Journal of Neuroscience, Vol 7, 2502-2509, Copyright © 1987 by Society for Neuroscience
Growth and morphogenesis of an autonomic ganglion. II. Establishment of neuron position
RD Heathcote and PB Sargent
The developmental events affecting the positioning of neurons were examined
in the frog cardiac ganglion. Use of a neuron-specific marker enabled the
position of all neurons in the ganglion to be quantified at different
developmental stages. Subsets of neurons born at specific times were
labeled with 3H-thymidine, and their positions were mapped at different
developmental stages. This technique identifies a subset of cells within a
seemingly homogeneous pool of neurons and provides an opportunity for
studying the position of individual neurons during ganglion morphogenesis.
Comparison of identified neurons in different animals has revealed several
unexpected results. First, during a period of dramatic ganglion and
cellular morphogenesis there is little or no cell death since the number of
identified neurons does not change during this time. Second, the
distinctive clusters that are characteristic of parasympathetic ganglia
have been shown to be ephemeral because identified cells that were
neighbors early in development become separated during ganglion
morphogenesis. Third, individual postmitotic neurons do not actively
migrate to produce the observed changes in neuron distribution, as
evidenced by the fact that their relative position in the ganglion is
maintained. Fourth, both ganglion and target undergo intercalary growth
since the absolute distance of identified neurons from one another
increases while the relative distance remains the same. Finally, the
differentiation of neurons is analogous to the inside-out pattern seen in
many parts of the CNS. Thus the ability to identify cells within a large
ensemble of seemingly equivalent neurons has made it possible to
investigate ganglion morphogenesis at the level of individual cells.