The Gem GTP-binding protein promotes morphological differentiation in neuroblastoma

Gem is a small GTP-binding protein within the Ras superfamily whose functio n has not been determined. We report here that ectopic Gem expression is su fficient to stimulate cell flattening and neurite extension in N1E-115 and SH-SY5Y neuroblastoma cells, suggesting a role for Gem in cytoskeletal rear rangement and/or morphological differentiation of neurons. Consistent with this potential function, in clinical samples of neuroblastoma, Gem protein was most highly expressed within cells which had differentiated to express ganglionic morphology. Gem was also observed in developing trigeminal nerve ganglia in 12.5 day mouse embryos, demonstrating that Gem expression is a property of normal ganglionic development. Although Gem expression is rare in epithelial and hematopoietic cancer cell lines, constitutive Gem levels were detected in several neuroblastoma cell lines and could be further indu ced as much as 10-fold following treatment with PMA or the acetylcholine mu scarinic agonist, carbachol.