Literature DB >> 2081459

Orientation of commissural axons in vitro in response to a floor plate-derived chemoattractant.

M Placzek1, M Tessier-Lavigne, T Jessell, J Dodd.   

Abstract

Developing axons are guided to their targets by molecular cues in their local environment. Some cues are short-range, deriving from cells along axonal pathways. There is also increasing evidence for longer-range guidance cues, in the form of gradients of diffusible chemoattractant molecules, which originate from restricted populations of target cells. The guidance of developing commissural axons within the spinal cord depends on one of their intermediate cellular targets, the floor plate. We have shown previously that floor plate cells secrete a diffusible factor(s) that can alter the direction of commissural axon growth in vitro. Here we show that the factor is an effective chemoattractant for commissural axons. It can diffuse considerable distances through a collagen gel matrix and through dorsal and ventral neural epithelium in vitro to reorient the growth of virtually all commissural axons. The orientation of axons occurs in the absence of detectable effects on the survival of commissural neurons or on the rate of commissural axon extension. The regionally restricted expression of the factor suggests that it is present in the embryonic spinal cord in a gradient with its high point at the floor plate. These observations support the idea that the guidance of commissural axons to the ventral midline of the spinal cord results in part from the secretion of a chemoattractant by the floor plate.

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Year:  1990        PMID: 2081459     DOI: 10.1242/dev.110.1.19

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  23 in total

1.  F-spondin is a contact-repellent molecule for embryonic motor neurons.

Authors:  V Tzarfati-Majar; T Burstyn-Cohen; A Klar
Journal:  Proc Natl Acad Sci U S A       Date:  2001-04-03       Impact factor: 11.205

2.  Widespread expression of netrin-1 by neurons and oligodendrocytes in the adult mammalian spinal cord.

Authors:  C Manitt; M A Colicos; K M Thompson; E Rousselle; A C Peterson; T E Kennedy
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling.

Authors:  Sara M Peyrot; John B Wallingford; Richard M Harland
Journal:  Dev Biol       Date:  2011-01-27       Impact factor: 3.582

4.  DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1.

Authors:  Alice Ly; Anatoly Nikolaev; Geetha Suresh; Yufang Zheng; Marc Tessier-Lavigne; Elke Stein
Journal:  Cell       Date:  2008-06-27       Impact factor: 41.582

5.  Differentiation of the chick embryo floor plate.

Authors:  C M Griffith; E J Sanders
Journal:  Anat Embryol (Berl)       Date:  1991

6.  Structure of the embryonic primate spinal cord at the closure of the first reflex arc.

Authors:  E Knyihar-Csillik; B Csillik; P Rakic
Journal:  Anat Embryol (Berl)       Date:  1995-06

7.  Axial structures control laterality in the distribution pattern of endothelial cells.

Authors:  S Klessinger; B Christ
Journal:  Anat Embryol (Berl)       Date:  1996-04

8.  Type Ib BMP receptors mediate the rate of commissural axon extension through inhibition of cofilin activity.

Authors:  Ken Yamauchi; Supraja G Varadarajan; Joseph E Li; Samantha J Butler
Journal:  Development       Date:  2013-01-15       Impact factor: 6.868

9.  The ventralizing effect of the notochord on somite differentiation in chick embryos.

Authors:  B Brand-Saberi; C Ebensperger; J Wilting; R Balling; B Christ
Journal:  Anat Embryol (Berl)       Date:  1993-09

10.  Spinal cord-notochord relationship in normal human embryos and in a human embryo with double spinal cord.

Authors:  M Saraga-Babić; V Stefanović; J Wartiovaara; E Lehtonen
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

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