Migration and aggregation of embryonic chicken neurons in vitro: possible functional implication of polysialogangliosides.

The presented study reports a primary culture system of embryonic chicken optic lobe neurons, which turned out to be a suitable model for cell migration and aggregation: Freshly dissociated neurons developed short processes, contacted one another and formed fasciculated bundles, on which neurons migrated as long-shaped cells, similar to migrating neurons in vivo. We used this system to study the possible involvement of c-pathway polysialogangliosides for neuronal migration and aggregation. These highly negative charged glycosphingolipids are the predominant gangliosides of migrating and outgrowing neurons in vivo. Addition of a purified ganglioside mixture (50 microM), extracted from brains of the corresponding embryonic stage, strongly enhanced neuronal migration and aggregation, while incubation of the cells with monoclonal antibody Q211, specifically binding c-polysialogangliosides, reduced aggregate formation in a dose-dependent manner. Cultures treated with 10 micrograms/ml Q211, instead, displayed a more divergent growth, leading to the formation of a fine network of single neuronal processes. These results suggest a functional implication of c-polysialogangliosides in neuronal fasciculation, migration and aggregation.