Literature DB >> 2359459

Polarizing activity and retinoid synthesis in the floor plate of the neural tube.

M Wagner1, C Thaller, T Jessell, G Eichele.   

Abstract

In many developing organisms the establishment of axial polarity and the patterning of cells depend on local signals that derive from restricted regions of the embryo. In vertebrate embryos, the origins of tissue polarity have been examined extensively in the developing limb. The anteroposterior pattern of the chick limb seems to be controlled by a morphogen, possibly retinoic acid, that is enriched in a region of the limb known as the zone of polarizing activity (ZPA). Certain tissues other than the ZPA have also shown polarizing activity experimentally in the chick limb, raising the possibility that signalling molecules involved in pattern formation in different embryonic tissues are conserved. Here we provide evidence that a similar polarizing activity is also present in a restricted region of the developing central nervous system (CNS). We show that a specialized group of neural cells termed the floor plate, but not other regions of the CNS, mimics the ZPA in respecifying the digit pattern in the developing chick limb. In addition, using an in vitro biochemical assay, we show that the floor plate can synthesize retinoic acid and 3,4-didehydroretinol, the precursor of a second morphogenetically active retinoid, 3,4-didehydroretinoic acid. These results show that the floor plate is a local source of a ZPA-like polarizing signal, possibly a retinoid, which may regulate the pattern of cell differentiation in the developing CNS.

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Year:  1990        PMID: 2359459     DOI: 10.1038/345819a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  37 in total

Review 1.  Retinoic acid, neoplasia, differentiation and development.

Authors:  C Berry
Journal:  Virchows Arch       Date:  1997-04       Impact factor: 4.064

2.  Development of floor plate, neurons and axonal outgrowth pattern in the early spinal cord of the notochord-deficient chick embryo.

Authors:  H W van Straaten; J W Hekking
Journal:  Anat Embryol (Berl)       Date:  1991

Review 3.  Retinoids and the control of growth/death decisions in human neuroblastoma cell lines.

Authors:  G Melino; C J Thiele; R A Knight; M Piacentini
Journal:  J Neurooncol       Date:  1997-01       Impact factor: 4.130

4.  Differentiation of the chick embryo floor plate.

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

5.  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

6.  The identification of a 9-cis retinol dehydrogenase in the mouse embryo reveals a pathway for synthesis of 9-cis retinoic acid.

Authors:  A Romert; P Tuvendal; A Simon; L Dencker; U Eriksson
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

7.  Segment-specific pattern of sympathetic preganglionic projections in the chicken embryo spinal cord is altered by retinoids.

Authors:  C J Forehand; E B Ezerman; J P Goldblatt; D L Skidmore; J C Glover
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

8.  Efficient differentiation of insulin-producing cells from skin-derived stem cells.

Authors:  W Guo; C Miao; S Liu; Z Qiu; J Li; E Duan
Journal:  Cell Prolif       Date:  2009-02       Impact factor: 6.831

Review 9.  The effect of vitamin A (retinoids) on pattern formation implies a uniformity of developmental mechanisms throughout the animal kingdom.

Authors:  M Maden
Journal:  Acta Biotheor       Date:  1993-12       Impact factor: 1.774

10.  Identification of a retinoic acid response element upstream of the murine Hox-4.2 gene.

Authors:  H Pöpperl; M S Featherstone
Journal:  Mol Cell Biol       Date:  1993-01       Impact factor: 4.272

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