Cytochemical Properties of Earthworm Coelomocytes Enriched by Percoll
Sherifa S. Hamed,
Edwin L. Cooper
Coelomocytes of E. fetida were separated by Percoll gradient and based
on cytomorphology and cytochemistry, classified into four major categories:
acidophils, basophils, chloragocytes cells and neutrophils. Basophils exhibited
heterogeneity with respect to staining properties of granules. The enzyme acid
phosphatase was present in all coelomocytes, but was especially abundant in
basophils and neutrophils. Alkaline phosphatase was detected in basophils and
acidophils and -esterase was found in all types except neutrophils. Acidophils
and basophils possessed the corresponding granules and neutrophils contained
both; acidophilic granules are often excreted. Basophils and neutrophils were
more active in killing the tumor target, K562, which partially reflects their
role in the earthworm`s immune system.
The earthworm's immune system is complex, composed of diverse cell types referred to as coelomocytes (leukocytes). These cells are suspended in Coelomic Fluid (CF), which contains humoral immune components (e.g. lysins, agglutinins) that are synthesized and secreted by coelomocytes. They display certain surface markers[2,3]. Coelomocytes have been separated into two major functional cell types by FACS basophils and lymphocytic coelomocytes[4-6]. Basophils, small in size and identified by light microscopy[7,8] are lymphocytic coelomocytes identified by electron microscopy and participate in graft rejection. Transplant destruction is initiated by inflammatory type, large neutrophilic coelomocytes that form granulomas in vitro after the tumor K562 by small basophils.
Despite these and other characteristics of coelomocytes, there have been no systematic attempts to develop methods for enriching and purifying any single coelomocyte type. Successful enrichment could then be used to analyze separate cell types with respect to their unique function as well as functional cell interactions. In this study we have combined three approaches that characterize coelomocytes: 1) Percoll separation; 2) cytochemistry; 3) 51Cr-release assay (cytotoxicity) which confirms that two of the enriched cell types at certain stage are actively involved in the killing of K562 tumor target cells.
MATERIALS AND METHODS
Earthworms and husbandry: Adult Eisenia foetida were purchased
from Carolina Biological Supply Company (Burlington, North Carolina) and maintained
at a constant temperature of 15°C in plastic boxes. Three days prior to
harvesting coelomocytes, earthworms were fasted and kept in plastic boxes on
wet paper towels. After coelomocyte extrusion earthworms were further maintained
in plastic boxes in a moist environment and fed oatmeal cereal.
Coelomocyte harvesting: Donor earthworms were first cleansed in distilled
water and dried on paper towels. They were handled with care to prevent premature
extrusion of coelomocytes, which results in lower yields. Several earthworms
(~3) were then placed in small Petri dishes (60x15 mm) containing 3 mL of PBS
with 0.25 mM EGTA to prevent coelomocyte aggregation. Extruded of coelomocytes
was achieved via electrical stimulation (6 V) of earthworms and cells were transferred
into conical glass centrifuge tubes previously "Sigmacote-Coated" (Sigma) to
avoid cell adherence.
Coelomocyte separation by Percoll gradient: Percoll (Pharmacia) was used as a cell separation media and was diluted with 0.15 M NaCI to the following concentrations (55-45, 35-25 and 15-5%). Two (2) mL of each concentration (55- 45, 35-25 and 15-5%) was carefully layered into a test tube to build a six-step gradient. Coelomocyte suspensions (3 mL in PBS) were transferred onto the Percoll gradient and centrifuged for 20 min at 1500 rpm, yielding four separate coelomocyte bands. The cell free supernatant was removed and transferred from each gradient using Pasteur pipettes into fresh, Sigma coated test tubes. Coelomocytes obtained from the respective bands in the Percoll gradient were pooled since they contained the same cell type. Coelomocytes were then washed twice in PBS (10 min at 1500 rpm) before further use.
