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Print version ISSN 0074-0276
Mem. Inst. Oswaldo Cruz vol.101 suppl.1 Rio de Janeiro Oct. 2006
Claudia Maria da Cunha Borges; Carine Machado Azevedo; Zilton A Andrade1
Laboratório de Patologia Experimental, Centro de Pesquisas Gonçalo Moniz-Fiocruz, Rua Valdemar Falcão 121, 40295-001 Salvador, BA, Brasil
This study attempts to investigate the relationship between the hemocytes in the two compartments: circulating peripheral lymph and the connective tissues. The hemocytes are compared with the vertebrate macrophages and constitute the principal line of defense against external aggression. The hemocytes were counted in circulating hemolymph and their phagocytic capability was evaluated in Schistosoma mansoni-infected Biomphalaria glabrata and the results were compared with those obtained from normal intact control snails. Although the number of circulating hemocytes revealed a mild increase in snails at the 6th week of infection, the overall findings were similar and pointed out that the cells in the two compartments are not functionally connected. However, the hemocytes found within the connective tissues of infected snails showed definite ultrastructural differences in the number and disposition of cytoplasmic prolongations and organelles in comparison with the hemocytes from non-infected snails. Histochemically, the staining for acid phosphatase activity served as a marker to hemocytes, sometimes being found in extracellular material at the foci of parasite-hemocyte interactions.
Key words: Biomphalaria glabrata - Schistosoma mansoni - hemocytes
During the interactions between the larval forms of the Schistosoma mansoni and its intermediate host Biomphalaria glabrata a pivot role is played by the snail defense cells - the hemocytes. These mobile phagocyte cells have been compared with the vertebrate macrophages, but although the similarities are many, there are also striking differences. It seems that the hemocytes are focally mobilized and act without cooperation from other cells or humoral factors. They are found in the circulating hemolymph and within the connective tissues, but the relationships between these two compartments are poorly understood. Abdul-Salam and Michelson (1980) observed an increase in the number of circulating hemocytes in B. glabrata after a 4 and 6-week S. mansoni infection. The same was also seen in B. glabrata during infection with Echinostoma liei (Mounkassa & Jourdane 1990). However, several factors may interfere with these results, such as the age of the snails (Stump & Gilbertson 1978) and even the temperature of the water were they are maintained (Feng 1965).
On the other hand, hemocytes represent cells with variable morphology and enzymatic contents, with sub-populations exhibiting different abilities for adhesion and phagocytosis (Van der Knaap & Loker 1990, Matricon-Gondran & Letocard 1999).
The present investigation considers the problems above mentioned and look for a correlation between the presence of hemocytes in tissue lesions and in the circulating hemolymph in B. glabrata infected with S. mansoni, and observes the main histological, histochemical and ultra structural features of the hemocytes within the snail tissues, in an attempt for a better understanding of its patho-biology.
MATERIALS AND METHODS
Groups and procedures - A stock of snails, originated from the region of Feira de Santana, BA, maintained at the Gonçalo Moniz Research Center for more that 20 years, has been used throughout the experiments. They measured from 8 to 14 mm in diameter and were maintained under controlled conditions of room temperature (26ºC) with free access to food. They were separated into two groups:
Group 1: normal, intact snails (Controls - 8 to 14 mm)
Group 2: snails submitted to infection with 20 miracidia, which were freshly obtained from the livers of mice infected with the Feira de Santana strain (Andrade & Sadigursky 1985) of S. mansoni. Thirty to 63 days later the snails were tested for cercarial elimination. The positive ones were transferred to individual recipients and maintained in the dark until the moment for another test or to be killed.
Counting of circulating hemocytes - Snails from both groups were submitted to this procedure. They had their shell perforated with a 26-G ½ insulin needle at the digestive gland level and the emerging hemolymph was aspirated, placed in siliconized tubes (Vacuum II Labnew®) and maintained at 4ºC. A total of hemolymph 30 µl to 100 µl of was collected from each snail. Cell count was performed in a mixture of 10 µl hemolymph with a 5% neutral red solution, and examined in Neubauer chamber. Red-stained cells were identified as granulocytes and the non-stained ones as hyalinocytes (Bezerra et al. 1997).
