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      A Reevaluation of X-Irradiation Induced Phocomelia and Proximodistal Limb Patterning

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      1 , 2 , 3 , 1
      Nature

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          Abstract

          Phocomelia is a devastating, rare congenital limb malformation in which the long bones are shorter than normal, with the upper portion of the limb being most severely affected. In extreme cases, the hands or fingers are attached directly to the shoulder and the most proximal elements (those closest to the shoulder) are entirely missing. This disorder, previously known in both autosomal recessive and sporadic forms, showed a dramatic increase in incidence in the early 1960’s due to the tragic toxicological effects of the drug thalidomide, which had been prescribed as a mild sedative 1, 2. This human birth defect is mimicked in developing chick limb buds exposed to X-irradiation 3- 5. Both X-irradiation 5 and thalidomide-induced phocomelia 5, 6 have been interpreted as patterning defects in the context of the Progress Zone Model, which states that a cell’s proximodistal (PD) identity is determined by the length of time spent in a distal limb region termed the “Progress Zone” 7. Indeed, studies of X-irradiation induced phocomelia have served as one of the two major experimental lines of evidence supporting the validity of the Progress Zone Model. Here, using a combination of molecular analysis and lineage tracing, we show that X-irradiation-induced phocomelia is fundamentally not a patterning defect, but rather results from a time-dependent loss of skeletal progenitors. As skeletal condensation proceeds from the shoulder to fingers (in a proximal to distal direction), the proximal elements are differentially affected in limb buds exposed to radiation at early stages. This conclusion changes the framework for considering the effect of thalidomide and other forms of phocomelia, suggesting the possibility that the etiology lies not in a defect in the patterning process, but rather in progenitor cell survival and differentiation. Moreover, molecular evidence that PD patterning is unaffected following X-irradiation does not support the predictions of the Progress Zone Model.

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          Most cited references30

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          Sonic hedgehog mediates the polarizing activity of the ZPA.

          The zone of polarizing activity (ZPA) is a region at the posterior margin of the limb bud that induces mirror-image duplications when grafted to the anterior of a second limb. We have isolated a vertebrate gene, Sonic hedgehog, related to the Drosophila segment polarity gene hedgehog, which is expressed specifically in the ZPA and in other regions of the embryo, that is capable of polarizing limbs in grafting experiments. Retinoic acid, which can convert anterior limb bud tissue into tissue with polarizing activity, concomitantly induces Sonic hedgehog expression in the anterior limb bud. Implanting cells that express Sonic hedgehog into anterior limb buds is sufficient to cause ZPA-like limb duplications. Like the ZPA, Sonic hedgehog expression leads to the activation of Hox genes. Sonic hedgehog thus appears to function as the signal for antero-posterior patterning in the limb.
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            Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

            M. McLeod (1980)
            The procedure described by Inouye ('76) for the staining of full-term mouse fetal skeletons has been adapted for use with mouse embryos and fetuses of days 14-18 of gestation. The main adaptations for younger specimens involve a longer time in acetone, in lieu of skinning, and omission of the aqueous KOH step. These adaptations require more time but result in consistently good staining of intact specimens.
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              Functions of FGF signalling from the apical ectodermal ridge in limb development.

              To determine the role of fibroblast growth factor (FGF) signalling from the apical ectodermal ridge (AER), we inactivated Fgf4 and Fgf8 in AER cells or their precursors at different stages of mouse limb development. We show that FGF4 and FGF8 regulate cell number in the nascent limb bud and are required for survival of cells located far from the AER. On the basis of the skeletal phenotypes observed, we conclude that these functions are essential to ensure that sufficient progenitor cells are available to form the normal complement of skeletal elements, and perhaps other limb tissues. In the complete absence of both FGF4 and FGF8 activities, limb development fails. We present a model to explain how the mutant phenotypes arise from FGF-mediated effects on limb bud size and cell survival.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                0028-0836
                1476-4687
                20 May 2009
                24 June 2009
                16 July 2009
                16 January 2010
                : 460
                : 7253
                : 400-404
                Affiliations
                [1 ]Department of Genetics Harvard Medical School 77 Avenue Louis Pasteur Boston, Massachusetts 02115, USA
                [2 ]Departamento de Anatomia y Biologia Celular Universidad de Cantabria C/ Herrera Oria s/n 39011 Santander, Espana
                [3 ]Instituto de Biomedicina y Biotecnología de Cantabria (CSIC-UC-IDICAN) C/ Herrera Oria s/n 39011 Santander. Spain
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                nihpa115631
                10.1038/nature08117
                2711994
                19553938
                1f7e72d3-1801-4598-899f-07cdfce34f2c
                History
                Funding
                Funded by: National Institute of Child Health & Human Development : NICHD
                Award ID: L40 HD057084-01 ||HD
                Funded by: National Institute of Child Health & Human Development : NICHD
                Award ID: F32 HD057701-02 ||HD
                Funded by: National Institute of Child Health & Human Development : NICHD
                Award ID: F32 HD057701-01 ||HD
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