Parallel expression level of dystrophin and contractile performances of rat aortic smooth muscle.

We have recently shown that the expression of dystrophin was in line with the conservation of contractility in primary and subcultured vascular smooth muscle cells (VSMC). In this report, we provide experimental evidence that shows the existence of a gradient in dystrophin expression from the aortic arch to the region just above the diaphragm, in line with a parallel gradient of contractility. On the contrary, there were no differences in caldesmon and smooth muscle myosin expression, as previously shown for vimentin and alpha-smooth muscle actin [Osborn, M., Caselitz, J., and Weber, K. (1981) Differentiation 20, 196-202]. Overall, this is the first demonstration, in a normal adult smooth muscle, of a differential expression of dystrophin, in line with its contractile performances. In addition, these results suggest that the experimental modulation of dystrophin expression in cultured VSMC in line with their contractility was the manifestation in vitro of an actual physiological property of those cells in vivo.

A simple method for the quantitative evaluation of functional effects of xenobiotics with cultured cells.

We present a simple, noninvasive, nondestructive all-purpose method for the quantitative evaluation of functional effects of xenobiotics with cultured cells and the work station for its routine, easy implementation. At present 1 to 150 cells growing in one to six dishes can be studied in parallel or otherwise at time intervals ranging from 10 s to 6 h or more, over periods of time ranging from a few tens of minutes to 3-4 days. Any aspect of cell physiological behavior can be studied (differentiation-dedifferentiation, migration, division, degeneration, death) without preliminary staining and/or fixation provided it results in optically visible changes.