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Volume 16, Number 24,
Issue of December 15, 1996
pp. 7981-7994
Copyright ©1996 Society for Neuroscience
Origin of Oligodendrocytes within the Human Spinal Cord
Received Aug. 5, 1996; revised Sept. 26, 1996; accepted Sept. 30, 1996.
Mohammad Hajihosseini,
To Nam Tham, and
Monique Dubois-Dalcq
Unité de Neurovirologie et Régénération du
Système Nerveux, Institut Pasteur, 75015 Paris, France
To determine the time and site of origin of the oligodendrocyte
lineage in the developing human spinal cord, we have examined tissues
from 45 to 83 d postconception (dpc) using sets of probes and
antibodies recognizing oligodendrocyte-specific glycolipids, transcripts, and proteins. We found that two clusters of
oligodendrocyte precursors appear on or before 45 dpc on each side of
the cord ventral ependyma above the floor plate. These precursors
express glycolipids recognized by the O4 and Rmab antibodies,
platelet-derived growth factor -receptor, myelin basic protein
(MBP), and 2 , 3 -cyclic nucleotide 3 phosphodiesterase as well as MBP
and proteolipid transcripts. Expression of the morphogen sonic hedgehog
was detected in the floor plate at 45 dpc and decreased at 58 dpc.
During this period, oligodendrocyte precursors emerged in the ventral
and lateral region of the forming white matter, a process occurring first in cervical and later in lumbar cord. The majority of
O4+ cells express the proliferating cell nuclear antigen
(PCNA), and their pattern of dispersion suggests that these cells
progressively populate the lateral and dorsal cord regions.
Oligodendrocytes expressing galactocerebroside appeared at 53 dpc and
did not express PCNA. Oligodendrocyte precursors were detected in
dorsal cord regions at 74 dpc and at 83 dpc when myelination started in
the ventral roots. Thus, oligodendrocyte precursors expressing myelin transcripts and proteins emerge in the ventral region of the embryonic cord several weeks before myelination.
Key words:
oligodendrocyte origin;
developing human spinal cord;
myelin gene transcripts;
in situ hybridization;
immunolabeling of myelin specific glycolipids and proteins;
platelet-derived growth factor receptor
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