Literature DB >> 3956867

Precardiac cell migration: fibronectin localization at mesoderm-endoderm interface during directional movement.

K K Linask, J W Lash.   

Abstract

The pathway of directional movement of chick precardiac mesoderm cells was studied by indirect immunofluorescence and by scanning electron microscopy. Directional movement of the precardiac cells begins at stage 6 from the lateral sides of the embryo at the level of Hensen's node. The cells move anteriorly in an arc to the embryo's midline. By stage 8 the cells arrive at the lateral sides of the anterior intestinal portal and movement ceases. The interval of this directional movement is approximately 10 hr. During migration the precardiac cells are in close association with the underlying endoderm. As migration proceeds, the cells encounter increasing amounts of fibrils in the substratum at the mesoderm-endoderm interface. Concomitant with increasing fibril formation there is an increase in fibronectin (FN) in the heart-forming region. During stage 5 FN first appears in the lateral heart-forming regions and increases in amount during the period of cell migration. By stage 7 a concentration difference of FN is apparent in the lateral regions with more FN cephalad and decreasing amounts caudad. At stages 7 and 8 large amounts of extracellular FN-associated fibrils are observed at the lateral sides of the anterior intestinal portal where the cells stop moving. The precardiac cells moving into this region are oriented perpendicular to the anterior intestinal portal and in close association with these fibrils. There is no evidence that the fibrillar meshwork forming the substratum of the precardiac mesoderm cells is physically oriented as a guide for directional movement. The correlations between FN distribution at the mesoderm-endoderm interface and directional cell movement suggest that the precardiac cells may migrate by haptotaxis, i.e., by moving along the substratum toward areas of greater adhesiveness.

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Year:  1986        PMID: 3956867     DOI: 10.1016/0012-1606(86)90385-4

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  25 in total

1.  Distribution of laminin, type IV collagen, and fibronectin in the cell columns and trophoblastic shell of early macaque placentas.

Authors:  T N Blankenship; A C Enders; B F King
Journal:  Cell Tissue Res       Date:  1992-11       Impact factor: 5.249

2.  Not just inductive: a crucial mechanical role for the endoderm during heart tube assembly.

Authors:  Victor D Varner; Larry A Taber
Journal:  Development       Date:  2012-05       Impact factor: 6.868

3.  Convective tissue movements play a major role in avian endocardial morphogenesis.

Authors:  Anastasiia Aleksandrova; Andras Czirók; Andras Szabó; Michael B Filla; M Julius Hossain; Paul F Whelan; Rusty Lansford; Brenda J Rongish
Journal:  Dev Biol       Date:  2012-01-04       Impact factor: 3.582

4.  Is chemotaxis a factor in the migration of precardiac mesoderm in the chick?

Authors:  H S Easton; R Bellairs; J W Lash
Journal:  Anat Embryol (Berl)       Date:  1990

5.  Effects of injecting fibronectin and antifibronectin antibodies on cushion mesenchyme formation in the chick. An in vivo study.

Authors:  J M Icardo; A Nakamura; M A Fernandez-Teran; F J Manasek
Journal:  Anat Embryol (Berl)       Date:  1992

6.  Cardiac looping in the chick embryo: the role of the posterior precardiac mesoderm.

Authors:  H Easton; M Veini; R Bellairs
Journal:  Anat Embryol (Berl)       Date:  1992

7.  Evidence for the involvement of receptors for fibronectin in the promotion of chick tail segmentation.

Authors:  C L Mills; O Ariyo; K M Yamada; J W Lash; R Bellairs
Journal:  Anat Embryol (Berl)       Date:  1990

8.  A new hypothesis for foregut and heart tube formation based on differential growth and actomyosin contraction.

Authors:  Hadi S Hosseini; Kara E Garcia; Larry A Taber
Journal:  Development       Date:  2017-05-19       Impact factor: 6.868

9.  Heart formative factor(s) is localized in the anterior endoderm of early Xenopus neurula.

Authors:  Akane Tonegawa; Megumi Moriya; Masazumi Tada; Shinichiro Nishimatsu; Chiaki Katagiri; Naoto Ueno
Journal:  Rouxs Arch Dev Biol       Date:  1996-02

10.  Why is cytoskeletal contraction required for cardiac fusion before but not after looping begins?

Authors:  Yunfei Shi; Victor D Varner; Larry A Taber
Journal:  Phys Biol       Date:  2015-01-30       Impact factor: 2.583

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