Growth of fibroblasts on linear and planar anchorages of limiting dimensions

BHK and 3T3 cells were grown on small glass fibres and platelets (size range 20–250 μm) in agar gel, over a layer of mouse primary feeder cells. Under these conditions the growth of colonies (4–20 cells) from single control cells, suspended freely in the gel, was less than 1 %, while cells attached...

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Veröffentlicht in:Experimental cell research 1973-09, Vol.81 (1), p.104-110
1. Verfasser: Maroudas, N.G.
Format: Artikel
Sprache:eng
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Zusammenfassung:BHK and 3T3 cells were grown on small glass fibres and platelets (size range 20–250 μm) in agar gel, over a layer of mouse primary feeder cells. Under these conditions the growth of colonies (4–20 cells) from single control cells, suspended freely in the gel, was less than 1 %, while cells attached to the larger platelets yielded more than 95 % colonies. Fibres (average diameter 0.625 μm) induced somewhat fewer colonies (45–70 %). However, there was a significant induction of single divisions by fibres as short as 30 μm, while on 60 μm fibres more than half the cells had gone through at least one division, compared with 4–12% of freely suspended controls. Longer fibres promoted multiple divisions. Colony formation increased sigmoidally with fibre length from 30 to 250 μm, with a d 50 around 115 μm. These figures resembled the observed range of lengths of freely growing BHK and 3T3 fibroblasts in tissue culture dishes. In another experiment, finer fibres (average diameter 0.075 μm) performed almost as well as platelets of equal length but of width 20–30 μm. Thus linear extension provides a stimulus for division of anchorage-dependent fibroblasts. It is suggested that this stimulus may arise from a change in conformation or tension in the cell membrane, rather than from increased surface, cell motility or interaction with substrate surface. The present results are discussed in relation to recent findings on the induction of tumours by solid particles.
ISSN:0014-4827
1090-2422
DOI:10.1016/0014-4827(73)90116-X