Literature DB >> 7604672

Formation of the cervical flexure: an experimental study on chick embryos.

J Männer1, W Seidl, G Steding.   

Abstract

It has been proposed that the cervical flexure of vertebrate embryos arises from the normal morphogenesis of the heart. This hypothesis is based on experiments in which the heart tube is removed or disrupted in early chick embryos. It has been reported that, in normal atmosphere, these embryos continued normal morphogenesis except for cervical flexure formation. In the present study, we performed similar experiments. In contrast to previous work, however, only one set of our heart-deprived chick embryos was reincubated in normal air. The other sets were reincubated in oxygen-enriched air. Under normoxia, heart removal resulted not only in prevention of the cervical flexure, but also in mesenchymal defects, and in a remarkable hypoplasia of the craniocervical region. Under hyperoxia, heart-deprived embryos developed no severe mesenchymal defects and the growth of the upper body portion was more normal, with the hypoplasia confined to the cranial region. The formation of the cervical flexure was now normalized. These results show that cervical flexure formation is not directly dependent on normal morphogenesis of the heart, but does depend on a sufficient oxygen supply to the cervical region. During early development, the cranio-cervical region of a chick embryo is more sensitive to circulatory failure than the trunk.

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Year:  1995        PMID: 7604672     DOI: 10.1159/000147677

Source DB:  PubMed          Journal:  Acta Anat (Basel)        ISSN: 0001-5180


  8 in total

1.  On the Biomechanics of Cardiac S-looping: insights from modeling and perturbation studies.

Authors:  Ashok Ramasubramanian; Xavier Capaldi; Sarah Bradner; Lianna Gangi
Journal:  J Biomech Eng       Date:  2019-03-06       Impact factor: 2.097

2.  Intravascular pillars and pruning in the extraembryonic vessels of chick embryos.

Authors:  Grace S Lee; Nenad Filipovic; Miao Lin; Barry C Gibney; Dinee C Simpson; Moritz A Konerding; Akira Tsuda; Steven J Mentzer
Journal:  Dev Dyn       Date:  2011-03-29       Impact factor: 3.780

3.  Intrauterine growth restriction results in persistent vascular mismatch in adulthood.

Authors:  Anderson H Kuo; Cun Li; Hillary F Huber; Geoffrey D Clarke; Peter W Nathanielsz
Journal:  J Physiol       Date:  2017-11-21       Impact factor: 5.182

4.  On the role of intrinsic and extrinsic forces in early cardiac S-looping.

Authors:  Ashok Ramasubramanian; Quynh B Chu-Lagraff; Takashi Buma; Kevin T Chico; Meagan E Carnes; Kyra R Burnett; Sarah A Bradner; Shaun S Gordon
Journal:  Dev Dyn       Date:  2013-06-05       Impact factor: 3.780

5.  Probing the Roles of Physical Forces in Early Chick Embryonic Morphogenesis.

Authors:  Yan Li; Hannah Grover; Eric Dai; Kevin Yang; Zi Chen
Journal:  J Vis Exp       Date:  2018-06-05       Impact factor: 1.355

6.  Blood flow shapes intravascular pillar geometry in the chick chorioallantoic membrane.

Authors:  Grace S Lee; Nenad Filipovic; Lino F Miele; Miao Lin; Dinee C Simpson; Barry Giney; Moritz A Konerding; Akira Tsuda; Steven J Mentzer
Journal:  J Angiogenes Res       Date:  2010-07-07

Review 7.  Investigating developmental cardiovascular biomechanics and the origins of congenital heart defects.

Authors:  William J Kowalski; Kerem Pekkan; Joseph P Tinney; Bradley B Keller
Journal:  Front Physiol       Date:  2014-10-21       Impact factor: 4.566

8.  Cardiac looping may be driven by compressive loads resulting from unequal growth of the heart and pericardial cavity. Observations on a physical simulation model.

Authors:  Meriç Bayraktar; Jörg Männer
Journal:  Front Physiol       Date:  2014-04-04       Impact factor: 4.566

  8 in total

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