HPLC-based Assay to Monitor Extracellular Nucleotide/Nucleoside Metabolism in Human Chronic Lymphocytic Leukemia Cells

Summary

The protocol described here represents an easy and reproducible method that employs reverse phase high-performance liquid chromatography (RP-HPLC) to measure purine metabolism on chronic lymphocytic leukemia (CLL) cells cultured under different conditions.

Abstract

This method describes a sensitive, specific, reliable and reproducible reverse phase high-performance liquid chromatography (RP-HPLC) assay developed and validated for the quantification of extracellular purine nucleotides and nucleosides produced by purified chronic lymphocytic leukemia (CLL) cells under different culture conditions. The chromatographic separation of adenosine 5'-monophosphate (AMP), adenosine (ADO) and inosine (INO) is performed at RT on a silica-based, reversed-phase column that is used for polar compound retention. The method includes a binary mobile phase, which consists of 7 mM ammonium acetate and acetonitrile with a flow rate of 1.00 ml/min. The eluates are monitored using a Photodiode Array UV detector set at 260 nm. A standard calibration curve is generated to calculate the equation for the analytical quantification of each purine compound. System control, data acquisition and analysis are then performed. Applying this protocol, AMP, INO and ADO elute at 7, 11 and 11.9 min, respectively, and the total run time for each sample is 20 min. This protocol may be applied to different cell types and cell lines (both suspension and adherent), using culture media as matrix. The advantages are easy and fast sample preparation and the requirement of a small amount of supernatant for analysis. Furthermore, the use of a serum-free medium allows skipping the protein precipitation step with acetonitrile that impacts the final concentration of purine compounds. One of the limitations of the method is the requirement of the equilibration column run before each single sample run, making the total run time of the experiment longer and preventing high throughput screening applications.

Introduction

Adenosine (ADO) is a purine nucleoside with an adenine molecule attached to a ribose sugar molecule moiety through a glycosidic bond. When present in the extracellular environment, it protects cells from excessive damage by the action of the immune system. This role has been highlighted using different disease models, such as colitis¹, diabetes², asthma³, sepsis⁴, and ischemic injury⁵. One of the main ADO functions is the inhibition of immune responses in the tumor microenvironment, contributing to tumor immune evasion⁶. For this reason, the mechanisms involved in ADO formation and signaling are of considerable therapeutic interest⁷.

ADO levels in the tissue microenvironment are relatively low under normal physiologic conditions and certainly below the sensitivity threshold of immune cells. However, during hypoxia, ischemia, inflammation, infection, metabolic stress and tumor transformation they rapidly increase⁸. The elevated extracellular ADO levels in response to tissue-perturbing signals have a dual function: to report tissue injury in an autocrine and paracrine way and to generate tissue responses that can be generally viewed as cytoprotective.

Extracellular ADO can be formed through a variety of mechanisms, which include release from intracellular compartments mediated by nucleoside transporters⁹ or accumulation because of impaired degradation operated by adenosine deaminase. The main pathway leading to increased extracellular ADO levels involves the action of a cascade of ectonucleotidases, which are membrane associated ectoenzymes generating ADO by phosphohydrolysis of nucleotides released from dead or dying cells. This pathway proceeds through the sequential action of CD39 (ectonucleoside triphosphate diphosphohydrolase-1) that converts extracellular adenosine 5'-triphosphate (ATP) or adenosine 5'-diphosphate (ADP) to adenosine 5'-monophosphate (AMP) and of CD73 (5'-nucleotidase), which converts AMP to ADO¹⁰.

Extracellular ADO elicits its physiological responses by binding to four transmembrane ADO receptors, namely A1, A2A, A2B and A3. Each receptor has different affinities for ADO and specific tissue distribution. All the receptors have seven transmembrane domains and are G-protein coupled to intracellular GTP-binding proteins (G proteins), that can induce (Gs protein) or inhibit (Gi protein) adenylate cyclase activity and, subsequently, the production of intracellular cAMP. Therefore, changes in cytoplasmic cAMP levels impact on intracellular protein kinase activity during physiological responses¹¹. Under physiological conditions extracellular ADO is below 1 µM, which can activate indiscriminately A1, A2A and A3 receptors. However, the activation of A2B subtype requires considerably higher concentrations of the nucleoside, such as those generated under pathophysiological conditions. Alternatively, extracellular ADO can be degraded to inosine (INO) by adenosine deaminase (ADA) and CD26, an ADA complexing protein localizing ADA on the cell surface. Another possibility is that ADO is internalized by the cell through the equilibrative nucleoside transporters (ENT) and phosphorylated to AMP by ADO kinase protein^12,13.

