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Slit-mediated repulsion is a key regulator of motor axon pathfinding in the hindbrain

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posted on 2023-06-09, 07:07 authored by Rachel Hammond, Valerie Vivancos, Arifa Naeem, John Chilton, Elvira Mambetisaeva, William Andrews, Vasi Sundaresan, Sarah GuthrieSarah Guthrie
The floor plate is known to be a source of repellent signals for cranial motor axons, preventing them from crossing the midline of the hindbrain. However, it is unknown which molecules mediate this effect in vivo. We show that Slit and Robo proteins are candidate motor axon guidance molecules, as Robo proteins are expressed by cranial motoneurons, and Slit proteins are expressed by the tissues that delimit motor axon trajectories, i.e. the floor plate and the rhombic lip. We present in vitro evidence showing that Slit1 and Slit2 proteins are selective inhibitors and repellents for dorsally projecting, but not for ventrally projecting, cranial motor axons. Analysis of mice deficient in Slit and Robo function shows that cranial motor axons aberrantly enter the midline, while ectopic expression of Slit1 in chick embryos leads to specific motor axon projection errors. Expression of dominant-negative Robo receptors within cranial motoneurons in chick embryos strikingly perturbs their projections, causing some motor axons to enter the midline, and preventing dorsally projecting motor axons from exiting the hindbrain. These data suggest that Slit proteins play a key role in guiding dorsally projecting cranial motoneurons and in facilitating their neural tube exit. Slit-mediated repulsion is a key regulator of motor axon pathfinding in the hindbrain (PDF Download Available). Available from: https://www.researchgate.net/publication/7599669_Slit-mediated_repulsion_is_a_key_regulator_of_motor_axon_pathfinding_in_the_hindbrain [accessed Jul 11, 2017].

History

Publication status

  • Published

File Version

  • Published version

Journal

Development

ISSN

0950-1991

Publisher

Company of Biologists

Issue

20

Volume

132

Page range

4483-4495

Department affiliated with

  • Neuroscience Publications

Full text available

  • Yes

Peer reviewed?

  • Yes

Legacy Posted Date

2017-07-11

First Open Access (FOA) Date

2017-07-11

First Compliant Deposit (FCD) Date

2017-07-11

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