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Culturing of human peripheral blood cells reveals unsuspected lymphocyte responses relevant to HIV disease

by: Bita Sahaf, Kondala Atkuri, Kartoosh Heydari, Meena Malipatlolla, Jay Rappaport, Emmanuel Regulier, Leonard A Herzenberg, Leonore A Herzenberg
Proceedings of the National Academy of Sciences, Vol. 105, No. 13. (1 April 2008), pp. 5111-5116.


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Recombinant HIV-Tat (Tat) induces extensive apoptosis in peripheral blood mononuclear cells (PBMCs) cultured in typical CO2 incubators, which are equilibrated with air (21% O2). However, as we show here, Tat apoptosis induction fails in PBMCs cultured at physiological oxygen levels (5% O2). Under these conditions, Tat induces PBMCs to divide, efficiently primes them for HIV infection, and supports virus production by the infected cells. Furthermore, Tat takes only 2 h to prime PBMCs under these conditions. In contrast, PHA/IL-2, which is widely used to prime cells for HIV infection, takes 23 days. These findings strongly recommend culturing primary cells at physiological oxygen levels. In addition, they suggest HIV-Tat as a key regulator of HIV disease progression. 10.1073/pnas.0712363105


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