Literature DB >> 3770301

Normal development of the skeleton in chick limb buds devoid of dorsal ectoderm.

P Martin, J Lewis.   

Abstract

It has been suggested that the ectoderm on the dorsal and ventral faces of the limb bud plays a part in controlling the pattern of cartilage differentiation. To test this, the dorsal wing bud ectoderm in the chick embryo was destroyed by irradiation with ultraviolet light at stage 17-19, at the very beginning of limb bud development, but the apical ectodermal ridge was spared. The irradiated ectoderm disappeared within 24 hr (by stage 23-24) and did not regenerate thereafter; thus the dorsal surface of the limb bud was kept denuded throughout most of the period of skeletal pattern formation. By 6 or 7 days after the irradiation (stage 35), when the rudiments of all the adult skeletal elements are normally present in recognizable form, the irradiated wings could be placed into two categories, those that were approximately normal in shape and those that had curled dorsally. All of these limbs were reduced in size, to varying degrees, when compared to their controls and lacked dorsal soft tissues. The limbs that were normal in shape, however, even though sometimes denuded over practically the whole extent of their dorsal surface, almost always had a complete and normally proportioned cartilage pattern, suggesting that ectoderm (other than the apical ectodermal ridge) does not exert any direct control over the development of the limb cartilage pattern. However, many of those limbs that had curled as a result of the irradiation did have major pattern deformities, suggesting that the topology of cartilage differentiation does depend on the shape of the limb bud.

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Mesh:

Year:  1986        PMID: 3770301     DOI: 10.1016/0012-1606(86)90091-6

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  5 in total

1.  A scanning electron microscopic study of the normal development of the chick wing from stages 19 to 36. A supplement to the Hamburger and Hamilton staging system.

Authors:  B M Murray; D J Wilson
Journal:  Anat Embryol (Berl)       Date:  1994-02

2.  Slit-Robo signalling establishes a Sphingosine-1-phosphate gradient to polarise fin mesenchyme.

Authors:  Harsha Mahabaleshwar; P V Asharani; Tricia Yi Loo; Shze Yung Koh; Melissa R Pitman; Samuel Kwok; Jiajia Ma; Bo Hu; Fang Lin; Xue Li Lok; Stuart M Pitson; Timothy E Saunders; Tom J Carney
Journal:  EMBO Rep       Date:  2022-06-09       Impact factor: 9.071

3.  The role of spatially controlled cell proliferation in limb bud morphogenesis.

Authors:  Bernd Boehm; Henrik Westerberg; Gaja Lesnicar-Pucko; Sahdia Raja; Michael Rautschka; James Cotterell; Jim Swoger; James Sharpe
Journal:  PLoS Biol       Date:  2010-07-13       Impact factor: 8.029

4.  Interdigital chondrogenesis and extra digit formation in the duck leg bud subjected to local ectoderm removal.

Authors:  D Macias; Y Gañan; J M Hurle
Journal:  Anat Embryol (Berl)       Date:  1992

Review 5.  Retinoic acid in limb-bud outgrowth: review and hypothesis.

Authors:  D F Paulsen
Journal:  Anat Embryol (Berl)       Date:  1994-11
  5 in total

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