Trypanosoma cruzi activates mouse cardiac fibroblasts in vitro leading to fibroblast-myofibroblast transition and increase in expression of extracellular matrix proteins
- Laura Lacerda Coelho1,
- Isabela Resende Pereira2,
- Mirian Claudia de Souza Pereira3,
- Liliane Mesquita3,
- Joseli Lannes-Vieira2,
- Daniel Adesse†4 and
- Luciana Ribeiro Garzoni†1Email author
© The Author(s). 2018
Received: 3 August 2017
Accepted: 2 January 2018
Published: 30 January 2018
Cardiac fibrosis is a consequence of chronic chagasic cardiomyopathy (CCC). In other cardiovascular diseases, the protagonist role of fibroblasts in cardiac fibrosis is well established. However, the role of cardiac fibroblasts (CFs) in fibrosis during the CCC is not clear. Here, our aim was to investigate the effect of Trypanosoma cruzi, the etiological agent of Chagas disease on CFs activation.
Cardiac fibroblasts were purified from primary cultures of mouse embryo cardiac cells. After two passages, cells were infected with T. cruzi (Y strain) and analyzed at different times for determination of infectivity, activation and production of extracellular matrix components (fibronectin, laminin and collagen IV) by immunofluorescence and western blot.
At second passage, cultures were enriched in CFs (95% of fibroblasts and 5% of cardiomyocytes), as revealed by presence of alpha-smooth muscle actin (α-SMA) and discoidin domain receptor 2 (DDR2) and absence of sarcomeric tropomyosin (ST) protein expression. Trypanosoma cruzi infection induced fibroblast-myofibroblast transition, with increased expression of α-SMA after 6 and 24 h post-infection (hpi). Fibronectin was increased at 6, 24 and 48 hpi, laminin was increased at 6 and 24 hpi and collagen IV was increased at 6 hpi.
Our results showed that T. cruzi activates CFs, inducing activation and exacerbates ECM production. Furthermore, our data raise the possibility of the involvement of CFs in heart fibrosis during Chagas disease.
Chagas disease (CD) caused by the protozoan Trypanosoma cruzi is endemic in Latin America, affects about 7 million people around the world  and is one of the most important causes of infectious cardiomyopathy . Thirty percent of infected people will develop the clinical symptoms of chronic CD, which include cardiac, digestive, cardio-digestive and neurological manifestations [3, 4]. The cardiac form of CD is the most significant clinical manifestation due to its gravity and frequency .
In chronic chagasic cardiomyopathy (CCC), the parasite persistence contributes to chronic inflammation and death of cardiac cells, resulting in fibrosis and heart failure [3–5]. In experimental CD, intracellular forms of T. cruzi and inflammatory infiltrates can be observed in association with fibrotic areas in the cardiac tissue [6, 7]. There are several previous studies that have suggested an increased expression of fibronectin, laminin and collagen IV expression upon T. cruzi infection  that was shown to be reversible after treatment with the trypanocidal agent posaconazole (L. R. Garzoni, personal communication). Such observations indicate that the infection per se, independently of the presence of inflammatory cells, contributes to tissue fibrosis. Moreover T. cruzi expresses a family of glycoproteins that bind to fibronectin and laminin. Upon adhesion to either of these proteins, a series of serine-, threonine- and tyrosine-kinases are activated that, in turn, phosphorylate flagellar tubulin from the parasite . Conversely, the parasite’s cysteine proteinases degrade fibronectin for successful invasion of the host cell .
Fibrosis can be induced by distinct stimuli such as infections, toxins, drugs, tissue injury and persistent inflammation. When exacerbated, fibrosis can cause organ dysfunction and death . Fibrosis is defined as excessive deposition of ECM proteins in organs and tissues, as a result of fibroblasts activation . When activated, mainly in response to cytokines and growth factors such as TNF and TGF-β, fibroblasts transition to myofibroblasts and start expressing smooth muscle α-actin (α-SMA) and produce high amounts of ECM proteins [11, 13]. Fibroblasts are mesenchymal cells found in the connective tissue in distinct organs  and the role of these cells on genesis of fibrosis is well established .
Fibroblasts are the most abundant cell type found in the heart tissue, along with myocytes, endothelial and smooth muscle cells . Cardiac fibroblasts (CFs) produce metalloproteases and their tissue inhibitors (TIMPs), growth factors, cytokines (including TNF, IL-1 and IL-6) as well as reactive oxygen and nitrogen species, contributing to the structure and function of the heart tissue [14, 17].