Cytocentrifugation and wright stain preparations: Percoll separated coelomocytes were placed on microscopic slide (Shadon cytoslides) for marking cytocentrifuged-stained preparations. Six to eight drops (5x105 coelomocytes/mL) of resuspended coelomocytes were added to the cytofunnels (Shadon), mixed with one drop of albumin, centrifuged for 5 min at 800 rpm and air-dried. After fixation in methanol for 1 min, the slides were transferred to a differential solution (Baxter B4 132-12) for 3 min, then rinsed in tap water for 10 min and stained with Giemsa for 5 min. Finally, they were rinsed by immersing them in tap water 10 times, air dried and mounted in Canada Balsam.
Cytochemical analyses to demonstrate enzymes
Acid phosphatase: A sigma assay kit, for demonstrating acid phosphatase
in leukocytes was used. According to instructions (Sigma No. 387), coelomocytes
on slides were incubated in a solution containing Naphthol AS-BI phosphoric
acid and freshly diazotized in fast garnet GBC at 37°C for 45 min. Controls
were done without adding substrate solution.
Alkaline phosphatase: Alkaline phosphatase was demonstrated by using a Sigma assay kit designed for leukocytes (Sigma procedure No. 86). To perform this assay, fixed coelomocytes on slides were incubated at 37°C for 45 min in a solution containing Naphthol AS-BI phosphate and freshly prepared fast blue BB salt at pH 9.5 with 2-amino-2-methyl-l, 3- propanediol (AMPD). Sites of phosphate activity appeared as blue granules. Controls were performed by adding PBS instead of substrate.
Naphthol AS-D chloroacetatesterase and alpha naphthyl acetate esterase: The presence of Naphthol AS-D chloroacetate esterase and alpha naphthyl acetate esterase were investigated using fixed coelomocytes on slides (Sigma kits). Enzyme detection was performed according to Sigma procedure 91 and controls without adding substrate.
Determination of cell and nuclear size: Cell size as well as nuclear diameter was measured with a calibrated ocular scale (10x), using a Zeiss microscope (40x) objective and a microcytometer (American Optical).
51Cr Release Assay (Cytotoxicity): As one single assay, which indicates normal coelomocyte function, we measured the cytotoxic activity of coelomocyte effectors derived from Percoll gradients against K562 tumor cell targets in a classical 4 h 51Cr release assay. Freshly collected coelomocytes from each Percoll band were resuspended at a concentration of 1x106/mL in PBS and maintained in complete media (RPMI 1640 + 5% FBS +1% antibiotic and 1% anti mycotic). Fifty micro liter of 51Cr was added to 100 μL of K562 (1x106) in complete media, incubated for 1 h at 37°C and washed three times with RPMI 1640. One hundred microliter of effector cells (coelomocytes) were added per well on microtiter plates to 100 μL of labeled K562 target cells. After effectors and targets were added to the wells, the microtiter plate was centrifuged (5 min, 200 rpm). Effector and targets were allowed to interact at 37°C for 4 h in an atmosphere of 5% C02 / 95% air. 51Cr release was determined by centrifuging the plates at 1000 g for 5 min and harvesting 100 μL of the culture supernatant for later counting in a Gamma counter (Beckman G50). Spontaneous release was determined by adding 100 μL of labeled K562 in complete media and total release was determined by adding 100 μL of K562 plus triton. The percent 51Cr release was determined from the experimental (Rc), spontaneous (Rs) and total (Rt) release by following the formula:
Cell separation by Percoll: Coelomocytes were separated on a Percoll
gradient (55-45, 35-25 and 15-5%) by centrifugation (20 min, 1500 rpm) resulted
in four separated bands visible at concentrations of 10, 25, 35 and 45% (Fig.
1). Acidophilic cells were present in the first band at 10%. The second
band, at 25%, was comprised of mainly basophils and few chloragocytes, which
were enriched at 35% in the third band.
||Cells from the CF were separated on a Percoll gradient (55+45,
35-25 and 15-5%) by centrifugation (20 min, 1500 rpm). Four separated cell
bands became visible at Percoll concentrations of 10, 25, 35 and 45%. The
first bands at 10%: mainly acidophilic cells; the second (25%) mainly basophils
and some chloragocytes; chloragocytes, 35% in the third band; fourth band
(45%) acidophils, basophils and neutrophils. Neutrophils appeared enriched
in the fourth band
||Mean±SD of percentage values of each coelomocyte type.
