- Research article
- Open Access
Heat shock cognate protein 70 contributes to Brucella invasion into trophoblast giant cells that cause infectious abortion
© Watanabe et al; licensee BioMed Central Ltd. 2008
Received: 21 April 2008
Accepted: 05 December 2008
Published: 05 December 2008
The cell tropism of Brucella abortus, a causative agent of brucellosis and facultative intracellular pathogen, in the placenta is thought to be a key event of infectious abortion, although the molecular mechanism for this is largely unknown. There is a higher degree of bacterial colonization in the placenta than in other organs and many bacteria are detected in trophoblast giant (TG) cells in the placenta. In the present study, we investigated mechanism of B. abortus invasion into TG cells.
We observed internalization and intracellular growth of B. abortus in cultured TG cells. A monoclonal antibody that inhibits bacterial internalization was isolated and this reacted with heat shock cognate protein 70 (Hsc70). Depletion and over expression of Hsc70 in TG cells inhibited and promoted bacterial internalization, respectively. IFN-γ receptor was expressed in TG cells and IFN-γ treatment enhanced the uptake of bacteria by TG cells. Administering the anti-Hsc70 antibody to pregnant mice served to prevent infectious abortion.
B. abortus infection of TG cells in placenta is mediated by Hsc70, and that such infection leads to infectious abortion.
Brucellosis is a widespread and economically important infectious disease of animals and humans caused by members of the genus Brucella. Brucella spp. are small gram-negative, facultative intracellular pathogens that cause abortion, retained placenta and infertility in numerous domestic and wild mammals, and a disease known as undulant fever in humans [1–3]. Transmission of Brucella spp. from infected animals to humans may be either direct or indirect. Direct transmission involves the respiratory, conjunctival and cutaneous routes, and is more important in people in close contact with infected animals. Indirect transmission is through the consumption of contaminated dairy products . Brucella spp. occasionally causes spontaneous abortion in pregnant women .
There have been several histological studies on the placentas of Brucella infected animals . Further, it has been found that Brucella internalizes into the caprine erythrophagocytic trophoblastic epithelial cells from the maternal circulation  and that the internalized bacteria replicate within the rough endoplasmic reticulum, resulting in secondary infection of adjacent trophoblastic epithelial cells [6, 7]. Researches have also shown that after necrosis of infected trophoblasts, large numbers of brucellae are released, and proximity of the fetal capillaries in the ulcerated placenta to the lumenal bacteria has been proposed as the source of the fetal bacteremia and further placental infection [6, 8]. However, the molecular mechanism of abortion induced by Brucella spp. remains unknown.
The mouse model, particularly that using the unpregnant mouse, has been used extensively to study some aspects of the pathogenesis of brucellosis . While brucellosis is known to primarily affect the reproductive tract in the natural host, little is known regarding the cellular and molecular mechanisms of Brucella infection in the pregnant mouse . Although the structure of bovine placenta is completely different from mouse placenta, the infectious abortion model using the pregnant mouse is a powerful tool for investigating the mechanisms of Brucella pathogenesis. In our previous study, we demonstrated that B. abortus causes abortion in pregnant mice by inoculating bacteria on day 4.5 of gestation . We found that there was a higher degree of bacterial colonization in the placenta than in other organs, that there were many bacteria in trophoblast giant (TG) cells in the placenta and that an intracellular replication-defective mutant did not induce abortion. These findings suggest that bacterial infection of TG cells plays a key role in abortion induced by B. abortus infection.
Pregnancy leads to a generalized suppression of the adaptive immune system, typified by significantly decreased cell-mediated immunity and reduced T helper cell (Th) 1 responsiveness [11–13]. This immunosuppressed state prevents maternal rejection of the fetus but has the unfortunate consequence of increasing maternal susceptibility to certain infectious agents [14, 15]. Our previous study showed that a transient increase in interferon (IFN)-γ due to Brucella infection contributes to abortion in pregnant mice . In addition to examining the balance of inflammatory and regulatory cytokines in bacteria infected pregnant mice, analysis of bacterial internalization into the TG cells, a specific host cells in placenta, will help to advance our knowledge regarding the control of Brucella-induced abortion.
In the present study, we investigated the internalization of B. abortus into TG cells and identified heat shock cognate protein 70 (Hsc70) as a candidate receptor against Brucella or bacterial uptake-associated molecule. We noted that IFN-γ enhances bacterial internalization into TG cells.
All B. abortus derivatives were from 544 (ATCC23448) smooth virulent B. abortus biovar 1 strains. GFP expressed 544 strain was used in this study [16, 17]. B. abortus strains were maintained as frozen glycerol stocks and cultured on Brucella broth (Becton Dickinson) or Brucella broth containing 1.5% agar.
