Cited by 49Neurogenesis and neuroplasticity mechanismsCell Adhesion Molecules ResearchGenetics and Neurodevelopmental Disorders

Flying under the radar: CDH2 (N-cadherin), an important hub molecule in neurodevelopmental and neurodegenerative diseases.

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László, Zsófia I., Lele, Zsolt·2022·Frontiers in Neuroscience

Abstract

CDH2 belongs to the classic cadherin family of Ca 2+ -dependent cell adhesion molecules with a meticulously described dual role in cell adhesion and β-catenin signaling. During CNS development, CDH2 is involved in a wide range of processes including maintenance of neuroepithelial integrity, neural tube closure (neurulation), confinement of radial glia progenitor cells (RGPCs) to the ventricular zone and maintaining their proliferation-differentiation balance, postmitotic neural precursor migration, axon guidance, synaptic development and maintenance. In the past few years, direct and indirect evidence linked CDH2 to various neurological diseases, and in this review, we summarize recent developments regarding CDH2 function and its involvement in pathological alterations of the CNS.

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  • Cadherin signaling has been linked to synaptic adhesion stability and neurodegeneration.

    “Cadherin signaling has also been linked to synaptic adhesion stability and neurodegeneration (Ando et al., 2011; Arikkath and Reichardt, 2008; Laszlo and Lele, 2022; Mysore et al., 2008), and APOE isoforms differentially modulate components of cadherin–catenin complexes (Ahmad et al., 2020; Zhang et al., 2024).”

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  1. Aaku-Saraste E. Hellwig A. Huttner W. B. (1996). Loss of occludin and functional tight junctions, but Not ZO-1, during neural tube closure-remodeling of the neuroepithelium prior to neurogenesis. Dev. Biol. 180 664– 679. 10.1006/dbio.1996.0336 8954735 · DOI
  2. Abdelhamed Z. Vuong S. M. Hill L. Shula C. Timms A. Beier D. (2018). A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice. Development 145: dev154500. 10.1242/dev.154500 29317443 PMC5825874 · DOI
  3. Accogli A. Calabretta S. St-Onge J. Boudrahem-Addour N. Dionne-Laporte A. Joset P. (2019). De Novo pathogenic variants in N-cadherin Cause a syndromic neurodevelopmental disorder with corpus collosum, axon, cardiac, ocular, and genital defects. Am. J. Hum. Genet. 105 854– 868. 10.1016/j.ajhg.2019.09.005 31585109 PMC6817525 · DOI
  4. Ajioka I. Nakajima K. (2005). Switching of α-catenin from αE-catenin in the cortical ventricular zone to αN-catenin II in the intermediate zone. Dev. Brain Res. 160 106– 111. 10.1016/j.devbrainres.2005.08.004 16185771 · DOI
  5. Anderson S. A. Eisenstat D. D. Shi L. Rubenstein J. L. R. (1997). Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science 278 474– 476. 10.1126/science.278.5337.474 9334308 · DOI · Paper page
  6. Ando K. Uemura K. Kuzuya A. Maesako M. Asada-Utsugi M. Kubota M. (2011). N-cadherin regulates p38 MAPK signaling via association with JNK-associated leucine zipper protein: implications for neurodegeneration in Alzheimer disease. J. Biol. Chem. 286 7619– 7628. 10.1074/jbc.M110.158477 21177868 PMC3045016 · DOI · Paper page
  7. Andrews W. D. Barber M. Parnavelas J. G. (2007). Slit-Robo interactions during cortical development. J. Anat. 211 188– 198. 10.1111/j.1469-7580.2007.00750.x 17553100 PMC2375773 · DOI
  8. Andreyeva A. Nieweg K. Horstmann K. Klapper S. Müller-Schiffmann A. Korth C. (2012). C-terminal fragment of N-cadherin accelerates synapse destabilization by amyloid-β. Brain 135 2140– 2154. 10.1093/brain/aws120 22637581 · DOI
  9. Arteaga-bracho E. E. Gulinello M. Winchester M. L. Pichamoorthy N. Gokhan S. Mehler M. F. (2016). Neurobiology of disease postnatal and adult consequences of loss of huntingtin during development: implications for Huntington’s disease. Neurobiol. Dis. 96 144– 155. 10.1016/j.nbd.2016.09.006 27623015 PMC5102778 · DOI
  10. Asada-Utsugi M. Uemura K. Kubota M. Noda Y. Tashiro Y. Uemura T. M. (2021). Mice with cleavage-resistant N-cadherin exhibit synapse anomaly in the hippocampus and outperformance in spatial learning tasks. Mol. Brain 14 1– 16. 10.1186/s13041-021-00738-1 33494786 PMC7831172 · DOI
  11. Baki L. Marambaud P. Efthimiopoulos S. Georgakopoulos A. Wen P. Cui W. (2001). Presenilin-1 binds cytoplasmic epithelial cadherin, inhibits cadherin/p120 association, and regulates stability and function of the cadherin/catenin adhesion complex. Proc. Natl. Acad. Sci. U.S.A. 98 2381– 2386. 10.1073/pnas.041603398 11226248 PMC30147 · DOI
  12. Barnat M. Capizzi M. Aparicio E. Boluda S. Wennagel D. Kacher R. (2020). Huntington’s disease alters human neurodevelopment. Science 3338: eaax3338. 10.1126/science.aax3338 32675289 PMC7859879 · DOI · Paper page
  13. Barnat M. Le Friec J. Benstaali C. Humbert S. (2017). Huntingtin-Mediated multipolar-bipolar transition of newborn cortical neurons is critical for their postnatal neuronal morphology. Neuron 93 99– 114. 10.1016/j.neuron.2016.11.035 28017473 · DOI
  14. Basu R. Taylor M. R. Williams M. E. (2015). The classic cadherins in synaptic specificity. Cell Adhes. Migr. 9 193– 201. 10.1080/19336918.2014.1000072 25837840 PMC4594527 · DOI
  15. Bekirov I. H. Needleman L. A. Zhang W. Benson D. L. (2002). Identification and localization of multiple classic cadherins in developing rat limbic system. Neuroscience 115 213– 227. 10.1016/S0306-4522(02)00375-5 12401335 · DOI
  16. Bhandari R. Ferri S. Whittaker B. Liu M. Lazzaro D. R. (2011). Peters anomaly: review of the literature. Cornea 30 939– 944. 10.1097/ICO.0b013e31820156a9 21448066 · DOI
  17. Bixby J. L. Zhang R. (1990). Purified N-cadherin is a potent substrate for the rapid induction of neurite outgrowth. J. Cell Biol. 110 1253– 1260. 10.1083/jcb.110.4.1253 2324197 PMC2116071 · DOI
  18. Borrell V. Cárdenas A. Ciceri G. Galcerán J. Flames N. Pla R. (2012). Slit/Robo signaling modulates the proliferation of central nervous system progenitors. Neuron 76 338– 352. 10.1016/j.neuron.2012.08.003 23083737 PMC4443924 · DOI
  19. Botella-López A. Burgaya F. Gavín R. García-Ayllón M. S. Gómez-Tortosa E. Peña-Casanova J. (2006). Reelin expression and glycosylation patterns are altered in Alzheimer’s disease. Proc. Natl. Acad. Sci. U.S.A. 103 5573– 5578. 10.1073/pnas.0601279103 16567613 PMC1414634 · DOI · Paper page
