Previous studies using cell culture systems to evaluate LAT expression demo
nstrated that the LAT promoter expresses at much higher levels in neuroblas
toma cell lines than fibroblast lines. The high level of LAT expression in
neuronal-derived cell lines correlates with the high level of LAT accumulat
ion observed in sensory ganglia neurons during a latent infection. We have
found that using LAT promoters to express reporter genes from recombinant v
iruses in vivo produces high levels of LAT promoter activity in the epithel
ium of the mouse foot. An analysis of LAT promoter activity during an acute
infection in the mouse clearly demonstrates that in contrast to studies pe
rformed with selected cell lines, the LAT promoter expresses similar levels
of reporter gene product in peripheral cells and in neurons. In addition,
the amount of reporter gene product is higher when the LAT promoter is loca
ted within the R-L as compared to the U-L region, and when expression is ad
justed for copy number of the reporter construct, expression is roughly the
same. These results suggest the activity of the LAT promoter varies greatl
y according to cell type and that high levels of expression is not limited
solely to neurons, especially in the in vivo setting. (C) 1999 Academic Pre
ss.