The involvement of CFs in fibrosis formation associated to hypertrophy in cardiovascular diseases including myocardial infarct, hypertension and heart failure is well established [14, 18]. However, the role of CFs in the genesis of cardiac fibrosis during CD has not been addressed. In this context, the aim of the present study was to investigate the effects of T. cruzi on activation of CFs trying to shed light on the involvement of these cells in the formation of cardiac fibrosis during CD. For this purpose, we established a purified culture of CFs that was successfully infected with T. cruzi and observed fibroblast-myofibroblast transition in infected cells. Trypanosoma cruzi also increased the expression of ECM proteins in the course of the infection, indicating that the direct infection of CFs in vivo, especially in the acute phase, may participate in the initiation of a fibrotic event, contributing to the pathogenesis of the chagasic cardiomyopathy.
Reagents and antibodies
Trypsin and ethylenediaminetetracetic acid (EDTA) were acquired from Gibco (Carlsbad, CA, USA). Type II collagenase was obtained from Worthington Biochemical Corporation (Lakewood, NJ, USA). Phosphate buffered saline (PBS), fetal bovine serum (FBS), L-glutamine, penicillin, streptomycin, CaCl2, Dulbecco’s Modified Eagle’s Medium (DMEM), RPMI, acetone and bovine serum albumin (BSA), were obtained from Sigma-Aldrich (St. Louis, MO, USA). Giemsa solution was obtained from Merck (Frankfurt, Germany). Primary antibodies, rabbit polyclonal antibodies anti-fibronectin and anti-laminin, mouse monoclonal antibody anti-α-SMA and mouse anti-ST were obtained from Sigma-Aldrich. Goat polyclonal antibody anti-DDR2 was obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and mouse monoclonal antibody anti-GAPDH was acquired from Fitzgerald (Acton, MA, USA). Secondary antibodies, goat anti-mouse IgG Alexa Fluor 594 or 488, goat anti-rabbit IgG and goat anti-mouse IgG HRP-labeled were obtained from Invitrogen (Carlsbad, CA, USA). BCA protein assay reagent (bicinchoninic acid) and 4′-6-Diamidino-2-phenylindole (DAPI) were acquired from Thermo Fisher Scientific (Rockford, IL, USA). 1,4-diazabicyclo [2.2.2] octane (DABCO) was obtained from Sigma-Aldrich. The Protease Inhibitor Cocktail was purchased from Roche Molecular Biochemicals (Indianapolis, IN, USA) and the chemiluminescent kit ECL from Pierce (Rockford, IL, USA).
Isolation and purification of mouse cardiac fibroblasts
Heart ventricles were obtained from 18 day-old fetuses of Swiss Webster mice. Cells were isolated by mechanical and enzymatic dissociation methods using 0.05% trypsin and 0.01% collagenase in PBS (pH 7.2) at 37 °C, as previously described . Cells were plated on 0.02% gelatin-coated 25 mm2 flasks and maintained at 37 °C in 5% CO2 atmosphere in DMEM supplemented with 10% FBS, 2.5 mM CaCl2, 1 mM L-glutamine, 2% chick embryo extract, 1000 U/ml penicillin and streptomycin 50 μg/ml. CF-enriched cultures were established from 3-day old primary cardiac cultures by dissociation with trypsin/ EDTA in HBSS without calcium and magnesium. The isolated cells were plated at a density of 106 cells in 25 mm2 cell-culture flasks. Fully confluent cultures were split every 3–4 days and cells were used for experiments at second passage at the density of 5 × 105 cells/dish for 60 mm culture dishes or 5 × 104 cells/well in 13 mm round glass coverslips in 24-well plates. CFs were maintained at 37 °C in 5% CO2 atmosphere in DMEM supplemented with 10% FBS and 1000 U/ml penicillin and streptomycin 50 μg/ml (CF Medium).
Infection with Trypanosoma cruzi (Y strain)
Trypomastigotes forms of the Y strain (MHOM/BR/1950/Y) were obtained from previously infected cultures of Vero cell. After 4 days of infection, the parasites released in the supernatant were harvested and centrifuged at 800 g for 20 min at 4 °C. CFs were infected after 24 h of plating at a multiplicity of infection of 10:1 (parasites: host cell) in 500 μl of DMEM without FBS. After 24 h of interaction, extracellular parasites were washed out and fresh medium with 10% FBS was added in case of long-term infection.