Chloragocytes show the highest, basophils second, followed by acidophils,
with neutrophils showing the lowest
The fourth band, at 45%, was composed of acidophils and basophils as well
as neutrophils, which displayed an enriched appearance (Fig. 1).
Characteristics of coelomocytes without Percoll separation revealed varying
percentages of cell and nuclear sizes for each coelomocyte type (Fig.
2-4). The percentage of coelomocytes and cell size of
each type per band after Percoll separation also revealed variation (Fig.
5 and 6).
||Mean±SD of cell size of all coelomocytes. The two types
of chloragocytes, large and small, have the largest cell size. Two acidophil
cell types are next in cell size, followed by basophils and neutrophils,
which are the smallest
||Mean±SD of nuclear size of all coelomocytes. The nuclear
size of both acidophil types, small and large, is larger than the nuclear
size of the entire population; however, the small acidophils have larger
nuclei than large acidophils. Basophils have the second largest nucleus,
followed by neutrophils. The two types of chloragocytes (small and large)
have more or less the same nuclear size, but they are also the smallest
compared to all coelomocytes
||Acid phosphatase, alkaline phosphatase, specific and non-specific
esterases activities of the general population of coelomocytes
|The acid phosphatase showed the highest intensity in basophil
while the alkaline phosphatase was moderate in basophil and acidophil and
the α-esterase was ranged from low to moderate in all types except
||Mean±SD of percentage of coelomocytes types in each
fraction. The greatest percentage of acidophils was present in fraction
1, basophils in fraction 2 and 4 and neutrophils in fraction 4: most chloragocytes
in fraction 3. A stands for acidophils; B stands for basophils; N stands
for neutrophils; C stands for chloragocytes
||Mean±SD of cell size of each fraction after Percoll-gradient
separation of coelomocytes. The cell size of small acidophil was present
in levels 1, 2 and 3, while the large size was in level 4. Small basophil
was in level 1 and 2 and large basophil in level 3 and 4. Small neutrophil
was in level 2 and 3 and the large neutrophil in level 1 and 4. Small chloragocyte
was in level 2 and 3 and large chloragocyte was in level 1 and 4
Four cell types in the CF: In E. fetida four major coelomocyte types were differentiated: basophils, acidophils, neutrophils and chloragogen cells based on light microscopy and Wright staining (Fig. 7).
Basophils: Basophils were the most numerous coelomocyte types, staining
strongly basophilic with occasional small, dark blue granules. The more abundant
cytoplasm was lighter blue and clear vacuoles were frequently present. The smaller
basophils, 12.8±0.8 μm, displayed a strong tendency to aggregate.
With respect to the nucleus, we found it to be compact, about 6.4±0.9
μm in diameter and either centrally or peripherally located. Chromatin
was condensed, stained dark blue violet and the nucleolus was not visible (Fig.
8 a-d). The cell size of large basophils was about ±21
μm and their nuclear size ±6.5 μm. We observed three enzymes
in the cytoplasm: acid phosphatase was present in large amounts (Fig.
8b); alkaline phosphatase as deep blue granules of different sizes (Fig.
8g); α-esterase mainly as brown granules (Fig. 8b
and Table 1).
Acidophils: Acidophils were usually granular cells with distinct outlines
and usually occurred in two types based upon granules and cell size; both types
stained pink to red. In type I, large cells, 20±2.3 μm, although
there were few granules, still filled the cells completely (Fig.
8 e-h). The nucleus was always in an eccentric position
and its size was about 6.7±0.6 μm.
||All cell types obtained from Eisenia foetida. Nearly
50% of the whole cell population is chloragocyte, which were seen to be
different sizes, small (chs) and large (chl), with a small nucleus (nu).
The cytoplasm contains numerous vacuoles (v) and lipid inclusions (arrows).
