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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682On-line version ISSN 1678-9849

Rev. Soc. Bras. Med. Trop. vol.30 n.6 Uberaba Nov./Dec. 1997

http://dx.doi.org/10.1590/S0037-86821997000600001 

ARTIGOS

FLOW CYTOMETRIC QUANTITATION OF PHAGOCYTOSIS IN HEPARINIZED COMPLETE BLOOD WITH LATEX PARTICLES AND CANDIDA ALBICANS

Jesús M. Egido and Juan Viñuelas

 

 

We report a rapid method for the flow cytometric quantitation of phagocytosis in heparinized complete peripherial blood (HCPB), using commercially available phycoerythrin-conjugated latex particles of 1µm diameter. The method is faster and shows greater reproducibility than Bjerknes' (1984) standard technique using propidium iodide-stained Candida albicans, conventionally applied to the leukocytic layer of peripherial blood but here modified for HCPB. We also report a modification of Bjerknes' Intracellular Killing Test to allow its application to HCPB.
Key-words: Phagocytosis. Flow cytometry. Latex particles. Candida albicans.

 

 

The phagocytic capacity of granulocytes 11 was until recently quantitated by extracting the leukocytic layer of peripheric blood, incubating it with Candida albicans and estimating phagocytosis through staining and examination under the light microscope13. The introduction of flow cytometry led to the development of more objective methods: in 1984, Bjerknes5 described such a method using Candida albicans, with similar sensitivity to that obtained using the classical method. Bjerknes' test has since been applied in various experimental contexts6 8 16 17. In related studies2 10, Staphylococcus aureus has been used for the measurement of both phagocytosis and hydrogen peroxide production, with similar results.

Bjerknes' test is conventionally applied to the leukocytic layer of peripherial blood. Here, we used heparinized complete peripherial blood (HCPB), to preveny the need for a cell separation step. We compared flow cytometric quantitation of phagocytosis using: a) propidium iodide-stained Candida albicans and b) commercially available phycoerythrin-conjugated 1µm diameter latex particles. Both tests were modified for a one-hour incubation period.

We are currently applying our modification of Bjerknes' test in routine analysis of the phagocytic capacity of polymorphonuclear leucocyte (PMNs) in peripherial blood of patients with immune disturbances.

 

MATERIAL AND METHODS

Human leukocytes. We used 125µl of heparinized complete human peripheral blood (from 3ml of blood containing 0.05ml of heparin lithium salt at 10IU/ml), less than 3h postextraction, maintained at 20oC, with a granulocyte count between 3,000 and 5,000 per mm3.

Candida albicans. A sample of human origin was cultured in Sabouraud-chloramphenicol agar (Bio-Merieux®), and a subsample was harvested in PBS, pH 7.4, washed twice for 5 min at 500xg (Beckman J-6B). Viability was determined by trypan blue vital staining in a Neubauer chamber, and by flow cytometry with propidium iodide (PI) staining. Only batches with greater viability than 95% were used.

Opsonization was carried out, when required, by incubating 5ml of human pooled serum with 1ml of Candida suspension (250 x 107 cells/ml) for 45 min at 37oC.

Fixation was carried out by mixing 70% ethanol with the Candida suspension (45:5 v/v) and incubating overnight at -20oC. This fixation method was compared with three others, using an alkalin cation fixative, Triton 0.1% and Triton 0.5%. Viability was determined by PI staining and Epics Profile II (Coulter®) cytometre.

Propidium iodide labelling was carried out by incubating 100µl of the Candida suspension (both opsonized and non-opsonized) for 30 min with one of a series of mixtures containing 20, 40, 80, 160, 240, 400 or 600µg/ml of PI (in volumes of between 50 and 400µl) and 100µl of RNAse (1mg/ml). Flow cytometry showed the 400µg/ml concentration to be most effective (data not show). Aliquots of the suspensions containing Candida labelled with PI at this concentration were stored at -20oC until use.

Candida phagocytosis test (CPT). A mixture containing 125µl of HCPB and 25µl of the Candida suspension (containing 1 x 107 PI-labelled cells/ml, fixed with 70% ethanol as described above) was incubated at 37oC with continuous mechanical stirring for 30, 60, 90 and 120 min, and then fixed using the Epics Q-Prep leukocyte preparation system (Coulter®) prior to flow cytometry. Parallel experiments, all with 60 min incubation, were run with 15, 10 and 5µl of the Candida suspension. Phagocytosis was measured by flow cytometry (Coulter Profile II) of 1ml samples of the Q-Prep-fixed HCPB/PI-labelled Candida mixtures, with recording of red fluorescence.

