Isolation and characterization of a neural progenitor cell line from tilapia brain

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 149, Issue 2, 2008, Pages 167-180

  Wen, Chiu Ming ^a   Cheng, Yeong Hsiang ^b   Huang, Ya Fen ^a   Wang, Chung Shung ^a  

^a NATIONAL UNIVERSITY OF KAOHSIUNG   (Taiwan)

^b NATIONAL ILAN UNIVERSITY   (Taiwan)

Author keywords

A2B5; Connexin; GFAP; Glutamine synthetase; Oligodendrocyte; Tyrosine hydroxylase

Indexed keywords

CARBOXYLYASE; CONNEXIN 43; DOPAMINE; GALACTOSYLCERAMIDE; GLIAL FIBRILLARY ACIDIC PROTEIN; GLUTAMATE AMMONIA LIGASE; KERATIN; LIPID BINDING PROTEIN; MEMBRANE ANTIGEN; MICROTUBULE ASSOCIATED PROTEIN 2; MYELIN BASIC PROTEIN; POLYLYSINE; PROTEIN S 100; PROTEOLIPID PROTEIN; SUBSTANCE P; TRANSCRIPTION FACTOR SOX2; TYROSINE 3 MONOOXYGENASE; VIMENTIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL ISOLATION; CELL LINE; CELL MATURATION; CELL STRUCTURE; CONTROLLED STUDY; NEURAL STEM CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN EXPRESSION; REAL TIME POLYMERASE CHAIN REACTION; TILAPIA;

BOVINAE; TILAPIA;

EID: 38649121149     PISSN: 10956433     EISSN: 15314332     Source Type: Journal    
DOI: 10.1016/j.cbpa.2007.11.005     Document Type: Article

References (71)

