Persistence of multipotential progenitors in the juvenile rat subventricular zone?

Developmental Neuroscience

Volumn 18, Issue 4, 1996, Pages 255-265

  Young, Greg M ^a   Levison, Steven W ^a  

^a PENN STATE COLLEGE OF MEDICINE   (United States)

Author keywords

Astrocytes; Cell culture; Differentiation; Lineage; Neurons; Oligodendrocytes; Retroviral vectors

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ANTIGEN EXPRESSION; ASTROCYTE; CELL STRUCTURE; CONFERENCE PAPER; NERVE CELL CULTURE; NERVE CELL DIFFERENTIATION; NONHUMAN; OLIGODENDROGLIA; PRIORITY JOURNAL; RAT; STEM CELL;

EID: 0029761696     PISSN: 03785866     EISSN: 14219859     Source Type: Journal    
DOI: 10.1159/000111415     Document Type: Article

References (38)

1. Lcvison SW. Goldman JE: Both oligodendrocytes and astrocytes develop from progenitors in the subvcntricular zone of postnatal rat fore-brain. Neuron 1993:10:201-212.
2. Zerlin M. Levison SW, Goldman JE: Early stages of dispersion and differentiation of glial progenitors in the postnatal mammalian fore-brain. J Neurosci 1995;15:7238-7249.
3. Levison SW. Chuang C. Abramson BJ. Goldman JE: The migrational patterns and developmental fates of glial precursors in the rat sub-ventricular zone are temporally regulated. Development 1993:119:611-623.
4. Privat A. Lcblond CP: The subependymal layer and neighboring region in the brain of the young rat. J Comp Neurol 1972.146:227-302.
5. Ling EA. Leblond CP: Investigation of glial cells in semithin sections. II. Variation with age-in the numbers of the various glial cell types in rat cortex and corpus callosum. J Comp Neurol 1973:149:73-82.
6. Paterson JA. Privat A. Ling EA. Leblond CP: Investigation of glial cells in semithin sections. III. Transformation of subependymal cells into glial cells as shown by radioautography after 'H-thymidinc injection into the lateral ventricle of the brain of young rats. J Comp Neurol 1973:149:83-102.
7. Luskin MB. Pearlman AL. Sancs JR: Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus. Neuron 1988:1:635-647.
8. Luskin MB, Pamavclas JG, Barfield JA: Neurons. Astrocytes, and oligodendrocytes of literal cerebral cortex originate from separate progenitor cells: An ultrastructural analysis of clonally related cells. J Neurosci 1993:13: 1730-1750.
9. Luskin MB. McDermott K: Divergent lineages for oligodendrocytes and astrocytes originating in the neonatal forebrain subvcntricular zone. Glia 1994:11:211-226.
10. Grove EA, Williams BP. Da-Qing L, Hajihos-seini M. Friedrich A, Price J: Multiple restricted lineages in the embryonic rat cerebral cortex. Development 1993:117:553-561.
11. Price J. Thurlow L: Cell lineage in the rat cerebral cortex: A study using retroviral-mediated gene transfer. Development 1988:104:473-482.
12. Williams BP, Abney ER, Raff MC: Macroglial cell development in embryonic rat brain: Studies using monoclonal antibodies, fluorescence activated cell sorting, and cell culture. Dev Biol 1985;112:126-134.
13. Luskin MB: Restricted proliferation and migration of postnatally generated neurons derived from the forebrain subventricular zone. Neuron 1993:11:173-189.
14. Lois C, Alvarez-Buylla A: Long-distance neuronal migration in the adult mammalian brain. Science 1994:264:1145-1148.
15. Galileo DS, Gray GE. Owens GC. Majors J. Sancs JR: Neurons and glia arise from a common progenitor in chicken optic tectum: Demonstration with two retroviruses and cell type-specific antibodies. Proc Natl Acad Sci USA 1990:87:458-462.
16. Mann R. Mulligan RC. Baltimore D: Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus. Cell 1983:33:153-159.
17. Price J, Turner DL, Cepko CL: Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. Proc Natl Acad Sci USA 1987:84:156-160.
