The Mesenchymal Cadherin-11 is Expressed in Restricted Sites during the Ontogeny of the Rat Brain in Modes Suggesting Novel Functions

References

• Anderson S. A., Eisenstat D. D., Shi L., Rubenstein J. L.R. a. lnterneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science 1997; 278: 474–476
   PubMed Web of Science ®Google Scholar
• Anderson S. A., Qiu M., Bulfone A., Eisenslat D. D., Meneses J., Pederson R., Rubenstein J. L.R. b. Mutations of the homcobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons. Neuron 1997; 19: 27–37
   PubMed Web of Science ®Google Scholar
• Barami K., Kirschembaum B., Lemmon V., Goldman S. A. N-cadherin and Ng-CAM/8D9 are involved serially in the migration of newly generated neurons into the adult songbird brain. Neuron 1994; 13: 567–582
   Web of Science ®Google Scholar
• Bayer S. A., Altman J. Neocorlical Development. Raven, New York 1991
   Google Scholar
• Bixby J. L., Zhang R. Purified N-cadherin is a potent substratfor rapid induction of neurite outgrowth. J. Cell Biol. 1990; 110: 1253–1260
   PubMed Web of Science ®Google Scholar
• Bloch-Gallego E., Millet S., Alvarado-Mallart R. M. Further observations on the susceptibility of diencephalic prosomeres to En-2 induction and on the resulting histogenetic capabilities. Mecli. Dev. 1996; 58: 51–63
   PubMed Web of Science ®Google Scholar
• Buisseret-Delmas C., Angaut P. The cerebellar olivo-corticonuclear connections in the rat. Progress in Neurobiol. 1993; 40: 63–87
   PubMed Web of Science ®Google Scholar
• Cepek K. L., Shaw S. K., Parker C M, Russel G. J., Morrow J. S, Rimm D. L., Brenner M. B. Adhesion between epithelial cells and T lymphocytes mediated by E-cadherin and the tvE/37 integrin. Nature 1994; 372: 190–193
   PubMed Web of Science ®Google Scholar
• Chedotal A., Pourquie O., Ezan F., San Clemente H., Sotelo C. BEN as a presumptive target recognition molecule during the development of the olivocerebellar system. J. Ncurosci. 1996; 16: 3296–3310
   PubMed Web of Science ®Google Scholar
• Detrick R. J., Dickey D., Kintner C. R. The effects of N-cadherin misexpression on morphogenesis in Xenopus embryos. Neuron 1990; 4: 493–506
   PubMed Web of Science ®Google Scholar
• Doherty P., Ashton S. V., Moore S. E., Walsh F. S. Morphoregulatory activities of N-CAM and N-cadherin can be accounted by G-protein-dependant activation of L- and N-type neuronal Ca2+ channels. Cell 1991; 67: 21–33
   PubMed Web of Science ®Google Scholar
• Doherty P., Walsh F. S. Signal transduction events underlying neurite outgrowth stimulated by cell adhesion molecules. Curr. Opin. Neurohiol. 1994; 4: 49–55
   PubMedGoogle Scholar
• Espeseth A., Johnson E., Kintner C. Xenopus F-cadherin, a novel member of the cadherin family of cell adhesion molecules, is expressed at boundaries in the neural tube. Mol. Cell Neurosci. 1995; 6: 199–211
   PubMed Web of Science ®Google Scholar
• Ffrench-Constant C, Miller R. H., Burne J. F., Raff M. C. Evidence that migratory oligodentrocyte-type-2 astrocyte (0-2A)progenitorcellsare kept out of the rat retina by a barrier at the eye-end of the optic nerve. J. Neurocytol. 1988; 17: 13–25
   PubMedGoogle Scholar
• Figdor M. C., Stern C D. Segmental organization of embryonic diencephalon. Nature 1993; 363: 630–634
   PubMed Web of Science ®Google Scholar
• Finkelstein R., Boncinelli E. From fly head to mammalian forebrain: the story of otd and Otx. Trends Genet. 1994; 10: 310–315
   PubMed Web of Science ®Google Scholar
• Fredette B. J., Ranscht B. T-cadherin expression delineates specific region of the developing motor axon-hindlimb projection pathway. J. Neurosci. 1994; 14: 7331–7346
   PubMed Web of Science ®Google Scholar
• Fujimori T., Miyatani S., Takeichi M. Ectopic expression of N-cadherin perturbs histogenesis in Xenopus laevis embryos. Development 1990; 110: 97–104
   PubMed Web of Science ®Google Scholar
• Gänzler S. I., Redies C. R-cadherin expression during nucleus formation in chicken forebrain neuromeres. J. Neurosci. 1995; 15: 4157–4172
   PubMed Web of Science ®Google Scholar
• Geiger B., Ayalon O. Cadherins. Annu. Rev. Cell Biol. 1992; 8: 307–332
   PubMedGoogle Scholar
• Hatta K., Takeichi M. Expression of N-cadherin adhesion molecules associated with early morphogenetic events in chick development. Nature 1986; 320: 447–449