  20. Bozdagi O. Wang X. Nikitczuk J. S. Anderson T. R. Bloss E. B. Radice G. L. (2010). Persistence of coordinated long-term potentiation and dendritic spine enlargement at mature hippocampal CA1 synapses requires N-cadherin. J. Neurosci. 30 9984– 9989. 10.1523/JNEUROSCI.1223-10.2010 20668183 PMC2921177 · DOI · Paper page
  21. Brayshaw L. L. Price S. R. (2016). “ Cadherins in neural development,” in The Cadherin Superfamily, eds Hirano S Suzuki S T. (Tokyo: Springer Japan), 315– 1340. 10.1007/978-4-431-56033-3_12 · DOI
  22. Budday S. Steinmann P. Kuhl E. (2015). Physical biology of human brain development. Front. Cell. Neurosci. 9: 257. 10.3389/fncel.2015.00257 26217183 PMC4495345 · DOI
  23. Carter M. G. Johns M. A. Zeng X. Zhou L. Zink M. C. Mankowski J. L. (2000). Mice deficient in the candidate tumor suppressor gene Hic1 exhibit developmental defects of structures affected in the Miller-Dieker syndrome. Hum. Mol. Genet. 9 413– 419. 10.1093/hmg/9.3.413 10655551 · DOI
  24. Caserta M. T. Sullivan E. (2009). Late-onset huntington’s disease masquerading as normal pressure hydrocephalus. J. Neuropsychiatry Clin. Neurosci. 21 97– 98. 10.1176/jnp.2009.21.1.97 19359459 · DOI
  25. Castaneyra-Ruiz L. Morales D. M. McAllister J. P. Brody S. L. Isaacs A. M. Strahle J. M. (2018). Blood exposure causes ventricular zone disruption and glial activation in vitro. J. Neuropathol. Exp. Neurol. 77 803– 813. 10.1093/jnen/nly058 30032242 PMC6927874 · DOI
  26. Cen C. Luo L. Da Li W. Q. Li G. Tian N. X. Zheng G. (2018). PKD1 promotes functional synapse formation coordinated with N-cadherin in hippocampus. J. Neurosci. 38 183– 199. 10.1523/JNEUROSCI.1640-17.2017 29133434 PMC6705812 · DOI
  27. Chai X. Förster E. Zhao S. Bock H. H. Frotscher M. (2009). Reelin stabilizes the actin cytoskeleton of neuronal processes by inducing n-cofilin phosphorylation at serine. J. Neurosci. 29 288– 299. 10.1523/JNEUROSCI.2934-08.2009 19129405 PMC6664910 · DOI · Paper page
  28. Chazeau A. Garcia M. Czöndör K. Perrais D. Tessier B. Giannone G. (2015). Mechanical coupling between transsynaptic N-cadherin adhesions and actin flow stabilizes dendritic spines. Mol. Biol. Cell 26 859– 873. 10.1091/mbc.E14-06-1086 25568337 PMC4342023 · DOI
  29. Choi J. Y. Cho S. J. Park J. H. Yun S. M. Jo C. Kim E. J. (2020). Elevated cerebrospinal fluid and plasma N-Cadherin in Alzheimer disease. J. Neuropathol. Exp. Neurol. 79 484– 492. 10.1093/jnen/nlaa019 32296844 · DOI
  30. Clandinin T. R. Zipursky S. L. (2002). Making connections in the fly visual system. Neuron 35 827– 841. 10.1016/S0896-6273(02)00876-0 12372279 · DOI
  31. Coles E. G. Taneyhill L. A. Bronner-Fraser M. (2007). A critical role for Cadherin6B in regulating avian neural crest emigration. Dev. Biol. 312 533– 544. 10.1016/j.ydbio.2007.09.056 17991460 PMC2266065 · DOI
  32. D’Arcangelo G. Homayouni R. Keshvara L. Rice D. S. Sheldon M. Curran T. (1999). Reelin is a ligand for lipoprotein receptors. Neuron 24 471– 479. 10.1016/S0896-6273(00)80860-0 10571240 · DOI · Paper page
  33. D’Arcangelo G. Miao G. Chen S.-C. Scares H. D. Morgan J. I Curran T. (1995). A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374 719– 723. 10.1038/374719a0 7715726 · DOI · Paper page
  34. Das R. M. Storey K. G. (2014). Apical abscission alters cell polarity and dismantles the primary cilium during neurogenesis. Science 343 200– 204. 10.1126/science.1247521 24408437 PMC4066580 · DOI · Paper page
  35. de Agustín-Durán D. Mateos-White I. Fabra-Beser J. Gil-Sanz C. (2021). Stick around: cell–cell adhesion molecules during neocortical development. Cells 10: 118. 10.3390/cells10010118 33435191 PMC7826847 · DOI
  36. Del Bigio M. R. (1995). The ependyma: a protective barrier between brain and cerebrospinal fluid. Glia 14 1– 13. 10.1002/glia.440140102 7615341 · DOI
  37. Dennhardt J. Ledoux M. S. (2010). Huntington disease in a nonagenarian mistakenly diagnosed as normal pressure hydrocephalus. J. Clin. Neurosci. 17 1066– 1067. 10.1016/j.jocn.2009.11.011 20488711 · DOI
  38. Dietrich P. Shanmugasundaram R. Shuyu E. Dragatsis I. (2009). Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages. Hum. Mol. Genet. 18 142– 150. 10.1093/hmg/ddn324 18838463 PMC3298867 · DOI
  39. Dlugosz P. Nimpf J. (2018). The reelin receptors apolipoprotein e receptor 2 (ApoER2) and VLDL receptor. Int. J. Mol. Sci. 19 1– 22. 10.3390/ijms19103090 30304853 PMC6213145 · DOI · Paper page
  40. Dodman N. H. Karlsson E. K. Moon-Fanelli A. Galdzicka M. Perloski M. Shuster L. (2010). A canine chromosome 7 locus confers compulsive disorder susceptibility. Mol. Psychiatry 15 8– 10. 10.1038/mp.2009.111 20029408 · DOI
  41. Edwards-Lee T. Wen J. Bell J. Hardy J. Chung J. Momeni P. (2006). A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer’s disease. Neurosci. Lett. 398 251– 252. 10.1016/j.neulet.2006.01.006 16469444 · DOI
  42. Elder G. A. Tezapsidis N. Carter J. Shioi J. Bouras C. Li H. C. (1996). Identification and neuron specific expression of the S182/presenilin I protein in human and rodent brains. J. Neurosci. Res 45 308– 320. 10.1002/(sici)1097-4547(19960801)45:3<308::aid-jnr13<3.0.co;2-# 8841992 · DOI
  43. Elia L. P. Yamamoto M. Zang K. Reichardt L. F. (2006). P120 catenin regulates dendritic spine and synapse development through rho-family GTPases and cadherins. Neuron 51 43– 56. 10.1016/j.neuron.2006.05.018 16815331 PMC2587166 · DOI
  44. Elste A. M. Benson D. L. (2006). Structural basis for developmentally regulated changes in cadherin function at synapses. J. Comp. Neurol. 495 324– 335. 10.1002/cne.20876 16440298 · DOI
  45. Erdmann B. Kirsch F.-P. Rathjen F. G. Moré M. I. (2003). N-Cadherin is essential for retinal lamination in the zebrafish. Dev. Dyn. 226 570– 577. 10.1002/dvdy.10266 12619142 · DOI
  46. Escamilla-Ayala A. A. Sannerud R. Mondin M. Poersch K. Vermeire W. Paparelli L. (2020). Super-resolution microscopy reveals majorly mono-and dimeric presenilin1/γ-secretase at the cell surface. Elife 9: e56679. 10.7554/eLife.56679 32631487 PMC7340497 · DOI
