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JAIDS Journal of Acquired Immune Deficiency Syndromes:
doi: 10.1097/QAI.0b013e3181fb1cb3
Letter to the Editor

Effects of HIV-1 gp120 and Protease Inhibitors on Apoptotic Susceptibility of CD34+ Hematopoietic Progenitor Cells

MacEneaney, Owen J PhD*; Connick, Elizabeth MD†; DeSouza, Christopher A PhD†

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*Integrative Vascular Biology Laboratory, Department of Integrative Physiology, University of Colorado, Boulder, CO; †Department of Medicine, University of Colorado Denver, Aurora, CO.

To the Editors:

HIV-1 infection is associated with several immunological disturbances, including a reduction in circulating CD34+ hematopoietic progenitor cells.1 Depletion of CD34+ cells may have far-reaching consequences, given their role in immune reconstitution and their association with vascular repair and cardiovascular disease.2,3 Although CD34+ cells are generally resistant to HIV-1 infection,4 uninfected CD34+ cells from patients with AIDS demonstrate a commitment to apoptosis.5 This adverse effect is likely due in large part to direct cytotoxic interactions with HIV-1 and, in particular, the envelope glycoprotein gp120.6

The advent of highly active antiretroviral therapy (HAART) in the treatment of HIV-1 infection has dramatically slowed the rate of progression of HIV-1 to AIDS and improved patient outcomes.7 As HIV-1-infected patients are living longer, HIV-1-related metabolic and cardiovascular complications are growing in this population,8 which may be linked to numerical or functional deficits in circulating progenitors. Treatment with protease inhibitors (PIs), an important component of many HAART regimens, generally results in improved viability of CD34+ cells from HIV-1-infected individuals.9,10 However, this may be largely driven by the antiviral activity of these medications, although the direct effects on CD34+ cells are less clear. One prior investigation reported that ritonavir (RTV) had antiapoptotic effects on CD34+ cells.9 Accordingly, we hypothesized that other common PIs would also reduce CD34+ cell apoptosis at physiological concentrations (ie, typical maximum plasma levels) in vitro.

Freshly isolated CD34+ cells from healthy G-CSF-treated human donors (n = 3) were obtained from an independent supplier (Allcells, LLC, Berkeley, CA). Donors tested negative for HIV-1, hepatitis B, and hepatitis C. Viability of cells determined by trypan blue exclusion tests was 95.7% ± 0.4%. Purity, as assessed by flow cytometric analysis with propidium iodide, was 97.7% ± 0.4%.

CD34+ cells were cultured in serum-free medium (StemCell Technologies, Inc, Vancouver, Canada) supplemented with 100 ng/mL of thrombopoietin, Flt3 ligand, and stem cell factor. Cells were treated for 48 hours with 1 μg/mL RTV,11 5.2 μg/mL atazanavir (ATV),11 or 9.8 μg/mL lopinavir (LPV)11 (obtained through the AIDS Research and Reference Reagent Program, Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health). Positive control experiments were performed using 100 ng/mL HIV-1Bal gp120 (R5 trophic) (AIDS Research and Reference Reagent Program) and HIV-1Lav gp120 (X4 trophic)12 (Protein Sciences Corporation, Meriden, CT).

Activation of caspase-3 was induced in CD34+ cells by incubating with staurosporine (1 μmol/L for 3 hours; Sigma Aldrich, St Louis, MO). The concentration of active caspase-3 large subunit in cell lysates was determined using enzyme immunoassays (R&D Systems, Minneapolis, MN). The intra- and interassay coefficients of variation for this assay in our laboratory are <10%.

Experimental points were performed in duplicate with 3 independent experiments. Differences between treatments were determined by analysis of variance. Where indicated by a significant F value, post hoc tests, with Bonferroni correction for multiple comparisons, were performed to determine differences between treatment groups. Results are expressed as mean ± standard error of the mean. Statistical significance was set at P < 0.05.