CFs infection was interrupted at desired time-points (6 to 96 h) with Bouin’s fixative solution (picric acid-formalin-acetic acid mixture). The samples were dehydrated in acetone/xylene gradient and stained in Giemsa solution. Coverslips were mounted with Permount resin and the images were acquired using bright field microscopy (Nikon Eclipse E200, Nikon, Tokyo, Japan) and analyzed with the software Nis-Elements BR 4.0.
CF cultures were washed with PBS and fixed for 5 min at 20 °C with 4% paraformaldehyde in PBS. After washing, cells were permeabilized with 0.5% Triton X-100 and non-specific antibody binding was blocked with PBS containing 4% BSA. Then, the cells were incubated overnight at 4 °C with primary antibodies including mouse anti α-SMA, mouse anti-ST, rabbit anti-fibronectin, rabbit anti-laminin (all from Sigma-Aldrich) and rabbit anti-collagen IV (Millipore, Massachusetts, USA). Cells were washed and incubated with the appropriated secondary polyclonal antibodies for 1 h at 37 °C. DNA staining was performed with DAPI 0.2 mg/ml, incubated for 5 min at 20 °C and samples were mounted in DABCO/Glycerol solution. For α-SMA, slides were observed in a Nikon Eclipse Ci-E microscope (Nikon). The microscope was coupled to the fluorescence system Intensilight C-HGFI and to the Digital Sight DS-U3 acquisition image system (Nikon). For ECM proteins, slides were analyzed under confocal microscope Zeiss 601 from the Plataforma de Microscopia Óptica de Luz Gustavo de Oliveira Castro (Universidade Federal do Rio de Janeiro, UFRJ). For determination of percentage of SMA-positive cells, fluorescence micrographs were obtained using a 40× objective and a total of 60 microscopic fields per experimental condition (control and T. cruzi-infected, 24 hpi) from three independent experiments were analyzed. The number of positive SMA cells was divided by the number of DAPI-positive cells per field and multiplied by 100. Statistical analyses were performed with GraphPad Prism software 5.0 using the Student’s t-test. Changes were considered statistically significant when P < 0.05.
At desired time-points (6 to 72 hpi), cells were washed with PBS and scraped with 200 μl of RIPA lysis buffer (50 mM Tris-HCl, pH 7.5; 150 mM NaCl; 0.1% SDS; 1% deoxycholate sodium) containing 10% protease inhibitor cocktail (Roche) and phosphatase inhibitor cocktail (Sigma-Aldrich) and samples were frozen at -80 °C until used. Lysates were sonicated and protein concentration was determined using the BCA protein quantification kit (Pierce). Ten micrograms of protein was loaded and resolved in 10% SDS-polyacrylamide gels. The proteins were transferred to nitrocellulose membranes (Bio Rad, Hercules, CA, USA) and incubated with 5% skim milk in TBST (TBS and 0.5% Tween 20) for 30 min followed by incubation with primary rabbit polyclonal anti-fibronectin, anti-laminin and anti-collagen IV antibodies, mouse monoclonal anti-α-SMA and anti-ST antibodies, or goat polyclonal anti-DDR2 antibody diluted in TBST with 5% skim milk overnight at 4 °C. Mouse anti-GAPDH monoclonal antibody was used as loading control. Membranes were washed with TBST followed by incubation with secondary goat anti-rabbit IgG and goat anti-mouse IgG HRP-labeled antibodies for 1 h at 25 °C. Membranes were washed with TBST, incubated with the chemiluminescent kit ECL (Pierce) and exposed to X-Ray film (Thermo Fisher Scientific). The densitometry of bands was performed with the software Image Studio Lite v.4.0. Relative expression of the target proteins (α-SMA, fibronectin, laminin and collagen IV) was determined by the ratio between values of intensity of its band by the values of GAPDH band. Relative expression values from infected samples were normalized by the values of uninfected cultures in the same time point. Statistical analyses were performed with GraphPad Prism software 5.0 using unpaired Student's t-test and one-way ANOVA test with Tukey post-hoc test. Changes were considered statistically significant when P < 0.05.
