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      Wnt11 Is Required for Oriented Migration of Dermogenic Progenitor Cells from the Dorsomedial Lip of the Avian Dermomyotome

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          Abstract

          The embryonic origin of the dermis in vertebrates can be traced back to the dermomyotome of the somites, the lateral plate mesoderm and the neural crest. The dermal precursors directly overlying the neural tube display a unique dense arrangement and are the first to induce skin appendage formation in vertebrate embryos. These dermal precursor cells have been shown to derive from the dorsomedial lip of the dermomyotome (DML). Based on its expression pattern in the DML, Wnt11 is a candidate regulator of dorsal dermis formation. Using EGFP-based cell labelling and time-lapse imaging, we show that the Wnt11 expressing DML is the source of the dense dorsal dermis. Loss-of-function studies in chicken embryos show that Wnt11 is indeed essential for the formation of dense dermis competent to support cutaneous appendage formation. Our findings show that dermogenic progenitors cannot leave the DML to form dense dorsal dermis following Wnt11 silencing. No alterations were noticeable in the patterning or in the epithelial state of the dermomyotome including the DML. Furthermore, we show that Wnt11 expression is regulated in a manner similar to the previously described early dermal marker cDermo-1. The analysis of Wnt11 mutant mice exhibits an underdeveloped dorsal dermis and strongly supports our gene silencing data in chicken embryos. We conclude that Wnt11 is required for dense dermis and subsequent cutaneous appendage formation, by influencing the cell fate decision of the cells in the DML.

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          Most cited references52

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          A series of normal stages in the development of the chick embryo. 1951.

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            Derivation of completely cell culture-derived mice from early-passage embryonic stem cells.

            Several newly generated mouse embryonic stem (ES) cell lines were tested for their ability to produce completely ES cell-derived mice at early passage numbers by ES cell tetraploid embryo aggregation. One line, designated R1, produced live offspring which were completely ES cell-derived as judged by isoenzyme analysis and coat color. These cell culture-derived animals were normal, viable, and fertile. However, prolonged in vitro culture negatively affected this initial totipotency of R1, and after passage 14, ES cell-derived newborns died at birth. However, one of the five subclones (R1-S3) derived from single cells at passage 12 retained the original totipotency and gave rise to viable, completely ES cell-derived animals. The total in vitro culture time of the sublines at the time of testing was equivalent to passage 24 of the original line. Fully potent early passage R1 cells and the R1-S3 subclone should be very useful not only for ES cell-based genetic manipulations but also in defining optimal in vitro culture conditions for retaining the initial totipotency of ES cells.
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              A Pax3/Pax7-dependent population of skeletal muscle progenitor cells.

              During vertebrate development, successive phases of embryonic and fetal myogenesis lead to the formation and growth of skeletal muscles. Although the origin and molecular regulation of the earliest embryonic muscle cells is well understood, less is known about later stages of myogenesis. We have identified a new cell population that expresses the transcription factors Pax3 and Pax7 (paired box proteins 3 and 7) but no skeletal-muscle-specific markers. These cells are maintained as a proliferating population in embryonic and fetal muscles of the trunk and limbs throughout development. Using a stable green fluorescent protein (GFP) reporter targeted to Pax3, we demonstrate that they constitute resident muscle progenitor cells that subsequently become myogenic and form skeletal muscle. Late in fetal development, these cells adopt a satellite cell position characteristic of progenitor cells in postnatal muscle. In the absence of both Pax3 and Pax7, further muscle development is arrested and only the early embryonic muscle of the myotome forms. Cells failing to express Pax3 or Pax7 die or assume a non-myogenic fate. We conclude that this resident Pax3/Pax7-dependent progenitor cell population constitutes a source of myogenic cells of prime importance for skeletal muscle formation, a finding also of potential value in the context of cell therapy for muscle disease.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                26 March 2014
                : 9
                : 3
                : e92679
                Affiliations
                [1 ]Department of Anatomy and Molecular Embryology, Ruhr-University of Bochum, Bochum, Germany
                [2 ]Department of Molecular Embryology, Freiburg University, Freiburg, Germany
                [3 ]Faculty of Biology, Freiburg University, Freiburg, Germany
                [4 ]Institute for Molecular Biology, Medizinische Hochschule Hannover, Hannover, Germany
                [5 ]Institute of Anatomy and Cell Biology, Department of Molecular Embryology, Albert-Ludwigs University, Freiburg, Germany
                Heart Science Centre, Imperial College London, United Kingdom
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: GMP BBS FY FD. Performed the experiments: GMP ABR JC. Analyzed the data: GMP BBS FY GZ JC. Contributed reagents/materials/analysis tools: THWL AK. Wrote the paper: GMP BBS FY. Immunostaining and sample preparation: GMP MAK. Time-lapse imaging: CT. Supervision: BBS.

                [¤a]

                Current address: Medizinische Klinik III, Universitätsklinikum Bergmannsheil, Bürkle-de-la-Camp-Platz 1, Bochum, Germany

                [¤b]

                Current address: Department of Craniofacial Development, King’s College London, London, United Kingdom

                [¤c]

                Current address: Neuroonkologie, Neurozentrum, Uniklinikum Freiburg, Freiburg, Germany

                [¤d]

                Current address: Department of Molecular and Cellular Neuroscience, York University, Toronto, Canada

                [¤e]

                Current address: Department of Anatomy and Embryology, Faculty of Veterinary Medicine, South Valley University, Qena, Egypt

                Article
                PONE-D-13-43631
                10.1371/journal.pone.0092679
                3966816
                24671096
                32f3094a-c942-4634-a2d0-4736040610ca
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 23 October 2013
                : 24 February 2014
                Page count
                Pages: 16
                Funding
                The project was supported by an EU’s Sixth Framework Program grant to Prof. Dr. B. Brand-Saberi (MYORES, 511978) and by the DFG (GRK 1104). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Agriculture
                Livestock
                Poultry
                Chickens
                Cell Biology
                Signal Transduction
                Cell Signaling
                Developmental Signaling
                Signaling Cascades
                Molecular Cell Biology
                Developmental Biology
                Organism Development
                Organogenesis
                Limb Development
                Cell Differentiation
                Cell Fate Determination
                Embryology
                Morphogenesis
                Medicine and Health Sciences
                Dermatology
                Research and Analysis Methods
                Model Organisms
                Animal Models

                Uncategorized
                Uncategorized

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