Béchade C., Colin I., Kirsch J., Betz H., Triller A. Expression of glycine receptor alpha subunits and gephyrin in cultured spinal neurons. Eur. J. Neurosci. 8:1996;429-435.
4. Benson D.L., Colman D.R., Huntley G.W. Molecules, maps and synapse specificity. Nat. Rev. Neurosci. 2:2001;899-909.
5. Bozdagi O., Shan W., Tanaka H., Benson D.L., Huntley G.W. Increasing numbers of synaptic puncta during late-phase LTP. N-cadherin is synthesized, recruited to synaptic sites, and required for potentiation Neuron. 28:2000;245-259.
6. Carlin R.K., Grab D.J., Cohen R.S., Siekevitz P. Isolation and characterization of postsynaptic densities from various brain regions. enrichment of different types of postsynaptic densities J. Cell Biol. 86:1980;831-845.
7. DeOlmos J.S., Ingram W.R. An improved cupric-silver method for impregnation of axonal and terminal degeneration. Brain Res. 33:1971;523-529.
8. Dreyer W.J., Roman-Dreyer J. Cell-surface area codes. mobile-element related gene switches generate precise and heritable cell-surface displays of address molecules that are used for constructing embryos Genetica. 107:1999;249-259.
9. Frank M., Kemler R. Protocadherins. Curr. Opin. Cell Biol. 14:2002;557-562.
10. Gautam M., Noakes P.G., Moscoso L., Rupp F., Scheller R.H., Merlie J.P., Sanes J.R. Defective neuromuscular synaptogenesis in agrin-deficient mutant mice. Cell. 85:1996;525-535.
11. Hamada S., Yagi T. The cadherin-related neuronal receptor family. a novel diversified cadherin family at the synapse Neurosci. Res. 41:2001;207-215.
12. Inoue A., Sanes J.R. Lamina-specific connectivity in the brain. regulation by N-cadherin, neurotrophins, and glycoconjugates Science. 276:1997;1428-1431.
13. Iwai Y., Usui T., Hirano S., Steward R., Takeichi M., Uemura T. Axon patterning requires DN-cadherin, a novel neuronal adhesion receptor, in the Drosophila embryonic CNS. Neuron. 19:1997;77-89.
14. Kohmura N., Senzaki K., Hamada S., Kai N., Yasuda R., Watanabe M., Ishii H., Yasuda M., Mishina M., Yagi T. Diversity revealed by a novel family of cadherins expressed in neurons at a synaptic complex. Neuron. 20:1998;1137-1151.
15. Lee C.H., Herman T., Clandinin T.R., Lee R., Zipursky S.L. N-cadherin regulates target specificity in the Drosophila visual system. Neuron. 30:2001;437-450.
16. Levi S., Grady R.M., Henry M.D., Campbell K.P., Sanes J.R., Craig A.M. Dystroglycan is selectively associated with inhibitory GABAergic synapses but is dispensable for their differentiation. J. Neurosci. 22:2002;4274-4285.
17. Lowrie M.B., Lawson S.J. Cell death of spinal interneurones. Prog. Neurobiol. 61:2000;543-555.
18. Manabe T., Togashi H., Uchida N., Suzuki S.C., Hayakawa Y., Yamamoto M., Yoda H., Miyakawa T., Takeichi M., Chisaka O. Loss of cadherin-11 adhesion receptor enhances plastic changes in hippocampal synapses and modifies behavioral responses. Mol. Cell. Neurosci. 15:2000;534-546.
19. Nijhawan D., Honarpour N., Wang X. Apoptosis in neural development and disease. Annu. Rev. Neurosci. 23:2000;73-87.
20. Nollet F., Kools P., van Roy F. Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members. J. Mol. Biol. 299:2000;551-572.
21. Nornes H.O., Carry M. Neurogenesis in spinal cord of mouse. an autoradiographic analysis Brain Res. 159:1978;1-6.
22. Obata S., Sago H., Mori N., Davidson M., St. John T., Suzuki S.T. A common protocadherin tail. multiple protocadherins share the same sequence in their cytoplasmic domains and are expressed in different regions of brain Cell Adhes. Commun. 6:1998;323-333.
23. Oliveira A.L., Risling M., Negro A., Langone F., Cullheim S. Apoptosis of spinal interneurons induced by sciatic nerve axotomy in the neonatal rat is counteracted by nerve growth factor and ciliary neurotrophic factor. J. Comp. Neurol. 447:2002;381-393.
24. Pfenninger K.H. The cytochemistry of synaptic densities. I. An analysis of the bismuth iodide impregnation method. J. Ultrastruct. Res. 34:1971;103-122.