On stimulation with staurosporine, both R5 (6.0 ± 0.4 ng/mL) and X4 (6.0 ± 0.1 ng/mL) gp120 resulted in a 65% greater activation of caspase-3 compared with the control condition (3.6 ± 0.4 ng/mL; P < 0.05) (Fig. 1A). Within the PI group, the capacity of staurosporine to induce an apoptotic response was 40% higher in cells treated with ATV (4.9 ± 0.7 ng/mL) and LPV (5.1 ± 0.2 ng/mL) compared with the control condition (P < 0.05) (Fig. 1B). In contrast, treatment with RTV (4.1 ± 0.5 ng/mL) did not significantly alter intracellular active caspase-3.

Figure 1
Figure 1
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The novel findings of the present study are that the PIs, ATV and LPV, reduce the resistance of CD34+ cells to an apoptotic stimulus. To our knowledge, this is the first study to demonstrate the proapoptotic effects of PIs on CD34+ cells from healthy adults.

CD34+ cells from patients with AIDS demonstrate a marked predisposition toward apoptosis.5 Zauli et al13 showed that virus isolates from HIV-1-seropositive patients induced a dose-dependent inhibition on the growth of CD34+ cells in vitro, an effect blocked by pretreatment with an anti-gp120 antibody. Subsequent investigations further implicated gp120 (in concentrations ranging from 0.01 to 20 μg/mL) in the induction of CD34+ cell apoptosis.14,15 Our results extend these findings to broadly physiological concentrations of gp120 from 2 strains of the HIV-1 virus, HIV-1Bal and HIV-1Lav, and add to the growing evidence base that indicates a direct cytotoxic activity of HIV-1 gpl20 on human CD34+ cells.

HAART has been shown to restore CD34+ cell function in HIV-1-infected patients. For example, increased CD34+ cell colony formation has been documented after 3-6 months of HAART.10,16 In addition, the PI RTV lowered apoptosis in CD34+ cells from HIV-1-infected patients in vitro but only at a concentration of 5 nmol/L; no differences were recorded at concentrations between 5 and 20 nmol and a decrease was observed at concentrations >20 nmol.9 Interestingly, these effects have only been documented in CD34+ cells from HIV-1-infected patients and only after short-term HAART administration. Our results show that the PIs ATV and LPV reduce resistance to apoptosis in CD34+ cells from healthy adults. Although RTV had no effect in the present investigation, it should be noted that the concentration of RTV used in this study was that which is achieved in vivo to boost LPV levels through inhibition of cytochrome P450 CYP3A; although higher concentrations of RTV that mediate direct antiretroviral activity are no longer used clinically, an important question for future studies is whether higher concentrations of RTV and therapeutic doses of other PIs also induce a proapoptotic phenotype. It is plausible, therefore, that the prosurvival effects of PIs on CD34+ cells are secondary to their antiviral activity and that direct interaction with healthy cells is actually harmful, albeit less harmful than exposure to gp120. This information may have clinically relevant implications in the context of longer-term treatment given its potential to explain, at least in part, why some patients do not reconstitute their CD4+ T-cell population, despite HAART and the accelerated cardiovascular morbidity observed in patients on HAART.

Although we endeavored to confer physiological relevance on our study by using concentrations of PIs and gp120 found in the plasma of HIV-1-positive patients,11,12 it is important to be conservative in any attempt to generalize our results to an in vivo context. CD34+ cells are exposed to these agents continuously in the circulation in addition to the full complexity of vascular milieu. In addition, although our findings were similar in all subjects, our sample was small and further experiments will be required to delineate the mechanisms of the PI-induced apoptotic effect.

In conclusion, our results suggest that typical plasma concentrations of ATV and LPV can reduce resistance to apoptosis in healthy CD34+ cells, suggesting a role for PIs in poor immune reconstitution and accelerated cardiovascular disease in some HAART-treated patients.

Owen J. MacEneaney, PhD*

Elizabeth Connick, MD†

Christopher A. DeSouza, PhD*†

*Integrative Vascular Biology Laboratory, Department of Integrative Physiology, University of Colorado, Boulder, CO

†Department of Medicine, University of Colorado Denver, Aurora, CO

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