- Research article
- Open Access
- Open Peer Review
The osteoblast as an inflammatory cell: production of cytokines in response to bacteria and components of bacterial biofilms
© The Author(s). 2016
- Received: 18 December 2015
- Accepted: 19 May 2016
- Published: 2 June 2016
Implant infections are a major complication in the field of orthopaedics. Bacteria attach to the implant-surface and form biofilm-colonies which makes them difficult to treat. Not only immune cells exclusively respond to bacterial challenges, but also local tissue cells are capable of participating in defense mechanisms. The aim of this study was to evaluate the role of osteoblasts in the context of implant infections.
Primary osteoblasts were cultivated and stimulated with free-swimming bacteria at 4 °C and 37 °C. Supernatants were harvested for ELISA and expression of pro-inflammatory cytokines evaluated by RT-PCR. Bacterial binding to osteoblasts was evaluated using cytofluorometry and uptake was investigated by 3H thymidine-labelling of bacteria. Osteoblasts were additionally stimulated with the extracellular polymeric substance (EPS) of Staphylococcus epidermidis biofilms, as well as components of the EPS; the bacterial heat shock protein GroEL in particular.
We demonstrated that binding of bacteria to the osteoblast cell surface leads to an increased production of pro-inflammatory cytokines. Bacteria are capable of surviving intracellular. Furthermore, osteoblasts do not only respond to free-swimming, planktonic bacteria, but also to components of the EPS, including lipoteichoic acid and the heat shock protein GroEL.
In conclusion, local tissue cells, specifically osteoblasts, might contribute to the persistence of the inflammatory response associated with implant-infections.
- Biofilm infection
- Extracellular polymeric substance
Osteoblasts are primarily studied in the context of bone turnover and fracture healing. However, they can also acquire characteristics of inflammatory cells. For example, in response to bacterial challenge synthesis and release of pro-inflammatory cytokines is described, including generation of CXCL8 (interleukin 8, IL-8) or CCL2 (monocyte chemoattractant protein-1, MCP-1). Because both, CXCL8 and CCL2, attract leukocytes, the local inflammatory response might escalade [1–4] (for review see [5, 6]). Of note, osteoblasts also acquire properties of antigen presenting cells. Following uptake of Staphylococcus aureus, expression of MHC class II molecules and of co-stimulatory receptors was described [7, 8], as was the ability of MHC class II positive osteoblasts to present superantigens to T lymphocytes. Furthermore, osteoblasts produce defensin, a molecule with bactericidal activity that was initially described in leukocytes .
Osteoblasts take up bacteria by an active process [10, 11]. Whether this uptake is a host defence reaction, analogous to the bacteriophagocytosis by leukocytes is still an open question. Under experimental conditions, ingested bacteria survive within the cell, leading to the notion that the osteoblast might provide a safe hiding place, which - in consequence - might contribute to the persistence of an infection [12–16].
Interactions of bacteria, either with phagocytic cells or osteoblasts, are mainly studied with free-swimming, planktonic bacteria. However, this is not the only life-style of bacteria, and possibly not even the preferred one, which was recognised over the last few years. Rather, many bacteria species live in structured colonies, embedded in an extracellular polymeric substance, so-called “biofilms” [17–20]. By means of biofilm formation, opportunistic bacteria in particular may acquire a pathogenic potential.
Our research group is particularly interested in infections due to biofilm formation on orthopaedic implants. In these infections, staphylococci species are prevalent . Extensive inflammation around the implant occurs, which eventually results in bone degradation and in loosening of the prosthesis. Analysis of the local host response revealed infiltration of phagocytic cells, particularly of neutrophils, generation of pro-inflammatory cytokines and increased development of bone-resorbing osteoclasts [22–24].
A likely source for these cytokines are infiltrating neutrophils, which are activated by bacterial biofilms. Of note, entities within the extracellular substance of the biofilm activate neutrophils, among those peptidoglycan, lipoteichoic acid and the bacterial heat shock protein GroEL [25, 26]. Another source could be osteoblasts, which are also known to produce cytokines after appropriate stimulation [3–5]. We now addressed the question whether osteoblasts are not only activated by planktonic staphylococci, but by entities derived from bacterial biofilms.