1. Adolf B., Chapouton P., Lam C.S., Topp S., Tannhauser B., Strahle U., Gotz M., and Bally-Cuif L. Conserved and acquired features of adult neurogenesis in the zebrafish telencephalon. Dev. Biol. 295 (2006) 278-293
2. Akimoto J., Itoh H., Miwa T., and Ikeda K. Immunohistochemical study of glutamine synthetase expression in early glial development. Brain Res. Dev. Brain Res. 72 (1993) 9-14
3. Alunni A., Vaccari S., Torcia S., Meomartini M.E., Nicotra A., and Alfei L. Characterization of glial fibrillary acidic protein and astroglial architecture in the brain of a continuously growing fish, the rainbow trout. Eur. J. Histochem. 49 (2005) 157-166
4. Arochena M., Anadón R., and Díaz-Regueira S.M. Development of vimentin and glial fibrillary acidic protein immunoreactivities in the brain of gray mullet (Chelon labrosus), an advanced teleost. J. Comp. Neurol. 469 (2004) 413-436
5. Auclair F., Lund J.P., and Dubuc R. Immunohistochemical distribution of tachykinins in the CNS of the lamprey Petromyzon marinus. J. Comp. Neurol. 479 (2004) 328-346
6. Bass D., Dalencon D., Fressinaud C., Vitkovic L., and Sarlieve L.L. Oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells express glutamine synthetase: developmental and cell type-specific regulation. Mol. Psychiatry 3 (1998) 356-361
7. Bastmeyer M., Beckmann M., Nona S.M., Cronly-Dillon J.R., and Stuermer C.A. Identification of astrocyte- and oligodendrocyte-like cells of goldfish optic nerves in culture. Neurosci. Lett. 101 (1989) 127-132
8. Baumann N., and Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system. Physiol. Rev. 81 (2001) 871-927
9. Belliveau D.J., and Naus C.C. Cortical type 2 astrocytes are not dye coupled nor do they express the major gap junction genes found in the central nervous system. Glia 12 (1994) 24-34
10. Bittman K.S., and LoTurco J.J. Differential regulation of connexin 26 and 43 in murine neocortical precursors. Cereb. Cortex 9 (1999) 188-195
11. Blaugrund E., Cohen I., Shani Y., and Schwartz M. Glial fibrillary acidic protein in the fish optic nerve. Glia 4 (1991) 393-399
12. Bonfigli A., Zarivi O., Colafarina S., Cimini A.M., Ragnelli A.M., Aimola P., Natali P.G., Ceru M.P., Amicarelli F., and Miranda M. Human glioblastoma ADF cells express tyrosinase, l-tyrosine hydroxylase and melanosomes and are sensitive to l-tyrosine and phenylthiourea. J. Cell. Physiol. 207 (2006) 675-682
13. Bongarzone E.R., Fosterm L., Byravan S., Casaccia-Bonnefil P., Schonmann V., and Campagnoni A.T. Two neuronal cell lines expressing the myelin basic protein gene display differences in their in vitro survival and in their response to glia. J. Neurosci. Res. 54 (1998) 309-319
14. Cammer W. Glutamine synthetase in the central nervous system is not confined to astrocytes. J. Neuroimmunol. 26 (1990) 173-178
15. Candy J., and Collet C. Two tyrosine hydroxylase genes in teleosts. Biochim. Biophys. Acta 1727 (2005) 35-44
16. Chiba A. S-100 protein-immunoreactive structures in the brains of the elasmobranchs scyliorhinus torazame and mustelus manazo. Neurosci. Lett. 279 (2000) 65-68
17. Dahl D., and Bignami A. Immunochemical and immunofluorescence studies of the glial fibrillary acidic protein in vertebrates. Brain Res. 61 (1973) 279-293
18. Dahl D., Crosby C.J., Sethi J.S., and Bignami A. Glial fibrillary acidic (GFA) protein in vertebrates: immunofluorescence and immunoblotting study with monoclonal and polyclonal antibodies. J. Comp. Neurol. 239 (1985) 75-88
19. Deloulme J.C., Raponi E., Gentil B.J., Bertacchi N., Marks A., Labourdette G., and Baudier J. Nuclear expression of S100B in oligodendrocyte progenitor cells correlates with differentiation toward the oligodendroglial lineage and modulates oligodendrocytes maturation. Mol. Cell. Neurosci. 27 (2004) 453-465
20. Doetsch F. The glial identity of neural stem cells. Nat. Neurosci. 6 (2003) 1127-1133
21. Eddé B., Rossier J., Le Caer J.P., Berwald-Netter Y., Koulakoff A., and Gros F.P.D. A combination of posttranslational modifications is responsible for the production of neuronal alpha-tubulin heterogeneity. J. Cell. Biochem. 46 (1991) 134-142
22. Fressinaud C., Weinrauder H., Delaunoy J.P., Tholey G., Labourdette G., and Sarlieve L.L. Glutamine synthetase expression in rat oligodendrocytes in culture: regulation by hormones and growth factors. J. Cell. Physiol. 149 (1991) 459-468
23. Fröjdö E.M., Westerlund J., and Isomaa B. Culturing and characterization of astrocytes isolated from juvenile rainbow trout (Oncorhynchus mykiss). Comp. Biochem. Physiol. A 133 (2002) 17-28