The aim of this protocol is to describe an analytical method of reverse phase high-performance liquid chromatography (RP-HPLC) to quantify in a single run the substrate AMP and the products ADO and INO, as generated by human lymphocytes. Our experience was initially obtained using cells from chronic lymphocytic leukemia (CLL) patients, which are characterized by the expansion of a mature population of CD19⁺/CD5⁺ B lymphocytes constitutively expressing CD39^14,15. We showed approximately 30% of CLL patients express the CD73 ectoenzyme and that this phenotype correlates with a poor prognosis¹⁶. This subpopulation of leukemic cells co-expressing CD39 and CD73 can actively produce extracellular ADO from ADP and/or AMP. Preincubation of CD73⁺ CLL cells with α,β-methylene-ADP (APCP), a known inhibitor of CD73 enzymatic activity, completely blocks extracellular ADO synthesis confirming that CD73 represents the bottle-neck enzyme of that cascade¹⁶.

CLL cells also express ADA and the ADA complexing protein CD26, which are responsible for the conversion of ADO into INO. By using specific ADA inhibitors, such as erythro-9-(2-Hydroxy-3-nonyl)I wiadenine (EHNA) hydrochloride and deoxycoformycin (dCF), it is possible to block extracellular ADO degradation into INO. Furthermore, pretreatment with an ADA inhibitor in combination with dipyridamole, that blocks nucleoside transporters, enhances ADO accumulation in cell supernatants.

We have then extended this protocol to cells derived from other lineages, including T lymphocytes and myeloid cells, confirming CD73-dependent ADO production. These findings suggest that this HPLC protocol is highly versatile and that it can be applied to different cell lineages and to different culture conditions (Figure 1).

Figure 1. Schematic representation of the enzymatic machinery responsible for extracellular ADO production. Adenosine 5'-triphosphate (ATP) and/or adenosine 5'-diphosphate (ADP) can be degraded by CD39 to adenosine 5'-monophosphate (AMP), which in turn is converted by CD73 into the nucleoside adenosine (ADO). Once ADO is produced in the extracellular space, it may reenter the cell through the nucleoside transporters (ENT), be converted into inosine (INO) or bind to different types of P1 ADO receptors. Please click here to view a larger version of this figure.

Protocol

CLL blood samples are obtained in accordance with Institutional Guidelines and Declaration of Helsinki.

1. Isolation of Leukemic Lymphocytes from Blood Samples of CLL Patients 

1. Collect blood sample in sodium heparin (green-top) tube¹⁷.
2. Make 1: 3 dilution of whole blood with RT 1x phosphate buffered saline (PBS).
3. Purify peripheral blood mononuclear cells (PBMC) from blood samples by density gradient centrifugation.
   1. Underlay 5 ml of density centrifugation media (e.g., Ficoll) in a 15 ml centrifuge tube and carefully transfer 10 ml of diluted blood. Immediately centrifuge at 1,500 x g for 20 min at RT.
4. Aspirate part of the supernatant with a glass Pasteur pipette connected to a vacuum pump and collect the PBMC ring at the interphase between density centrifugation media and diluted plasma with a 5 ml pipette. Transfer to a 50 ml centrifuge tube and wash with PBS (50 ml final volume). Centrifuge at 500 x g for 5 min at 4 °C.
5. Aspirate the supernatant with a glass Pasteur pipette, resuspend the pellet in 50 ml of PBS and count the cells using a hemocytometer.
6. Stain PBMCs with anti-CD19 and -CD5 antibodies for flow cytometry following a standard protocol for immunostaining and check for PBMC subpopulation composition¹⁸.
   Note: CLL lymphocytes are CD19⁺/CD5⁺.
7. Check the % of CD19⁺/CD5⁺ cells using a flow cytometer¹⁸. Purify B lymphocytes from patients with a ≥95% of CD19⁺/CD5⁺ leukemic cells following the instructions detailed in step 2 for the negative isolation of B cells¹⁹.

