Literature DB >> 7276892

Cephalic flexure formation in the chick embryo.

G R Goodrum, A G Jacobson.   

Abstract

The cephalic flexure, found in all vertebrate brains, is a ventrally directed bend through the mesencephalon, and a ventral bulging and elongation of the prosencephalon. Most sources say the cephalic flexure is caused by differential growth. We have measured the changing angle of flexure through time and find that flexure occurs between chick embryo stages 10 to 15. We measured, during these stages, the lengths, thicknesses, and volumes of the floor and roof of the mesencephalon and of the prosencephalon. As expected, during flexure the mesencephalic roof elongates much more than the floor. Both roof and floor increase in thickness, and mesencephalic roof volume increases twice as much as floor volume. However, prosencephalon, which does not bend, also has differential growth between roof and floor, but the growth is taken up in complex changes of shape other than flexure. There are sufficient numbers of mitoses in the brain to account for the observed tissue growth, assuming accompanying cell enlargement. We deleted brain parts adjacent to the mesencephalon before flexure and the mesencephalon bent, so migration of cells from or to these adjacent parts to contribute to the differential growth of the mesencephalon is unlikely. We reduced cerebrospinal fluid pressure during flexure by explanting heads to the chorioallantoic membrane, or into New cultures. The mesencephalon of explanted heads bends, but the prosencephalon fails to elongate. We conclude that differential growth may be necessary for mesencephalic flexure in the chick embryo, but other factors that decide the disposition of the products of growth in space must determine the shape.

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Year:  1981        PMID: 7276892     DOI: 10.1002/jez.1402160308

Source DB:  PubMed          Journal:  J Exp Zool        ISSN: 0022-104X


  14 in total

1.  Mechanical stress as a regulator of cytoskeletal contractility and nuclear shape in embryonic epithelia.

Authors:  Benjamen A Filas; Philip V Bayly; Larry A Taber
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2.  Contraction and stress-dependent growth shape the forebrain of the early chicken embryo.

Authors:  Kara E Garcia; Ruth J Okamoto; Philip V Bayly; Larry A Taber
Journal:  J Mech Behav Biomed Mater       Date:  2016-08-15

3.  The development of the human brain from a closed neural tube at stage 13.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1988

4.  The development of the human brain, the closure of the caudal neuropore, and the beginning of secondary neurulation at stage 12.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1987

5.  The development of the human brain, including the longitudinal zoning in the diencephalon at stage 15.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1988

6.  The development of the human brain and the closure of the rostral neuropore at stage 11.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1986

7.  The first appearance of the major divisions of the human brain at stage 9.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1983

8.  The first appearance of the neural tube and optic primordium in the human embryo at stage 10.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1985

9.  The first appearance of the future cerebral hemispheres in the human embryo at stage 14.

Authors:  F Müller; R O'Rahilly
Journal:  Anat Embryol (Berl)       Date:  1988

10.  The mechanism of cervical flexure formation in the chick.

Authors:  M E Flynn; A S Pikalow; R S Kimmelman; R L Searls
Journal:  Anat Embryol (Berl)       Date:  1991
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