Adhesion molecules can improve hematopoietic cell survival; however, their role in leukemic cell resistance to drug-induced apoptosis is poorly documented. The CD44 adhesion molecule is strongly expressed on acute myeloid leukemia (AML) blasts. Using 2 myeloid cell lines, HL60 and NB4, evidence is presented that prior incubation with the CD44-specific monoclonal antibody (mAb) A3D8, reported to induce differentiation of AML blasts, significantly decreases apoptosis induced by 3 drugs used in AML chemotherapy: daunorubicin (DNR), mitoxantrone, and etoposide. In addition, in HL60 cells, CD44 ligation with A3D8 mAb fully abrogates the DNR-triggered generation of ceramide, a lipid second messenger involved in the DNR apoptotic signaling pathway. Moreover, results show that the A3D8 mAb and Bcl-2 additively inhibit DNR-induced apoptosis in HL60 cells overexpressing Bcl-2. These results suggest that, to eradicate AML blasts, the differentiation-inducing anti-CD44 mAb A3D8 should not be administered prior to apoptosis-inducing drugs.

Chemoresistance, a major cause of treatment failure in acute myeloid leukemia (AML), is a complex process involving various mechanisms. Among them, inhibition of drug-induced apoptosis1 is likely to be involved because chemoresistance of AML frequently correlates with increased expression of antiapoptotic molecules, such as Bcl-2.2 Interestingly, it was recently shown that AML cell apoptosis could be inhibited via integrins,3 suggesting a role for adhesive receptors in AML blasts chemoresistance.

The CD44 adhesion molecule, a receptor for hyaluronan,4 is strongly expressed on AML blasts.5 Recent reports suggest that CD44 can inhibit apoptosis; CD44 ligation with activating monoclonal antibodies (mAbs) or hyaluronan abrogates apoptosis of T lymphocytes and promotes survival of B lymphocytes.6 7Therefore, we investigated whether CD44 ligation could decrease drug-induced apoptosis of AML blasts.

We used 2 human myeloid cell lines, HL60 and NB4, and independently ligated CD44 with 2 activating mAbs.8,9 Interestingly, A3D8 mAb induces differentiation of fresh AML blasts, whereas J173 does not.10 Hyaluronan was not assayed because of its low affinity for CD44 expressed on HL60 and NB4.11 After CD44 ligation, apoptosis was induced by 3 drugs used in AML chemotherapy: daunorubicine (DNR), mitoxantrone, or etoposide. Our results show that preincubation with A3D8 inhibits apoptosis induced by all drugs tested, in both cell lines. Moreover, A3D8-mediated antiapoptotic effect is additive to that of Bcl-2, in HL60 cells overexpressing Bcl-2. These findings may have implications for designing treatments potentially associating CD44-targeted differentiation and chemotherapy.

Reagents and cells

The A3D8 (Sigma Chemical, St. Louis, MO) and J173 (Coulter-Immunotech, Marseille, France) antihuman CD44 mAbs were purchased uncoupled or as fluorescein isothiocyanate (FITC) conjugates. Murine IgG1 (isotype control) and FITC-conjugated goat antimurine IgG (GAM-FITC) were from Coulter-Immunotech.

Daunorubicin (Cerubidine) was obtained from Laboratoire Roger Bellon (Neuilly-sur-Seine, France) and mitoxantrone (Novantrone) from Lederle Parenterals (Carolina, Puerto Rico). Methyl-[3H]-thymidine (79 Ci/mmol) and 9,10(n)-[3H]-palmitic acid (53 Ci/mmol) were purchased from Amersham (Les Ulis, France), annexinV-FITC from Roche (Meylan, France), and other reagents from Sigma.

