E. Gaino et G. Magnino, Dissociated cells of the calcareous sponge Clathrina: a model for investigating cell adhesion and cell motility in vitro, MICROSC RES, 44(4), 1999, pp. 279-292
The study of cell-cell and cell-substratum adhesion in vitro is useful for
understanding cell behavior in a three-dimensional pattern. We have used di
ssociated cells (choanocytes represent the main fraction) from the calcareo
us sponge Clathrina, namely C. cerebrum and C. clathrus, to illustrate our
present understanding on three main aspects of cell-cell and cell-substratu
m adhesion in vitro: (1) cytoskeletal protrusions; (2) cell behaviours on o
rganic substrata; and (3) paths of locomotory sponge cell. Cell locomotion
occurs by the extensions of scleropodial and lamellipodial protrusions, by
way of actin polymerization. The extent to which cells produce these cytopl
asmic processes varies according to the substratum (e.g., collagen, fibrone
ctin, laminin, polylysine). It was found that more cell extensions were pro
duced on collagen substrata, and this led to greater cell movement. Advanci
ng choanocytes are not polarized. Their paths are particularly complicated,
showing linear segments, which produce a more efficent cellular translocat
ion, and winding tracts with frequent turns or loops. Small amoeboid cells
describe more linear paths with a wide range of speed variation than larger
cells. The presence of cell-derived substratum reduces the progressive dis
persion of cells and allows cells to encounter one another in such a way th
at the initial random walking later turns into non-random displacement. Eve
n though cAMP-treated cells exhibit different aggregative tactics, cAMP 10(
-8) M remarkably enhances cell encounters and supports the existing informa
tion that this cyclic nucleotide represents a signal that affects cell morp
hology and locomotion. The bulk of data on sponge cell-cell and cell-substr
atum adhesion has been evaluated by mentioning the significant advances and
references concerning studies of other cell systems. Microsc. Res. Tech. 4
4:279-292, 1999. (C) 1999 Wiley-Liss, Inc.