  47. Feng Y. Chen M. H. Moskowitz I. P. Mendonza A. M. Vidali L. Nakamura F. (2006). Filamin A (FLNA) is required for cell–cell contact in vascular development and cardiac morphogenesis. Proc. Natl. Acad. Sci. U.S.A. 103 19836– 19841. 10.1073/pnas.0609628104 17172441 PMC1702530 · DOI
  48. Ferland R. J. Batiz L. F. Neal J. Lian G. Bundock E. Lu J. (2009). Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Hum. Mol. Genet. 18 497– 516. 10.1093/hmg/ddn377 18996916 PMC2722192 · DOI
  49. Flanagan L. A. Chou J. Falet H. Neujahr R. Hartwig J. H. Stossel T. P. (2001). Filamin A, the Arp2/3 complex, and the morphology and function of cortical actin filaments in human melanoma cells. J. Cell Biol. 155 511– 518. 10.1083/jcb.200105148 11706047 PMC2198874 · DOI
  50. Franco S. J. Martinez-Garay I. Gil-Sanz C. Harkins-Perry S. R. Müller U. (2011). Reelin regulates cadherin function via Dab1/Rap1 to control neuronal migration and lamination in the neocortex. Neuron 69 482– 497. 10.1016/j.neuron.2011.01.003 21315259 PMC3056352 · DOI
  51. Friocourt G. Kanatani S. Tabata H. Yozu M. Takahashi T. Antypa M. (2008). Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis. J. Neurosci. 28 5794– 5805. 10.1523/JNEUROSCI.1067-08.2008 18509041 PMC6670801 · DOI
  52. Furey C. G. Choi J. Jin S. C. Zeng X. Timberlake A. T. Nelson-Williams C. (2018). De Novo mutation in genes regulating neural stem cell fate in human congenital hydrocephalus. Neuron 99 302.e4– 314.e4. 10.1016/j.neuron.2018.06.019 29983323 PMC7839075 · DOI
  53. Gallardo-Orihuela A. Hervás-Corpión I. Hierro-Bujalance C. Sanchez-Sotano D. Jiménez-Gómez G. Mora-López F. (2019). Transcriptional correlates of the pathological phenotype in a Huntington’s disease mouse model. Sci. Rep. 9: 18696. 10.1038/s41598-019-55177-9 31822756 PMC6904489 · DOI
  54. Gambello M. J. Darling D. L. Yingling J. Tanaka T. Gleeson J. G. Wynshaw-Boris A. (2003). Multiple dose-dependent effects of lis1 on cerebral cortical development. J. Neurosci. 23 1719– 1729. 10.1523/JNEUROSCI.23-05-01719.2003 12629176 PMC6741979 · DOI
  55. Gänzler-Odenthal S. I. I. Redies C. (1998). Blocking N-Cadherin function disrupts the epithelial structure of differentiating neural tissue in the embryonic chicken brain. J. Neurosci. 18 5415– 5425. 10.1523/JNEUROSCI.18-14-05415.1998 9651223 PMC6793493 · DOI
  56. Gärtner A. Fornasiero E. F. Munck S. Vennekens K. Seuntjens E. Huttner W. B. (2012). N-cadherin specifies first asymmetry in developing neurons. EMBO J. 31 1893– 1903. 10.1038/emboj.2012.41 22354041 PMC3343329 · DOI
  57. Gate D. Rodriguez J. Kim G. Breunig J. J. Town T. Danielpour M. (2012). Rapid genetic targeting of pial surface neural progenitors and immature neurons by neonatal electroporation. Neural Dev. 7: 26. 10.1186/1749-8104-7-26 22776033 PMC3479020 · DOI
  58. Geletu M. Adan H. Niit M. Arulanandam R. Carefoot E. Hoskin V. (2022). Erratum: modulation of Akt vs Stat3 activity by the focal adhesion kinase in non-neoplastic mouse fibroblasts (Experimental Cell Research (2021) 404(1), (S0014482721001336), (10.1016/j.yexcr.2021.112601)). Exp. Cell Res. 411: 112731. 10.1016/j.yexcr.2021.112731 33957118 · DOI
  59. Georgakopoulos A. Marambaud P. Efthimiopoulos S. Shioi J. Cui W. Li H. C. (1999). Presenilin-1 forms complexes with the cadherin/catenin cell-cell adhesion system and is recruited to intercellular and synaptic contacts. Mol. Cell 4 893– 902. 10.1016/S1097-2765(00)80219-1 10635315 · DOI
  60. Gil-Sanz C. Franco S. J. Martinez-Garay I. Espinosa A. Harkins-Perry S. Müller U. (2013). Cajal-Retzius cells instruct neuronal migration by coincidence signaling between secreted and contact-dependent guidance cues. Neuron 79 461– 477. 10.1016/j.neuron.2013.06.040 23931996 PMC3774067 · DOI
  61. Gil-Sanz C. Landeira B. Ramos C. Costa M. R. Muller U. (2014). Proliferative defects and formation of a double cortex in mice lacking Mltt4 and Cdh2 in the dorsal telencephalon. J. Neurosci. 34 10475– 10487. 10.1523/JNEUROSCI.1793-14.2014 25100583 PMC4200106 · DOI
  62. Gorlin J. B. Yamin R. Egan S. Stewart M. Stossel T. P. Kwiatkowski D. J. (1990). Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): a molecular leaf spring. J. Cell Biol. 111 1089– 1105. 10.1083/jcb.111.3.1089 2391361 PMC2116286 · DOI
  63. Guerra M. M. Henzi R. Ortloff A. Lichtin N. Vío K. Jiménez A. J. (2015). Cell junction pathology of neural stem cells is associated with ventricular zone disruption, hydrocephalus, and abnormal neurogenesis. J. Neuropathol. Exp. Neurol. 74 653– 671. 10.1097/NEN.0000000000000203 26079447 · DOI
  64. Hack I. Hellwig S. Junghans D. Brunne B. Bock H. H. Zhao S. (2007). Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons. Development 134 3883– 3891. 10.1242/dev.005447 17913789 · DOI
  65. Halperin D. Stavsky A. Kadir R. Drabkin M. Wormser O. Yogev Y. (2021). CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and mice. Nat. Commun. 12: 6187. 10.1038/s41467-021-26426-1 34702855 PMC8548587 · DOI
  66. Handley M. T. Morris-Rosendahl D. J. Brown S. Macdonald F. Hardy C. Bem D. (2013). Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and martsolf syndrome. Hum. Mutat. 34 686– 696. 10.1002/humu.22296 23420520 · DOI
  67. Hart A. W. Morgan J. E. Schneider J. West K. McKie L. Bhattacharya S. (2006). Cardiac malformations and midline skeletal defects in mice lacking filamin A. Hum. Mol. Genet. 15 2457– 2467. 10.1093/hmg/ddl168 16825286 · DOI
  68. Hartmann D. De Strooper B. Serneels L. Craessaerts K. Herreman A. Annaert W. (2002). The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for α-secretase activity in fibroblasts. Hum. Mol. Genet. 11 2615– 2624. 10.1093/hmg/11.21.2615 12354787 · DOI
  69. Hatakeyama J. Wakamatsu Y. Nagafuchi A. Kageyama R. Shigemoto R. Shimamura K. (2014). Cadherin-based adhesions in the apical endfoot are required for active Notch signaling to control neurogenesis in vertebrates. Development 141 1671– 1682. 10.1242/dev.102988 24715457 · DOI
  70. Hatta K. Takeichi M. (1986). Expression of N-cadherin adhesion molecules associated with early morphogenetic events in chick development. Nature 320 447– 449. 10.1038/320447a0 3515198 · DOI
  71. Hawi Z. Tong J. Dark C. Yates H. Johnson B. Bellgrove M. A. (2018). The role of cadherin genes in five major psychiatric disorders: a literature update. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 177 168– 180. 10.1002/ajmg.b.32592 28921840 · DOI