The next high number of coelomocytes is represented by basophilic cells,
large basophil (bl) and small basophil (bs), with an eccentric large nucleus
(head arrows). Neutrophils (N) appear in small numbers and size and the
cytoplasm contains many granules. Notice the acidophil cell (ac). (methanol-Wright
stain) (x, 400)
||Large basophil cell with eccentric compact nucleus (nu) with
heterochromatin. The cytoplasm was strongly basophilic and a large number
of granules (g) were recognized. Note the vacuole (v) (methanol-Wright stain).
||A large deep intensely stained granules were obtained in the cytoplasm
of basophil indicating an intense reaction of acid phosphatase, which was
higher than the general population (arrows).
||Alkaline phosphatase was detected as deep blue granules of different sizes
(head arrows) in basophil cells.
||A low to moderate "-esterase activity was obtained in the cytoplasm
of basophil (arrow) while the nucleus (nu) was negative.
||A large acidophilic cell with a distinct cell membrane, notes the pale
nucleus (nu) with eccentric position and the cytoplasm spreads with a number
of vacuoles (v) (methanol-Wright stain).
||Acid phosphatase was found as granules in low to moderate frequency in
the cytoplasm (arrows), but never in large amount in acidophil cell. Notice,
||Moderate alkaline phosphatase activity was obtained as dark blue granules
in the cytoplasm (arrows), while eccentric nucleus (nu) was a negative reaction.
||A non-specific esterase activity was obtained ranging from low to moderate
in the cytoplasm of acidophil arrow). Notice, nucleus (nu) gave no indication
to enzyme activity.
||A chloragocyte with a heterochromatin nucleus (nu) which in an eccentric
position. The cytoplasm contains numerous vacuoles (v) and lipid inclusions
(arrow) (methanol-Wright stain).
||The amount of acid phosphatase in chloragocyte was much smaller than acidophil,
basophil, neutrophil and was indicated as large granules (arrows) around
the nucleus (nu).
||A moderate α-esterase activity was shown in the chloragocytes as
granules of different sizes (head arrows).
||Neutrophilic cells (N) which are smaller than the other coelomocytes.
They possess relatively less cytoplasm, which is characterized by numerous
granules (g). The nucleus (nu) is more or less centric and relatively large
compared to the cytoplasm (methanol –Wright stain). All figures x,
||Mean±SD of 51Cr release assay using K562
targets and coelomocytes effectors. Coelomocytes were separated into 4 fractions
using Percoll gradients. Cells from these individual fractions were then
incubated together with K562 targets (4 h, 37°C) and the results were
obtained with a gamma counter. Fraction 2 and 4, which were enriched mainly
with basophil and neutrophil, displaced a very high percentage of cytotoxicity
The cytoplasm of smaller cells (type II) I3.9±1.8 μm sometimes
appeared homogeneous and without granulation whereas type II acidophils contained
mostly large granules which also completely filled the cytoplasm. The nucleus
(7±0.8 μm) was located either centrally or peripherally, appeared
flattened. The nucleolus was not visible. Three enzymes were detected in acidophil
cells: acid phosphatase in low to moderate frequency, distributed diffusely
throughout the cytoplasm (Fig. 8f); alkaline phosphatase
as deep blue cytoplasmic granules; the nucleus gave no indication of enzyme
activity (Fig. 8g); a-esterase activity was different from
low to moderate (Fig. 8h and Table 1).
Neutrophils: The most prominent characteristic of neutrophils, which
were easily observed and contrasted to those in acidophils was the profusion
of granules scattered throughout the cytoplasm (Fig. 8i).
Neutrophils (11.3±2 μm) contained both basophilic and acidophilic
granules of an intermediate color, neither red not blue. The nucleus measured
6.1±0.8 μm, stained medium to dark purple and displayed condensed
chromatin. Although indication of acid phosphatase was significant, they stained
less intensely. The percent of acid phosphatase in neutrophils was high and
was exceeded only by that of basophils (Fig. 8f). In contrast
to other coelomocytes, neutrophils contained neither alkaline phosphatase nor
α-esterase (Table 1).
