Regulation of Nogo and Nogo receptor during the development of the entorhino-hippocampal pathway and after adult hippocampal lesions

Molecular and Cellular Neuroscience

Volumn 26, Issue 1, 2004, Pages 34-49

  Mingorance, Ana ^a   Fontana, Xavier ^a   Solé, Marta ^a   Burgaya, Ferran ^a   Ureña, Jesús M ^a   Teng, Felicia Y H ^b   Tang, Bor Luen ^b   Hunt, David ^c   Anderson, Patrick N ^c   Bethea, John R ^d   Schwab, Martin E ^e   Soriano, Eduardo ^a   Del Río, José A ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b INSTITUTE OF MOLECULAR AND CELL BIOLOGY   (Singapore)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY OF MIAMI   (United States)

^e University of Zurich Brain Research Institute   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

KAINIC ACID; MESSENGER RNA; NOGO RECEPTOR; PROTEIN NOGO A; RECEPTOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASTROCYTE; BRAIN CELL; BRAIN DEVELOPMENT; BRAIN INJURY; CELL TYPE; CEREBELLUM; CONTROLLED STUDY; EMBRYO; ENTORHINAL CORTEX; FEMALE; FETUS; GRANULE CELL; HIPPOCAMPUS; MATURATION; MOUSE; NEWBORN; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RAT; REGULATORY MECHANISM;

ANIMALS; ANIMALS, NEWBORN; ANTIBODIES; ASTROCYTES; BRAIN INJURIES; COS CELLS; ENTORHINAL CORTEX; FETUS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GLIOSIS; GROWTH CONES; HIPPOCAMPUS; KAINIC ACID; MICE; MYELIN PROTEINS; NERVE REGENERATION; NEURONAL PLASTICITY; PERFORANT PATHWAY; RECEPTORS, CELL SURFACE; RECEPTORS, PEPTIDE; RNA, MESSENGER;

EID: 2342593377     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mcn.2004.01.001     Document Type: Article

References (74)