18. Eields-Berry SC. Halliday AL. Cepko CL: A recombinant retrovirus encoding alkaline phosphatase confirms clonal boundary assignment in lineage analysis of murine retina. Proc Natl Acad Sci USA 1992:89:693-697.
19. Abney ER. Williams BP. Raff MC: Tracing the development of oligodendrocytes from precursor cells using monoclonal antibodies, fluorescence-activated cell sorting, and cell culture. Dev Biol 1983;100:166-171.
20. Baimbridge KG, Miller JJ: Immunohistochem-ical localization of calcium-binding protein in the cerebellum, hippocampal formation and olfactory bulb of the rat. Brain Res 1982:245: 223-229.
21. Antanitus DS, Choi BH. Lapham LW: Immunofluorescence staining of astrocytes in vitro using antiserum to glial fibrillary acidic protein. Brain Res 1975:89:363-367.
22. Caccrcs A, Binder LI. Payne MR, Bender P. Rebhun L, Steward O: Differential subcellular localization of tubulin and the microtubule-associated protein MAP2 in brain tissue as revealed by immunocytochemistry with monoclonal hybridoma antibodies. J Neurosci 1984: 4:394-410.
23. Slallcup WB, Beasley L: Bipotential glial precursor cells of the optic nerve express the NG2 proteoglycan. J Neurosci 1987:7:2737-2744.
24. Schmcchel DE, Brighiman MW, Barker JL: Localization of ncuron-spccific enolasc in mouse spinal neurons grown in tissue culture. Brain Res 1980:181:391-400.
25. Bansal R. Warrington AE. Gard AL. Ranscht B. Pfeiffer SE: Characterization of monoclonal antibodies Ol, 04, and R-mAb used in the analysis of oligodendrocyte development. Ann NY Acad Sci 1990:605:409-411.
26. Raff MC. Mirsky R. Fields KL. Lisak RP. Dorfman SH, Silberberg DH, Gregson NA, Leibowitz S. Kennedy MC: Galactocerebro-side is a specific cell-surface antigenic marker for oligodendrocytes in culture. Nature 1978; 274:813-816.
27. Stemberger LA. Slernbcrger NM: Monoelonal antibodies distinguish phosphorylated and non-phosphorylated forms of ncurofilaments in situ. Proc Natl Acad Sci USA 1983:80: 6126-6130.
28. Lee MK. Tuttle JB, Rebhun LI. Cleveland DW. Frankfurter A: The expression and posttransla-tional modification of a ncuron-spccific P-tubulin isotype during chick embryogenesis. Cell Motil Cytoskeleton 1990; 17:118-132.
29. Acklin SE. van dcr Kooy D: Clonal heterogeneity in the germinal zone of the developing rat telencephalon. Development 1993:118: 175-192.
30. Davis AA. Temple S: A self-renewing multi-potential stem cell in embryonic rut cerebral cortex. Nature 1994:372:263-266.
31. Temple S: Division and differentiation of isolated CNS blast cells in microcullure. Nature 1989:340:471-473.
32. Morshead CM. Reynolds BA, Craig CG. McBumey MW. Staines WA. Morassutti D, Weiss S. van dcr Koov D: Neural stem cells in the adult mammalian forebrain: A relatively quiescent subpopulation of subependymal cells. Neuron 1994:13:1071-1082.
33. Pamavclas JG. Barfield JA. Frankc E. Luskin MB: Separate progenitor cells give rise to pyramidal and nonpyramidal neurons in the rat telencephalon. Ccreb Cortex 1991:1:463-468.
34. Homma S. Yaginuma H, Oppenheim RW: Programmed cell death during the earliest stages of spinal cord development in the chick embryo: A possible means of early phenotypic selection. J Comp Neurol 1994;345:377-395.
35. Smart I: The subependymal layer of the mouse brain and its cell production as shown by radioautography after’H-thymidine injection. J Comp Neurol 1961:116:325-347.
36. Morshead CM. van der Kooy D: Postmitotic death is the fate of constitutivcly proliferating cells in the subependymal layer of the adult mouse brain. J Ncurosci 1992:12:249-256.
37. Krueger BK, Bume JF. Raff MC: Evidence for large-scale astrocyte death in the developing cerebellum. J Ncurosci 1995:15:3366-3374.
38. Reynolds BA, Telzlaff W. Weiss S: A multipo-lent EGF-rcsponsive striatal embryonic progenitor cell produces neurons and astrocytes. J Ncurosci 1992;12:4565-4574.