Journal of Neuroscience, Vol 9, 25-37, Copyright © 1989 by Society for Neuroscience
Structural and functional properties of reticulospinal neurons in the early-swimming stage Xenopus embryo
P van Mier and HJ ten Donkelaar
Department of Anatomy and Embryology, University of Nijmegen, The Netherlands.
This study presents direct evidence that in Xenopus laevis embryos ipsi-
and contralaterally descending reticulospinal fibers from the caudal brain
stem project to the spinal cord, where they directly contact primary
motoneurons. At stage 30, occasional contacts between primary motoneurons
and descending axons are present. These contacts are possibly already
functional since presynaptic vesicles were sometimes observed. Furthermore,
the physiological data obtained in this study suggest that reticulospinal
neurons in the caudal brain stem are involved in the central generation of
early swimming. The first ingrowth of reticulospinal axons was observed in
the rostral spinal cord after application of HRP to the caudal brain stem
of stage 27/28 embryos. By stage 32, many supraspinal axons could be found
in the spinal cord at the level of the 12/13th myotome, near the time of
the first rhythmic swimming. Both lamellipodial and varicose growth cones
were found. Intracellular recordings from the brain stem and extracellular
recordings from the myotomal muscles in curarized embryos around stage 30
revealed neurons in the caudal brain stem which were active during early
fictive swimming. After intracellular staining with Lucifer yellow neurons
with descending axons were found in the brain- stem reticular formation.
These reticulospinal neurons showed "motoneuron-like" phasic activity,
producing one spike each swimming cycle. Rhythmically occurring spikes with
swimming periodicity were superimposed on a sustained depolarization level
of some 5-30 mV. Reticulospinal neurons in the brain stem resemble
descending interneurons in the spinal cord by their morphology, projection
pattern, and activity during early swimming. Reticulospinal neurons and
descending interneurons might therefore form one continuous population of
projecting interneurons with a different location but a similar function.
In support of this we propose that the embryonic brain-stem reticular
formation forms part of the swimming pattern generator.