Cells were cultured in RPMI 1640 containing 10% fetal calf serum, 2 mmol/L l-glutamine, 100 μg/mL streptomycin, and 200 U/mL penicillin (GIBCO, Grand Island, NY). HL60 was purchased from ATCC (CCL240; Rockville, MD). Bcl-2 overexpressing HL60/Bcl-2, HL60/Neo cells, and Western blotting for Bcl-2 detection have been described.12,13 NB4 cells were derived from an acute promyelocytic leukemia.14 

Cross-blocking of mAbs

Cells were preincubated with 20 μg/mL uncoupled A3D8, J173, or mouse IgG1, then stained with 2 μg/mL FITC-conjugated A3D8 or J173. Fluorescence was analyzed on a Profile II flow cytometer (Coulter Immunology, Hialeah, FL) equipped with a 15-mW argon laser (488 nm) on 3000 to 5000 cells.

CD44 ligation and induction of apoptosis

Cells (5 × 105 cells/mL) were preincubated at 37°C for 16 hours with 2.5 μg/mL A3D8, J173, mouse IgG1, or culture medium. Subsequently, DNR (0.5 μmol/L), mitoxantrone (0.3 μmol/L), or etoposide (10 μmol/L) was added, during 6 or 24 hours. Cell viability was evaluated by trypan blue dye exclusion.

Quantification of apoptosis

Apoptosis was quantified by 3 previously described methods: flow cytometry on cells labeled with annexinV-FITC and propidium iodide,15 microscopical examination of smears stained with May-Grünwald-Giemsa stain,13 and quantification of fragmented DNA, based on an [3H]-thymidine release assay.16 

Ceramide quantitation

Cells were metabolically labeled for 48 hours with 1 μCi/mL 9,10(n)-[3H]-palmitic acid. A3D8 mAb was added during the last 16 hours of labeling. Total cellular ceramide content was measured for 0 to 15 minutes after addition of 0.5 μmol/L DNR, as described.17 

Statistical analysis

A paired Student t test was used to assess differences between treated and control groups. A P value less than .05 was considered significant.

A3D8 anti-CD44 mAb inhibits drug-induced apoptosis

The HL60 and NB4 cells were preincubated with A3D8 or J173 mAbs, or culture medium, then treated with DNR, mitoxantrone, or etoposide. Apoptotic cells, labeled with annexinV-FITC and excluding propidium iodide, were quantified by flow cytometry. Drug treatment alone induced apoptosis of 24% to 34% HL60 and 34% to 40% NB4 cells (Figure1A,B). Preincubation with A3D8 mAb reduced apoptosis induced by all 3 drugs by over 50% in HL60 (Figure 1A) and by 75% to 100% in NB4 cells (Figure 1B). In contrast, J173 did not modulate drug-induced apoptosis in these cells.

Fig. 1.

A3D8 anti-CD44 mAb inhibits drug-induced apoptosis.

The inhibitory effect of CD44-specific A3D8 mAb on drug-induced apoptosis was determined in HL60, as shown in A, C, and D, and NB4 (B) myeloid cells. Cells were preincubated for 16 hours with 2.5 μg/mL anti-CD44 mAbs A3D8 or J173, control mouse IgG1, or culture medium only, then treated with DNR (0.5 μmol/L), mitoxantrone (0.3 μmol/L), or etoposide (10 μmol/L) for 24 hours (A-C) or 6 hours (D). Apoptosis was evaluated by measuring the percentage of annexinV-FITC-positive, propidium iodide-negative cells, by flow cytometry (A and B); the percentage of apoptotic cells, by microscopical observation of May-Grünwald-Giemsa stained cytosmears (C); and the percentage of fragmented DNA, in which the spontaneous DNA fragmentation of untreated cells (routinely < 5% DNA fragmentation) has been subtracted, by the [3H]-thymidine release assay (D), as described.16 Panels A and B show results from 1 representative experiment of 3. The mean ± SEM from triplicate samples are shown for panels C and D. (E) Analysis of cell survival in DNR-treated cultures preincubated with CD44-specific mAbs. HL60, HL60/Bcl-2 and NB4 cells were preincubated for 16 hours with culture medium, A3D8 or J173 mAbs, as indicated, then treated with 0.5 μmol/L DNR or culture medium alone (DNR-free control) for 24 hours. The total number of viable cells per milliliter was evaluated by trypan blue dye exclusion. For each preincubation, the percentage of surviving cells was calculated as follows: [number of viable cells/mL in DNR-treated culture] / [number of viable cells/mL in DNR-free culture] × 100. Results represent 1 of 2 independent experiments. (F) A3D8 and J173 anti-CD44 mAbs do not cross-block each other's binding to HL60 cells. HL60 cells were preincubated with a saturating concentration (20 μg/mL) of A3D8 or J173 mAbs, or IgG1 control isotype, and subsequently stained with 2 μg/mL FITC-conjugated A3D8 or J173. Cell fluorescence (black histograms) was analyzed by flow cytometry. Nonspecific background fluorescence was determined on cells incubated with control IgG1, followed by GAM-FITC (gray histograms).