2. Purification of Leukemic B Cells by Negative Isolation

1. Resuspend 10⁷ PBMCs/ml in PBS 0.1 % bovine serum albumin (BSA) 2 mM EDTA, pH 7.4 (isolation buffer).
2. Add 10 µg of mouse monoclonal anti-CD3, -CD14 and -CD16 primary antibodies for 10⁷ cells and incubate for 30 min at 4 °C.
3. Wash the cells with the isolation buffer and centrifuge at 500 x g for 5 min at 4 °C.
4. Resuspend the cells in the isolation buffer at 10⁷ PBMCs/ml.
5. Before incubating with the cells, resuspend sheep anti-mouse IgG magnetic beads in the vial. Transfer 100 µl of beads per 10⁷ cells to a tube.
6. Add 1 mL of isolation buffer and place the tube in a magnet holder for 1 min. Discard the supernatant with a 5 ml pipette.
7. Remove the tube from the magnet and resuspend the washed beads in 100 µl of isolation buffer.
8. Incubate 10⁷ cells with 100 µl of magnetic beads for 30 min at 4 °C with gentle tilting and rotation.
9. Place the tube in the magnet holder for 2 min and transfer the supernatant with the CD19⁺/CD5⁺ unbound cells to a fresh tube with a 5 ml pipette.
10. At the end of the isolation protocol, stain 100 µl of cells with anti-CD19 and -CD5 antibodies for flow cytometry and incubate 30 min at 4 °C. Wash the cells with 3 ml of PBS 1% BSA, discard the excess of supernatant and check B cell purity again by flow cytometry¹⁹.
    Note: Perform an additional negative isolation step if B cell purity is lower than 95%.

3. Preparation of Standard and Inhibitors Stock Solutions

1. To prepare AMP, weigh out 0.00345 g of AMP and dissolve it in 5 ml of serum-free medium to have a 2 mM standard solution of AMP.
2. To prepare ADO, weigh out 0.00265 g of ADO and dissolve it in 5 ml of serum-free medium to have a 2 mM standard solution of ADO.
3. To prepare INO, weigh out 0.00268 g of INO and dissolve it in 5 ml of serum-free medium to have a 2 mM standard solution of INO.
4. Prepare a 400 µM solution of AMP, ADO and INO by mixing 1 ml of the 2 mM stock solution in 4 ml of serum-free medium (5 ml final volume).
   1. Make 1:4 dilution of each 400 µM standard solution to obtain a 100 µM concentration by pipetting 500 µl of the 400 µM solution in 1,500 µl of serum-free medium (2 ml final volume).
   2. Prepare serial dilutions of each compound in serum-free medium to obtain the following concentrations: 100 µM - 50 µM - 25 µM - 10 µM - 5 µM - 2.5 µM - 1 µM - 0.5 µM - 0.25 µM.
      Note: For example, pipette 1 ml of the 100 µM solution in 1 ml of serum-free medium (1:2 dilution) to obtain 50 µM concentration and proceed with the remaining dilutions.
5. Prepare a 10 mM stock solution of APCP dissolved in PBS; aliquot and stock at - 30 °C.
6. Prepare 10 mM stock solutions of EHNA hydrochloride, dCF and dipyridamole dissolved in dimethyl sulfoxide (DMSO); aliquot and stock at -30 °C.

4. Program the HPLC Method

1. Prepare a 7 mM ammonium acetate buffer by dissolving 0.770 g of ammonium acetate in 2 L of double deionised water (Buffer A). Adjust to pH 3.0 with hydrochloric acid.
2. Prepare a glass bottle containing at least 2 L of ultrapure acetonitrile for HPLC (Buffer B) and connect the guard column and the column to the HPLC.
   Note: The columns and buffers are at RT while in use.
3. Log into the HPLC software and select the "browse project" button. Go to the "file" menu and select "new method" and then "instrument method".
4. Program the equilibration column method as per Table 1. Set a flow rate of 1.00 ml/min and program the UV detector to read at 260 nm. Save the instrument method and select again “new method” from the “file” menu and then “method set”. Choose the instrument method previously saved and save the current method set with the same name.

