Characterization of Prion Susceptibility in Neuro2a Mouse Neuroblastoma Cell Subclones

In this study, we established Neuro2a (N2a) neuroblastoma subclones and characterized their susceptibility to prion infection. The N2a cells were treated with brain homogenates from mice infected with mouse prion strain Chandler. Of 31 N2a subclones, 19 were susceptible to prion as those cells became positive for abnormal isoform of prion protein (PrP Sc ) for up to 9 serial passages, and the remaining 12 subclones were classified as unsusceptible. The susceptible N2a subclones expressed cellular prion protein (PrP C ) at levels similar to the parental N2a cells. In contrast, there was a variation in PrP C expression in unsusceptible N2a subclones. For example, subclone N2a‐1 expressed PrP C at the same level as the parental N2a cells and prion‐susceptible subclones, whereas subclone N2a‐24 expressed much lower levels of PrP mRNA and PrP C than the parental N2a cells. There was no difference in the binding of PrP Sc to prion‐susceptible and unsusceptible N2a subclones regardless of their PrP C expression level, suggesting that the binding of PrP Sc to cells is not a major determinant for prion susceptibility. Stable expression of PrP C did not confer susceptibility to prion in unsusceptible subclones. Furthermore, the existence of prion‐unsusceptible N2a subclones that expressed PrP C at levels similar to prion‐susceptible subclones, indicated that a host factor(s) other than PrP C and/or specific cellular microenvironments are required for the propagation of prion in N2a cells. The prion‐susceptible and ‐unsusceptible N2a subclones established in this study should be useful for identifying the host factor(s) involved in the prion propagation.