Culture of osteoblasts
Primary osteoblasts were cultivated from human bone marrow which was harvested either from the femoral bone using the RIA (reamer-irrigator-aspirator)-technique or from the iliac crest of patients undergoing surgery due to fracture malunion or non-union, and who required an autologous bone graft. Informed consent was obtained from the patients, and the study was approved by the local ethic committee of Heidelberg University (S-355/2010; October 28th 2010). Samples were grinded using sterile scalpels and cultivated in osteoblast growth medium (PromoCell, Heidelberg, Germany) containing 0.1 % penicillin/streptomycin (Gibco Life Technologies, Eggenstein, Germany). Outgrowth of cells occurred usually between 4 to 8 days. Cells were subcultivated following digestion with trypsin (0.05 % Trypsin-EDTA, Life Technologies) for 5 min at 37 °C and resuspended in osteoblast growth medium. After 10 to 14 days, homogenous cell layers were seen; osteoblasts were identified by expression of collagen type I and bone sialoglycoprotein, and lack of markers for myeloid cells (CD11b, CD68) (all from Beckman Coulter, Krefeld, Germany) as seen by laser scan microscopy and by cytofluorometry of detached cells. Expression of CD90 (Beckman Coulter, Krefeld, Germany) was used as a marker for de-differentiation. Osteoblasts were used for a maximum of two passages and experiments were carried out in 6 or 24-well dishes (NuncTM, Wiesbaden, Germany) at a concentration of 2 × 105 cells/mL in osteoblast growth medium.
Cytofluorometry and microscopy
Cytofluorometry was performed with paraformaldehyde-fixed osteoblasts using FACS Calibur and Cell quest pro as software (Becton and Dickinson, Heidelberg, Germany). Presence of collagen type I and bone sialoglycoprotein was assessed by indirect immunofluorescence. Slides were viewed by Laser scan microscopy (LSM, Leica).
Stimulation of osteoblasts by bacteria
Staphylococcus aureus (Seattle 1945, ATCC 25923, Wesel, Germany) and Staphylococcus epidermidis (RP62a, ATCC 35984) were grown overnight on a blood agar plate at 37 °C (number PB5039A, Thermo Scientific, Germany, Wesel). The following day, bacteria were scraped of the plate, suspended in phosphate buffered saline and adjusted to 1x108 cells/mL. Bacteria were added in a ratio of 1:20, 1:100 and 1:500 bacteria per osteoblast (2x105 cells per well in a 6-well culture dish in a volume of 4 mL) and incubated at either 4 °C or 37 °C for the times indicated in the respective experiments (two different temperatures were compared, because phagocytosis is impaired at 4 °C). The supernatant was discarded and 1600 μg vancomycin/4 mL osteoblast growth medium was added for 30 min. The supernatant was discarded and replaced with 4 mL osteoblast growth medium containing 80 μg vancomycin and culture was continued for the times indicated in the respective experiment. In another set of experiments, heparin 200 μg (Heparin Sodium 25000, Ratiopharm, Ulm, Germany) was added before stimulation with bacteria and pre-incubated at room temperature for 10 min. After that, bacteria were added and experiments carried out as described above.
For RT-PCR analysis, cells were collected in 400 μL lysis buffer from the MagnaPure mRNA Isolation Kit I containing 1 % DTT (v/w) (ROCHE Applied Sciences - RAS, Mannheim, Germany). To determine release of cytokines, culture was continued for 6 h, 24 h and 48 h at 37 °C. Supernatants were then harvested and stored at−20 °C for ELISA (see below).