Chloragocytes: These cells occurred in two forms of different cell size
and were sometimes arranged in clusters of four to six cells. Both types were
larger than acidophils, basophils and neutrophils (Fig.8j-l).
Large chloragocytes were oblong with a cell size of 32±1.8 μm; the
nucleus was 4.5±l.7 μm. The cytoplasmic granules, which were spheroid,
stained bright blue with Wright-stain. Small chloragocytes 23.4±3.4 μm
had circular nuclei which measured 4.1±0.7 μm in diameter. The nuclear
shape appeared uneven in a peripheral position. The amount of acid phosphatase
in chloragocytes (Fig. 8k) was less than in acidophils, basophils
and neutrophils. There was no indication of alkaline phosphatase. α-esterase
was moderately frequent in the cytoplasm as brown granules (Fig.
8 and Table 1).
Cell division: Mitotic divisions were not observed in any coelomocyte type and in all instances; the nuclei of acidophils and basophils were in the interphase stage.
51Cr release assay: The effect of coelomocytes on K562 targets was observed using 51Cr release assay. Coelomocytes were separated into 4 fractions using Percoll gradient and were incubated with K562 targets. Results showed an increase in 51Cr release in fractions 2 and 4, which were enriched with basophils and neutrophils (Fig. 9).
We have separated earthworms coelomocytes for the first time on Percoll
gradient and revealed four bands at Percoll concentrations of 10, 20, 35 and
45% (Fig. 1). The second band was composed mainly of basophils
and the fourth band at 45% Percoll appeared enriched with neutrophils. The separation
procedure is rapid, reproducible and the inert nature of the Percoll along with
its lack of toxicity makes it a useful medium. The lower viscosity of Percoll
allows for more rapid cell isolation, without cell death, suggests that it may
be superior for separating of particularly sensitive cell populations, or when
for some reason cells must remain in the separation medium for long periods
of time. Density separations have been widely used for many immunological
A method for separating of human blood monocytes and lymphocytes has been described.
Mononuclear leukocytes were centrifuged on a continuous gradient of colloidal
silica particles (Percoll) in phosphate -buffered saline. This leads to formation
of 4 bands: a layer containing dead material (if present) which did not enter
the gradient; a layer near the bottom of the tube containing granulocytes and
red cells and two other bands in between, of which the upper one is enriched
with monocytes (av. 78%). The final yields of these cell types were 73 and 79%,
respectively and their viability is greater than 95%. No functional impairments
could be detected by different functional assays including the ability of B
lymphocytes to produce immunoglobulins when stimulated with pokeweed mitogen
and the ability of monocytes to phagocytize opsonized red cells and latex particles.
Another method for isolation of eosinophils from human peripheral blood using
isomolar solution of polyvinylpyrrolidone-coated silica gel (Percoll) is described.
The purity ranged from 86 to 99% eosinophils in the final preparation and the
recovery was 38-56%. The separation technique did not affect the viability or
the metabolic capacities of the cells.
One important factor observed is the high degree of cell variability in invertebrate
leukocytes. Such variability results from the high polymorphic nature of these
cells and to a lesser degree, the presence of intermediate or transitional cell
forms. The range of variations encountered for each coelomocyte
type is an important indication of the diverse functional capabilities of each
cell type. All coelomocyte types display this variability to one degree or another.
Basophils are occasionally heterogeneous and also contain notable amounts of
cytoplasmic basophilia, which due primarily to their RNA content, in electron
micrographs of basophils, large numbers of ribosomes are observed, both as free
and membrane-associated forms[6,10].
In some Wrights-stained acidophils, the cells contain strongly acidophilic material, but lack observable granules. This reflects a particular developmental stage in which much of the granular material has been synthesized but not yet "packaged" into discrete granules. In cytochemical preparation, acidophils of both types have been observed and appear to have unknown secretory activity. In other invertebrates, substances secreted by granular cells range from clotting factors in Limulus and several species of crustaceans to lysosomal enzymes in the mollusc Mercenaria mercenaria. Although the coelomic fluid of Lumbricus is known to contain haemagglutinins, the specific cell responsible for synthesizing and secreting them has not been identified although specific agglutinins have been shown to be secreted in vitro in response to stimulate by rabbit erythrocytes in response to stimulation.
