Development of O4+/O1- immunopanned pro-oligodendroglia in vitro

Developmental Brain Research

Volumn 112, Issue 1, 1999, Pages 79-87

  Ingraham, Christine A ^a   Rising, Lisa J ^a   Morihisa, John M ^a  

^a ALBANY MEDICAL COLLEGE   (United States)

Author keywords

Astroglia; Cell culture; Development; Immunopanning; Myelin; Oligodendroglia

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN; MYELIN BASIC PROTEIN;

ANIMAL CELL; ANTIBODY SPECIFICITY; ARTICLE; CONTROLLED STUDY; IMMUNOCYTOCHEMISTRY; MACROGLIA; MYELINATION; NERVE CELL CULTURE; NERVE CELL DIFFERENTIATION; NEWBORN; NONHUMAN; OLIGODENDROGLIA; PRIORITY JOURNAL; RAT;

ANIMALS; ANIMALS, NEWBORN; ANTIBODIES, MONOCLONAL; CATTLE; CELL AGING; CELLS, CULTURED; FETAL BLOOD; GLIAL FIBRILLARY ACIDIC PROTEIN; IMMUNOLOGIC TECHNIQUES; MICROSCOPY, PHASE-CONTRAST; MYELIN BASIC PROTEINS; OLIGODENDROGLIA; RATS; RATS, SPRAGUE-DAWLEY; STEM CELLS; TIME FACTORS;

ANIMALIA; BOVINAE;

EID: 0033545199     PISSN: 01653806     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-3806(98)00163-1     Document Type: Article

References (45)

