In response to Marc Brande: We are using real-time confocal microscopy to
examine changes in fibroblasts of the eye after injury and to construct 3-D
images of cell layers of parts of the eye to determine changes in spatial
relaationships between cells. Using this method it has been possible to see
changes in nuclear configuration, and over hours and days to follow the
morphological changes in cells as they become activated by injury.
        As another question, I presume that you also have an active server
mediating 3D imaging. I will forward a request to subscribe.
Roger Beuerman [log in to unmask]