Six to ten-week-old ICR female mice were individually mated to 6- to 10-week-old ICR male mice. The parent mice were obtained from CLEA Japan. Day 0.5 of gestation was the day the vaginal plug was observed. The normal gestational time for these mice is 19 days.
Virulence in pregnant mice
Groups of five pregnant mice were infected intraperitoneally with approximately 104 colony forming unit (CFU) of brucellae in 0.1 ml saline on day 4.5 of gestation . On day 18.5 of gestation, placenta and spleen were removed and homogenized in phosphate buffered saline (PBS). Tissue homogenates were serially diluted with PBS and plated on Brucella agar to count the number of CFU in each organ. Fetuses were determined to be alive if there was a heartbeat, and dead if there was no heartbeat. The animal experiments were permitted by Animal Research Committee of Obihiro University of Agriculture and Veterinary Medicine.
Trophoblast stem (TS) cells were cultured in TS medium in the presence of FGF4, heparin and mouse embryonic fibroblast (MEFs)-conditioned medium as described previously . The TS medium was prepared by adding 20% fetal bovine serum (FBS), 1 mM sodium pyruvate, 100 μM β-mercaptoethanol, and 2 mM L-glutamine to RPMI 1640. To induce differentiation to trophoblast giant (TG) cells, the cells were cultured in the only TS medium alone for 3 days at 37°C in CO2 incubator. The TG cells were seeded (1–2 × 105 per well) in 48 well tissue culture plates for all assays.
Efficiency of bacterial internalization and replication within cultured cells
Bacterial infection and intracellular survival assays were performed according to a modified version of the method of Kim et al . B. abortus strains were deposited onto TS or TG cells at a multiplicity of infection (MOI) of 100 which had been grown on 48-well microtiter plates containing TS medium but no antibiotics by centrifugation at 150 × g for 10 min at room temperature. To measure bacterial internalization efficiency after 30 min of incubation at 37°C, the cells were washed once with TS medium and then incubated with TS medium containing gentamicin (30 μg/ml) for 30 min. Next, cells were washed three times with PBS and lysed with cold distilled water. CFU values were determined by serial dilution on Brucella plates. To measure intracellular replication efficiency, infected cells were incubated at 37°C for 30 min, washed once with TS medium and then incubated with TS medium containing gentamicin (30 μg/ml) for 2, 24, 48 and 72 h. The cell washing, lysis and plating procedures were the same as for the bacterial internalization efficiency assay. Percentage protection was determined by dividing the number of bacteria surviving by the number in the infectious inoculum. The purified the R2–25 antibody or recombinant IFN-γ (Cedarlane Laboratories) was added to the TS medium at the indicated concentrations 2 or 12 h before infection.
GFP-expressing bacteria were deposited onto the cultured cells by centrifugation and the incubation was conducted at 37°C for 30 min. The infected cells were incubated with TS medium containing gentamicin (30 μg/ml) at 37°C for 30 min to kill extracellular bacteria and were then fixed in 4% paraformaldehyde for 30 min at room temperature. Next, samples were permeabilized in 0.2% Triton X-100, washed three times with PBS and incubated with Alexa Fluor 594-phalloidin (Molecular Probes) at 20 μg/ml for 30 min at 37°C. After three washes with PBS, samples were placed in mounting medium (90% glycerol containing 1 mg/ml phenylenediamene in PBS, pH 9.0) and visualized by fluorescence microscopy.
Isolation of monoclonal antibodies
Hybridomas producing monoclonal antibodies that inhibit bacterial internalization into TG cells were obtained from fusions of BALB/c P3-X63-Ag8.653 (8-azaguanine-resistant and non-producer cell line) myeloma cells with spleen cells from Wister rats that had been immunized with TG cells. The screening of hybridoma supernatants for inhibiting antibodies was performed by adding antibodies to the TS medium in a bacterial internalization assay. Monoclonal antibodies obtained from hybridoma supernatants were purified using a protein G column (GE Healthcare Life Science) and the class and subclass of the purified monoclonal antibodies were determined using an Immunogloblin Typing Kit (WAKO Pure Chemical). The R2–25 monoclonal antibody used in this study was typed as IgG1.
Subcellular fractionation of TS and TG cells
TS and TG cells (3 × 105/ml) were seeded into each well of a 6-well plate. Protein isolation for the cytoskeleton, nuclear, membrane, and cytosol fraction was performed using a ProteoExtract Subcellular Proteome Extraction Kit as described by the manufacturer (Calbiochem).
