Literature DB >> 2592304

Locomotory behavior of fibroblasts in "sail-sheets".

S C Tripathi1.   

Abstract

The locomotory behavior of fibroblasts in two-dimensional cultures (e.g., on culture dishes, cover slips, etc.) was first reported by Abercrombie's group. This paper describes some of the features of movement of fibroblasts in a unique culture system known as sail-sheet cultures (SSCs). Cells in SSCs grow mostly on one another in a three-dimensional form that resembles, to some extent, the in vivo situation. We grew chicken heart fibroblasts (CHFs) as SSCs and studied their locomotory behavior by time-lapse filming extended for periods ranging from 12 h to several days. It was found that CHFs grown as sail-sheets exhibit many features of movement as observed in conventional two-dimensional cultures (CCs). However, we observed that CHFs in SSCs, like those in vivo, lack leading lamella directing their movement. Furthermore, locomotion is significantly slower in SSCs than in CCs. Based on data on the movement of CHFs within the mesh holes of inert grids, we suggest that the mesenchymal cells in SSCs, in addition to their individual movement, move in sheets and that their movement in sheets results in the closure of the mesh holes, a situation that resembles the phenomenon of healing of wounds. Thus SSCs provide a model system for the study of healing of wounds. The presence of collagenlike extracellular matrix (CLECM) between cellular layers in SSCs suggests that CLECM may be involved in guiding the locomotory behavior of CHFs in SSCs.

Entities:  

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Year:  1989        PMID: 2592304     DOI: 10.1007/bf02624130

Source DB:  PubMed          Journal:  In Vitro Cell Dev Biol        ISSN: 0883-8364


  17 in total

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Authors:  A S CURTIS; M VARDE
Journal:  J Natl Cancer Inst       Date:  1964-07       Impact factor: 13.506

2.  Some new data concerning the formation of the definitive endoblast in the chick embryo.

Authors:  L VAKAET
Journal:  J Embryol Exp Morphol       Date:  1962-03

3.  Social behaviour of cells in tissue culture. III. Mutual influence of sarcoma cells and fibroblasts.

Authors:  M ABERCROMBIE; J E HEAYSMAN; H M KARTHAUSER
Journal:  Exp Cell Res       Date:  1957-10       Impact factor: 3.905

4.  The growth of cells on a transparent gel of reconstituted rat-tail collagen.

Authors:  R L EHRMANN; G O GEY
Journal:  J Natl Cancer Inst       Date:  1956-06       Impact factor: 13.506

5.  Cytoplasmic microtubules in tissue culture cells appear to grow from an organizing structure towards the plasma membrane.

Authors:  M Osborn; K Weber
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

6.  A sponge matrix method for tissue culture; formation of organized aggregates of cells in vitro.

Authors:  J LEIGHTON
Journal:  J Natl Cancer Inst       Date:  1951-12       Impact factor: 13.506

7.  Cell locomotion and contact inhibition of normal and neoplastic rat cells.

Authors:  P Veselý; R A Weiss
Journal:  Int J Cancer       Date:  1973-01-15       Impact factor: 7.396

8.  Contact guidance on oriented collagen gels.

Authors:  G A Dunn; T Ebendal
Journal:  Exp Cell Res       Date:  1978-02       Impact factor: 3.905

9.  Surface distribution of LETS protein in relation to the cytoskeleton of normal and transformed cells.

Authors:  V Mautner; R O Hynes
Journal:  J Cell Biol       Date:  1977-12       Impact factor: 10.539

10.  The behavior of fibroblasts from the developing avian cornea. Morphology and movement in situ and in vitro.

Authors:  J B Bard; E D Hay
Journal:  J Cell Biol       Date:  1975-11       Impact factor: 10.539

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