   PubMed Web of Science ®Google Scholar
• Hoffmann I., Balling R. Cloning and expression analysis of a novel mesodermallv expressed cadherin. Dev. Biol. 1995; 169: 337–346
   PubMed Web of Science ®Google Scholar
• Inuzuka H., Redies C., Takeichi M. Differential expression of R- and N-cadherin in neural and mesodermal tissues during early chicken development. Development. 1991; 113: 959–967
   PubMed Web of Science ®Google Scholar
• Jessel T. M. Adhesion molecules and the hierarchy of neural development. Neuron 1988; 1: 3–13
   PubMed Web of Science ®Google Scholar
• Kemler R. From cadherins to catenins: cytoplasmic protein interactions and regulation of cell adhesion. Trends Genet. 1993; 9: 317–321
   PubMed Web of Science ®Google Scholar
• Kimura Y., Matsunami H, Inoue T., Shimamura K., Uchida N., Ueno T., Miyazaki T., Takeichi M. Cadherin-11 expressed in association with mesenchymal morphogenesis in the head, somite, and limb bud of early mouse embryos. Dev. Biol. 1995; 169: 347–358
   PubMed Web of Science ®Google Scholar
• Kimura Y., Matsunami H., Takeichi M. Expression of cadherin-11 delineates boundaries, neuromeres, and nuclei in the developing mouse brain. Dev. Dyn. 1996; 206: 455–462
   Web of Science ®Google Scholar
• Lumsden A. A cellular basis of segmentation in the developing hindbrain. Trends Neurosci. 1990; 13: 329–335
   PubMed Web of Science ®Google Scholar
• Lumsden A., Krumlauf R. Patterning the vertebrate neuraxis. Science 1996; 274(5290)1109–1115
   PubMed Web of Science ®Google Scholar
• Martinez S., Wassef M., Alvarado-Mallart R. M. Induction of a mesencephalic phenotype in the 2-days old chick prosencephalon is preceded by the early expression of the homeobox gene. en. Neuron 1991; 6: 971–981
   PubMed Web of Science ®Google Scholar
• Matsugana M., Hatta K., Nagafuchi A., Takeichi M. Guidance of optic nerve fibers by N-cadherin adhesion molecules. Nature 1988; 334: 62–64
   PubMed Web of Science ®Google Scholar
• Matsunami H., Miyatani S., Inoue T., Copeland N. G., Gilbert D. J., Jenkins N. A., Takeichi M. Cell binding specificity of mouse R-cadherin and chromosomal mapping of the gene. J. Cell Sci. 1993; 106: 401–409
   PubMed Web of Science ®Google Scholar
• Matsunami H., Takeichi M. Fetal brain subdivisions defined by R- and E-cadherin expressions: evidence for the role of cadherin activity in region-specific, cell-cell adhesion. Dev. Biol. 1995; 172: 466–478
   PubMed Web of Science ®Google Scholar
• Millen K. J., Hui C. C., Joyner A. L. A role for En-2 and other murine homologues of Drosophila segment polarity genes in regulating positional information in the developing cerebellum. Development 1995; 121: 3935–3945
   PubMed Web of Science ®Google Scholar
• Murphy-Erdosh C, Napolitano E. W., Reichardy L. F. The expression of B-cadherin during embryonic chick development. Dev. Biol. 1994; 161: 107–125
   PubMed Web of Science ®Google Scholar
• Murphy-Erdosh C, Yoshida C. K., Paradies N., Reichardt L. F. The cadherin-bindjng specificity of B-cadherin and L-CAM. J. Cell Biol 1995; 129: 1379–1390
   PubMed Web of Science ®Google Scholar
• Nakagawa S., Takeichi M. Neural crest cell-cell adhesion controlled by sequential and subpopulation-specific expression of novel cadherins. Development 1995; 121: 1321–1332
   PubMed Web of Science ®Google Scholar
• Ono K., Yasui Y., Rutishauser U., Miller R. H. Focal ventricular origin and migration of oligodendrocyte precursors into the chick optic nerve. Neuron 1997; 19: 283–292
   PubMed Web of Science ®Google Scholar
• Otteson D. C., Shelden E., Jones J. M., Kameoka J., Hitchcock P. F. Pax2 expression and retinal morphogenesis in the normal and. Krdmome. Dev. Biol. 1998; 193: 209–224
   PubMed Web of Science ®Google Scholar
• Paxinos G. The Rat Nervous Sytem, 2nd ed. Academic Press, San Diego, CA 1995
   Google Scholar
• Rakic P. Specification of cerebral cortical areas. Science 1988; 241: 170–176
   PubMed Web of Science ®Google Scholar
• Ranscht B. Cadherin and catenins: interactions and functions in embryonic development. Curr. Opin. Cell Biol. 1994; 6: 740–746
   PubMed Web of Science ®Google Scholar