24. Hachem S., Aguirre A., Vives V., Marks A., Gallo V., and Legraverend C. Spatial and temporal expression of S100B in cells of oligodendrocyte lineage. Glia 51 (2005) 81-97
25. Hinsch K., and Zupanc G.K.H. Isolation, cultivation, and differentiation of neural stem cells from adult fish brain. J. Neurosci. Methods 158 (2006) 75-88
26. Itoh T., Satou T., Nishida S., Hashimoto S., and Ito H. Cultured rat astrocytes give rise to neural stem cells. Neurochem. Res. 31 (2006) 1381-1387
27. Jeserich G., and Rauen T. Cell cultures enriched in oligodendrocytes from the central nervous system of trout in terms of phenotypic expression exhibit parallels with cultured rat Schwann cells. Glia 3 (1990) 65-74
28. Jeserich G., and Stratmann A. In vitro differentiation of trout oligodendrocytes: evidence for an A2B5-positive origin. Brain Res. Dev. Brain Res. 67 (1992) 27-35
29. Jeserich G., Strelau J., and Tönnies R. An immunomagnetic cell separation technique for isolating oligodendroglial progenitor cells of trout CNS. NeuroProtocols 2 (1993) 219-224
30. Kálmán M. Astroglial architecture of the carp (Cyprinus carpio) brain as revealed by immunohistochemical staining against glial fibrillary acidic protein (GFAP). Anat. Embryol. 198 (1998) 409-433
31. Kálmán M., and Gould R.M. GFAP-immunopositive structures in spiny dogfish, Squalus acanthias, and little skate, Raia erinacea, brains: differences have evolutionary implications. Anat. Embryol. 204 (2001) 59-80
32. Kinoshita M., Fukaya M., Tojima T., Kojima S., Ando H., Watanabe M., Uranom A., and Ito E. Retinotectal transmission in the optic tectum of rainbow trout. J. Comp. Neurol. 484 (2005) 249-259
33. Kondo T., and Raff M. Oligodendrocyte precursor cells reprogrammed to become multipotential CNS stem cells. Science 289 (2000) 1754-1757
34. Kristen B.C., and McCarthy K.D. GFAP-positive progenitor cells produce neurons and oligodendrocytes throughout the CNS. Mol. Cell. Neurosci. 31 (2006) 676-684
35. Kubrusly R.C.C., da Cunha M.C.C., Reis R.AdM., Soares H., Ventura A.L.M., Kurtenbach E., de Mello M.C.F., and de Mello F.G. Expression of functional receptors and transmitter enzymes in cultured Müller cells. Brain Res. 1038 (2005) 141-149
36. Laywell E.D., Rakic P., Kukekov V.G., Holland E.C., and Steindler D.A. Identification of a multipotent astrocytic stem cell in the immature and adult mouse brain. Proc. Natl. Acad. Sci. U. S. A. 97 (2000) 13883-13888
37. Laywell E.D., Kearns S.M., Zheng T., Chen K.A., Deng J., Chen H.X., Roper S.N., and Steindler D.A. Neuron-to-astrocyte transition: phenotypic fluidity and the formation of hybrid asterons in differentiating neurospheres. J. Comp. Neurol. 493 (2005) 321-333
38. Lazzari M., and Franceschini V. Glial fibrillary acidic protein and vimentin immunoreactivity of astroglial cells in the central nervous system of the African lungfish, Protopterus annectens (Dipnoi: Lepidosirenidae). J. Morphol. 262 (2004) 741-749
39. Li H., Babiarz J., Woodbury J., Kane-Goldsmith N., and Grumet M. Spatiotemporal heterogeneity of CNS radial glial cells and their transition to restricted precursors. Dev. Biol. 271 (2004) 225-238
40. Lin R.C. Reactive astrocytes express substance-P immunoreactivity in the adult forebrain after injury. NeuroReport 29 (1995) 310-312
41. Mack A.F., Germer A., Janke C., and Reichenbach A. Müller (glial) cells in the teleost retina: consequences of continuous growth. Glia 22 (1998) 306-313
42. Marone M., Quiñones-Jenab V., Meiners S., Nowakowski R.S., Ho S.Y., and Geller H.M. An immortalized mouse neuroepithelial cell line with neuronal and glial phenotypes. Dev. Neurosci. 17 (1995) 311-323
43. Mastronardi F.G., Boulias C., Roots B.I., and Moscarello M.A. Characterization of basic proteins from goldfish myelin. J. Neurochem. 60 (1993) 153-160
44. Michel J.P., Sakamoto N., Bouvier R., Tommasi M., and Pearson J. Substance P-immunoreactive astrocytes related to deep white matter and striatal blood vessels in human brain. Brain Res. 377 (1986) 383-387
45. Müller R., Heinrich M., Heck S., Blohm D., and Richter-Landsberg C. Expression of microtubule-associated proteins MAP2 and tau in cultured rat brain oligodendrocytes. Cell Tissue Res. 288 (1997) 239-249
46. Nona S., Swhab S.A.S., Stafford C.A., and Cronly-Dillon J.R. Glial fibrillary acidic protein (GFAP) from the goldfish: its localization in the visual pathways. Glia 2 (1989) 189-200
47. Pellegrini E., Mouriec K., Anglade I., Menuet A., Page Y.L., Gueguen M.M., Marmignon M.H., Brion F., Pakdel F., and Kah O. Identification of aromatase-positive radial glial cells as progenitor cells in the ventricular layer of the forebrain in zebrafish. J. Comp. Neurol. 501 (2007) 150-167