The phagocytosis activity of the circulating hemocytes was also evaluated in these snails. To samples of hemolymph containing 105 cells and hemolymph soluble factors, it was added 40 µl of RPMI-1640 medium, Zimozan A (0,624 mg/ml) and diluted Indian ink in RPMI (1:1000). After 3h incubation in a water bath at 37ºC, it was added 5 mg/ml PBS, pH 7.2, of MTT (3-4,5 dimetil tetrazolium bromide, Sigma, US), and the water bath continued for more 2 h, at 37ºC. After that, 1 ml of isopropanol-HCl 0,04 N was added, homogenized, centrifuged and the supernatant analyzed with a Hitachi U-2000 spectophotomer, under 570 nm wave-length (Bezerra et al. 1997).
Histopathology - Snails were anesthetized with menthol crystals during 4 h, and the soft parts were removed from the crushed shells and fixed either in Bouin fluid. Five to 10 micrometer thick sections were stained with Hematoxilyn and eosin, PAS-Schiff for sugars, and Sirius-red for collagen. Hemocyte reactions were considered as focal (granulomatous) or diffuse, and a semi-quantitative estimation of their grades as mild, moderate and intense was made by two independent observers.
Electron microscopy - Tiny fragments taken from several regions of both infected and non-infected snails, were immediately fixed in 2% glutaraldehyde in 0.2 M cacodylate buffer, pH 7.4, and postfixed with 1% osmium tetroxide. Fragments were dehydrated in graded concentrations of acetone and embedded in Poly-bed 812 (Embedding Media Polysciences, IVC). Selected ultrathin sections (50-70 nm) were made with a Reichert (Ultratome Supernova Leica) ultramicrotome and mounted on uncoated copper grids, contrasted with uranyl acetate and lead citrate. Specimens were examined in a transmission Zeiss EM-9 electron microscope, which was operated at an acceleration voltage of 50 kV.
Histochemistry - The infected snails were killed at 42, 49, and 63 days following miracidial exposition for the histochemical demonstration of two enzymes: one representative of the respiratory chain - dehydrogenase; and a lysossome enzyme - acid phosphatase. After removal of the soft parts, fresh fragments were immediately taken from the regions of digestive glands and ovo-testis and immersed in Tissue-tek (Sakura, Japan) and snap frozen with liquid nitrogen and preserved in air-tight bottles in a freezer at -70ºC until the moment the blocks were cut in a Reichert-Jung (2.800 Frigocut) cryostat, at -21ºC.
Acetone-fixed cryostat sections were submitted to a tetrazolium histochemical method for the demonstration of dehydrogenase, using di-sodium succinate as substrate (Pearse 1960).
The presence of acid phosphatase was revealed by using Naphtol AS-BI (BioChemika - 70491, US) as substrate, and pararosaniline as indicator, according to the method described by Barka (1960).
Statistical analysis - A one-way ANOVA test followed by a Neuman-Keuls Multiple Comparison Test was used to compare the data from hemocyte counting and phagocytosis activity analysis.
The snail infection rate reached 80%, with cercarial elimination varying from 50 to 80 per snail, without much variation with time after exposure to miracidia. The smaller snails (8-11 mm shell diameter) presented slightly, but statistically significant, higher elimination in comparison with larger (12-14 mm) adult snails (Fig. 1A).
The counting of hemocytes in the circulating hemolymph revealed a statistically significant increase in number at the 6th week following miracidial exposure, but from then on the variations observed were not significant, even when the comparison included snails from the 7th-9th week after miracidial exposure, and normal intact controls (Fig. 1C).
The histological sections examined disclosed many parasitic forms with variable degree of tissue reaction. The major concentration of parasites appeared at the digestive gland region and the ovotestis, but they could be found throughout the snail tissues. The host reaction was represented by mild to moderate, usually diffuse, and rarely focal hemocyte infiltration around the abundant multiplying S. mansoni forms. Only rarely an encapsulating type of reaction was seen surrounding parasite forms. Sometimes sporocysts and developing cercariae were found without any sign of host reaction (Fig. 2).