  72. Hickman R. A. Faust P. L. Rosenblum M. K. Marder K. Mehler M. F. Vonsattel J. P. (2021). Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains. Acta Neuropathol. 141 399– 413. 10.1007/s00401-021-02269-4 33517535 PMC7882590 · DOI
  73. Hirano S. Takeichi M. (2012). Cadherins in brain morphogenesis and wiring. Physiol. Rev. 92 597– 634. 10.1152/physrev.00014.2011 22535893 · DOI
  74. Hirotsune S. Fleck M. W. Gambello M. J. Bix G. J. Chen A. Clark G. D. (1998). Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat. Genet. 19 333– 339. 10.1038/1221 9697693 · DOI
  75. Hoe H. S. Kea J. L. Carney R. S. E. Lee J. Markova A. Lee J. Y. (2009). Interaction of reelin with amyloid precursor protein promotes neurite outgrowth. J. Neurosci. 29 7459– 7473. 10.1523/JNEUROSCI.4872-08.2009 19515914 PMC2759694 · DOI · Paper page
  76. Hooli B. V. Kovacs-Vajna Z. M. Mullin K. Blumenthal M. A. Mattheisen M. Zhang C. (2014). Rare autosomal copy number variations in early-onset familial Alzheimer’s disease. Mol. Psychiatry 19 676– 681. 10.1038/mp.2013.77 23752245 · DOI · Paper page
  77. Hor C. H. H. Goh E. L. K. (2018). Rab23 regulates radial migration of projection neurons via N-cadherin. Cereb. Cortex 28 1516– 1531. 10.1093/cercor/bhy018 29420702 PMC6093454 · DOI
  78. Hung C. O. Y. Livesey F. J. (2018). Altered γ-Secretase Processing of APP disrupts lysosome and autophagosome function in monogenic Alzheimer’s disease. Cell Rep. 25 3647.e2– 3660.e2. 10.1016/j.celrep.2018.11.095 30590039 PMC6315085 · DOI · Paper page
  79. Husain M. A. Laurent B. Plourde M. (2021). APOE and Alzheimer’s disease: from lipid transport to physiopathology and therapeutics. Front. Neurosci. 15: 630502. 10.3389/fnins.2021.630502 33679311 PMC7925634 · DOI · Paper page
  80. Iefremova V. Manikakis G. Krefft O. Jabali A. Weynans K. Wilkens R. (2017). An organoid-based model of cortical development identifies non-cell-autonomous defects in wnt signaling contributing to miller-dieker syndrome. Cell Rep. 19 50– 59. 10.1016/j.celrep.2017.03.047 28380362 · DOI · Paper page
  81. Itoh Y. Moriyama Y. Hasegawa T. Endo T. A. Toyoda T. Gotoh Y. (2013). Scratch regulates neuronal migration onset via an epithelial-mesenchymal transition-like mechanism. Nat. Neurosci. 16 416– 425. 10.1038/nn.3336 23434913 · DOI
  82. Jang C. Choi J. Na Y. Jang B. Wasco W. Buxbaum J. D. (2011). Calsenilin regulates presenilin 1/γ−secretase-mediated N-cadherin ∈-cleavage and β−catenin signaling. FASEB J. 25 4174– 4183. 10.1096/fj.11-185926 21852538 · DOI
  83. Jiang Y. J. Brand M. Heisenberg C. P. Beuchle D. Furutani-Seiki M. Kelsh R. N. (1996). Mutations affecting neurogenesis and brain morphology in the zebrafish, Danio rerio. Development 123 205– 216. 10.1242/dev.123.1.205 9007241 · DOI
  84. Jontes J. D. (2018). The cadherin superfamily in neural circuit assembly. Cold Spring Harb. Perspect. Biol. 10: a029306. 10.1101/cshperspect.a029306 28778868 PMC6028066 · DOI
  85. Jorissen E. Prox J. Bernreuther C. Weber S. Schwanbeck R. Serneels L. (2010). The disintegrin/metalloproteinase ADAM10 is essential for the establishment of the brain cortex. J. Neurosci. 30 4833– 4844. 10.1523/JNEUROSCI.5221-09.2010 20371803 PMC2921981 · DOI · Paper page
  86. Jossin Y. (2020). Reelin functions, mechanisms of action and signaling pathways during brain development and maturation. Biomolecules 10: 964. 10.3390/biom10060964 32604886 PMC7355739 · DOI
  87. Jüngling K. Eulenburg V. Moore R. Kemler R. Lessmann V. Gottmann K. (2006). N-cadherin transsynaptically regulates short-term plasticity at glutamatergic synapses in embryonic stem cell-derived neurons. J. Neurosci. 26 6968– 6978. 10.1523/JNEUROSCI.1013-06.2006 16807326 PMC6673917 · DOI
  88. Juric-sekhar G. Hevner R. F. (2019). Malformations of cerebral cortex development: molecules and mechanisms. Annu. Rev. Pathol. 14 293– 318. 10.1146/annurev-pathmechdis-012418-012927 30677308 PMC6938687 · DOI
  89. Kadowaki M. Nakamura S. Machon O. Krauss S. Radice G. L. Takeichi M. (2007). N-cadherin mediates cortical organization in the mouse brain. Dev. Biol. 304 22– 33. 10.1016/j.ydbio.2006.12.014 17222817 · DOI
  90. Kahle K. T. Kulkarni A. V, Jr. Limbrick D. D. Warf B. C. (2016). Hydrocephalus in children. Lancet 387 788– 799. 10.1016/S0140-6736(15)60694-8 26256071 · DOI
  91. Kanjee M. Yuce Kahraman C. Ercoskun P. Tatar A. Kahraman M. (2022). A Novel nonsense variant in the CDH2 gene associated with ACOGS: a case report. Am. J. Med. Genet. Part A 188 2815– 2818. 10.1002/ajmg.a.62861 35708058 · DOI
  92. Kawauchi T. Sekine K. Shikanai M. Chihama K. Tomita K. Kubo K. I. (2010). Rab GTPases-dependent endocytic pathways regulate neuronal migration and maturation through N-cadherin trafficking. Neuron 67 588– 602. 10.1016/j.neuron.2010.07.007 20797536 · DOI
  93. Keryer G. Pineda J. R. Liot G. Kim J. Dietrich P. Benstaali C. (2011). Ciliogenesis is regulated by a huntingtin-HAP1-PCM1 pathway and is altered in Huntington disease. J. Clin. Invest. 121 4372– 4382. 10.1172/JCI57552 21985783 PMC3223861 · DOI · Paper page
  94. Khalesi R. Razmara E. Asgaritarghi G. Tavasoli A. R. Riazalhosseini Y. Auld D. (2021). Novel manifestations of Warburg micro syndrome type 1 caused by a new splicing variant of RAB3GAP1: a case report. BMC Neurol. 21: 180. 10.1186/s12883-021-02204-w 33910511 PMC8080372 · DOI
  95. Kim W. Shen J. (2008). Presenilins are required for maintenance of neural stem cells in the developing brain. Mol. Neurodegener. 3: 2. 10.1186/1750-1326-3-2 18182109 PMC2235867 · DOI
  96. Kitamura K. Yanazawa M. Sugiyama N. Miura H. Iizuka-Kogo A. Kusaka M. (2002). Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans. Nat. Genet. 32 359– 369. 10.1038/ng1009 12379852 · DOI
  97. Ko H. Kim S. Jin C. H. Lee E. Ham S. Yook J. I. (2012). Protein kinase casein kinase 2-mediated upregulation of N-cadherin confers anoikis resistance on esophageal carcinoma cells. Mol. Cancer Res. 10 1032– 1038. 10.1158/1541-7786.MCR-12-0261 22767590 · DOI
  98. Kwon Y. T. Gupta A. Zhou Y. Nikolic M. Tsai L. (2000). Regulation of N-cadherin-mediated adhesion by the p35–Cdk5 kinase. Curr. Biol. 10 363– 372. 10.1016/S0960-9822(00)00411-5 10753743 · DOI
