Retinoids and binding proteins in the cerebellum during lifetime

Cerebellum

Volumn 3, Issue 1, 2004, Pages 16-20

  Parenti, Rosalba ^a   Cicirata, Federico ^a  

^a UNIVERSITY OF CATANIA   (Italy)

Author keywords

Cerebellum; CRABP I; CRBP I; Retinoic acid; Retinoids

Indexed keywords

CELLULAR RETINOIC ACID BINDING PROTEIN I; CELLULAR RETINOIC ACID BINDING PROTEIN II; FIBROBLAST GROWTH FACTOR 8; RETINOIC ACID; RETINOID; RETINOL BINDING PROTEIN; TRANSCRIPTION FACTOR EN1; TRANSCRIPTION FACTOR EN2; TRANSCRIPTION FACTOR OTX2; TRANSCRIPTION FACTOR PAX2; TRANSCRIPTION FACTOR PAX5; UNCLASSIFIED DRUG; WNT1 PROTEIN;

ANIMAL CELL; CEREBELLUM; GENE EXPRESSION REGULATION; GRANULE CELL; MESENCEPHALON; MUTANT; NERVOUS SYSTEM DEVELOPMENT; NEWBORN; NONHUMAN; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RAT; REGULATOR GENE; REVIEW; VERTEBRATE;

ANIMALS; CARRIER PROTEINS; CEREBELLUM; HUMANS; RECEPTORS, RETINOIC ACID; RETINOIDS;

EID: 1642350920     PISSN: 14734222     EISSN: None     Source Type: Journal    
DOI: 10.1080/14734220310017186     Document Type: Review

References (51)