Intracellular killing test (IKT). To determine optimum incubation time for the IKT, twenty-five-µl samples of unfixed Candida (1 x 107 cells/ml, viability by trypan blue vital staining > 95%) were incubated with 125µl of HCPB at 37oC with mechanical shaking for 30, 60, 90 or 120 min. Granulocytes were then fixed, and erythrocytes lysed, using the Q-Prep system, and the preparation was washed at 500xg with phosphate-bulfered saline (PBS), pH 7.4. The pellet was incubated for 5 min with 1ml of lysis buffer (2.5% sodium desoxycholate, pH 8.7, in sterile distilled water) to lyse granulocytes, then washed twice at 10,000xg with PBS. The pellet was resuspended in 1ml of PBS then incubated with 50µl of PI (400µg/ml) and 100µl of RNAse (1mg/ml) for 30 min at room temperature in a darkroom, to allow differentiation of dead and live cells. Analysis was by flow cytometry with measurement of red fluorescence.

Latex phagocytosis test (LPT). One-hundred-µl aliquots of 1µm diameter phycoerythrin (PE)-labelled latex particles (Polyscience®) 7 were washed twice with washing buffer (0.054 M glycine/saline, pH 8.2) at 13,000xg for 10 min (Beckman Microfuge 11). The pellet was resuspended in 5ml of washing buffer and sonicated for 30 sec with three 50W pulses (Branson Sonifier 250). The concentration of latex particles in this suspension according to the manufacturer's instruction was 9 x 108 particles per ml. Opsonization was achieved by adding 200µl of ammonium sulphate-purified immunoglobulins at 25mg/ml to 5ml of the suspension of sonicated latex particles, then incubating at 20oC with mechanical stirring for one hour. Following 2 - 3 washes in a washing buffer, the resulting pellet was resuspended in 5ml of storage buffer (0.27 M glycine/saline and 0.1% bovine serum albumin - BSA) and stored at 4oC. Phagocytosis of both opsonized and non-opsonized particles was quantitated by incubation of 5, 10, 20, 30 and 40µl of this suspension (containing 45 x 105, 9 x 106, 18 x 106, 27 x 106 and 36 x 106 latex particles respectively) with 125µl of HCPB at 37oC for 60 min, followed by fixation using the Q-Prep system. Flow cytometry measurement (FCM) was of orange fluorescence.

 

RESULTS

Candida phagocytosis test. The fixation method leading to the successful fixation of most Candida cells was with 70% ethanol at -20oC overnight (Table 1); 0.1% Triton and 0.5% Triton fixation methods were less effective. With a granulocyte-to-Candida cell ratio of 1:5, cell suspensions which had been labelled with a PI solution of 400µg/ml were found to give the most homogenous fluorescence peak (data no shows). The variation in phagocytosis percentages with different incubation times (Table 2) are in accordance with Bjerknes' results with the leukocytic layer of non-heparinized peripheric blood5. The optimum granulocyte-to-Candida cell ratio was 1:5 (i.e. 25µl of Candida suspension to 125µl of HCPB), with higher ratios leading to reduced phagocytosis (Table 3).

 

 

 

Latex phagocytosis test. Different volumes of a suspension containing 9 x 107 latex particles/ml were added to HCPB, with subsequent measurement of phagocytosis (Figure 1). The optimum granulocyte-to-latex particle ratio was 1:32 (20µl of the suspension containing 18 x 106 particles to 125µl of HCPB. The phagocytosis was much higher in HCPB (3ml of blood containing 0.05ml of the lithium salt of heparin at 10IU/ml) than in ethylenediaminetetraacetate, tripotassium salt (EDTA)-treated complete peripheric blood (3ml of blood containing 0.06ml of EDTA (K3) at 85g/l), in opsonized (OPS) and non-opsonized particles after 60 min incubation at 37oC (Table 4).

 

 

 

We have adapted Bjerknes' flow cytometric method for the quantitation of phagocytosis, which uses Candida albicans and the leukocytic layer of peripheric blood4 5, for use with HCPB. This obviates the need for prior separation, washing and quantitation of the leukocytic layer, and is thus simpler and more rapid than Bjerknes' original method.