The histochemical search for enzymatic activity revealed that dehydrogenase was negative from the hemocytes, but was noted in several other snail structures of the digestive glands and ovotestis, although always presenting a rather faint staining. A more strong reaction was seen in the parasites (Fig. 3A). On the contrary, the mark for acid phosphatase activity appeared well distinct. Besides being present in the hemocyte cytoplasm, acid phosphatase was also revealed in several snail cells in the digestive glands and ovotestis, as well as in the schistosome sporocysts and developing cercariae (Fig. 3B). Also, some hemocytes appeared devoid of acid phosphatase. During accumulations of hemocytes around dead or dying parasites a staining for acid phosphatase was sometimes found extra-cellularly, forming a halo around the disintegrating parasite.
Under the electron microscope the hemocytes were frequently found in the connective tissues of the digestive glands and ovotestis. In infected snails the hemocytes presented denser and larger cytoplasm, with many organelles, and more numerous philopodia, when compared with the hemocytes seen in normal snails. Not only dark bodies (lysossomes) and phagosomes (myelin figures), but also mitochondria and granular endoplasmic reticulum appeared more prominent in infected snails when compared with hemocytes from normal snails (Figs 3C, D). The spaces between the numerous cytoplasmic prolongations appeared filled with slightly dense granules. These prolongations formed a characteristic labyrinthine picture. Glycogens granules were also frequentely concentrated in the cytoplasm of hemocytes from infected snails.
The expectation that changes involving the hemocytes within the B. glabrata tissues would have a repercussion on the peripheral hemolymph did not come true. Although the snails used were very susceptible to S. mansoni infection, large areas of hemocyte infiltrations did occur in some specimens, but variations in hemocyte counting and in their signs of increased phagocytic activity were always scarce. Probably the two compartments are independent, and nothing similar to a vertebrate leukocytosis is to be expected during the occurrence of inflammatory-like changes in the snail tissues. Actually, some mild variations did occur in hemocyte counting, but this applied more to the size of the snail (shell diameter), rather than to the presence of schistosome infection. Regarding this latter finding our data only confirm those of Stumpf and Gilbertson (1978), and Dikkeboom et al. (1984). The shell size is related to the age of the snail, and probably the variation in hemocyte concentration in the hemolymph may be under the influence of several factors, among them sexual maturity (Sminia et al. 1974). In the present study, especial attention was paid in order to previously determine the concentration of hemocyte in the hemolymph of normal snails with different ages (shell diameter). It was noted that normal snails measuring 10 mm of shell diameter presented the lowest hemocyte count, what was probably related to their stage of sexual maturity (Fig. 1B). The stage of the schistosome infection also is important. Abdul-Salam and Michelson (1980) observed significant increase in peripheral hemocyte number in snails with 4-6-week old infection as compared to normal controls. On the other hand, Granath and Yoshino (1983) found the contrary, a decrease in hemocyte number, that they attributed to a migration of hemolymph cells to the interior of the tissues.
Another tested parameter was phagocytosis activity to zymosan. It did not presented differences when peripheral hemocytes from infected snails were compared to non-infected controls. This has been interpreted as another line of evidences that B. glabrata hemocytes from the lymph and tissues depend on independent and peculiar types of stimulation during S. mansoni infection.
B. glabrata hemocytes have frequently been compared with the vertebrate macrophages. The macrophages are cells specially adapted to intracellular digestion. So they frequently present lysossomes ready to pour their digestive enzymes, among them several acid hydrolyses, into phagocytic vacuoles. These aspects have already been studied (Carter & Bogitsh 1975, Folley & Cheng 1977, Cheng 1983, Borges & Andrade 2003). However, two aspects now observed deserve comments. The presence of acid phosphatase activity found free within the tissues, denoting the possibility of this enzyme to act extracellularly, being secreted and eliminated at some reaction zones. Another aspect refers to the finding of acid phosphatase positive and negative hemocytes, which suggests cells at different stages of functional activity.
Present ultrastructural findings reveal mild but definite differences between hemocytes present in the tissues of infected and non-infected snails. The formal present signs of activation in the number, size and disposition of cytoplasmic prolongations, and in the number and size of organelles. On this later aspect, the tissue hemocytes also differ from their peripheral counterpart.
To Dr Joseph Schrevel chief the Laboratoire de Biologie Parasitaire, Protistologie, Helminthologie (Museum National D¢Histoire Naturelle) for receiving one of us (CMC Borges) in his Laboratory, where the studies with electron microscopy were undertaken.
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Received 25 May 2006
Accepted 26 June 2006