  99. László Z. I. Bercsényi K. Mayer M. Lefkovics K. Szabó G. Katona I. (2020a). N-cadherin (Cdh2) maintains migration and postmitotic survival of cortical interneuron precursors in a cell-type-specific manner. Cereb. Cortex 30 1318– 1329. 10.1093/cercor/bhz168 31402374 PMC7219024 · DOI
  100. László Z. I. Lele Z. Zöldi M. Miczán V. Mógor F. Simon G. M. (2020b). ABHD4-dependent developmental anoikis safeguards the embryonic brain. Nat. Commun. 11: 4363. 10.1038/s41467-020-18175-4 32868797 PMC7459116 · DOI
  101. Lazarov O. Peterson L. D. Peterson D. A. Sisodia S. S. (2006). Expression of a familial Alzheimer’s disease-linked presenilin-1 variant enhances perforant pathway lesion-induced neuronal loss in the entorhinal cortex. J. Neurosci. 26 429– 434. 10.1523/JNEUROSCI.3961-05.2006 16407539 PMC6674394 · DOI
  102. Lefkovics K. Mayer M. Bercsényi K. Szabó G. Lele Z. (2012). Comparative analysis of type II classic cadherin mRNA distribution patterns in the developing and adult mouse somatosensory cortex and hippocampus suggests significant functional redundancy. J. Comp. Neurol. 520 1387– 1405. 10.1002/cne.22801 22102170 · DOI
  103. Lele Z. Folchert A. Concha M. Rauch G.-J. Geisler R. Rosa F. (2002). Parachute/N-Cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube. Development 129 3281– 3294. 10.1242/dev.129.14.3281 12091300 · DOI
  104. Lelièvre E. C. Plestant C. Boscher C. Wolff E. Mège R.-M. Birbes H. (2012). N-Cadherin mediates neuronal cell survival through bim down-regulation. PLoS One 7: e33206. 10.1371/journal.pone.0033206 22427990 PMC3299760 · DOI
  105. Li M. Cui Z. Niu Y. Liu B. Fan W. Yu D. (2010). Synaptogenesis in the developing mouse visual cortex. Brain Res. Bull. 81 107– 113. 10.1016/j.brainresbull.2009.08.028 19751806 · DOI
  106. Li W. Q. Luo L. Hu Z. W. Lyu T. J. Cen C. Wang Y. (2019). PLD1 promotes dendritic spine morphogenesis via activating PKD1. Mol. Cell. Neurosci. 99: 103394. 10.1016/j.mcn.2019.103394 31356881 · DOI
  107. Liegel R. P. Handley M. T. Ronchetti A. Brown S. Langemeyer L. Linford A. (2013). Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and warburg micro syndrome in humans. Am. J. Hum. Genet. 93 1001– 1014. 10.1016/j.ajhg.2013.10.011 24239381 PMC3852926 · DOI
  108. Lien W.-H. (2006). E-Catenin controls cerebral cortical size by regulating the hedgehog signaling pathway. Science. 311 1609– 1612. 10.1126/science.1121449 16543460 PMC2556178 · DOI
  109. Linford A. Yoshimura S. Bastos R. N. Langemeyer L. Gerondopoulos A. Rigden D. J. (2012). Rab14 and its exchange factor FAM116 link endocytic recycling and adherens junction stability in migrating cells. Dev. Cell 22 952– 966. 10.1016/j.devcel.2012.04.010 22595670 PMC3383995 · DOI
  110. Liu D. Cao H. Kural K. C. Fang Q. Zhang F. (2019). Integrative analysis of shared genetic pathogenesis by autism spectrum disorder and obsessive-compulsive disorder. Biosci. Rep. 39: BSR20191942. 10.1042/BSR20191942 31808517 PMC6928520 · DOI
  111. Lopez-Font I. Iborra-Lazaro G. Sánchez-Valle R. Molinuevo J. L. Cuchillo-Ibanez I. Sáez-Valero J. (2019). CSF-ApoER2 fragments as a read-out of reelin signaling: distinct patterns in sporadic and autosomal-dominant Alzheimer disease. Clin. Chim. Acta 490 6– 11. 10.1016/j.cca.2018.12.012 30552869 · DOI
  112. Luccardini C. Hennekinne L. Viou L. Yanagida M. Murakami F. Kessaris N. (2013). N-Cadherin sustains motility and polarity of future cortical interneurons during tangential migration. J. Neurosci. 33 18149– 18160. 10.1523/JNEUROSCI.0593-13.2013 24227724 PMC3858641 · DOI
  113. Luccardini C. Leclech C. Viou L. Rio J.-P. Métin C. (2015). Cortical interneurons migrating on a pure substrate of N-cadherin exhibit fast synchronous centrosomal and nuclear movements and reduced ciliogenesis. Front. Cell. Neurosci. 9: 286. 10.3389/fncel.2015.00286 26283922 PMC4522564 · DOI
  114. Luo L. Da Li G. Wang Y. (2017). PLD1 promotes dendritic spine development by inhibiting ADAM10-mediated N-cadherin cleavage. Sci. Rep. 7: 6035. 10.1038/s41598-017-06121-2 28729535 PMC5519554 · DOI
  115. Luo Y. Ferreira-Cornwell M. C. Baldwin H. S. Kostetskii I. Lenox J. M. Lieberman M. (2001). Rescuing the N-cadherin knockout by cardiac-specific expression of N- or E-cadherin. Development 128 459– 469. 10.1242/dev.128.4.459 11171330 · DOI
  116. Malicki J. Jo H. Pujic Z. (2003). Zebrafish N-cadherin, encoded by the glass onion locus, plays an essential role in retinal patterning. Dev. Biol. 259 95– 108. 10.1016/S0012-1606(03)00181-7 12812791 · DOI
  117. Marambaud P. Wen P. H. Dutt A. Shioi J. Takashima A. Siman R. (2003). A CBP binding transcriptional repressor produced by the PS1/ε-cleavage of N-Cadherin is inhibited by PS1 FAD mutations. Cell 114 635– 645. 10.1016/j.cell.2003.08.008 13678586 · DOI
  118. Martinez-Garay I. (2020). Molecular mechanisms of cadherin function during cortical migration. Front. Cell Dev. Biol. 8: 588152. 10.3389/fcell.2020.588152 33043020 PMC7523180 · DOI
  119. Masai I. (2003). N-cadherin mediates retinal lamination, maintenance of forebrain compartments and patterning of retinal neurites. Development 130 2479– 2494. 10.1242/dev.00465 12702661 · DOI
  120. Masai I. Lele Z. Yamaguchi M. Komori A. Nakata A. Nishiwaki Y. (2003). N-cadherin mediates retinal lamination, maintenance of forebrain compartments and patterning of retinal neurites. Development 130 2479– 2494. 12702661
  121. Matsunaga M. Hatta K. Takeichi M. (1988). Role of N-cadherin cell adhesion molecules in the histogenesis of neural retina. Neuron 1 289– 295. 10.1016/0896-6273(88)90077-3 3078519 · DOI
  122. Matsunaga Y. Noda M. Murakawa H. Hayashi K. Nagasaka A. Inoue S. (2017). Reelin transiently promotes N-cadherin-dependent neuronal adhesion during mouse cortical development. Proc. Natl. Acad. Sci. U.S.A. 114 2048– 2053. 10.1073/pnas.1615215114 28174271 PMC5338414 · DOI
  123. Mayer M. Bercsényi K. Géczi K. Szabó G. Lele Z. (2010). Expression of two type II cadherins, Cdh12 and Cdh22 in the developing and adult mouse brain. Gene Expr. Patterns 10 351– 360. 10.1016/j.gep.2010.08.002 20723620 · DOI
  124. McGregor N. W. Lochner C. Stein D. J. Hemmings S. M. J. (2015). Polymorphisms within the neuronal cadherin (CDH2) gene are associated with obsessive-compulsive disorder (OCD) in a South African cohort. Metab. Brain Dis. 31 191– 196. 10.1007/s11011-015-9693-x 26093892 · DOI
