HSP70 production and inhibition of cell proliferation in molt-4 T-cells after cell-to-cell transmission of HTLV-I: Effect of PGA1

Infection with HTLV-I is associated with leukemic transformation of mature CD4(+) T lymphocytes. PGA(1), a powerful inhibitor of tumour cell proliferation, can prevent the clonal expansion of HTLV-I-infected cells following acute infection of cord blood-derived mononuclear cells. Since the antiproliferative effect of PGA(1) on HTLV-I transformed, chronically infected MT-2 cell line was associated with induction of HSP70, we have investigated the effect of PGA(1) on cell cycle progression and HSP70 production in a leukemic T-cell line (Molt-4) shortly after exposure to HTLV-I in a cell-to-cell transmission model. rate of cell proliferation and HSP70 expression were studied within one duplication cycle of Molt-4 cells after exposure to HTLV-I. growth of both control and virus-exposed cultures was inhibited by treatment with PGA(1) (4 mu g/ml) and cell cycling was arrested preferentially at the G(1)/S interphase. synthesis of HSP70 was induced within 3 h by PGA(1) in control and virus-exposed Molt-4 cells and became undetectable from overnight onward, though the protein accumulated in the cells. the arrest of growth was observed from overnight up to 48 h so that treated cells almost missed one cycle. Interestingly, HSP70 transcript and protein persisted at remarkably high levels in molt-4 cells exposed to HTLV-I in the absence of PGA(1), showing that HSP70 expression can be directly activated during primary infection with this human retrovirus. moreover, in these cocultures, treatment with PGA(1) or heat shock was not able to increase further the elevated level of HSP70 found in untreated cocultures, suggesting that during the early period of the virus-transmission phase, HTLV-I could interfere with HSP70 induction by other inducers.