48. Pepperell C., and Levine R.L. Nonspecific esterase activity in astrocytes of the goldfish brain. J. Histochem. Cytochem. 44 (1996) 1195-1203
49. Peterson R.E., Fadool J.M., Mcclintock J., and Linser P.J. Müller cell differentiation in the zebrafish neural retina: evidence of distinct early and late stages in cell maturation. J. Comp. Neurol. 429 (2001) 530-540
50. Raff M.C., Miller R.H., and Noble M. A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium. Nature 303 (1983) 390-396
51. Raff M.C., Williams B.P., and Miller R.H. The in vitro differentiation of a bipotential glial progenitor cell. EMBO J. 3 (1984) 1857-1864
52. Rash J.E., Yasumura T., Davidson K.G., Furman C.S., Dudek F.E., and Nagy J.I. Identification of cells expressing Cx43, Cx30, Cx26, Cx32 and Cx36 in gap junctions of rat brain and spinal cord. Cell Commun. Adhes. 8 (2001) 315-320
53. Raymond P., Barthel L.K., Bernardos R.L., and Perkowski J.J. Molecular characterization of retinal stem cells and their niches in adult zebrafish. BMC Dev. Biol. 6 (2006) 36
54. Richter-Landsberg C., and Heinrich M. S-100 immunoreactivity in rat brain glial cultures is associated with both astrocytes and oligodendrocytes. J. Neurosci. Res. 42 (1995) 657-665
55. Rosser A.E., Tyers P., ter Borg M., Dunnett S.B., and Svendsen C.N. Co-expression of MAP-2 and GFAP in cells developing from rat EGF responsive precursor cells. Brain Res. Dev. Brain Res. 98 (1997) 291-295
56. Schinstine M., and Iacovitti L. Expression of neuronal antigens by astrocytes derived from EGF-generated neuroprogenitor cells. Exp. Neurol. 141 (1996) 67-78
57. Shioda S., Honma Y., Yoshie S., and Hosoya Y. Scanning electron microscopy of the third ventricular wall in the lamprey, Lampetra japonica. Arch. Histol. Jpn. 40 (1977) 41-49
58. Sivron T., Jeserich G., Nona S., and Schwartz M. Characteristics of fish glial cells in culture: possible implications as their lineage. Glia 6 (1992) 52-66
59. Smith D.D., Ritter N.M., and Campbell J.W. Glutamine synthetase isozymes in elasmobranch brain and liver tissues. J. Biol. Chem. 262 (1987) 198-202
60. Sueiro C., Carrera I., Rodriguez-Moldes I., Molist P., and Anadon R. Development of catecholaminergic systems in the spinal cord of the dogfish Scyliorhinus canicula (Elasmobranchs). Dev. Brain Res. 142 (2003) 141-150
61. Tansey F.A., Farooq M., and Cammer W. Glutamine synthetase in oligodendrocytes and astrocytes: new biochemical and immunocytochemical evidence. J. Neurochem. 56 (1991) 266-272
62. Tlhyama T., Lee V.M., and Trojanowski J.Q. Co-expression of low molecular weight neurofilament protein and glial fibrillary acidic protein in established human glioma cell lines. Am. J. Pathol. 142 (1993) 883-892
63. Tocher D.R., and Wilson R. Primary culture of astrocytic glial cells from rainbow trout, Salmo gairdneri L., brain. J. Neurosci. Methods 33 (1990) 93-100
64. Vecino E., Velasco A., Caminos E., and Aijon J. Distribution of S-100 immunorecativity in the retina and optic nerve head of the teleost Tinca tinca L. Microsc. Res. Tech. 36 (1997) 17-25
65. Von Visger J.R., Yeon D.S., Oh T.H., and Markelonis G.J. Differentiation and maturation of astrocytes derived from neuroepithelial progenitor cells in culture. Exp. Neurol. 70 (2007) 1079-1090
66. Wai M.S.M., Lorke D.E., Zhang A., Kung H.-F., and Yew D.T. Study of the spinal cords of the sturgeon Acipenser schrenckii, gar Lepisosteus oculatus, and goldfish Carassius auratus by morphological, immunohistochemical, and biochemical approaches. Microsc. Res. Tech. 70 (1997) 1079-1090
67. Wallraff A., Odermatt B., Willecke K., and Steinhäuser C. Distinct types of astroglial cells in the hippocampus differ in gap junction coupling. Glia 48 (2004) 36-43
68. Wang, I.D., 2001. Establishment of the cell line derived from tilapia (Oreochromis mossambica × Oreochromis nilotica) brain and characteristics of its differentiation. Master's Thesis. National Taipei University of Education, Taipei, Taiwan. 69 p.
69. Wicht H., Derouiche A., and Korf H.W. An immunocytochemical investigation of glial morphology in the Pacific hagfish: radial and astrocyte-like glia have the same phylogenetic age. J. Neurocytol. 23 (1994) 565-576
70. Xu Y., Tamamaki N., Noda T., Kimura K., Itokazu Y., Matsumoto N., Dezawa M., and Ide C. Neurogenesis in the ependymal layer of the adult rat 3rd ventricle. Exp. Neurol. 192 (2005) 251-264
71. Yavin Z., and Yavin E. Survival and maturation of cerebral neurons on poly-l-lysine surfaces in the absence of serum. Dev. Biol. 75 (1980) 454-459