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Journal of Neuroscience, Vol 1, 204-217, Copyright © 1981 by Society for Neuroscience
Separation of cell types from embryonic chicken and rat spinal cord: characterization of motoneuron-enriched fractions
RI Schnaar and AE Schaffner
Single cell suspensions prepared from embryonic chick or rat spinal cords
were separated into morphologically and functionally distinct subpopulation
based on their buoyant densities The lightest fraction (F- 1) was highly
enriched for cells containing the enzyme choline acetyltransferase (CAT), a
marker for developing motoneurons. The morphology biochemistry, and in
vitro development of this and other spinal cord cell fractions isolated by
the outlined procedure were investigated. Spinal cords, dissected from
6-day chick or 12-day rat embryos, were dissociated with trypsin and
applied to iso-osmotic metrizamide density gradients. After brief
centrifugation, biochemical analysis revealed that cholinergic cells
migrated to lower densities than other spinal cord cells. The use of
discontinuous density gradients allowed rapid and simple isolation of three
fractions of viable cells (designated F-1 to F-3, lowest to highest
density). Characterization of chicken and rat embryo cell fractions gave
similar results. The cells in Fraction 1 were large with prominent nuclei
and nucleoli, while those in F-2 and F-3 were distinctly smaller. Fraction
1 was highly enriched for cholinergic cells. The CAT specific activity
(CAT/cell) was increased 400% in Fraction 1 compared to unfractionated
cells, while CAT specific activity in F-2 and F-3 was reduced to 25% and
less than 4% that of unfractionated cells, respectively. The recovery of
cholinergic cells using this procedure was much better than with other
published procedures; greater than half the spinal cord CAT activity was
routinely recovered in the enriched fraction. The cholinergic-enriched
cells (F-1) were unique in their in vitro growth characteristics. All
fractions had neuronal cells, while non-neuronal cells were distributed
primarily in F-3, fewer in F-2, and were essentially absent from F-1.
Neurons in F-2 and F-3 remained viable under a variety of conditions, most
of which were not supportive of F-1 cell survival. The cholinergic-enriched
F-1 cells survived and developed only in the presence of muscle cells or in
muscle-conditioned medium on highly adhesive substrata. Large, multipolar
neurons predominated under these conditions. The method described provides
a means of characterizing the factors involved in the development of
distinct populations of cells from the embryonic spinal cord.
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