1. Morriss-Kay G. Retinoic acid and craniofacial development: molecules and morphogenesis. Bioessays 1993; 15: 9-15.
2. Ong DE. A novel retinol-binding protein from rat. Purification and partial characterization. J Biol Chem 1984; 259: 1476-1482.
3. Ong DE. Purification and partial characterization of cellular retinol-binding protein from human liver. Cancer Res 1982; 42: 1033-1037.
4. Eriksson U, Das K, Busch C, Nordlinder H, Rask L, Sundelin J, et al. Cellular retinol-binding protein. Quantitation and distribution. J Biol Chem 1984; 259: 13464-13470.
5. Eriksson U, Hansson E, Nordlinder H, Busch C, Sundelin J, Peterson PA. Quantitation and tissue localization of the cellular retinoic acid-binding protein. J Cell Physiol 1987; 133: 482-490.
6. Crow JA, Ong DE. Cell-specific immunohistochemical localization of a cellular retinol-binding protein (type two) in the small intestine of rat. Proc Natl Acad Sci USA 1985; 82: 4707-4711.
7. Bailey JS, Siu CH. Purification and partial characterization of a novel binding protein for retinoic acid from neonatal rat. J Biol Chem 1988; 263: 9326-9332.
8. Boylan JF, Gudas LJ. Overexpression of the cellular retinoic acid binding protein-I (CRABP I) results in a reduction in differentiation-specific gene expression in F9 teratocarcinoma cells. J Cell Biol 1991; 112: 965-979.
9. Gustafson AL, Donovan M, Annerwall E, Dencker L, Eriksson U. Nuclear import of cellular retinoic acid-binding protein type I in mouse embryonic cells. Mech Dev 1996; 58: 27-38.
10. Fiorella PD, Napoli JL. Expression of cellular retinoic acid binding protein (CRABP) in Escherichia coli. Characterization and evidence that holo-CRABP is a substrate in retinoic acid metabolism. J Biol Chem 1991; 266: 16572-16579.
11. Dollè P, Ruberte E, Leroy P, Morris-Kay GM, Chambon P. Retinoic acid receptors and cellular retinoid binding proteins. I. A systematic study of their differential pattern of transcription during mouse organogenesis. Development 1990; 110: 1133-1151.
12. Ruberte E, Friederich V, Morriss-Kay G, Chambon P. Differential distribution patterns of CRABP I and CRABP II transcripts during mouse embryogenesis. Development 1992; 115: 973-987.
13. Ruberte E, Friederich V, Chambon P, Morriss-Kay G. Retinoic acid receptors and cellular retinoid binding proteins. III. Their differential transcript distribution during mouse nervous system development. Development 1993; 118: 267-282.
14. Avantaggiato V, Acampora D, Tuorto F, Simeone A. Retinoic acid induces stage-specific repatterning of the rostral central nervous system. Dev Biol 1996; 175: 347-357.
15. Zetterstrom RH, Simon A, Giacobini MM, Eriksson U, Olson L. Localization of cellular retinoid-binding proteins suggests specific roles for retinoids in the adult central nervous system. Neuroscience 1994; 62: 899-918.
16. Parenti R, Wassef M, Cicirata F. Expression of CRABP I mRNA in fastigial cells of the developing cerebellum. Eur J Neurosci 2002; 15: 211-215.
17. Yamamoto M, Ullman D, Drager UC, McCaffery P. Postnatal effects of retinoic acid on cerebellar development. Neurotoxicol Teratol 1999; 21: 141-146.
18. Yamamoto M, Drager UC, Ong DE, McCaffery P. Retinoid-binding proteins in the cerebellum and choroid plexus and their relationship to regionalized retinoic acid synthesis and degradation. Eur J Biochem 1998; 257: 344-350.
19. Donovan M, Olofsson B, Gustafson AL, Dencker L, Eriksson U. The cellular retinoic acid binding proteins. Review. J Steroid Biochem Mol Biol 1995; 53: 459-465.
20. Boylan JF, Gudas LJ. The level of CRABP-I expression influences the amounts and types of all-trans-retinoic acid metabolites in F9 teratocarcinoma stem cells. J Biol Chem 1992; 267: 21486-21491.
21. Albus SS. A theory of cerebellar function. Math Biosci 1971; 10: 25-69.
22. Marr D. A theory of cerebellar cortex. J Physiol (London) 1969; 202: 437-470.
23. Le Marec N, Dahhaoui M, Stelz T, Bakalian A, Delhaye-Bouchaud N, Caston J, et al. Effect of cerebellar granule cell depletion on spatial learning and memory and in an avoidance conditioning task: studies in postnatally X-irradiated rats. Brain Res Dev Brain Res 1997; 99: 20-28.
24. Martinez S, Alvarado-Mallart RM. Transplanted mesencephalic quail cells colonize selectively all primary visual nuclei of chick diencephalon: a study using heterotopic transplants. Brain Res Dev Brain Res 1989; 47: 263-274.
