PUBLICATION
Pathfinding by identified zebrafish motoneurons in the absence of muscle pioneers
- Authors
- Melançon, E., Liu, D.W.C., Westerfield, M., and Eisen, J.S.
- ID
- ZDB-PUB-971013-1
- Date
- 1997
- Source
- The Journal of neuroscience : the official journal of the Society for Neuroscience 17(20): 7796-7804 (Journal)
- Registered Authors
- Eisen, Judith S., Liu, Dennis, Melançon (Brandenburg), Ellie, Westerfield, Monte
- Keywords
- acetylcholine receptors; neuromuscular junctions; axogenesis; zebrafish motoneurons; muscle pioneers; pathway navigation
- MeSH Terms
-
- Animals
- Axons/physiology
- Embryo, Nonmammalian/cytology
- Interneurons/physiology
- Motor Neurons/physiology*
- Muscles/cytology
- Muscles/physiology*
- Neural Pathways/physiology
- Zebrafish/embryology
- Zebrafish/physiology*
- PubMed
- 9315900 Full text @ J. Neurosci.
Citation
Melançon, E., Liu, D.W.C., Westerfield, M., and Eisen, J.S. (1997) Pathfinding by identified zebrafish motoneurons in the absence of muscle pioneers. The Journal of neuroscience : the official journal of the Society for Neuroscience. 17(20):7796-7804.
Abstract
To identify the cellular cues that guide zebrafish neuronal growth cones to their targets, we examined interactions between identified motor growth cones and identified muscle fibers and tested whether these fibers were required for growth cone navigation. Caudal primary motoneurons (CaPs) and middle primary motoneurons (MiPs) are identified motoneurons that innervate cell-specific regions of the myotome. Growth cones of both cells initially extend along a common pathway and then pause at a set of identified muscle fibers, called muscle pioneers, before diverging along cell-specific pathways. Muscle pioneers are intermediate targets of both CaP and MiP (Westerfield et al., 1986; Liu and Westerfield, 1990); both motoneurons extend their growth cones directly to the muscle pioneers on which the first functional neuromuscular contacts form, suggesting that muscle pioneers may provide guidance information to these growth cones. We tested this idea by ablating muscle pioneers and observing the resulting motor axonal trajectories. Both CaP and MiP ultimately formed normal axonal arbors after muscle pioneer ablation, showing that muscle pioneers are unnecessary for formation of correct axonal trajectories; however, although final cellular morphology was correct in the absence of muscle pioneers, MiP growth cones branched abnormally or extended ventrally beyond the common pathway. Ablation of CaP and the muscle pioneers together increased the aberrant behavior of the MiP growth cone. Our results provide evidence that an intermediate target, the muscle pioneers, affects motor axonal extension without altering target choice, suggesting that other cues also contribute to proper pathway navigation.
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