Fig. 1.

A3D8 anti-CD44 mAb inhibits drug-induced apoptosis.

The inhibitory effect of CD44-specific A3D8 mAb on drug-induced apoptosis was determined in HL60, as shown in A, C, and D, and NB4 (B) myeloid cells. Cells were preincubated for 16 hours with 2.5 μg/mL anti-CD44 mAbs A3D8 or J173, control mouse IgG1, or culture medium only, then treated with DNR (0.5 μmol/L), mitoxantrone (0.3 μmol/L), or etoposide (10 μmol/L) for 24 hours (A-C) or 6 hours (D). Apoptosis was evaluated by measuring the percentage of annexinV-FITC-positive, propidium iodide-negative cells, by flow cytometry (A and B); the percentage of apoptotic cells, by microscopical observation of May-Grünwald-Giemsa stained cytosmears (C); and the percentage of fragmented DNA, in which the spontaneous DNA fragmentation of untreated cells (routinely < 5% DNA fragmentation) has been subtracted, by the [3H]-thymidine release assay (D), as described.16 Panels A and B show results from 1 representative experiment of 3. The mean ± SEM from triplicate samples are shown for panels C and D. (E) Analysis of cell survival in DNR-treated cultures preincubated with CD44-specific mAbs. HL60, HL60/Bcl-2 and NB4 cells were preincubated for 16 hours with culture medium, A3D8 or J173 mAbs, as indicated, then treated with 0.5 μmol/L DNR or culture medium alone (DNR-free control) for 24 hours. The total number of viable cells per milliliter was evaluated by trypan blue dye exclusion. For each preincubation, the percentage of surviving cells was calculated as follows: [number of viable cells/mL in DNR-treated culture] / [number of viable cells/mL in DNR-free culture] × 100. Results represent 1 of 2 independent experiments. (F) A3D8 and J173 anti-CD44 mAbs do not cross-block each other's binding to HL60 cells. HL60 cells were preincubated with a saturating concentration (20 μg/mL) of A3D8 or J173 mAbs, or IgG1 control isotype, and subsequently stained with 2 μg/mL FITC-conjugated A3D8 or J173. Cell fluorescence (black histograms) was analyzed by flow cytometry. Nonspecific background fluorescence was determined on cells incubated with control IgG1, followed by GAM-FITC (gray histograms).

Close modal

These results were confirmed by cell morphology analysis and DNA fragmentation. Indeed, preincubation of HL60 with A3D8 significantly decreased DNR-induced apoptosis (from 62.9 ± 2.8% to 41.5 ± 1.7%, P < .01, Figure 1C) and DNA fragmentation (from 42.5 ± 1.6% to 23.1 ± 1.5%,P < .001, Figure 1D). Apoptosis inhibition was specifically mediated by A3D8 anti-CD44 mAb, because both a control isotype (IgG1) and another anti-CD44 mAb (J173) were inactive (Figure 1C,D). Note that culture medium or antibodies alone induced less than 2% apoptosis (Figure 1A-C).