We have also developed an alternative test for the quantitation of phagocytosis in HCPB using commercially available PE-labelled latex particles, of smaller size and more homogenous morphology than Candida cells. Our results show that this test is considerably simpler, faster and more reliable than either Bjerknes' original method or our adaptation of it to HCPB, and we thus propose it as a valid alternative for routine quantitation of the phagocytic capacity of granulocytes in peripheric blood. Clearly, more complex methods are still necessary for detailed studies of patients with phagocytic disturbances1.

Optimum granulocyte-particle ratio was found to be 1:5 in the case of the Candida test, and 1:36 in the case of the latex test.

The Candida test was additionally optimized with respect to incubation time, with the aim of ensuring sufficient phagocytosis to provide a strong fluorescent signal which is clearly differentiated from the background noise due to other forms of granulocyte-particle binding. In other respects, it was found that any departure from the standard incubation conditions (37oC with continuous mechanical stirring) led to considerable increases in background noise.

We also attempted to determine the best PI concentration for Candida labelling such that the fluorescence signal was as strong and homogenous as possible. As has been noted in previous studies17, homogeneity of staining is very difficult to achieve. Different batches of Candida cells fixed and stained under identical conditions respond unpredictably to storage, making it necessary to run controls every time the test is required. Likewise, the dispersion of both forward angle light scatter (FALS) and 90-degree light scater (90LS) diagrams were considerable even after filtration and homogenization with low-power ultrasound, giving high variability in granulocyte size once phagocytosis had occurred. All these problems are minimized when PE-labelled latex particles, which stain much more homogenously and have a much more constant size distribution (and consequently scatter diagrams which are easier to interpret)12, are used.

Given the possibility that free (non-phagocytosed) labelled particles may cause fluorescence, leading to false positive results, we also ran controls in which suspensions containing labelled Candida cells (2.5 x 106 cells/ml) or latex particles (18 x 106 particles/ml) were treated and subjected to flow cytometry, as in the respective phagocytosis tests (CPT or LPT) but without incubation with blood. Counts of less than 1% of those obtained in the respective phagocytosis tests were recorded over periods of more than 120s (note that the standard phagocytosis test samples, containing about 15,000 PMNs, require between 90 and 120s to pass through the cytometer).

Our results confirm that blood treated with EDTA (K3) is not useful for phagocytosis quantitation because of the resulting complexation of calcium and consequent inhibition of calcium-dependent phagocytosis14 15. Our data likewise confirm the absence of phagocytosis by lympocytes.

The intracellular killing test depends upon the maintenance of a live Candida population in order to obtain a suspension of cells with viability greater than 90%. Propidium iodide will only stain those Candida cells with an altered cell wall which permits its diffusion. The two-stage lysis eliminates the problems associated with staining of cell debris, and the false positives which arise as a result.

We propose the use of the latex phagocytosis test for routine screening purposes, since it shows greater reproducibility than the Candida Phagocytosis Test and is less affected by differences in particle size and labelling/ storage conditions. Continued use of Candida for the intracellular killing test is, however, necessary. Under the test conditions described here, we observed no significant differences between phagocytosis of opsonized and non-opsonized latex particles; however, the application of both forms of the LPT during routine screening may be of value in showing up deficiencies in the opsonization capacity of the patient's serum.

 

 

RESUMEN

Se da cuenta de un método rápido para la cuantización del flujo citométrico de la fagocitosis en sangre periférica completamente heparinizada (HCPB), mediante la utilización de partículas de látex phycoerythrin-conjugadas de 1µm de diámetro disponibles comercialmente. El método es más rápido y presenta mayor reproducibilidad que la técnica estandar de Bjerknes' (1984) utilizando propidium iodide-teñida Candida albicans, aplicada convencionalmente a la capa leucocitica de sangre periférica pero modificada por HCPB. Tambien damos cuenta de una modificación de Bjerknes' Intracellular Killing Test para permitir su aplicación a HCPB.
Palavras-chaves: Fagocitosis. Flujo citométrico. Partículas de látex. Candida albicans.

 

 

REFERENCES

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Department of Microbiology and Inmunology, Santiago University, Spain. Department of Inmunology, Hospital Xeral, Santiago, Spain.
Address to: Dr. J. Egido. PO Box 8121, 28080 Madrid, Spain.
Recebido para publicação em 17/01/96.

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