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In this study the contribution of the ERK1/2 pathway to sphingosine-induced death and morphological changes of the actin cytoskeleton in glioma C6 cells was investigated. Surprisingly, the level of ERK1/2 phosphorylation does not change after incubation of cells with sphingosine. Despite this, sphingosine induces rounding and detachment of cells without formation of apoptotic bodies. To shed light on this process, a specific inhibitor of ERK1/2 phosphorylation, U0126, was used. Cells incubated simultaneously with sphingosine and U0126 not only detached, but also exhibited formation of apoptotic-like blebs. These data suggest that during sphingosine-induced glioma C6 cell death apoptotic blebbing is dependent on ERK1/2 signalling and occurs only when ERK1/2 activity is decreased or abolished.
The ultrastructure of the tegumental cytoskeleton of Fasciola hepatica has been examined following various extraction fixations. Microtubules were found throughout the tegument. They run parallel to the basal and apical tegumental borders, and have a pre-dominant basal-to-apical orientation in the central parts of the distal cytoplasm. Microtubules are also found in the cytoplasmic bridges which connect the distal and perikaryal tegumental parts.
The actin and the tubulin cytoskeleton organization during the differentiation of the embryo-suspensor in Alisma plantago-aquatica was studied in comparison with the development of embryo, using immunofluorescence detection and rhodamine-phalloidin assay. At the early stage of the suspensor basal cell development (from 2- to ~10-celled embryos) microfilaments form an abundant network in the cytoplasm of the basal cell, while the microtubules form a delicate network. At the mature stage of development (from a dozen to several dozen-celled embryos), in the suspensor basal cell, the microfilaments and microtubules were localized from micropylar to chalazal pole of the cell. At the micropylar end of the basal cell a high amount of actin and tubulin material was observed. The microfilaments were mainly arranged parallel whereas numerous bundles of microtubules distributed longitudinally or transversally to the long axis of the cell. At this stage of basal cell functioning, some bundles of microtubules appeared to pass close to the nucleus surface. Microtubules were also observed distributed at the chalazal pole of the basal cell. At the senescence stage of the suspensor basal cell (>100-celled embryos) the actin and tubulin filaments disorganize, some disrupted microfilaments and microtubules were observed in the cytoplasm of the basal cell. At all stages of the suspensor basal cell development in the embryo cells an extensive actin and tubulin network was observed.
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