1. Alcántara S., Ruiz M., De Castro F., Soriano E., Sotelo C. Netrin 1 acts as an attractive or as a repulsive cue for distinct migrating neurons during the development of the cerebellar system. Development. 127:2000;1359-1372
2. Amaral D.G., Witter M.P. Hippocampal formation. Paxinos G. The Rat Nervous System. 1995;443-493 Academic Press, San Diego
3. Ben-Ari Y., Represa A. Brief seizure episodes induce long-term potentiation and mossy fibre sprouting in the hippocampus. Trends Neurosci. 13:1990;312-318
4. Ben-Ari Y., Tseeb V., Raggozzino D., Khazipov R., Gaiarsa J.L. Gamma-aminobutyric acid (GABA): a fast excitatory transmitter which may regulate the development of hippocampal neurones in early postnatal life. Prog. Brain Res. 102:1994;261-273
5. Bovolenta P., Wandosell F., Nieto-Sampedro M. Neurite outgrowth inhibitors associated with glial cells and glial cell lines. NeuroReport. 5:1993;345-348
6. Bregman B.S., Kunkel-Bagden E., Schnell L., Dai H.N., Gao D., Schwab M.E. Recovery from spinal cord injury mediated by antibodies to neurite growth inhibitors. Nature. 378:1995;498-501
7. Brosamle C., Huber A.B., Fiedler M., Skerra A., Schwab M.E. Regeneration of lesioned corticospinal tract fibers in the adult rat induced by a recombinant, humanized IN-1 antibody fragment. J. Neurosci. 20:2000;8061-8068
8. Buffo A., Zagrebelsky M., Huber A.B., Skerra A., Schwab M.E., Strata P., Rossi F. Application of neutralizing antibodies against NI-35/250 myelin-associated neurite growth inhibitory proteins to the adult rat cerebellum induces sprouting of uninjured Purkinje cell axons. J. Neurosci. 20:2000;2275-2286
9. Calbet M., Guadano-Ferraz A., Spier A.D., Maj M., Sutcliffe J.G., Przewlocki R., de Lecea L. Cortistatin and somatostatin mRNAs are differentially regulated in response to kainate. Brain Res. Mol. Brain Res. 72:1999;55-64
10. Chedotal A., Del Rio J.A., Ruiz M., He Z., Borrell V., de Castro F., Ezan F., Goodman C.S., Tessier-Lavigne M., Sotelo C., Soriano E. Semaphorins III and IV repel hippocampal axons via two distinct receptors. Development. 125:1998;4313-4323
11. Chen M.S., Huber A.B., van der Haar M.E., Frank M., Schnell L., Spillmann A.A., Christ F., Schwab M.E. Nogo-A is a myelin-associated neurite outgrowth inhibitor and an antigen for monoclonal antibody IN-1. Nature. 403:2000;434-439
12. Cherubini E., Gaiarsa J.L., Ben-Ari Y. GABA: an excitatory transmitter in early postnatal life. Trends Neurosci. 14:1991;515-519
13. De Lecea L., Soriano E., Criado J.R., Steffensen S.C., Henriksen S.J., Sutcliffe J.G. Transcripts encoding a neural membrane CD26 peptidase-like protein are stimulated by synaptic activity. Brain Res. Mol. Brain Res. 25:1994;286-296
14. Del Rio J.A., Heimrich B., Soriano E., Schwegler H., Frotscher M. Proliferation and differentiation of glial fibrillary acidic protein-immunoreactive glial cells in organotypic slice cultures of rat hippocampus. Neuroscience. 43:1991;335-347
15. Del Rio J.A., Heimrich B., Super H., Borrell V., Frotscher M., Soriano E. Differential survival of Cajal-Retzius cells in organotypic cultures of hippocampus and neocortex. J. Neurosci. 16:1996;6896-6907
16. Del Rio J.A., Heimrich B., Borrell V., Forster E., Drakew A., Alcantara S., Nakajima K., Miyata T., Ogawa M., Mikoshiba K., Derer P., Frotscher M., Soriano E. A role for Cajal-Retzius cells and reelin in the development of hippocampal connections. Nature. 385:1997;70-74
17. Del Rio J.A., Sole M., Borrell V., Martinez A., Soriano E. Involvement of Cajal-Retzius cells in robust and layer-specific regeneration of the entorhino-hippocampal pathways. Eur. J. Neurosci. 15:2002;1881-1890
18. Deller T., Frotscher M. Lesion-induced plasticity of central neurons: sprouting of single ficres in the rat hippocampus after unilateral entorhinal cortex lesion. Prog. Neurobiol. 53:1997;687-727
19. Domeniconi M., Cao Z., Spencer T., Sivasankaran R., Wang K., Nikulina E., Kimura N., Cai H., Deng K., Gao Y., He Z., Filbin M. Myelin-associated glycoprotein interacts with the Nogo66 receptor to inhibit neurite outgrowth. Neuron. 35:2002;283-290
20. Fagan A.M., Gage F.H. Cholinergic sprouting in the hippocampus, a proposed role for IL-1. Exp. Neurol. 110:1990;105-120
21. Fournier A.E., Strittmatter S.M. Repulsive factors and axon regeneration in the CNS. Curr. Opin. Neurobiol. 11:2001;89-94
22. Fournier A.E., GrandPre T., Strittmatter S.M. Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration. Nature. 409:2001;341-346
23. Fournier A.E., Gould G.C., Liu B.P., Strittmatter S.M. Truncated soluble Nogo receptor binds Nogo-66 and blocks inhibition of axon growth by myelin. J. Neurosci. 22:2002;8876-8883