Time	Flow rate (ml/min)	%A	%B
	1.00	100	0
1.24	1.00	100	0
6.22	1.00	2	98
18.65	1.00	2	98

Table 1: Equilibration column method. Schematic representation of solvent changes for the equilibration of the column. Buffer A: 7 mM ammonium acetate, pH 3.0. Buffer B: acetonitrile.

5. Repeat the step 4.3 to program the run sample method indicated in Table 2. Set a flow rate of 1.00 mL/min and program the UV detector to read at 260 nm. Save the instrument method and repeat the same procedure as described in step 4.4 to save the method set..

Time	Flow rate (ml/min)	%A	%B
	1.00	0	100
3.74	1.00	0	100
13.71	1.00	15	85
17.00	1.00	100	0
20.00	1.00	100	0

Table 2: Run sample method. Schematic representation of solvent changes for HPLC measurement of purine compounds. Buffer A: 7 mM ammonium acetate, pH 3.0. Buffer B: acetonitrile. 

6. Select the "run samples" button, choose "new sample set method" from the "file" menu.
7. Select the "empty" option and enter the number of the vial (in the autosampler), the sample name, the injection volume (50 µl). Select the method set saved before for the "method set" column and enter the total run time (min).
   Note: Enter the equilibration column method (Table 1) in the "method set" column before each sample run and enter the total run time (min).

5. Generation of a Standard Calibration Curve for Each Compound

1. Inject 50 µl of blank (specific serum-free medium, which does not contain adenosine deaminase) and of each standard sample following the methods described in Table 1 and Table 2.
   1. Use the equilibration column method (Table 1) prior to each sample run and set the gradient conditions described in Table 2 to obtain adequate peak separation. Refer to Table 3 for reported retention times of AMP, ADO and INO under these HPLC conditions.

	Retention Time	λmax
AMP	8.00 min	260
INO	11.00 min	260
ADO	11.90 min	260

Table 3: Retention times of purine compounds. Typical retention times observed for AMP, ADO and INO. The UV detector is programmed to read at 260 nm. 

2. Determine the peak area of AMP, ADO and INO at different concentrations choosing the "process" button in the HPLC software and next the "integrate" option. Alternatively select manually the starting and end points of each peak.
3. Plot the peak areas against the nominal concentration of each standard to obtain the nine-point calibration curve (100, 50, 25, 10, 5, 2.5, 1, 0.5, 0.25 µM).
4. Calculate the equation of a straight line for AMP, ADO and INO: y = mx + b,
   where x is the µM concentration and y correspond to the peak area.

Figure 2. Generation of an internal standard curve. Representative calibration standard curve for ADO and the relative equation obtained. Please click here to view a larger version of this figure.

