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Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture

The shapes of homologous skeletal elements in the vertebrate forelimb and hindlimb are distinct, with each element exquisitely adapted to their divergent functions. Many of the signals and signalling pathways responsible for patterning the developing limb bud are common to both forelimb and hindlimb...

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Autores principales: Butterfield, Natalie C., Qian, Chen, Logan, Malcolm P. O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528256/
https://www.ncbi.nlm.nih.gov/pubmed/28746404
http://dx.doi.org/10.1371/journal.pone.0180453
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author Butterfield, Natalie C.
Qian, Chen
Logan, Malcolm P. O.
author_facet Butterfield, Natalie C.
Qian, Chen
Logan, Malcolm P. O.
author_sort Butterfield, Natalie C.
collection PubMed
description The shapes of homologous skeletal elements in the vertebrate forelimb and hindlimb are distinct, with each element exquisitely adapted to their divergent functions. Many of the signals and signalling pathways responsible for patterning the developing limb bud are common to both forelimb and hindlimb. How disparate morphologies are generated from common signalling inputs during limb development remains poorly understood. We show that, similar to what has been shown in the chick, characteristic differences in mouse forelimb and hindlimb cartilage morphology are maintained when chondrogenesis proceeds in vitro away from the endogenous limb bud environment. Chondrogenic nodules that form in high-density micromass cultures derived from forelimb and hindlimb buds are consistently different in size and shape. We described analytical tools we have developed to quantify these differences in nodule morphology and demonstrate that characteristic hindlimb nodule morphology is lost in the absence of the hindlimb-restricted limb modifier gene Pitx1. Furthermore, we show that ectopic expression of Pitx1 in the forelimb is sufficient to generate nodule patterns characteristic of the hindlimb. We also demonstrate that hindlimb cells are less adhesive to the tissue culture substrate and, within the limb environment, to the extracellular matrix and to each other. These results reveal autonomously programmed differences in forelimb and hindlimb cartilage precursors of the limb skeleton are controlled, at least in part, by Pitx1 and suggest this has an important role in generating distinct limb-type morphologies. Our results demonstrate that the micromass culture system is ideally suited to study cues governing morphogenesis of limb skeletal elements in a simple and experimentally tractable in vitro system that reflects in vivo potential.
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spelling pubmed-55282562017-08-07 Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture Butterfield, Natalie C. Qian, Chen Logan, Malcolm P. O. PLoS One Research Article The shapes of homologous skeletal elements in the vertebrate forelimb and hindlimb are distinct, with each element exquisitely adapted to their divergent functions. Many of the signals and signalling pathways responsible for patterning the developing limb bud are common to both forelimb and hindlimb. How disparate morphologies are generated from common signalling inputs during limb development remains poorly understood. We show that, similar to what has been shown in the chick, characteristic differences in mouse forelimb and hindlimb cartilage morphology are maintained when chondrogenesis proceeds in vitro away from the endogenous limb bud environment. Chondrogenic nodules that form in high-density micromass cultures derived from forelimb and hindlimb buds are consistently different in size and shape. We described analytical tools we have developed to quantify these differences in nodule morphology and demonstrate that characteristic hindlimb nodule morphology is lost in the absence of the hindlimb-restricted limb modifier gene Pitx1. Furthermore, we show that ectopic expression of Pitx1 in the forelimb is sufficient to generate nodule patterns characteristic of the hindlimb. We also demonstrate that hindlimb cells are less adhesive to the tissue culture substrate and, within the limb environment, to the extracellular matrix and to each other. These results reveal autonomously programmed differences in forelimb and hindlimb cartilage precursors of the limb skeleton are controlled, at least in part, by Pitx1 and suggest this has an important role in generating distinct limb-type morphologies. Our results demonstrate that the micromass culture system is ideally suited to study cues governing morphogenesis of limb skeletal elements in a simple and experimentally tractable in vitro system that reflects in vivo potential. Public Library of Science 2017-07-26 /pmc/articles/PMC5528256/ /pubmed/28746404 http://dx.doi.org/10.1371/journal.pone.0180453 Text en © 2017 Butterfield et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Butterfield, Natalie C.
Qian, Chen
Logan, Malcolm P. O.
Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title_full Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title_fullStr Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title_full_unstemmed Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title_short Pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
title_sort pitx1 determines characteristic hindlimb morphologies in cartilage micromass culture
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528256/
https://www.ncbi.nlm.nih.gov/pubmed/28746404
http://dx.doi.org/10.1371/journal.pone.0180453
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