  125. Mège R. M. Ishiyama N. (2017). Integration of cadherin adhesion and cytoskeleton at adherens junctions. Cold Spring Harb. Perspect. Biol. 9: a028738. 10.1101/cshperspect.a028738 28096263 PMC5411698 · DOI
  126. Mendez P. De Roo M. Poglia L. Klauser P. Muller D. (2010). N-cadherin mediates plasticity-induced long-term spine stabilization. J. Cell Biol. 189 589– 600. 10.1083/jcb.201003007 20440002 PMC2867305 · DOI
  127. Miyamoto Y. Sakane F. Hashimoto K. (2015). N-cadherin-based adherens junction regulates the maintenance, proliferation, and differentiation of neural progenitor cells during development. Cell Adh. Migr. 9 183– 192. 10.1080/19336918.2015.1005466 25869655 PMC4594476 · DOI
  128. Molero A. E. Arteaga-bracho E. E. Chen C. H. Gulinello M. (2016). Selective expression of mutant huntingtin during development recapitulates characteristic features of Huntington’s disease. Proc. Natl. Acad. Sci. U.S.A. 113 5736– 5741. 10.1073/pnas.1603871113 27140644 PMC4878495 · DOI
  129. Molina-Calavita M. Barnat M. Elias S. Aparicio E. Piel M. Humbert S. (2014). Mutant huntingtin affects cortical progenitor cell division and development of the mouse neocortex. J. Neurosci. 34 10034– 10040. 10.1523/JNEUROSCI.0715-14.2014 25057205 PMC6608303 · DOI
  130. Morris-Rosendahl D. J. Segel R. Born A. P. Conrad C. Loeys B. Brooks S. S. (2010). New RAB3GAP1 mutations in patients with warburg micro syndrome from different ethnic backgrounds and a possible founder effect in the Danish. Eur. J. Hum. Genet. 18 1100– 1106. 10.1038/ejhg.2010.79 20512159 PMC2987448 · DOI
  131. Moya P. R. Dodman N. H. Timpano K. R. Rubenstein L. M. Rana Z. Fried R. L. (2013). Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes. Eur. J. Hum. Genet. 21 850– 854. 10.1038/ejhg.2012.245 23321619 PMC3722668 · DOI
  132. Mysore S. P. Tai C. Y. Schuman E. M. (2007). Effects of N-cadherin disruption on spine morphological dynamics. Front. Cell. Neurosci. 1: 1. 10.3389/neuro.03.001.2007 18946519 PMC2525931 · DOI
  133. Nadarajah B. Brunstrom J. E. Grutzendler J. Wong R. O. L. Pearlman A. L. (2001). Two modes of radial migration in early development of the cerebral cortex. Nat. Neurosci. 4 143– 150. 10.1038/83967 11175874 · DOI
  134. Nakagawa S. Takeichi M. (1995). Neural crest cell-cell adhesion controlled by sequential and subpopulation-specific expression of novel cadherins. Development 121 1321– 1332. 10.1242/dev.121.5.1321 7540531 · DOI
  135. Nakagawa S. Takeichi M. (1998). Neural crest emigration from the neural tube depends on regulated cadherin expression. Development 125 2963– 2971. 9655818
  136. Nazaryan L. Bertelsen B. Padmanabhuni S. S. Debes N. M. LuCamp, Have C. T. (2015). Association study between CDH2 and Gilles de la Tourette syndrome in a Danish cohort. Psychiatry Res. 228 974– 975. 10.1016/j.psychres.2015.05.010 26032459 · DOI
  137. Neugebauer K. M. Tomaselli K. J. Lilien J. Reichardt L. F. (1988). N-cadherin, NCAM, and integrins promote retinal neurite outgrowth on astrocytes in vitro. J. Cell Biol. 107 1177– 1187. 10.1083/jcb.107.3.1177 3262111 PMC2115273 · DOI
  138. Niethammer M. Smith D. S. Ayala R. Peng J. Ko J. Lee M. (2000). NUDEL Is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein. Neuron 28 697– 711. 10.1016/S0896-6273(00)00147-1 11163260 · DOI
  139. Noctor S. C. Martinez-Cerdeño V. Ivic L. Kriegstein A. R. (2004). Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nat. Neurosci. 7 136– 144. 10.1038/nn1172 14703572 · DOI · Paper page
  140. Nuriya M. Huganir R. L. (2006). Regulation of AMPA receptor trafficking by N-cadherin. J. Neurochem. 97 652– 661. 10.1111/j.1471-4159.2006.03740.x 16515543 · DOI
  141. OECD/EU (2018). Health at a Glance: Europe 2018: State of Health in the EU Cycle. Paris: OECD Publishing. 10.1787/health_glance_eur-2018-en · DOI
  142. Okamura K. Tanaka H. Yagita Y. Saeki Y. Taguchi A. Hiraoka Y. (2004). Cadherin activity is required for activity-induced spine remodeling. J. Cell Biol. 167 961– 972. 10.1083/jcb.200406030 15569714 PMC2172468 · DOI
  143. Oliver C. González C. A. Alvial G. Flores C. A. Rodríguez E. M. Bátiz L. F. (2013). Disruption of CDH2/N-cadherin-based adherens junctions leads to apoptosis of ependymal cells and denudation of brain ventricular walls. J. Neuropathol. Exp. Neurol. 72 846– 860. 10.1097/NEN.0b013e3182a2d5fe 23965744 · DOI
  144. Padmanabhan P. Kneynsberg A. Götz J. (2021). Super-resolution microscopy: a closer look at synaptic dysfunction in Alzheimer disease. Nat. Rev. Neurosci. 22 723– 740. 10.1038/s41583-021-00531-y 34725519 · DOI
  145. Pagnamenta A. T. Khan H. Walker S. Gerrelli D. Wing K. Bonaglia M. C. (2011). Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. J. Med. Genet. 48 48– 54. 10.1136/jmg.2010.079426 20972252 PMC3003876 · DOI
  146. Paoli P. Giannoni E. Chiarugi P. (2013). Anoikis molecular pathways and its role in cancer progression. Biochim. Biophys. Acta Mol. Cell Res. 1833 3481– 3498. 10.1016/j.bbamcr.2013.06.026 23830918 · DOI · Paper page
  147. Park C. Falls W. Finger J. H. Longo-Guess C. M. Ackerman S. L. (2002). Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation. Nat. Genet. 31 279– 284. 10.1038/ng908 12089526 · DOI
  148. Park K. S. Gumbiner B. M. (2010). Cadherin 6B induces BMP signaling and de-epithelialization during the epithelial mesenchymal transition of the neural crest. Development 137 2691– 2701. 10.1242/dev.050096 20610481 PMC2910385 · DOI
  149. Peglion F. Llense F. Etienne-manneville S. (2014). Adherens junction treadmilling during collective migration. Nat. Cell. Biol. 16 639– 651. 10.1038/ncb2985 24929360 · DOI
  150. Picascia M. Zangaglia R. Bernini S. Minafra B. Sinforiani E. Pacchetti C. (2015). A review of cognitive impairment and differential diagnosis in idiopathic normal pressure hydrocephalus. Funct. Neurol. 30 217– 228. 10.11138/fneur/2015.30.4.217 26727700 PMC4758774 · DOI
  151. Pielarski K. N. van Stegen B. Andreyeva A. Nieweg K. Jüngling K. Redies C. (2013). Asymmetric N-Cadherin expression results in synapse dysfunction. Synapse elimination, and axon retraction in cultured mouse neurons. PLoS One 8: e54105. 10.1371/journal.pone.0054105 23382872 PMC3561303 · DOI
  152. Piprek R. P. Kolasa M. Podkowa D. Kloc M. Kubiak J. Z. (2019). N-Cadherin is critical for the survival of germ cells, the formation of steroidogenic cells, and the architecture of developing mouse gonads. Cells 8: 1610. 10.3390/cells8121610 31835801 PMC6952792 · DOI
