Journal of Histochemistry & Cytochemistry · 2003 · 103 citations · 56 references
Life SciencesCell BiologyNeuroscienceCell AdhesionCell ProliferationStem Cell BiologyActin FilamentsMicroscopic Cell MorphologyNervous TissueNeural Stem Cell BiologyNeural Stem CellsCell ProcessesFibroblast Growth Factor Receptor SignalingNecrotic MorphologyNeural Stem Cell AdhesionNeural Stem Cell NichePhagocytic ActivityPhagocytic Recognition
Neural stem cells proliferate in liquid culture as cell clusters (neurospheres). This study was undertaken to characterize the epidermal growth factor (EGF)-expanded free-floating neurospheres derived from rat fetal striatum. We examined the ultrastructural and antigenic characteristics of these spheres. They consisted of two cell types, electron-dense and electron-lucent cells. Lucent cells were immunopositive to actin, vimentin, and nestin, whereas dense cells were immunopositive to actin, weakly positive to vimentin, and nestin-negative. Neurospheres contained healthy, apoptotic, and necrotic cells. Healthy cells were attached to each other by adherens junctions. They showed many pseudopodia and occasionally a single cilium. Sphere cells showed phagocytic capability because healthy cells phagocytosed the cell debris derived from dead cells in a particular process that involves the engulfment of dying cells by cell processes from healthy cells. Sphere cells showed a cytoplasmic and a nuclear pool of fibroblast growth factor (FGF) receptors. They expressed E- and N-cadherin, alpha- and beta-catenin, EGF receptor, and a specific subset of FGF receptors. Because sphere cells expressed this factor in the absence of exogenous FGF-2, we propose that they are able to synthesize FGF-2.
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