24. GrandPre T., Nakamura F., Vartanian T., Strittmatter S.M. Identification of the Nogo inhibitor of axon regeneration as a reticulon protein. Nature. 403:2000;439-444
25. GrandPre T., Li S., Strittmatter S.M. Nogo-66 receptor antagonist peptide promotes axonal regeneration. Nature. 417:2002;547-551
26. Hass C.A., Rauch U., Thon N., Merten T., Deller T. Entorhinal cortex lesion in adult rats induces the expression of the neuronal chondroitin sulfate proteoglycan neurocan in reactive astrocytes. J. Neurosci. 19:1999;9953-9963
27. Hailer N.P., Jarhult J.D., Nitsch R. Resting microglial cells in vitro: analysis of morphology and adhesion molecule expression in organotypic hippocampal slice cultures. Glia. 18:1996;319-331
28. He X.L., Bazan J.F., McDermott G., Park J.B., Wang K., Tessier-Lavigne M., He Z., Garcia K.C. Structure of the nogo receptor ectodomain. A recognition module implicated in myelin inhibition. Neuron. 38:2003;177-185
29. Hjorth-Simonsen A., Jeune B. Origin and termination of the hippocampal perforant path in the rat studied by silver impregnation. J. Comp. Neurol. 144:1972;215-232
30. Horner P.J., Gage F.H. Regenerating the damaged central nervous system. Nature. 407:2000;963-970
31. Hu W.H., Hausmann O.N., Yan M.S., Walters W.M., Wong P.K., Bethea J.R. Identification and characterization of a novel Nogo-interacting mitochondrial protein (NIMP). J. Neurochem. 81:2002;36-45
32. Huber A.B., Weinmann O., Brosamle C., Oertle T., Schwab M.E. Patterns of Nogo mRNA and protein expression in the developing and adult rat and after CNS lesions. J. Neurosci. 9:2002;3553-3567
33. Hunt D., Mason M.R., Campbell G., Coffin R., Anderson P.N. Nogo receptor mRNA expression in intact and regenerating CNS neurons. Mol. Cell. Neurosci. 20:2002;537-552
34. Hunt D., Coffin R.S., Anderson P.N. The Nogo receptor, its ligands and axonal regeneration in the spinal cord; a review. J. Neurocytol. 31:2003;93-120
35. Jessen M.B., Finsen B., Zimmer J. Morphological and microglial changes in the denervated fascia dentata: correlation with blood-brain-barrier damage and astroglial reactions. Exp. Neurol. 143:1997;103-116
36. Jin W.L., Liu Y.Y., Liu H.L., Yang H., Wang Y., Jiao X.Y., Ju G. Intraneuronal localization of Nogo-A in the rat. J. Comp. Neurol. 458:2003;1-10
37. Josephon A., Widenfalk J., Widmer H.W., Olson L., Spenger C. NOGO mRNA expression in adult and fetal human and rat nervous tissue and in weight drop injury. Exp. Neurol. 169:2001;319-328
38. Josephon A., Trifunovski A., Widmer H.R., Widenfalk J., Olson L., Spenger C. Nogo-receptor gene activity: cellular localization and developmental regulation of mRNA in mice and humans. J. Comp. Neurol. 453:2002;292-304
39. Josephon A., Trifunovski A., Scheele C., Widenfalk J., Wahlestedt C., Brene S., Olson L., Spenger C. Activity-induced and developmental downregulation of the Nogo receptor. Cell Tissue Res. 311:2003;333-342
40. Kottis V., Thibault P., Mikol D., Xiao Z.C., Zhang R., Dergham P., Braun P.E. Oligodendrocyte-myelin glycoprotein (OMgp) is an inhibitor of neurite outgrowth. J. Neurochem. 6:2002;1566-1569
41. Li D., Field P.M., Raisman G. Failure of axon regeneration in postnatal rat entorhinohippocampal slice coculture is due to maturation of the axon, not that of the pathway or target. Eur. J. Neurosci. 7:1995;1164-1171
42. Li Q., Qi B., Oka K., Shimakage M., Yoshioka N., Inoue H., Hakura A., Kodama K., Stanbridge E.J., Yutsudo M. Link of a new type of apoptosis-inducing gene ASYNogo-B to human cancer. Oncogene. 20:2001;3929-3936
43. Li Q., Ng C.E., Tang B.L. Nogo-A expression in mouse central nervous system neurons. Neurosci. Lett. 328:2002;257-260
44. McKerracher L., David S., Jackson D.L., Kottis V., Dunn R.J., Braun P.E. Identification of myelin-associated glycoprotein as a major myelin-derived inhibitor of neurite growth. Neuron. 4:1994;805-811
45. Meier S., Brauer A.U., Heimrich B., Schwab M.E., Nitsch R., Savaskan N.E. Molecular analysis of Nogo expression in the hippocampus during development and following lesion and seizure. FASEB J. 17:2003;1153-1155
46. Michel A., Fischer U., Meese E. Novel glioma expressed antigen immunogenic in glioblastoma and pilocytic astrocytoma. Electron. J. Pathol. Histol. 5:1999;993-997
47. Mukhopadhyay G., Doherty P., Walsh F.S., Crocker P.R., Filbin M.T. A novel role for myelin-associated glycoprotein as an inhibitor of axonal regeneration. Neuron. 13:1994;757-767
48. Niederost B., Oertle T., Fritsche J., McKinney R.A., Bandtlow C.E. Nogo-A and myelin-associated glycoprotein mediate neurite growth inhibition by antagonistic regulation of RhoA and Rac1. J. Neurosci. 22:2002;10368-10376
49. Oerthle T., Schwab M.E. Nogo and its paRTNers. Trends Cell Biol. 4:2003;187-194
50. Oerthle T., Merkler D., Schwab M.E. Do cancer cells die because of Nogo-B? Oncogene. 22:2003;1390-1399