1. E.R. Abney, P.P. Bartlett, M.C. Raff, Astrocytes, ependymal cells and oligodendrocytes develop on schedule in dissociated cell cultures of embryonic rat brain, Dev. Biol. 83 (1981) 301-310.
2. C. Agresti, F. Aloisi, G. Levi, Heterotypic and homotypic cellular interactions influencing the growth and differentiation of bipotential oligodendrocyte-type 2 astrocyte progenitors in culture, Dev. Biol. 144 (1991) 16-29.
3. F. Aloisi, C. Agresti, D. D'Urso, G. Levi, Differentiation of bipotential glial precursors into oligodendrocytes is promoted by interaction with type-1 astrocytes in cerebellar cultures, Proc. Natl. Acad. Sci. U.S.A. 85 (1988) 6167-6171.
4. R. Bansal, A.L. Gard, S.E. Pfeiffer, Multiple and novel specificities of monoclonal antibodies O1, O4 and R-mAb used in the analysis of oligodendrocyte development, J. Neurosci. Res. 21 (1989) 260-267.
5. R. Bansal, K. Stefansson, S.E. Pfeiffer, Proligodendroblast antigen (POA), a developmental antigen expressed by A007/O4-positive oligodendrocyte progenitors prior to the appearance of sulfatide and galactocerebroside, J. Neurochem. 58 (1992) 2221-2229.
6. A. Baron-Van Evercooren, Future prospects in transplantation, Ann. Neurol. 36 (1994) S151-S156.
7. T. Behar, F.A. McMorris, E.A. Novotny, J.L. Barker, M. Dubois-Dalcq, Growth and differentiation properties of O-2A progenitors purified from rat cerebral hemispheres, J. Neurosci. Res. 21 (1988) 168-180.
8. A. Bignami, L.F. Eng, D. Dahl, C.T. Uyeda, Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence, Brain Res. 43 (1972) 429-435.
9. M. Dubois-Dalcq, Regeneration of oligodendrocytes and myelin, Trends Neurosci. 18 (1995) 289-291.
10. M. Dubois-Dalcq, Characterization of a slowly proliferative cell along the oligodendrocyte differentiation pathway, EMBO J. (1987) 2587-2595.
11. M. Dubois-Dalcq, T. Behar, L. Hudson, R.A. Lazzarini, Emergence of three myelin proteins in oligodendrocyte cultures without neurons, J. Cell Biol. 120 (1986) 384-392.
12. I.D. Duncan, Glial cell transplantation and remyelination of the central nervous system, Neuropathol. Appl. Neurobiol. 22 (1996) 87-100.
13. I.D. Duncan, C. Paino, D.R. Archer, P.M. Wood, Functional capacities of transplanted cell-sorted adult oligodendrocytes, Dev. Neurosci. 14 (1992) 114-122.
14. A. Espinosa de los Monteros, M.S. Zhang, M. Gordon, M. Aymie, J. De Vellis, Transplantation of cultured premyelinating oligodendrocytes into normal and myelin-deficient rat brain, Dev. Neurosci. 14 (1992) 98-104.
15. C. Ffrench-Constant, B.W. Kiernan, R. Milner, S. Scott-Drew, Developmental studies of oligodendrocyte precursor cell migration and their implications for transplantation as therapy for multiple sclerosis, Eye 8 (1994) 221-223.
16. R.J.M. Franklin, S.A. Bayley, W.F. Blakemore, Transplanted CG4 cells (an oligodendrocyte progenitor cell line) survive, migrate and contribute to repair of areas of demyelination in X-irradiated and damaged spinal cord but not in normal spinal cord, Exp. Neural. 137 (1996) 263-276.
17. R.J.M. Franklin, S.A. Bayley, R. Milner, C. Ffrench-Constant, W.F. Blakemore, Differentiation of the O-2A progenitor cell line CG-4 into oligodendrocytes and astrocytes following transplantation into glia-deficient areas of CNS white matter, Glia 13 (1995) 39-44.
18. R.J.M. Franklin, W.F. Blakemore, Glial cell transplantation and plasticity in the O-2A lineage - implications for CNS repair, Trends Neurosci. 18 (1995) 151-156.
19. R.J.M. Franklin, A.J. Crang, W.F. Blakemore, Transplanted type 1 astrocytes facilitate repair of demyelinating lesions by host oligodendrocytes in adult rat spinal cord, J. Neurocytol. 20 (1991) 420-430.
20. A.L. Gard, S.E. Pfeiffer, W.C. Williams II, Immunopanning and developmental stage-specific primary culture of oligodendrocyte progenitors (O4+GalC-) directly from postnatal rodent cerebrum, Neuroprotocols: A Companion to Methods in Neurosciences 2 (1993) 209-218.
21. A.L. Gard, W.C. Williams II, M.R. Burrell, Oligodendroblasts distinguished from O-2A glial progenitors by surface phenotype (O4+ GalC-) and response to cytokines using signal transducer LIFRβ, Dev. Biol. 167 (1995) 596-608.
22. C. Godfraind, V.L. Friedrich, K.V. Holmes, M. Dubois-Dalcq, In vivo analysis of glial cell phenotypes during a viral demyelinating disease in mice, J. Cell Biol. 109 (1989) 2405-2416.