The cell lysates (500 μg/ml) and fractionated proteins (50 μg/ml) were separated on 10% polyacrylamide gels and transferred to a PVDF membrane, which was incubated for 1 h at room temperature with primary antibody (0.5 μg/ml) in 5% skim milk. It was then washed three times in Tris buffered saline (TBS) with 0.02% Tween 20, incubated for 30 min with a horseradish peroxidase (HRP)-conjugated secondary antibody at 0.01 μg/ml and then washed again. Immunoreactions were visualized by ECL (GE Healthcare Life Science). Antibodies for β-actin, β-tublin and histone H1 were purchased from SIGMA or Abcam. Anti-IFN-γ receptor rabbit polyclonal antibody was purchased from Santa Cruz Biotechnology.
Mass spectrometry analysis
Identification of proteins reacting with monoclonal antibodies that inhibited bacterial internalization into TG cells was conducted by means of nano LC-MS/MS analysis and a search of MASCOT database (APRO life Science Institute, Japan).
RNA isolation and RT-PCR
The total RNA of TG cells was isolated using an RNA Purification Kit (Qiagen) and purified RNA samples were stored at -30°C until use. The RNA was quantified by absorption at 260 nm using a SmartSpec3000 spectrophotometer (Bio-Rad). RT-PCR was carried out using a Sperscript II Kit (Invitrogen). The primers used for mouse Hsc70 or β-actin amplification had the following sequence 5'-GCAGCTGGGCCTACACACAAG-3' and 5'-CCCTGTGGAACAAAGCTACAC-3', or 5'-CGTGACATTAAGGAGAAGCTGTGC-3' and 5'-CTCAGGAGGAGCAATGATCTTGAT.
Expression and purification of recombinant proteins
Mouse Hsc70 cDNA (GenBank Accession No. BC066191) was amplified from RNA isolated from TG cells by means of RT-PCR with the pair of primers described above. The product was cloned into the pCR2.1-TOPO vector (Invitrogen) (pCR-Hsc70). To achieve expression of recombinant Hsc70 protein, amplified DNA encoding Hsc70 from pCR-Hsc70 in PCR was cloned into pCold TF vector (Takara Bio Inc.). The His-tagged Hsc70 was expressed in the E. coli strain DH5α, and its purification and cleavage of His-tagged by HRV 3C protease were performed as described by the manufacturer (Novagen). Bovine Hsc70 and the rat anti-Hsc70 monoclonal antibody (SPA-815) were obtained from Stressgen for use as control materials.
To achieve expression of Hsc70 in TG cells, amplified DNA encoding Hsc70 from pCR-Hsc70 in PCR was cloned into the pcDNA4/TO vector in the T-Rex System (Invitrogen). pcDNA4/TO-Hsc70 was transfected into TG cells using the FuGENE 6 Transfection Reagent (Roche) with a final concentration of 1.2 μg/ml.
The siRNA duplexes used for silencing mouse Hsc70 (target sequence: AACAAGTAACATGGAATAATA), and β-actin (target sequence: CACTGACTTGAGACCAATAAA) and AllStars Negative Control siRNA were purchased from QIGEN. TG cells were transiently transfected using oligofectamine (Invitrogen) with or without a final concentration of 10 nM for siRNAs.
Samples grown on coverslips were washed twice with PBS, fixed with 4% paraformaldehyde in PBS for 30 min at room temperature, and permeabilized with or without 0.2% Triton X-100 in PBS for 20 min at room temperature. After blocking with 5% BSA in PBS, the cells were incubated with primary antibody (25 μg/ml) for 1 h at 37°C, and detection was conducted with TRITC-labeled goat anti-rat IgG (0.01 μg/ml) (Chemicon). Fluorescent images were taken using an Olympus BX51 microscope and a cooled CCD camera Olympus DP70.
In vivo depletion of Hsc70
Hsc70 was neutralized in the mice by administering an anti-mouse Hsc70 monoclonal antibody (clone R2–25)in vivo using 100 or 200 μg of antibody in a volume of 0.3 or 0.6 ml intraperitoneally 24 h before infection. Control mice were given 100 μg of normal rat IgG in a volume of 0.1 ml according to the same injection schedule as used for the anti-Hsc70 monoclonal antibody treated groups. Bacterial infection was conducted as described previously. On day 18.5 of gestation, fetuses were removed from the mice and a judgment made as to whether they were pregnant or not. Fetuses were determined to be alive if there was a heartbeat, and dead if there was no heartbeat.
All statistical analysis was conducted using the Student t test.
B. abortus internalizes and replicates in trophoblast giant cells
Several intracellular pathogens attached to the host plasma membrane induce actin polymerization around the site of bacterial attachment and the process is essential for bacterial entry . We therefore examined actin polymerization by means of fluorescence microscopy after 30 min and 48 h of incubation of TS and TG cells infected with B. abortus. It has been noted that differentiated TG cells dramatically rearrange their actin cytoskeleton into thick bundles of stress fibers . There was no apparent actin polymerization around the site of the bacterial entry after 30 min incubation on TG cells or 48 h of incubation of infected TG cells (Fig. 1C).