• Redies C. Cadherin expressions in the developing vertebrate CNS: from neuromeres to brain nuclei and neural circuits. Exp. Cell Res. 1995; 220: 243–256
   PubMed Web of Science ®Google Scholar
• Redies C., Takeichi M. a. N- and R-cadherin expression in the optic nerve of the chicken embryo. Glia 1993; 8: 161–171
   PubMed Web of Science ®Google Scholar
• Redies C., Takeichi M. b. Expression of N-cadherin mRNA during development of the mouse bram. Dev. Dyn. 1993; 197: 26–39
   PubMed Web of Science ®Google Scholar
• Redies C., Takeichi M. Cadherins in the developing central nervous system: an adhesive code for segmental and functional subdivisions. Dev. Biol. 1996; 180: 413–423
   Web of Science ®Google Scholar
• Rubenstein J. L.R., Martinez S., Shimamura K., Puelles L. The embryonic vertebrate forebrain: the prosomeric model. Science 1994; 266: 578–580
   PubMed Web of Science ®Google Scholar
• Sano K., Tanihara H., Heimark R., Obata S., Davidson M. St., John T., Takenati S., Suzuki S. Protocadherins: a large family of cadherin-related molecules in central nervous system. EMBO J. 1993; 12: 2249–2256
   PubMed Web of Science ®Google Scholar
• Shimamura K., Takeichi M. Local and transient expression of E-cadherin in mouse embryonic brain morphogenesis. Development 1992; 116: 1011–1019
   PubMed Web of Science ®Google Scholar
• Shimamura K., Hartigan D. A., Martinez S., Puelles L., Rubenstein L. R. Longitudinal organization of the anterior neural plate and neural tube. Development 1995; 121: 3923–3933
   PubMed Web of Science ®Google Scholar
• Simonneau L., Broders F., Thiery J. P. N-cadherin transcripts in Xenopus laevis tialbud to tadpole. Dev. Dvn. 1992; 194: 247–260
   PubMed Web of Science ®Google Scholar
• Simonneau L., Kitagawa M., Suzuki S., Thiery J. P. Cadherin-11 expression marks the mesenchymal phenotype: towards new functions for cadherins?. Cell Adhes. d'Commun. 1995; 3: 115–130
   PubMed Web of Science ®Google Scholar
• Steinberg M. S., Takeichi M. Experimental specification of cell sorting, tissue spreading, and specific spatial patterning by quantitatives differences in cadherin expression. Proc. Natl. Acad. Sci. USA 1994; 91: 206–209
   PubMed Web of Science ®Google Scholar
• Stoykova A., Fritsch R., Walther D., Gruss P. Forebrain patterning defects in Small eye mutant mice. Development 1996; 122: 3453–3465
   PubMed Web of Science ®Google Scholar
• Suzuki S. C., Inoue T., Kimura Y., Tanaka T., Takeichi M. Neuronal circuits are subdivided by differential expression of type-Il classic cadherins in neonatal mouse brains. Mol. and Cell. Neuroscience, (in press).
   Web of Science ®Google Scholar
• Suzuki S., Sano K., Tanihara H. Diversity of the cadherin family: evidence for height new cadherin in nervous tissue. Cell Regul 1991; 2: 261–270
   PubMedGoogle Scholar
• Tamamaki N., Fujimori K. E., Takauji R. Origin and route of tangentially migrating neurons in the developing neocortical intermediate zone. J. Neurosci. 1997; 17: 8313–8323
   PubMed Web of Science ®Google Scholar
• Takeichi M. Cadherin cell adhesion receptor as a morphogenetic regulator. Science 1991; 251: 1451–1455
   PubMed Web of Science ®Google Scholar
• Takeichi M. Morphogenetic roles of classic cadherins. Curr. Opin. Cell Biol. 1995; 1: 619–627
   Web of Science ®Google Scholar
• Tan S. S., Morris-Kay G. M. The development and distribution of the cranial neural crest in the rat embryo. Cell Tissue Research 1985; 240: 403–416
   PubMed Web of Science ®Google Scholar
• Tanihara H., Sano K., Heimark R., John T. S., Suzuki S. Cloning of five cadherins clarifies characteristic features of cadherins extracellular domain and provides further evidence for two structurally different types of cadherin. Cell Adhes. d'Commun. 1994; 1: 15–26
   Google Scholar
• Torres M., Gomez-Pardo E., Gruss P. Pax2 contributes to inner ear patterning and optic nerve trajectory. Development 1996; 122: 3381–3391
   PubMed Web of Science ®Google Scholar
• Uchida N., Honjo Y., Johnson K. R., Wheelock M. J., Takeichi M. The catenin/cadherin adhesion system is localized in synaptic junctions bordering transmitter release zones. J. Cell Biol 1996; 135: 767–779
   PubMed Web of Science ®Google Scholar
• Wilkinson D. G. In Situ Hybridization. A Practical Approach, D. G. Wilkinson. IRL Press. 1992
   Google Scholar