25. Price S.R., De Marco Garcia N.V., Ranscht B., Jessell T.M. Regulation of motor neuron pool sorting by differential expression of type II cadherins. Cell. 109:2002;205-216.
26. Rao A., Cha E.M., Craig A.M. Mismatched appositions of presynaptic and postsynaptic components in isolated hippocampal neurons. J. Neurosci. 20:2000;8344-8353.
27. Redies C. Cadherins in the central nervous system. Prog. Neurobiol. 61:2000;611-648.
28. Ridet J.L., Malhotra S.K., Privat A., Gage F.H. Reactive astrocytes. cellular and molecular cues to biological function Trends Neurosci. 20:1997;570-577.
29. Riehl R., Johnson K., Bradley R., Grunwald G.B., Cornel E., Lilienbaum A., Holt C.E. Cadherin function is required for axon outgrowth in retinal ganglion cells in vivo. Neuron. 17:1996;837-848.
30. Sano K., Tanihara H., Heimark R.L., Obata S., Davidson M., St. John T., Taketani S., Suzuki S. Protocadherins. a large family of cadherin-related molecules in central nervous system EMBO J. 12:1993;2249-2256.
31. Senzaki K., Ogawa M., Yagi T. Proteins of the CNR family are multiple receptors for Reelin. Cell. 99:1999;635-647.
32. Serpinskaya A.S., Feng G., Sanes J.R., Craig A.M. Synapse formation by hippocampal neurons from agrin-deficient mice. Dev. Biol. 205:1999;65-78.
33. Serafini T. Finding a partner in a crowd. neuronal diversity and synaptogenesis Cell. 98:1999;133-136.
34. Shapiro L., Colman D.R. The diversity of cadherins and implications for a synaptic adhesive code in the CNS. Neuron. 23:1999;427-430.
35. Sugino H., Hamada S., Yasuda R., Tuji A., Matsuda Y., Fujita M., Yagi T. Genomic organization of the family of CNR cadherin gene in mice and humans. Genomics. 63:2000;75-87.
36. Tang L., Hung C.P., Schuman E.M. A role for the cadherin family of cell adhesion molecules in hippocampal long-term potentiation. Neuron. 20:1998;1165-1175.
37. Takeichi M. Morphogenetic roles of classic cadherins. Curr. Opin. Cell Biol. 7:1995;619-627.
38. Tasic B., Nabholz C.E., Baldwin K.K., Kim Y., Rueckert E.H., Ribich S.A., Cramer P., Wu Q., Axel R., Maniatis T. Promoter choice determines splice site selection in protocadherin alpha and gamma pre-mRNA splicing. Mol. Cell. 10:2002;21-33.
39. Togashi H., Abe K., Mizoguchi A., Takaoka K., Chisaka O., Takeichi M. Cadherin regulates dendritic spine morphogenesis. Neuron. 35:2002;77-89.
40. Tomaselli K.J., Neugebauer K.M., Bixby J.L., Lilien J., Reichardt L.F. N-cadherin and integrins. two receptor systems that mediate neuronal process outgrowth on astrocyte surfaces Neuron. 1:1988;33-43.
41. Verhage M., Maia A.S., Plomp J.J., Brussaard A.B., Heeroma J.H., Vermeer H., Toonen R.F., Hammer R.E., van den Berg T.K., Missler M.et al. Synaptic assembly of the brain in the absence of neurotransmitter secretion. Science. 287:2000;864-869.
42. Wang X., Su H., Bradley A. Molecular mechanisms governing Pcdh-γ gene expression. evidence for a multiple promoter and cis-alternative splicing model Genes Dev. 16:2002;1890-1905.
43. Wolverton T., Lalande M. Identification and characterization of three members of a novel subclass of protocadherins. Genomics. 76:2001;66-72.
44. Wu Q., Maniatis T. A striking organization of a large family of human neural cadherin-like cell adhesion genes. Cell. 97:1999;779-790.
45. Wu Q., Zhang T., Cheng J.F., Kim Y., Grimwood J., Schmutz J., Dickson M., Noonan J.P., Zhang M.Q., Myers R.M.et al. Comparative DNA sequence analysis of mouse and human protocadherin gene clusters. Genome Res. 11:2001;389-404.
46. Yagi T., Takeichi M. Cadherin superfamily genes. functions, genomic organization, and neurologic diversity Genes Dev. 14:2000;1169-1180.
47. Yamagata M., Herman J.-P., Sanes J.R. Lamina-specific expression of adhesion molecules in developing chick optic tectum. J. Neurosci. 15:1995;4556-4571.
48. Yap A.S., Brieher W.M., Gumbiner B.M. Molecular and functional analysis of cadherin-based adherens junctions. Annu. Rev. Cell Dev. Biol. 13:1997;119-146.