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PMID: 9763477 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Multiple restricted origin of oligodendrocytes.

Spassky N, Goujet-Zalc C, Parmantier E, Olivier C, Martinez S, Ivanova A, Ikenaka K, Macklin W, Cerruti I, Zalc B, Thomas JL

Abstract

The plp gene encodes the proteolipid protein and its alternatively spliced product DM-20, major proteins of CNS myelin. In the mouse, plp/dm-20 transcripts are expressed beginning at embryonic day 9.5 (E9.5) by restricted foci of germinative neuroepithelial cells. To determine the identity of the neural precursors expressing plp/dm- 20, a zeomycin resistance gene fused to the lacZ reporter was expressed in transgenic mice under the control of the plp regulatory sequences. In the three different lines generated, the pattern of beta-galactosidase expression was similar and superimposable on the expression pattern of endogenous plp/dm-20. Both in vivo and in vitro, the transgene was expressed by O4(+) pre-oligodendrocytes, and later by RIP+ differentiated oligodendrocytes, but not by neuronal cells, astrocytes, or radial glial cells. After zeomycin selection, a dramatic enrichment in O4(+) pre-oligodendrocytes was observed in cultures derived from E12.5 transgenic embryos. This enrichment indicates the oligodendroglial specification of neural precursors that continuously express plp/dm-20. Early plp/dm-20-expressing precursors, however, appear to be a separate population from previously described PDGFRalpha oligodendrocyte precursors, as shown by the striking differences in their (1) patterns of distribution and (2) responsiveness to PDGF. These data suggest that oligodendrocytes have a plural origin and that early plp/dm-20 defines one of the neural lineages generating oligodendrocytes.

MeSH Terms
Animals Biomarkers Bleomycin/pharmacology Brain Chemistry/genetics Cell Differentiation/physiology Cell Lineage/physiology Cells, Cultured Central Nervous System/cytology,embryology Cloning, Molecular DNA-Binding Proteins/analysis,genetics,metabolism Drug Resistance, Microbial Female Gene Expression Regulation, Developmental Lac Operon Male Mice Mice, Transgenic Neurons/chemistry,cytology,physiology Oligodendroglia/chemistry,cytology,physiology Receptors, Platelet-Derived Growth Factor/analysis,genetics Stem Cells/chemistry,cytology,physiology Transcription Factors/analysis,genetics,metabolism Transgenes/physiology beta-Galactosidase/genetics
Chemicals
Biomarkers DNA-Binding Proteins Myt1 protein, mouse Transcription Factors Bleomycin Zeocin Receptors, Platelet-Derived Growth Factor beta-Galactosidase
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Spassky N
Biologie des Interactions Neurones/Glie, Institut National de la Santé et de la Recherche Médicale U-495, Université Pierre Marie Curie, Hôpital de la Salpêtrière, 75651 Paris Cedex 13, France.
Goujet-Zalc C
Parmantier E
Olivier C
Martinez S
Ivanova A
Ikenaka K
Macklin W
Cerruti I
Zalc B
Thomas J L
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Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
0270-6474
Published
1998-10-15
Pages
8331-43
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6792828
Subset
IM
Grants
NINDS NIH HHS · R01 NS025304 · United States
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