6. Pretreatment with the Inhibitors and Incubation with the Substrate (AMP)

1. To test AMP consumption, ADO and INO generation without inhibition of CD73, ADA and nucleoside transporters, resuspend 2 x 10⁶ CD19⁺/CD5⁺ CLL cells (isolated and purified in steps 1 and 2) in 250 µl of serum-free medium and plate cells in a 48 well plate (or in a 1.5 ml microcentrifuge tube).
2. To block CD73 enzymatic activity, dilute 1:1,000 the stock solution of APCP (10 mM) in the culture medium to obtain a 10 µM final concentration. Resuspend 2 x 10⁶ CLL cells in 250 µl of culture medium containing APCP and pretreat 60 min at 37 °C in a cell culture incubator.
3. To block the conversion of ADO into INO, dilute 1:1,000 the stock solution of EHNA hydrochloride and/or dCF (both 10 mM) in serum-free medium to have a 10 µM final concentration. Resuspend 2 x 10⁶ CLL cells in 250 µl of culture medium containing EHNA and/or dCF. Incubate for 30 min at 37 °C in the cell culture incubator.
4. To block the uptake of ADO through the nucleoside transporters, dilute 1:1,000 the stock solution of dipyridamole (10 mM) in serum-free medium to have a 10 µM final concentration. Resuspend 2 x 10⁶ CLL cells in 250 µl of culture medium containing dipyridamole and incubate for 30 min at 37 °C in the cell culture incubator.
5. Prepare single solutions of APCP, EHNA, dCF and dipyridamole diluted 1:1,000 in 400 µM AMP.
6. Add 250 µl of 400 µM AMP or AMP plus inhibitors to obtain a final concentration of 200 µM AMP. Include a condition in the absence of the substrate to be used as blank sample.
7. Incubate from 30 to 60 min at 37 °C.
   Note: The optimal concentration of AMP and the incubation time were experimentally determined.
8. At the end of the incubation time, collect 500 µl of the supernatants in cold microcentrifuge tubes (on ice) and immediately centrifuge at 17,000 x g at 4 °C for 5 min.
9. Transfer the supernatants in new 1.5 ml microcentrifuge tubes and immediately store at -80 °C or proceed to sample preparation for the HPLC runs.

7. Samples Preparation for HPLC

1. Filter the supernatants in new 1.5 ml microcentrifuge tubes with the 0.2 µm syringe filters. Use 1 ml syringes for filtering.
2. If the HPLC system is provided with an autosampler, prepare the glass vials for HPLC and use the 0.1 ml micro-inserts for small volumes of sample.
3. Transfer at least 100 µl of sample in the glass vial with a micropipette or a glass Pasteur pipette. Be careful to transfer without bubbles and close the vial with the screw cap.
4. Samples are now ready for analysis by RP-HPLC.

8. HPLC Measurements of Purines 

1. Select the "run samples" button; choose "new sample set method" from the "file" menu.
2. Select the "empty" option and indicate: the number of the vial (in the autosampler), the sample name, the injection volume (50 µl).
3. Select the equilibration column method and the run sample method described in Table 1 and Table 2, respectively, for all the blank and sample runs that follow.
   Note: Set the equilibration column method (Table 1) before each sample run.
4. Inject 50 µl of blank (serum-free medium) and of each sample.
5. Determine the concentration of purines in each sample, quantify the AMP, ADO and INO by obtaining the peak areas at the retention times described in Table 3.
   1. Select the "process" button and next the "integrate" option. Alternatively choose manually the start and end points of each single peak to obtain the area measurement. This is done by tracing a line between the start and end points of the peak.
   2. Determine the µM concentration applying the equation obtained for the standard curve: y = mx + b, where x represents the µM concentration and y is the area of the peak measured from the unknown sample.
      Note: An example of the ADO calibration standard curve is reported in Figure 2, where: x = (y area - 981.02)/40026
6. Considering that 2 x 10⁶ cells were resuspended in 0.500 ml of medium, calculate the µmoles of AMP, ADO and INO consumed and/or produced by 10⁶ CLL cells applying the following proportion:
   µmoles : 1,000 ml = x µmoles : 0.250 ml
   Note: The µmoles in 1,000 ml (number µmoles in 1 L) of are equivalent to the µM concentration and x are the µmoles of nucleotide or nucleoside produced by 10⁶ cells.
   1. Lastly, convert the µmoles into nmoles consumed and/or produced by 10⁶ CLL cells:
      nmoles = µmoles x 1,000

Representative Results

To evaluate the percentage (%) of leukemic cells in freshly purified PBMCs from a representative CLL patient, cells are marked with anti-CD19 and anti-CD5 antibodies. The left panel of Figure 3 represents a cytofluorimetric dot plot with a selective gate on live cells. Figure 3 shows an example of PBMC from a CLL patient before (middle panel) and after (right panel) B cell purification.

An example of HPLC quantification of purine compounds in CD73⁺ CLL cells is represented in Figure 4A. The different retention times of AMP, INO and ADO at 260 nm allow the simultaneous quantification of the compounds. When the assay is run correctly, all the nucleotides and nucleosides have an adequate peak separation. Starting from a concentration of 200 µM AMP as substrate, the peaks obtained for ADO and INO are clearly visible and the concentrations are in the range of the standard calibration curve. However, using also lower concentrations of the substrate (e.g., 100 µM) will give good results. After peak integration, the areas of each peak are converted into µM concentration and finally in nmoles of compound produced by 10⁶ CLL lymphocytes through the use of standard curves.