25. Alvarez Otero R, Sotelo C, Alvarado-Mallart RM. Chick/quail chimeras with partial cerebellar grafts: an analysis of the origin and migration of cerebellar cells. J Comp Neurol 1993; 333: 597-615.
26. Alvarado-Mallart RM. Fate and potentialities of the avian mesencephalic/metencephalic neuroepithelium. Review. J Neurobiol. 1993; 24: 1341-1355.
27. Wassef M, Joyner AL. Early mesencephalon/metencephalon patterning and development of the cerebellum. Review. Perspect Dev Neurobiol 1997; 5: 3-16.
28. Joyner AL, Liu A, Millet S. Otx2, Gbx2 and Fgf8 interact to position and maintain a mid-hindbrain organizer. Review. Curr Opin Cell Biol 2000; 12: 736-741.
29. Crossley PH, Martin GR. The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo. Development 1995; 121: 439-451.
30. Crossley PH, Martinez S, Martin GR. Midbrain development induced by FGF8 in the chick embryo. Nature 1996; 380: 66-68.
31. Martinez S, Marin F, Nieto MA, Puelles L. Induction of ectopic engrailed expression and fate change in avian rhombomeres: intersegmental boundaries as barriers. Mech Dev 1995; 51: 289-303.
32. Martinez S, Crossley PH, Cobos I, Rubenstein JL, Martin GR. FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. Development 1999; 126: 1189-1200.
33. Liu A, Losos K, Joyner AL. FGF8 can activate Gbx2 and transform regions of the rostral mouse brain into a hindbrain fate. Development 1999; 126: 4827-4838.
34. Sato T, Araki I, Nakamura H. Inductive signal and tissue responsiveness defining the tectum and the cerebellum. Development 2001; 128: 2461-2469.
35. Nusse R, Varmus HE. Wnt genes. Review. Cell 1992; 69: 1073-1087.
36. Parr BA, Shea MJ, Vassileva G, McMahon AP. Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds. Development 1993; 119: 247-261.
37. Joyner AL, Martin GR. En-1 and En-2, two mouse genes with sequence homology to the Drosophila engrailed gene: expression during embryogenesis. Genes Dev 1987; 1: 29-38.
38. Joyner AL. Engrailed, Wnt and Pax genes regulate midbrain-hindbrain development. Review. Trends Genet 1996; 12: 15-20.
39. Urbanek P, Fetka I, Meisler MH, Busslinger M. Cooperation of Pax2 and Pax5 in midbrain and cerebellum development. Proc Natl Acad Sci USA 1997; 94: 5703-5708.
40. Schwarz M, Alvarez-Bolado G, Urbanek P, Busslinger M, Gruss P. Conserved biological function between Pax-2 and Pax-5 in midbrain and cerebellum development: evidence from targeted mutations. Proc Natl Acad Sci USA 1997; 94: 14518-14523.
41. Millet S, Bloch-Gallego E, Simeone A, Alvarado-Mallart RM. The caudal limit of Otx2 gene expression as a marker of the midbrain/hindbrain boundary: a study using in situ hybridisation and chick/quail homotopic grafts. Development 1996; 122: 3785-3797.
42. Millet S, Campbell K, Epstein DJ, Losos K, Harris E, Joyner AL. A role for Gbx2 in repression of Otx2 and positioning the mid/ hindbrain organizer. Nature 1999; 401: 161-164.
43. Liu A, Joyner AL. EN and GBX2 play essential roles downstream of FGF8 in patterning the mouse mid/hindbrain region. Development 2001; 128: 181-191.
44. Matsunaga E, Katahira T, Nakamura H. Role of Lmx1b and Wnt1 in mesencephalon and metencephalon development. Development. 2002; 129: 5269-5277.
45. Bevans CG, Kordel M, Rhee SK, Harris AL. Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules. J Biol Chem 1998; 273: 2808-2816.
46. Irving C, Mason I. Signalling by FGF8 from the isthmus patterns anterior hindbrain and establishes the anterior limit of Hox gene expression. Development 2000; 127: 177-186.
47. Altman J, Bayer SA. Development of the Cerebellar System in Relation to its Evolution, Structure and Functions. Boca Raton: CRC Press, 1997.
48. Bourrat F, Sotelo C. Neuronal migration and dendritic maturation of the medial cerebellar nucleus in rat embryos: an HRP in vitro study using cerebellar slabs. Brain Res 1986; 378: 69-85.
49. Gorry P, Lufkin T, Dierich A, Rochette-Egly C, Decimo D, Dolle P, et al. The cellular retinoic acid binding protein I is dispensable. Proc Natl Acad Sci USA 1994; 91: 9032-9036.
50. Lampron C, Rochette-Egly C, Gorry P, Dolle P, Mark M, Lufkin T, et al. Mice deficient in cellular retinoic acid binding protein II (CRABPII) or in both CRABPI and CRABPII are essentially normal. Development 1995; 121: 539-548.
51. Chambon P. The retinoid signaling pathway: molecular and genetic analyses. Semin Cell Biol 1994; 5: 115-125.