Journal of Neuroscience, Vol 12, 1351-1362, Copyright © 1992 by Society for Neuroscience
Does lineage determine the dopamine phenotype in the tadpole hypothalamus?: A quantitative analysis
S Huang and SA Moody
Department of Anatomy & Cell Biology, University of Virginia, Charlottesville 22908.
The ancestry of dopaminergic (DA) neurons in the Xenopus laevis
hypothalamus was investigated by combining intracellular lineage dye
injections of 16- and 32-cell blastomeres with the immunofluorescent
detection of tyrosine hydroxylase at tadpole stages. At these stages, DA
neurons in the hypothalamus comprise a discrete nucleus that contains from
22 to 45 cells on each side [mean = 32.6 +/- 6.6 (SD)]. The DA nucleus
descends from only four of the 16-cell blastomeres. The two dorsal midline
blastomeres (D1.1) are the major progenitors, and in all embryos studied
they contributed to the DA nucleus. The two dorsal lateral blastomeres
(D1.2) contribute to the DA nucleus in only about half of the embryos.
Thus, the DA nucleus descends only from a discrete group of progenitors,
and the participation of some of the progenitors in the DA lineage is only
probabilistic. The number of DA neurons generated by the same blastomere
varied greatly in different animals. This variation in cell number
correlated with the degree of coherence and the density of the clone in the
hypothalamus, rather than with clonal ancestry. Bilateral deletion of the
major 32-cell progenitor (D1.1.1) resulted in a nearly complete restitution
of the DA nucleus in 74% of the embryos that successfully completed
gastrulation and neurulation. In the rest, the hypothalamus was smaller
than normal or missing, and the DA nucleus was significantly reduced in
size or absent. These results show that the DA nucleus can be restored
after its normal lineage is deleted, but complete regulation is not always
accomplished. Several blastomere progenitors dramatically altered their
contribution to the DA nucleus after D1.1.1 ablation, including two
blastomeres that normally do not contribute to the DA lineage. Thus, the
fate to produce DA neurons is not determined at cleavage stages.