The HPLC chromatogram of ADO produced by CD73⁺ cells after 60 min of pretreatment with 10 µM APCP indicates a complete blockade of extracellular ADO synthesis (Figure 4A). Because of the rapid enzymatic conversion of ADO into INO operated by the ADA/CD26 complex, pretreatment of CLL cells with 10 µM EHNA hydrochloride or 10 µM dCF is required to inhibit ADA degradation. Under these conditions extracellular ADO concentrations are significantly increased. Representative chromatograms of Figure 4 highlights how pretreatment with EHNA hydrochloride and/or dCF (Figure 4B-C) completely inhibits ADO conversion into INO.

Figure 3. Cytofluorimetric analysis of the % of CD19⁺/CD5⁺ leukemic cells in freshly purified PBMCs of a representative CLL patient. After gating on live cells (left panel), the % of CD19⁺/CD5⁺ CLL cells is evaluated. Before the negative isolation of B cells (middle panel), the % of leukemic cells corresponds to the 75%. After purification (right panel) the % of CLL B lymphocytes reaches 95%. Please click here to view a larger version of this figure.

Figure 4. Quantification of extracellular purine nucleotides and nucleosides consumed and produced by leukemic cells after exposure to AMP and different inhibitors. (A) Representative chromatograms of ADO and INO generated by CD73⁺ leukemic lymphocytes with or without pretreatment with α,β-methylene-ADP (APCP, 10 µM, 60 min), a specific inhibitor of CD73 enzymatic activity. (B) Representative HPLC chromatogram obtained from supernatants of CD73⁺ CLL cells pretreated or not with the adenosine deaminase (ADA) inhibitor erythro-9-(2-Hydroxy-3-nonyl)adenine (EHNA) hydrochloride (10 µM, 30 min) before incubation with AMP as substrate (200 µM, 30 min). (C) Representative chromatogram obtained from supernatants of CD73⁺ CLL cells after pretreatment or not with the ADA inhibitor deoxycoformycin (dCF, 10 µM, 30 min) before incubation with AMP (200 µM, 30 min). Data shown in panel (B) and (C) are obtained from a patient with a 98% of CD73 expression. Please click here to view a larger version of this figure.

Discussion

The protocol described here permits to evaluate the activity of the CD39/CD73 adenosinergic machinery in cell culture media from purified human leukemic cells. Through this HPLC method we can follow and quantitatively measure the enzymatic generation of ADO (CD73-dependent) and its subsequent degradation to INO (CD26/ADA dependent). The use of enzyme inhibitors allows to control the protocol and to have internal controls. The advantages and novelties of this protocol are that i) it may be applied to cells that are growing in culture, that ii) it requires a small amount of culture media and that iii) the sample preparation is extremely easy.

Our system consists of a separation module equipped with a quaternary low-pressure mixing pump and inline vacuum degassing along with an autosampler. The chromatographic separation of AMP, ADO and INO is achieved on a silica-based, reversed-phase column that is used for polar compound retention. The binary mobile phase system consists of a Buffer A (7 mM ammonium acetate in double deionised water, pH 3.0 adjusted with hydrochloric acid) and Buffer B (acetonitrile).

This HPLC method is sensitive, reliable and reproducible and can be applied to different cell culture models, both adherent and suspension cells. It could be also applied to compare different culture conditions, such as normoxia (21% of O₂) and hypoxia (1-3% O₂) or to compare different activation states of cells. Here we perform treatment of cells with purine compounds in cell culture plates, but can be also used microcentrifuge tubes for short time treatments.