Isolation of monoclonal antibodies that inhibit bacterial internalization into TG cells
Antibody inhibiting bacterial internalization reacts with heat shock cognate protein 70
Hsc70 contributes to bacterial internalization into TG cells
IFN-γ enhances bacterial uptake by TG cells
Preventing abortion by inoculating pregnant mice with anti-Hsc70 antibody
Previous mouse model studies have shown that Brucella abortus specifically replicates in trophoblast giant (TG) cells in the placenta [9, 10]. TG cells are polyploid cells that play a crucial role in implantation, in remodeling of the embryonic cavity, and preventing maternal blood flow to the implantation site . Since B. abortus internalizes into TG cells and replicates in them, cell functions are not exhibited completely, which leads to abortion since implantation and placental development are inhibited. Therefore, it is thought that bacterial infection of TG cells is a key event in inducing abortion. To analyze the molecular mechanisms of B. abortus infection of TG cells in vitro, we used trophoblast stem (TS) cells and TG cells differentiated from TS cells for the infection assay in this study. Although TG cell differentiation is fairly well understood at the morphological and molecular level , the role of immune responses in fighting against pathogens of TG cells is poorly understood and in this regard a model of host-pathogen interaction using TG cells would be useful for obtaining new information of the effect of TG cell functions on pregnancy.
Hsc70 has been reported to be present on the surface of several types of cells . In this regard, though Hsc70 congregates on the surface of TG cells, it is present to a much lesser extent on the surface of TS cells (data not shown). This may be a reason that the internalization of B. abortus into TG cells was greater than that into TS cells. As Hsc70 and many other factors will be present on TG cells differentiated from TS cells, there is a possibility that other receptors or bacterial uptake-associated molecules may contribute to B. abortus infection of TG cells. Little is known about how Hsc70, a protein with no signal sequence for secretion, exits cells by mechanisms other than escape from cells undergoing necrotic lysis. In previous studies, Hsc70 has seen to be released from a late endsomal lysosomal location where it participates in protein degradation [25, 26]. Further, the secretion of the Hsp70 family and its association with lipid rafts have also been observed in epithelial cells under normal conditions, and a lipid raft-based mechanism has been suggested for the membrane delivery and release of Hsp70 family . Although receptors for the extracellular Hsp70 family have still not been fully defined, several cell surface receptors have been suggested, such as CD14, CD40, CD91 and scavenger receptor Lox-1 [28–31]. Since it has also been noted that class A scavenger receptor (SR-A) contributes to B. abortus infection in macrophages , SR-A may be receptors for Hsc70, and the mechanism for B. abortus internalization into TG cells may be the same pathway as that for Hsc70 uptake by TG cells. Hsc70 may have a function that is catching antigens and anti-Hsc70 would inhibit binding between Hsc70 and antigens. IFN-γ treatment enhanced bacterial internalization into TG cells and these observations agreed with results obtained in pregnant mice model , and thus expression of unidentified receptors against Hsc70 may be upregulated by IFN-γ treatment. IFN-γ should therefore promote internalization of B. abortus into TG cells in vivo and this would be one of ways in which infectious abortion is induced.
The finding of this study that the anti-Hsc70 antibody prevents abortion caused by B. abortus infection is expected to be applied in the development of methods of preventing abortion. Since intracellular bacteria such as Brucella replicate in host cells, it is difficult to completely eliminate them from the host through treatment with antibiotics and develop effective vaccines against them. An alternative strategy in treating infection due to Brucella would be inhibition of bacterial internalization into TG cells and this could be an effective means of protecting against abortion due to brucellosis. Recently, Carvalho Neta et al. reported that B. abortus modulates innate immune response by bovine trophoblastic cells . Although the structure of bovine placenta is completely different from mouse placenta, bovine and mouse trophoblastic cells may have similar function in the immune system. However, it is not known whether the mechanism of host-pathogen interaction observed in this study could be used to develop protective methods against other abortion-inducing pathogen infections, and thus further analysis of TG cell function in the immune system will be needed to clarify host defense mechanisms in the placenta and those contributing to the success of pregnancy.
We thank Dr. Alexander Cox for critical reading of the manuscript, and Dr. Suk Kim for valuable discussion. This work was supported, in part, by grants from Program for Promotion of Basic Research Activities for Innovative Biosciences (PROBRAIN), and grants from the Naito Fundation, and Institute for Fermentation, Osaka.
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