Using PCR to monitor HIV-1 RNA genome reverse transcription and nuclear imp
ort of preintegration complexes, we found that memory, but not naive, CD4() T cells could support transport of HIV-1 DNA to nuclei upon TCR/CD3 and I
L-2 stimulation. Moreover, memory CD4(+) T cells, unlike naive CD4(+) T cel
ls, express high levels of phosphodiesterase 4 (PDE4) constitutively. Selec
tive blocking of PDE4 activity inhibited IL-2R expression and thereby led t
o abolishing HIV-1 DNA nuclear import in memory T cells; however, full-leng
th viral DNA synthesis was not affected. Thus, blocking PDE4 prevents initi
ation of HIV-1 DNA circle formation in T cells. The fact that PDE4 is expre
ssed constitutively at higher levels in memory vs naive CD4(+) T cells may
help HIV-1 readily infect memory T cells.