The method here described allows the quantification of extracellular purine nucleotides and nucleosides consumed and produced in the reaction avoiding the use of radiolabeled compounds such as those employed in the thin-layer chromatography (TLC) assays¹⁰. Moreover, the HPLC system is also more sensitive and selective as compared to the TLC method. However, a RP-HPLC system with tandem mass spectrometric (MS/MS) detection is now considered the best choice for quantitative measurements of nucleotides and nucleosides. A limitation of this HPLC method is the requirement of an equilibration column run before each single sample run, making the total run time of the experiment longer and significantly limiting the possibilities for high throughput screenings. Faster alternative methods are represented by the Malachite Green Phosphate assay, a colorimetric method that allows the indirect measurement of AMP conversion into ADO, and bythe luciferase-based method²⁰. However, both these methods do not offer a direct measurement of adenosine.

The sample processing for this assay is minimal and protein precipitation with acetonitrile is not required, because the protocol is based on the use of a serum-free medium. An alternative to the serum-free medium could be to resuspend cells in PBS 5 mM glucose before the incubation with the substrate.

The main critical step within the protocol is to obtain a pure population of B cells. Indeed, the measurements of AMP, ADO and INO can be false due to the presence of other cell populations expressing the ectoenzymes involved in this cascade (e.g., T lymphocytes). A second critical point is to inject filtered culture media into the HPLC system without any cell contamination that can affect the integrity and the life of the column.

In conclusion, this assay is relatively fast and highly reliable, allowing for real-time monitoring of nucleotide consumption and nucleoside generation in different cell populations.

Materials

Name	Company	Catalog Number	Comments
Human blood
Milli-Q water	Millipore		double deionised water
Ficoll-Paque Plus	GE-Healthcare	17-1440-03
purified anti-CD3, -CD14, -CD16	made in-house		mouse monoclonal
PE-labeled anti-CD19	Miltenyi Biotec	120-014-229
FITC-labeled anti-CD5	Miltenyi Biotec	130-096-574
Dynabeads sheep anti-mouse IgG	Invitrogen	11031
Phosphate-buffered saline (PBS)	Amresco	E404-200TABS	tablets
bovine serum albumin (BSA)	ID bio	1000-70	standard grade
isolation buffer			PBS 0.1% BSA 2 mM EDTA, pH 7.4
AIM V serum free medium	GIBCO	12055-091	liquid (research grade)
adenosine 5’-diphosphate (ADP)	Sigma-Aldrich	A2754
adenosine 5’-monosphate (AMP)	Sigma-Aldrich	A1752
adenosine (ADO)	Sigma-Aldrich	A9251
inosine (INO)	Sigma-Aldrich	I4125
α,β-methylene-ADP (APCP)	Sigma-Aldrich	M8386	CD73 inhibitor
EHNA hydrochloride	Sigma-Aldrich	E114	adenosine deaminase inhibitor
Deoxycoformycin (dCF)	Tocris	2033	adenosine deaminase inhibitor
Dimethyl sulfoxide (DMSO)	Sigma-Aldrich	D2650
Dipyridamole	Sigma-Aldrich	D9766	nucleoside transporter inhibitor
acetonitrile (CHROMASOLV Plus)	Sigma-Aldrich	34998	HPLC-grade
ammonium acetate	Sigma-Aldrich	9688	7 mM, pH 3.0
hydrochloric acid	Sigma-Aldrich	30721-1L	min. 37%
Name	Company	Catalog Number	Comments
Equipment
Bürker cell counter	VWR	631-0920	hemocytometer
DynaMag-15 Magnet	Invitrogen	12301D	Dynal magnetic bead separator
microcentrifuge safe-lock tubes	Eppendorf	030-120-0086	1.5 ml
PET centrifuge tubes	Corning	430053/430304	15 – 50 ml
Minisart RC4 syringe filters	Sartorius Stedim Biotech	17821	membrane 0.2 µm
short thread vials	VWR	548-0029	1.5 ml/glass
micro-inserts	VWR	548-0006	0.1 ml/glass
screw caps	VWR	548-0085	9 mm/PP blue
Atlantis dC18 Column	Waters	186001344	5 µm, 4.6 mm x 150 mm
Atlantis dC18 Guard Column	Waters	186001323	5 µm, 4.6 mm x 20 mm
Waters Alliance 2965 Separations Module	Waters		HPLC separation module
Waters 2998 Photodiode Array (PDA) Detector	Waters		UV detector
Waters Empower2 software	Waters