  153. Plachez C. Andrews W. Liapi A. Knoell B. Drescher U. Mankoo B. (2008). Robos are required for the correct targeting of retinal ganglion cell axons in the visual pathway of the brain. Mol. Cell. Neurosci. 37 719– 730. 10.1016/j.mcn.2007.12.017 18272390 · DOI
  154. Plump A. S. Erskine L. Sabatier C. Brose K. Epstein C. J. Goodman C. S. (2002). Slit1 and Slit2 cooperate to prevent premature midline crossing of retinal axons in the mouse visual system. Neuron 33 219– 232. 10.1016/S0896-6273(01)00586-4 11804570 · DOI
  155. Pollarolo G. Schulz J. G. Munck S. Dotti C. G. (2011). Cytokinesis remnants define first neuronal asymmetry in vivo. Nat. Neurosci. 14 1525– 1534. 10.1038/nn.2976 22081156 · DOI
  156. Priller C. Dewachter I. Vassallo N. Paluch S. Pace C. Kretzschmar H. A. (2007). Mutant presenilin 1 alters synaptic transmission in cultured hippocampal neurons. J. Biol. Chem. 282 1119– 1127. 10.1074/jbc.M605066200 17088253 · DOI
  157. Qian S. Jiang P. Guan X. M. Singh G. Trumbauer M. E. Yu H. (1998). Mutant human presenilin 1 protects presenilin 1 null mouse against embryonic lethality and elevates Aβ1-42/43 expression. Neuron 20 611– 617. 10.1016/S0896-6273(00)80999-X 9539133 · DOI
  158. Quillé M. L. Carat S. Quéméner-Redon S. Hirchaud E. Baron D. Benech C. (2011). High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies. PLoS One 6: e25181. 10.1371/journal.pone.0025181 21966449 PMC3178625 · DOI
  159. Radice G. L. Rayburn H. Matsunami H. Knudsen K. A. Takeichi M. Hynes R. O. (1997). Developmental defects in mouse embryos lacking N-cadherin. Dev. Biol. 181 64– 78. 10.1006/dbio.1996.8443 9015265 · DOI
  160. Rajendran L. Paolicelli R. C. (2018). Microglia-mediated synapse loss in Alzheimer’s disease. J. Neurosci. 38 2911– 2919. 10.1523/JNEUROSCI.1136-17.2017 29563239 PMC6596066 · DOI · Paper page
  161. Ramsden C. E. Keyes G. S. Calzada E. Horowitz M. S. Zamora D. Jahanipour J. (2022). Lipid peroxidation induced ApoE receptor-ligand disruption as a unifying hypothesis underlying sporadic Alzheimer’s disease in humans. J. Alzheimers Dis. 87 1251– 1290. 10.3233/JAD-220071 35466940 PMC9268955 · DOI · Paper page
  162. Ranscht B. Dours-Zimmermann M. T. (1991). T-cadherin, a novel cadherin cell adhesion molecule in the nervous system lacks the conserved cytoplasmic region. Neuron 7 391– 402. 10.1016/0896-6273(91)90291-7 1654948 · DOI
  163. Rasin M.-R. Gazula V.-R. Breunig J. J. Kwan K. Y. Johnson M. B. Liu-Chen S. (2007). Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors. Nat. Neurosci. 10 819– 827. 10.1038/nn1924 17589506 · DOI
  164. Ray H. Chang C. (2020). The transcription factor Hypermethylated in Cancer 1 (Hic1) regulates neural crest migration via interaction with Wnt signaling. Dev. Biol. 463 169– 181. 10.1016/j.ydbio.2020.05.012 32502469 PMC7437249 · DOI
  165. Rebman J. K. Kirchoff K. E. Walsh G. S. (2016). Cadherin-2 is required cell autonomously for collective migration of facial branchiomotor neurons. PLoS One 11: e0164433. 10.1371/journal.pone.0164433 27716840 PMC5055392 · DOI
  166. Redies C. (1997). Cadherins and the formation of neural circuitry in the vertebrate CNS. Cell Tissue Res. 290 405– 413. 10.1007/s004410050947 9321704 · DOI
  167. Redies C. Hertel N. Hübner C. A. (2012). Cadherins and neuropsychiatric disorders. Brain Res. 1470 130– 144. 10.1016/j.brainres.2012.06.020 22765916 · DOI
  168. Reis L. M. Houssin N. S. Zamora C. Abdul-Rahman O. Kalish J. M. Zackai E. H. (2020). Novel variants in CDH2 are associated with a new syndrome including Peters anomaly. Clin. Genet. 97 502– 508. 10.1111/cge.13660 31650526 PMC7028510 · DOI
  169. Reiss K. Maretzky T. Ludwig A. Tousseyn T. De Strooper B. Hartmann D. (2005). ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling. EMBO J. 24 742– 752. 10.1038/sj.emboj.7600548 15692570 PMC549617 · DOI
  170. Rhee J. Buchan T. Zukerberg L. Lilien J. Balsamo J. (2007). Cables links Robo-bound Abl kinase to N-cadherin-bound β-catenin to mediate Slit-induced modulation of adhesion and transcription. Nat. Cell Biol. 9 883– 892. 10.1038/ncb1614 17618275 · DOI
  171. Rhee J. Mahfooz N. S. Arregui C. Lilien J. Balsamo J. VanBerkum M. F. A. (2002). Activation of the repulsive receptor roundabout inhibits N-cadherin-mediated cell adhesion. Nat. Cell Biol. 4 798– 805. 10.1038/ncb858 12360290 · DOI
  172. Riehl R. Johnson K. Bradley R. Grunwald G. B. Cornel E. Lilienbaum A. (1996). Cadherin function is required for axon outgrowth in retinal ganglion cells in vivo. Neuron 17 837– 848. 10.1016/S0896-6273(00)80216-0 8938117 · DOI
  173. Rivero O. Selten M. M. Sich S. Popp S. Bacmeister L. Amendola E. (2015). Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition. Transl. Psychiatry 5: e655. 10.1038/tp.2015.152 26460479 PMC4930129 · DOI
  174. Rousso D. L. Pearson C. A. Gaber Z. B. Miquelajauregui A. Li S. Portera-Cailliau C. (2012). Foxp-Mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS. Neuron 74 314– 330. 10.1016/j.neuron.2012.02.024 22542185 PMC3444171 · DOI
  175. Roy A. Murphy R. M. Deng M. MacDonald J. W. Bammler T. K. Aldinger K. A. (2019). PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice. Elife 8: e45961. 10.7554/eLife.45961 31094678 PMC6544437 · DOI
  176. Sáez-Valero J. Costell M. Sjögren M. Andreasen N. Blennow K. Luque J. M. (2003). Altered levels of cerebrospinal fluid reelin in frontotemporal dementia and Alzheimer’s disease. J. Neurosci. Res. 72 132– 136. 10.1002/jnr.10554 12645087 · DOI
  177. Saglietti L. Dequidt C. Kamieniarz K. Rousset M. C. Valnegri P. Thoumine O. (2007). Extracellular interactions between GluR2 and N-Cadherin in spine regulation. Neuron 54 461– 477. 10.1016/j.neuron.2007.04.012 17481398 · DOI · Paper page
  178. Sakai N. Insolera R. Sillitoe R. V. Shi S. H. Kaprielian Z. (2012). Axon sorting within the spinal cord marginal zone via Robo-mediated inhibition of N-cadherin controls spinocerebellar tract formation. J. Neurosci. 32 15377– 15387. 10.1523/JNEUROSCI.2225-12.2012 23115176 PMC3511830 · DOI
  179. Sanes J. R. Zipursky S. L. (2020). Synaptic specificity, recognition molecules, and assembly of neural circuits. Cell 181 536– 556. 10.1016/j.cell.2020.04.008 32359437 · DOI