23. R.J. Hardy, V.L. Friedrich, Progressive remodeling of the oligodendrocyte process arbor during myelinogenesis, Dev. Neurosci. 18 (1996) 243-254.
24. C.A. Ingraham, K.D. McCarthy, Plasticity of process-bearing glial cell cultures from neonatal rat cerebral cortical tissue, J. Neurosci. 9 (1989) 63-69.
25. S.U. Kim, F.A. McMorris, T.J. Sprinkle, Immunofluorescence demonstration of 2′,3′-cyclic-nucleotide 3′-phosphodiesterase in cultured oligodendrocytes of mouse, rat, calf and human, Brain Res. 300 (1984) 195-199.
26. P.E. Knapp, W.P. Bartlett, R.P. Skoff, Cultured oligodendrocytes mimic in vivo phenotypic characteristics: cell shape, expression of myelin-specific antigens and membrane production, Dev. Biol. 120 (1987) 356-365.
27. G. Levi, F. Aloisi, G.P. Wilkin, Differentiation of cerebellar bipotential glial precursors into oligodendrocytes in primary culture: developmental profile of surface antigens and mitotic activity, J. Neurosci. Res. 18 (1987) 407-417.
28. G. Levi, V. Gallo, M.T. Ciotti, Bipotential precursors of putative fibrous astrocytes and oligodendrocytes in rat cerebellar cultures express distinct features and 'neurone-like' gamma-aminobutyric acid transport, Proc. Natl. Acad. Sci. U.S.A. 83 (1986) 1504-1508.
29. S.M. Levine, J.E. Goldman, Embryonic divergence of oligodendrocyte and astrocyte lineages in developing rat cerebrum, J. Neurosci. 8 (1988) 3992-4006.
30. M. Mayer-Pröschel, Isolation and generation of oligodendrocytes by immunopannning, in: J.N. Crawley, C.R. Gerfen, R. McKay, M.A. Rogawski, D.R. Sibley, P. Skolnick (Eds.), Current Protocols in Neuroscience, Wiley, New York, 1998, pp. 3.13.1-3.13.11.
31. M.C. Raff, R.H. Miller, M. Noble, A glial progenitor cell that develops in vitro into an astrocyte or an oligodendrocyte depending on culture medium, Nature 303 (1983) 390-396.
32. M.C. Raff, R. Mirsky, K.L. Fields, R.P. Lisak, S.H. Dorfman, D.H. Silberberg, N.A. Gregson, S. Liebowitz, M. Kennedy, Galactocerebroside: a specific cell surface antigenic marker for oligodendrocytes in culture, Nature 274 (1978) 813-816.
33. B. Ranscht, P.A. Clapshaw, J. Price, M. Noble, W. Siefert, Development of oligodendrocytes and Schwann cells studied with a monoclonal antibody against galactocerebroside, Proc. Natl. Acad. Sci. U.S.A. 79 (1982) 2709-2713.
34. C.L. Rosen, R.P. Bunge, M. Ard, P.M. Wood, Type 1 astrocytes inhibit myelination by rat oligodendrocytes in vitro, J. Neurosci. 9 (1989) 3371-3379.
35. M. Schachner, S.K. Kim, R. Zehnle, Developmental expression in central and peripheral nervous system of oligodendrocyte cell surface antigens (O antigens) recognized by monoclonal antibodies, Dev. Biol. 83 (1981) 328-338.
36. I. Sommer, M. Schachner, Cells that are O4 antigen-positive and O1 antigen-negative differentiate into O1 antigen-positive oligodendrocytes, Neurosci. Lett. 29 (1982) 183-188.
37. I. Sommer, M. Schachner, Monoclonal antibodies (O1 and O4) to oligodendrocyte cell surfaces: an immunocytochemical study in the central nervous system, Dev. Biol. 83 (1981) 311-327.
38. S. Temple, M.C. Raff, Clonal analysis of oligodendrocyte development in culture: evidence for a developmental clock that counts cell divisions, Cell 44 (1986) 773-779.
39. S. Temple, M.C. Raff, Differentiation of a bipotential glial progenitor cell in a single cell microculture, Nature 313 (1985) 223-225.
40. J. Trotter, M. Schachner, Cells positive for the O4 surface antigen isolated by cell sorting are able to differentiate into astrocytes or oligodendrocytes, Dev. Brain Res. 46 (1989) 115-122.
41. A.E. Warrington, E. Barbarese, S.E. Pfeiffer, Differential myelinogenic capacity of specific developmental stages of the oligodendrocyte lineage upon transplantation into hypomyelinating hosts, J. Neurosci. Res. 34 (1993) 1-13.
42. A.E. Warrington, S.E. Pfeiffer, Morphology, proliferation and differentiation of oligodendrocytes in unfixed postnatal rat cerebellum, J. Neurosci. Res. 33 (1992) 338-353.
43. B.P. Williams, E.R. Abney, M.C. Raff, Macroglial cell development in embryonic rat brain: studies using monoclonal antibodies, fluorescence activated cell sorting and cell culture, Dev. Biol. 112 (1985) 126-134.
44. P.M. Wood, R.P. Bunge, The origin of remyelinating cells in the adult central nervous system: the role of the mature oligodendrocyte, Glia 4 (1991) 225-232.
45. P.M. Wood, J. Mora, Source of remyelinating oligodendrocytes, Adv. Neurol. 59 (1993) 113-123.