To determine whether A3D8 antiapoptotic effect was associated with increased cell viability, we compared cell survival in DNR-treated cultures preincubated with A3D8, J173, or culture medium. Only A3D8 improved survival of HL60, HL60/Bcl-2, and NB4 cells to DNR treatment (Figure 1E). However, no viable cells were recovered after 5 days.

Inactivity of J173 was not due to poor binding because it bound CD44 as strongly as A3D8 (Figure 1F, left panels). Moreover, J173 and A3D8 did not cross-block each other's binding (Figure 1F), suggesting that they recognize distinct epitopes of CD44. Because of its inactivity, J173 subsequently served as surface-binding, isotype-matched control.

A3D8 inhibits proliferation of myeloid leukemia cells

To investigate the mechanisms of A3D8 antiapoptotic activity, we first examined its effect on cell viability. We noticed that, in DNR-free cultures, A3D8 inhibited proliferation of HL60 (Figure2A), HL60/Bcl-2 (Figure 2B), and NB4 cells (not shown). As expected, J173 was inactive.

Fig. 2.

Mechanisms of A3D8-mediated inhibition of apoptosis.

(A and B) Inhibitory effect of anti-CD44 A3D8 mAb on myeloid leukemia cell proliferation. HL60 (A) and HL60/Bcl-2 (B) cells in exponential growth phase were seeded at 5 × 105/mL in culture medium in the absence (medium) or presence of 2.5 μg/mL anti-CD44 mAbs (A3D8 or J173). Cell viability was evaluated by trypan blue dye exclusion. (C) Inhibitory effect of A3D8 anti-CD44 mAb on DNR-induced ceramide generation in HL60 cells. Cellular lipids were metabolically labeled by incubating cells with [3H]-palmitic acid for 48 hours. A3D8 mAb or control medium was added during the last 16 hours of this incubation. DNR (0.5 μmol/L) was then added and the amount of cellular ceramide was quantitated through 15 minutes, as described.13 Results shown represent the mean ± SEM from 3 independent experiments. The difference between A3D8-treated and untreated cells is statistically significant (Student t test, P < .05). (D) Additive inhibitory effects of A3D8 anti-CD44 mAb and Bcl-2 on DNR-induced apoptosis. HL60/Bcl-2 (Bcl-2 overexpressing) and HL60/Neo (control) cells were preincubated for 16 hours with 2.5 μg/mL anti-CD44 mAb A3D8 or J173, or with culture medium only; cells were then treated with 0.5 μmol/L DNR for 24 hours, and the percentage of apoptotic cells was evaluated by microscope examination. Results represent the mean ± SEM from 3 independent experiments. (E) Western blot analysis of Bcl-2 expression in HL60/Neo and HL60/Bcl-2 cells.

Fig. 2.

Mechanisms of A3D8-mediated inhibition of apoptosis.

(A and B) Inhibitory effect of anti-CD44 A3D8 mAb on myeloid leukemia cell proliferation. HL60 (A) and HL60/Bcl-2 (B) cells in exponential growth phase were seeded at 5 × 105/mL in culture medium in the absence (medium) or presence of 2.5 μg/mL anti-CD44 mAbs (A3D8 or J173). Cell viability was evaluated by trypan blue dye exclusion. (C) Inhibitory effect of A3D8 anti-CD44 mAb on DNR-induced ceramide generation in HL60 cells. Cellular lipids were metabolically labeled by incubating cells with [3H]-palmitic acid for 48 hours. A3D8 mAb or control medium was added during the last 16 hours of this incubation. DNR (0.5 μmol/L) was then added and the amount of cellular ceramide was quantitated through 15 minutes, as described.13 Results shown represent the mean ± SEM from 3 independent experiments. The difference between A3D8-treated and untreated cells is statistically significant (Student t test, P < .05). (D) Additive inhibitory effects of A3D8 anti-CD44 mAb and Bcl-2 on DNR-induced apoptosis. HL60/Bcl-2 (Bcl-2 overexpressing) and HL60/Neo (control) cells were preincubated for 16 hours with 2.5 μg/mL anti-CD44 mAb A3D8 or J173, or with culture medium only; cells were then treated with 0.5 μmol/L DNR for 24 hours, and the percentage of apoptotic cells was evaluated by microscope examination. Results represent the mean ± SEM from 3 independent experiments. (E) Western blot analysis of Bcl-2 expression in HL60/Neo and HL60/Bcl-2 cells.