Establishment of culture enriched in cardiac fibroblast
To confirm the enrichment in CFs, the expression of sarcomeric tropomyosin (ST), a protein specific of striated muscle cells, was evaluated in the second passage cultures (Fig. 1g, h). Immunofluorescence analysis showed that less than 5% of cells were positive for ST, indicating a high enrichment in CFs (Fig. 1g). Additionally, immunoblotting analysis showed the expression of ST only in samples of cardiac tissue (positive control) but it was undetectable in the second passage of cardiac cell cultures (Fig. 1h). Although no general marker for cardiac fibroblasts has been identified to date, a tyrosine kinase receptor named discoidin domain receptor 2 (DDR2), which is activated by collagen, is specifically expressed by CFs but not by the other cell types . The expression of DDR-2 was evaluated during the establishment of CF cultures and was found to be expressed in all time points analyzed (24, 48 and 72 h) (Fig. 1i).
Trypanosoma cruzi successfully completes its intracellular cycle in enriched cardiac fibroblasts cultures
Trypanosoma cruzi induces fibroblast-myofibroblast transition
Infected CFs produce higher levels of extracellular matrix proteins
In this study, we investigated the effect of T. cruzi on the activation of cardiac fibroblasts in vitro, trying to understand the contribution of these cells in cardiac fibrosis during Chagas disease. We observed that T. cruzi infection activated CFs, inducing differentiation to myofibroblasts and increasing ECM proteins synthesis.
Crucially, fibroblasts take part in the genesis and maintenance of fibrosis during injury situations, when the tissue repair machinery is necessary . The involvement of CFs in fibrosis and tissue remodeling in cardiovascular diseases such as myocardial infarct, hypertension and heart failure, has been described [12, 14, 17]. Moreover, cardiac fibrosis causes electrical alterations and heart failure [11, 13, 21]. The persistence of pro-fibrotic stimulation then results in an activated phenotype of fibroblasts and, consequently, an increase in the production and accumulation of ECM proteins .
The cardiac fibrosis is an important manifestation of Chagas disease  and the role of CFs in this process is understudied. However, the association of CFs with inflammatory cells, myofibroblasts and collagen deposits was demonstrated in an experimental model of CCC , suggesting a possible participation CFs on heart tissue remodeling during T. cruzi infection.
Our first step in this study was to settle and characterize cell cultures enriched in CFs. Such enrichment was confirmed by the absence of sarcomeric tropomyosin expression, a protein of striated muscle cells including cardiomyocytes  and by the presence of DDR-2, a collagen receptor expressed exclusively in CFs . Moreover, the CFs in culture preserved the morphological and functional characteristics as previously observed in vivo  and in vitro [20, 24]. These cells were capable of differentiating into myofibroblasts, as revealed by the expression of α-SMA and were able to produce ECM proteins, including laminin, fibronectin and collagen IV, similarly to what is observed in vivo [13, 16]. Indeed, in an experimental model of chronic Chagas disease in mice, the expression of α-SMA was increased in the heart tissue .
The establishment of T. cruzi infection in CFs-enriched cultures was based on previous studies of our group approaching aspects of the interaction of T. cruzi with cardiac cells . Herein, we observed that trypomastigote forms of T. cruzi successfully invaded CFs. Furthermore, the parasite completed its intracellular cycle inside CFs. These data are in agreement with previous data of our group supporting the infection and intracellular cycle of T. cruzi parasites in CFs of primary cultures of cardiac cells enriched in cardiomyocytes . Interestingly, using this mixed culture of cardiac cells , a group described that infected CFs were refractory to infection-induced apoptosis, indicating that these cells may be activated in such an inflammatory environment.
Our data showed that T. cruzi infection led to a transient increase in expression of SMA, thus indicating fibroblast-to-myofibroblast transition. Although the overall increase in SMA content was of only 9–12%, our immunofluorescence analyses showed that at the same time point (24 hpi) the number of highly stained cells for SMA was higher than in uninfected controls. However, when a protein lysate is generated for western blotting, this effect might be diluted. Additionally, at the final times of infection, as the parasite replicates in the cytoplasm, there was a reduction in α-SMA expression and disorganization of this protein, suggesting a breakdown of the cytoskeleton, as previously shown in cardiomyocytes [28, 29]. However, paracrine effects of secreted factor by infected CFs could maintain the culture in an activated state. Previous studies using mixed cultures of mouse and human cardiac cells have shown that T. cruzi induce the activation of TGF-beta  and pro-fibrotic proteins  as well as inflammatory cytokines .