51. Oerthle T., van der Haar M.E., Bandtlow C.E., Robeva A., Burfeind P., Buss A., Huber A.B., Simonen M., Schnell L., Brosamle C., Kaupmann K., Vallon R., Schwab M.E. Nogo-A inhibits neurite outgrowth and cell spreading with three discrete regions. J. Neurosci. 23:2003;5393-5406
52. Pozas E., Pascual M., Nguyen Ba-Charvet K.T., Guijarro P., Sotelo C., Chedotal A., Del Rio J.A., Soriano E. Age-dependent effects of secreted Semaphorins 3A, 3F, and 3E on developing hippocampal axons, in vitro effects and phenotype of Semaphorin 3A (-) mice. Mol. Cell. Neurosci. 18:2001;26-43
53. Prang P., Del Turco D., Kapfhammer J.P. Regeneration of entorhinal fibers in mouse slice cultures is age dependent and can be stimulated by NT-4, GDNF, and modulators of G-proteins and protein kinase C. Exp. Neurol. 169:2001;135-147
54. Pratt T., Sharp L., Nichols J., Price D.J., Mason J.O. Embryonic stem cells and transgenic mice ubiquitously expressing a tau-tagged green fluorescent protein. Dev. Biol. 228:2000;19-28
55. Prinjha R., Moore S.E., Vinson M., Blake S., Morrow R., Christie G., Michalovich D., Simmons D.L., Walsh F.S. Inhibitor of neurite outgrowth in humans. Nature. 403:2000;383-384
56. Przewlocki R., Kaminska B., Lukasiuk K., Nowicka D.Z., Przewlocka B., Kaczmarek L., Lason W. Seizure related changes in the regulation of opioid genes and transcription factors in the dentate gyrus of rat hippocampus. Neuroscience. 68:1995;73-81
57. Sambrook J., Fritsch E.F., Maniatis T. Molecular Cloning: A Laboratory Manual. second ed. 1989;Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
58. Savaskan N.E., Plaschke M., Ninnemann O., Spillmann A.A., Schwab M.E., Nitsch R., Skutella T. Myelin does not influence the choice behaviour of entorhinal axons but strongly inhibits their outgrowth length in vitro. Eur. J. Neurosci. 11:1999;316-326
59. Schnell L., Schwab M.E. Axonal regeneration in the rat spinal cord produced by an antibody against myelin-associated neurite growth inhibitors. Nature. 343:1990;269-272
60. Schwab M.E., Bartholdi D. Degeneration and regeneration of axons in the lesioned spinal cord. Physiol. Rev. 76:1996;319-370
61. Skutella T., Nitsch R. New molecules for hippocampal development. Trends Neurosci. 24:2001;107-113
62. Stoppini L., Buchs P.A., Muller D. A simple method for organotypic cultures of nervous tissue. J. Neurosci. Methods. 37:1991;173-182
63. Taketomi M., Kinoshita N., Kimura K., Kitada M., Noda T., Asou H., Nakamura T., Ide C. Nogo-A expression in mature oligodendrocytes of rat spinal cord in association with specific molecules. Neurosci. Lett. 332:2002;37-40
64. Tang B.L. Inhibitors of neuronal regeneration: mediators and signaling mechanisms. Neurochem. Int. 42:2003;189-203
65. Thallmair M., Metz G.A., Z'Graggen W.J., Raineteau O., Kartje G.L., Schwab M.E. Neurite growth inhibitors restrict plasticity and functional recovery following corticospinal tract lesions. Nat. Neurosci. 1:1998;124-131
66. Tozaki H., Kawasaki T., Takagi Y., Hirata T. Expression of Nogo protein by growing axons in the developing nervous system. Brain Res. Mol. Brain Res. 104:2002;111-119
67. Trifunovski A., Galter D., Josephson A., Widmer H.R., Olson L., Spenger C. Nogo-receptor in developing and adult rat and human brain and spinal cord. 2003 Abstract ViewerItinerary Planner. 2003;Society for Neuroscience, Washington, DC. Program No. 358.14. Online
68. Turner D.A., Buhl E.H., Hailer N.P., Nitsch R. Morphological features of the entorhinal-hippocampal connection. Prog. Neurobiol. 55:1998;537-562
69. Walter J., Kern-Veits B., Huf J., Stolze B., Bonhoeffer F. Recognition of position-specific properties of tectal cell membranes by retinal axons in vitro. Development. 101:1987;685-696
70. Wang X., Chun S.J., Treloar H., Vartanian T., Greer C.A., Strittmatter S.M. Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact. J. Neurosci. 22:2002;5505-5515
71. Watari A., Yutsudo M. Multi-functional gene ASYNogoRTN-XRTN4: apoptosis, tumor suppression, and inhibition of neuronal regeneration. Apoptosis. 1:2003;5-9
72. Wong S.T., Henley J.R., Kanning K.C., Huang K.H., Bothwell M., Poo M.M. A p75(NTR) and Nogo receptor complex mediates repulsive signaling by myelin-associated glycoprotein. Nat. Neurosci. 5:2002;1302-1308
73. Woodhams P.L., Prinjha R., Moore S.E., Walsh F.S. Differential distribution of Nogo isoforms in the rat central nervous system. Soc. Neurosci. Abstr. 27:2001;670
74. Zagrebelsky M., Buffo A., Skerra A., Schwab M.E., Strata P., Rossi F. Retrograde regulation of growth-associated gene expression in adult rat Purkinje cells by myelin-associated neurite growth inhibitory proteins. J. Neurosci. 18:1998;7912-7929