Close modal

A3D8 abrogates the DNR-induced generation of ceramide

We next examined how A3D8 could affect DNR-induced apoptotic signaling.17 We found that A3D8 totally abrogated the generation of ceramide, a lipid second messenger involved in the apoptotic signaling of cytotoxic agents18 (Figure 2C). Note that, like A3D8, protein kinase C (PKC) activators inhibit both DNR-induced ceramide generation and apoptosis in HL60 cells.19 Because CD44 ligation can activate PKC,20 this suggests that A3D8 might inhibit ceramide generation via PKC activation.

CD44 and Bcl-2 additively inhibit DNR-induced apoptosis

We previously demonstrated that, unlike A3D8, Bcl-2 inhibits DNR-induced apoptosis in HL60 cells without affecting ceramide generation,13 suggesting different antiapoptotic mechanisms. Using HL60/Bcl-2 cells, we first checked Bcl-2 anti-apoptotic activity; significant apoptosis inhibition was observed in HL60/Bcl-2, compared to HL60/Neo cells (26.8 ± 2.3% versus 64.8 ± 3.5% apoptotic cells, P < .001, Figure 2D). Strikingly, preincubation of HL60/Bcl-2 cells with A3D8 further decreased DNR-induced apoptosis in these cells (13.3 ± 3.2% versus 26.8 ± 2.3%, P < .01, Figure 2D), thus demonstrating additive anti-apoptotic effects of A3D8 and Bcl-2. As expected, J173 (Figure 2D) or control IgG1 (not shown) were inactive. These results suggest that A3D8 and Bcl-2 inhibit apoptosis signaling at different levels, upstream and downstream of ceramide, respectively. In agreement, we found that A3D8 did not inhibit apoptosis induced by exogenous, cell permeant ceramide in HL60 cells (data not shown).

In conclusion, we demonstrate that prior treatment of AML cell lines NB4 and HL60 with A3D8 anti-CD44 mAb significantly reduces drug-induced apoptosis. The A3D8 antiapoptotic effect may be related to its antiproliferative and differentiating activity on AML cells, as shown for patients' blasts,10 and HL60 and NB4 cells (Charrad and coworkers, article in preparation). Indeed, several authors reported that differentiating agents inhibit drug-induced apoptosis of AML.21-23 Moreover, in agreement with our present experiments, prior administration of all-transretinoic acid in patients with acute promyelocytic leukemia decreased chemotherapy efficiency.24 Taken together, these considerations suggest that, in a therapy combining A3D8-induced differentiation and drug-induced apoptosis, A3D8 should not be administered first.

We wish to acknowledge Dr Michel Lanotte for the gift of NB4 cells, Dr Jacqueline Bréard and Dr Pierre Brousset for helpful suggestions on the manuscript, and Prof Georges Delsol for his scientific support and critical discussion of this work.

Supported by INSERM, the Association pour la Recherche sur le Cancer, and the Association Nouvelles Recherches Biomédicales. R.S.C. received a fellowship from the Association pour la Recherche sur le Cancer.

Reprints:Michèle Allouche, CNRS-UPCM, UPR2163, CHU Purpan, avenue de Grande Bretagne, 31059 Toulouse Cedex 03, France; e-mail: allouche@cict.fr.

The publication costs of this article were defrayed in part by page charge payment. Therefore, and solely to indicate this fact, this article is hereby marked “advertisement” in accordance with 18 U.S.C. section 1734.

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