Trypanosoma cruzi secrete soluble factors that may also induce production of ECM proteins in fibroblast cultures . Moreover, cytokines produced by infected cells may contribute to fibroblast-myofibroblast transition. The consequence of myofibroblast differentiation is the increased expression and deposition of ECM proteins that further contribute to the fibrotic process . Inflammation and fibrosis are hallmarks of CCC [6, 34–36], with production of cytokines that contribute to pathogenesis  and co-localization of T. cruzi DNA or antigens with inflammatory infiltrate and fibrosis in cardiac tissue was also observed [6, 7, 38].
We were interested in verifying whether in our system of purified CFs T. cruzi would stimulate ECM (fibronectin, laminin and collagen IV) deposition as seen in the cardiac tissue during in vivo infection [7, 39–42]. In the present study, we showed that T. cruzi infection, without the presence of inflammatory cells, increased the production of both fibronectin and laminin at 6 and 24 hpi, being reduced at the later time points. Although in the chagasic heart the levels of ECM proteins is extremely higher compared with what we observed in our CF cultures, the fact that fibronectin needs a three-dimensional microenvironment to establish a firbillar network  must be taken into consideration when analyzing data from monolayer cultures. This transient increase in ECM proteins in infected CF differs from what was shown in mixed cultures of cardiac cells . Cytoskeleton breakdown can also be responsible for ECM decrease in heavily infected cells in this 2D system, since previous work done on mixed cultures of cardiac cells showed that these two proteins are decreased at late stages of infection . Increased production of ECM proteins by T. cruzi infection or T. cruzi secreted factors in skeletal muscle cells (C2C12) and adipose tissue fibroblasts (L929) have also been demonstrated in the early stages of infection/treatment . In addition, our group had previously shown that T. cruzi induces fibrosis, hypertrophy and changed the distribution pattern of ECM proteins in a three-dimensional (3D) cardiac cells culture system .
ECM deposition observed in fibrosis leads to tissue stiffness, which contributes to cardiac electrical alterations . In fact, electrocardiographic (ECG) abnormalities are found in chronically infected mice and humans, concomitantly with the presence of fibronectin increase and myocardial scars that correlate with a worse prognosis in chronic patients [42, 46].
In conclusion, our study showed that T. cruzi is able to activate CFs, possibly contributing to cardiac fibrosis in Chagas disease. Therefore, the utilization of therapeutic strategies including trypanocidal compounds could contribute to inhibit the activation of CFs, reducing the synthesis of ECM proteins and consequently the fibrosis, improving the prognosis of patients with chronic Chagas cardiomyopathy.
Based on our results we conclude that (i) the culture of purified cardiac fibroblasts will serve as an important tool to deepen the knowledge of the pathogenesis of chagasic cardiomyopathy and (ii) T. cruzi infection activates these cells, which in turn contributes further to ECM deposition in response to infection. In the context of the in vivo infection we believe that cardiac fibroblasts may serve as an important cellular target to prevent exacerbation of tissue fibrosis.
The authors would like to thank Alanderson da Rocha Nogueira for the technical support with handling of T. cruzi.
Departamento de Ciência e Tecnologia/Ministério da Saúde/Ministério da Ciência, tecnologia e inovação/Conselho Nacional de Desenvolvimento Científico e Tecnológico (DECIT/MS/MCTI/CNPq) - 403979/2012–9 (JLV). Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) - Edital Universal (JLV, DA, MCSP); Programa de Objetivos e Metas - Fiocruz (POM/Fiocruz) (LRG, JLV, MCP), Fundação Carlos Chagas de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ) (JLV).
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author upon reasonable request.
Designed the experiments: LRG, LLC and JLV. Performed the experiments: LLC, DA, LBM, ISP and MCSP. Data analysis: LLC, LRG, DA and JLV. Discussed the major findings: LLC, LRG, JLV and DA. Wrote the manuscript: LLC, LRG and DA. Reviewed the manuscript: MCSP, LRG and JLV. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All procedures were approved by the Oswaldo Cruz Foundation Animal Welfare Committee (License number: LW-40/13) and were consistent with the USA National Institute of Health Guide for the Care and Use of Laboratory Animals (NIH Publication No. 85–23, revised 1996).
Consent for publication
The authors declare that they have no competing interests.
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