  180. Sasaki S. Shionoya A. Ishida M. Gambello M. J. Yingling J. Wynshaw-Boris A. (2000). A LIS1/NUDEL/Cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron 28 681– 696. 10.1016/S0896-6273(00)00146-X 11163259 · DOI
  181. Schiffmacher A. T. Padmanabhan R. Jhingory S. Taneyhill L. A. (2014). Cadherin-6B is proteolytically processed during epithelial-to-mesenchymal transitions of the cranial neural crest. Mol. Biol. Cell 25 41– 54. 10.1091/mbc.E13-08-0459 24196837 PMC3873892 · DOI
  182. Schirinzi T. Sancesario G. M. Ialongo C. Imbriani P. Madeo G. Toniolo S. (2015). A clinical and biochemical analysis in the differential diagnosis of idiopathic normal pressure hydrocephalus. Front. Neurol. 6: 86. 10.3389/fneur.2015.00086 25954245 PMC4407581 · DOI
  183. Schmid M.-T. Weinandy F. Wilsch-Bräuninger M. Huttner W. B. Cappello S. Götz M. (2014). The role of α-E-catenin in cerebral cortex development: radial glia specific effect on neuronal migration. Front. Cell. Neurosci. 8: 215. 10.3389/fncel.2014.00215 25147501 PMC4124588 · DOI
  184. Schrick C. Fischer A. Srivastava D. P. Tronson N. C. Penzes P. Radulovic J. (2007). N-Cadherin regulates cytoskeletally associated IQGAP1/ERK signaling and memory formation. Neuron 55 786– 798. 10.1016/j.neuron.2007.07.034 17785185 PMC2064867 · DOI
  185. Sekine K. Honda T. Kawauchi T. Kubo K. Nakajima K. (2011). The outermost region of the developing cortical plate is crucial for both the switch of the radial migration mode and the dab1-dependent “inside-out” lamination in the neocortex. J. Neurosci. 31 9426– 9439. 10.1523/JNEUROSCI.0650-11.2011 21697392 PMC6623472 · DOI
  186. Sela-Donenfeld D. Kalcheim C. (1999). Regulation of the onset of neural crest migration by coordinated activity of BMP4 and Noggin in the dorsal neural tube. Development 126 4749– 4762. 10.1242/dev.126.21.4749 10518492 · DOI
  187. Shen J. Bronson R. T. Chen D. F. Xia W. Selkoe D. J. Tonegawa S. (1997). Skeletal and CNS defects in presenilin-1-deficient mice. Cell 89 629– 639. 10.1016/S0092-8674(00)80244-5 9160754 · DOI · Paper page
  188. Shieh J. C. Schaar B. T. Srinivasan K. Brodsky F. M. McConnell S. K. (2011). Endocytosis regulates cell soma translocation and the distribution of adhesion proteins in migrating neurons. PLoS One 6: e17802. 10.1371/journal.pone.0017802 21445347 PMC3062553 · DOI
  189. Shikanai M. Nakajima K. Kawauchi T. (2011). N-Cadherin regulates radial glial fiber-dependent migration of cortical locomoting neurons. Commun. Integr. Biol. 4 326– 330. 10.4161/cib.4.3.14886 21980571 PMC3187899 · DOI
  190. Shoval I. Ludwig A. Kalcheim C. (2006). Antagonistic roles of full-length N-cadherin and its soluble BMP cleavage product in neural crest delamination. Development 134 491– 501. 10.1242/dev.02742 17185320 · DOI
  191. Singh S. Solecki D. J. (2015). Polarity transitions during neurogenesis and germinal zone exit in the developing central nervous system. Front. Cell. Neurosci. 9: 62. 10.3389/fncel.2015.00062 25852469 PMC4349153 · DOI
  192. Sival D. A. Guerra M. Den Dunnen W. F. A. Bátiz L. F. Alvial G. Castañeyra-Perdomo A. (2011). Neuroependymal denudation is in progress in full-term human foetal spina bifida aperta. Brain Pathol. 21 163– 179. 10.1111/j.1750-3639.2010.00432.x 21269337 PMC8094240 · DOI
  193. Soriano E. Del Río J. A. (2005). The cells of cajal-retzius: still a mystery one century after. Neuron 46 389– 394. 10.1016/j.neuron.2005.04.019 15882637 · DOI
  194. Southwell D. G. Paredes M. F. Galvao R. P. Jones D. L. Froemke R. C. Sebe J. Y. (2012). Intrinsically determined cell death of developing cortical interneurons. Nature 491 109– 113. 10.1038/nature11523 23041929 PMC3726009 · DOI · Paper page
  195. Spassky N. (2005). Adult ependymal cells are postmitotic and are derived from radial glial cells during embryogenesis. J. Neurosci. 25 10– 18. 10.1523/JNEUROSCI.1108-04.2005 15634762 PMC6725217 · DOI · Paper page
  196. Stan A. Pielarski K. N. Brigadski T. Wittenmayer N. Fedorchenko O. Gohla A. (2010). Essential cooperation of N-cadherin and neuroligin-1 in the transsynaptic control of vesicle accumulation. Proc. Natl. Acad. Sci. U.S.A. 107 11116– 11121. 10.1073/pnas.0914233107 20534458 PMC2890764 · DOI
  197. Stocker A. M. Chenn A. (2009). Focal reduction of αE-catenin causes premature differentiation and reduction of β-catenin signaling during cortical development. Dev. Biol. 328 66– 77. 10.1016/j.ydbio.2009.01.010 19389371 PMC2674140 · DOI
  198. Subramanian J. Savage J. C. Tremblay M. È (2020). Synaptic loss in Alzheimer’s disease: mechanistic insights provided by two-photon in vivo imaging of transgenic mouse models. Front. Cell. Neurosci. 14: 592607. 10.3389/fncel.2020.592607 33408613 PMC7780885 · DOI
  199. Szabó A. Mayor R. (2018). Mechanisms of neural crest migration. Annu. Rev. Genet. 52 43– 63. 10.1146/annurev-genet-120417-031559 30476447 · DOI
  200. Tabrizi S. J. Flower M. D. Ross C. A. Wild E. J. (2020). Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities. Nat. Rev. Neurol. 16 529– 546. 10.1038/s41582-020-0389-4 32796930 · DOI

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Sorted by citations

Authors
László, Z. I., & Lele, Z.
Affiliations
  • University of Dundee (GB)
  • HUN-REN Institute of Experimental Medicine (HU)
Corresponding author
Lele, Zsolt
Venue
Frontiers in Neuroscience
Published
2022-09-23
Volume
16
Pages
972059-972059
ISSN
1662-453X (ISSN-L)
OpenAlex
W4296995576
Cited by
49
References
8
Citations by year
2026: 15 · 2025: 15 · 2024: 13 · 2023: 6
FWCI
1.33
Type
journal article
Language
en
Open access
Locations
  • Frontiers in Neuroscience (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Repository of the Academy's Library (Library of the Hungarian Academy of Sciences) (acceptedVersion)
  • Discovery Research Portal (University of Dundee) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Motor Neurone Disease Association (Laszlo/Oct21/977-799)
  • Nemzeti Kutatási, Fejlesztési és Innovaciós Alap (2017-1.2.1-NKP-2017-00002)
Topics
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
N-cadherin, adhesion molecules, β-catenin signaling, brain development, neurodegenerative diseases, neural tube closure, axon guidance, synaptic development

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