Neutrophils contain a large nucleus and less heterochromatic than those of other coelomocytes, which is a characteristic usually associated with relatively undifferentiated cells. Neutrophils are of particular interest to invertebrate immunologists. In addition to being highly phagocytic, they are responsible for the invasion and destruction of foreign tissue grafts. Basophils have been found at the graft site, but they appear to play a secondary or scavenger role and are not the primary agent of graft rejection. In experiments involving chemotaxis toward foreign tissue or bacteria, it has been found that neutrophils, the major coelomocyte type, comprise 92-94% of the responding cells, although they comprise an average of only 18% of the total coelomocyte population.
Basophils and neutrophils also contain significant amounts of the enzyme acid phosphatase in discrete granules or vesicles, which are presumed to be lysosomes. Using electron micrographs, very large (4-6 μm) acid phosphatase-positive vacuoles are found in basophils and neutrophils and are thought to be phagosomes. Acid phosphatase is not as abundant in acidophils as in basophils and neutrophils.
Chloragogen cells have been compared to the liver of vertebrates and postulated to have a trophic function and two types of phospholipids. Our investigations have confirmed the presence of these substances. In electron micrographs of chloragogen cells, certain granules contain crystalline structures, which interpreted as hemoglobin.
Although no cell division was observed, newer findings in relation to coelomocyte multiplication have been observed during cytotoxic activity against the erythromyeloid human tumor cell line K562. In vitro cultures, two cell types (i.e. small and large coelomocytes) retained their morphological features, their FNA content was significantly less than that of human K562 and significant percentages of coelomocytes were found to be in S or G@/M phases of the cell cycle. When cultivated alone for up to three hours, coelomocytes formed no aggregates, but upon mixing with K562, coelomocytes spontaneously killed tumor cells and cytoxic reactivity was accompanied by the formation of multiple aggregates similar to granulomas. These results are described as non-specific inflammatory" responses of earthworms in vitro against tumor cells.
Earthworm coelomocytes affect cytotoxicity at significantly high levels against
the NK-sensitive, human tumor cell line, K562 and the NK-resistant targets (U937,
BSM, OEM). Release of 51Cr was weakly dependent on the effector/target
ratios, decreasing from 80% lysis at 25:1 to 50% at 1:1 and the activity of
earthworm coelomocytes was significantly higher than that of human PBE.
Using K562 as a target for earthworm effector coelomocytes suggests the possibility
that, these cells kill by mechanisms akin to those of vertebrate NK cells, so
that they are trivial to the immune system. Although NK cells can kill after
they acquire Ig through Fc receptors on their cell surface, they also can kill
cells spontaneously in the absence of Ig or any prior activation[4,26,27].
Present results revealed that the cytotoxic activity was observed in all four
levels after Percoll separation, but the highest values were obtained in levels
2 and 4, which were enriched with neutrophils and basophils.
Present results suggest that the gradients we described here demonstrate that the Percoll preparation was valuable in several types of cell separations and it was a rapid method for the separation of coelomocytes cell populations. This material is inexpensive and non-toxic for immunocyte function. Small numbers of cells with good yields has made this a routine tool in our laboratory.
In the present investigation, certain cytochemical properties of each of the different coelomocyte type separated by Percoll gradient have been described. Since these are the first cytochemical and 51Cr- release observations to be made on Percoll separation of earthworm coelomocytes, a number of specific points remain unresolved: 1) the nature and the enzymatic changes that takes place in both small and large cells during phagocytosis and killing; 2) at What stage exactly, the cell start to be active in both two activities. The cytochemical information reported here should serve as a foundation for further studies those related to immune responses.
The authors express appreciation to volunteers from the Student Research Program: Andrew Vuong performed the statistical analyses and Lizbeth Miranda-Kuhn, assisted in research.
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