TY - JOUR
T1 - Effects of transforming growth factor-β and platelet-derived growth factor on oligodendrocyte precursors
T2 - Insights gained from a neuronal cell line
AU - Asakura, Kunihiko
AU - Hunter, Samuel F.
AU - Rodriguez, Moses
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 1997/6
Y1 - 1997/6
N2 - Conditioned medium derived from a rat central nervous system neuronal cell line B1O4 (B104 CM) was shown previously to contain uncharacterized potent mitogen(s) for oligodendrocyte/type-2 astrocyte (O-2A) progenitor cells. In this study, we demonstrated that B104 cells produce and secrete platelet-derived growth factor (PDGF)-AA homodimer, but not PDGF-B chain. B104 cells did not express other known potent mitogens for O-2A progenitor cells, including fibroblast growth factor-2 and neurotrophin-3. Unexpectedly, B104 cells also expressed transcripts of transforming growth factor-β1 (TGF- β1) and -β2 (TGF-β2), which are known to regulate O-2A progenitor cell differentiation and proliferation, and secreted exclusively the 25-kDa active forms of TGF-β1 and TGF-β2. Neutralization of B104 CM with anti-PDGF-AA antibody decreased proliferation of O-2A progenitor cells, whereas neutralization with anti-TGF-β antibodies had no effect. The combination of PDGF and TGF-β on proliferation was not equivalent to the effect of B104 CM, indicating the possibility of an unidentified growth factor. B104 CM maintained a high expression of PDGF-α receptor in oligodendrocytes. The observation that both a stimulatory factor (PDGF-AA) and a regulatory factor (TGF-β) for O-2A progenitor cell proliferation and differentiation are produced from a single neuronal cell line emphasizes the potential critical interaction between neurons and O-2A progenitor cells in myelination and possibly in remyelination.
AB - Conditioned medium derived from a rat central nervous system neuronal cell line B1O4 (B104 CM) was shown previously to contain uncharacterized potent mitogen(s) for oligodendrocyte/type-2 astrocyte (O-2A) progenitor cells. In this study, we demonstrated that B104 cells produce and secrete platelet-derived growth factor (PDGF)-AA homodimer, but not PDGF-B chain. B104 cells did not express other known potent mitogens for O-2A progenitor cells, including fibroblast growth factor-2 and neurotrophin-3. Unexpectedly, B104 cells also expressed transcripts of transforming growth factor-β1 (TGF- β1) and -β2 (TGF-β2), which are known to regulate O-2A progenitor cell differentiation and proliferation, and secreted exclusively the 25-kDa active forms of TGF-β1 and TGF-β2. Neutralization of B104 CM with anti-PDGF-AA antibody decreased proliferation of O-2A progenitor cells, whereas neutralization with anti-TGF-β antibodies had no effect. The combination of PDGF and TGF-β on proliferation was not equivalent to the effect of B104 CM, indicating the possibility of an unidentified growth factor. B104 CM maintained a high expression of PDGF-α receptor in oligodendrocytes. The observation that both a stimulatory factor (PDGF-AA) and a regulatory factor (TGF-β) for O-2A progenitor cell proliferation and differentiation are produced from a single neuronal cell line emphasizes the potential critical interaction between neurons and O-2A progenitor cells in myelination and possibly in remyelination.
KW - Myelination
KW - Oligodendrocyte/type-2 astrocyte progenitor
KW - Platelet-derived growth factor
KW - Platelet-derived growth factor-α receptor
KW - Remyelination
KW - Transforming growth factor- β
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U2 - 10.1046/j.1471-4159.1997.68062281.x
DO - 10.1046/j.1471-4159.1997.68062281.x
M3 - Article
C2 - 9166720
AN - SCOPUS:0030929911
VL - 68
SP - 2281
EP - 2290
JO - Journal of Neurochemistry
JF - Journal of Neurochemistry
SN - 0022-3042
IS - 6
ER -