I'm currently culturing the NS20Y mouse neuroblastoma cell line on 100mm poly-L-ornithine coated culture dishes in the appropriate medium, but I'm finding that the cells tend to form aggregate clusters that grow up rather than spread out across the dish. I've read this could be due to unfavourability of the substrate, however, the literature routinely cites use of P-L-O coated dishes for this line. Does anyone know how to avoid this clustering? I've tried pelleting and resuspending, trituration, and other simple measures to reduce clumping, but I'm still left with the same issue. We use 0.25% Trypsin-EDTA to dissociate the cells. Any suggestions are welcome.