Binding of bacteria to osteoblasts
FITC-labelled dead S. aureus were purchased (Molecular probes, S-2851, ThermoFisher Scientific, Schwerte, Germany). S. epidermidis were labelled with fluorescein isothiocyanate (FITC) according to the following protocol: FITC isomer I was purchased (Sigma- Aldrich, Darmstadt, Germany; F7250). A 5 mg/mL DMSO stock solution was diluted in phosphate buffered saline 1:10 (end concentration 0.5 mg/mL) and was incubated with bacteria (8x107) for 45 min at 37 °C. Following repeated washing, the bacteria were suspended in 4 % formaldehyde. FITC-labelling of bacteria was evaluated by cytofluorometry. Binding of FITC-labeled bacteria to osteoblasts was determined by incubating with bacteria at a ratio of 1:100 bacteria per osteoblast for 2 h at either 37 °C or 4 °C, followed by cytofluorometry and by laser scan microscopy.
To visualise uptake of bacteria, osteoblasts were incubated with FITC-labelled bacteria (see below) at a ratio of 1:100 for 2 h. The cells were fixed and viewed by LSM.
Uptake of 3H thymidine-labelled bacteria
An overnight culture of S. epidermidis in trypticase soy broth was performed. The next morning 2 mL of the overnight culture were added to 20 mL fresh trypticase soy broth containing 100 μL 3H Thymidin (Amersham, UK, TRA120 1 mCi/mL) and culture was continued for 4 h. Radioactivity associated with the bacteria was quantified. Osteoblasts were then incubated with the labelled bacteria as described above for 3 h. Then cell-associated radioactivity was measured in an aliquot, the remaining cells were treated with vancomycin to kill adherent, but not internalised cells (as described above), then lysed. An aliquot of the lysate was placed onto agar plates, and colonies were counted after 24 h.
Formation of biofilms and extraction of the extracellular polymeric substance (EPS)
S. epidermidis was added to 1.5 L of pre-warmed Trypticase Soy Broth (TSB) to reach a final concentration of 3x106 CFU/mL, then transferred to 30 polysterol dishes (Nunc 150x20, Thermo Fisher Scientific, Roskilde, Denmark) with a final volume of 50 mL per dish. After incubation for 2 days at 37 °C without shaking, the medium was removed and the remaining biofilm was scrapped off. The following treatment was adapted from Liu et al. (2002) : per 10 mL of slime, 60 μL of 37 % formaldehyde was added and mixed for 1 h at 4 °C, followed by the addition of 4 mL 1 M NaCl and mixing for another 3 h at 4 °C. The resulting suspension was then centrifuged (Sorvall 5B Plus) for 15 min (18000 rpm at 4 °C). The pellet was discarded, the supernatant filtrated (Millex Syringe-driven Filter Unit 0.22um, Merck Milipore Ltd, Tullagreen, Ireland) and then dialysed overnight against Milipore water at 4 °C (membrane cut off 3600 Da; Spectrum Labs, Rancho Dominguez, CA, USA). The water was replaced and the isolated EPS was again dialysed for another 3 h, then concentrated using Vivaspin 20 (Sartorius Stedim Biotech, Göttingen, Germany) to a final volume of 4 mL and frozen at−20 °C until use. Extraction of EPS from 1.79 square meters biofilm yielded on average 44.9 mg of protein.
To detect possible endotoxin contamination a limulus assay was performed (Pierce LAL Chromogenic Endotoxin Quantitation Kit, Thermo Scientific, Bonn, Germany) following the instructions provided by the manufacturer. The adsorption of LPS was accomplished using Pierce High Capacity Endotoxin Removal Spin Column following the instructions provided but adjusting the incubation time to 2 h in order to maximize LPS-removal.
Stimulation of osteoblasts
LTA (Sigma Aldrich) and recombinant GroEL (Enzo Life Sciences) were purchased. Osteoblasts were cultivated with LTA1 or LTA5 (1 μg/mL and 5 μg/mL, respectively), GroEL1 and GroEL5 (1 μg/mL and 5 μg/mL, respectively) or EPS2 and EPS10 (2 % and 10 % (v/v)). Supernatants were collected after 6 h and 24 h incubation time at 37 °C and cells were collected in lysis buffer for RT-PCR-analysis (see below).
Quantitative real-time polymerase chain reaction
Cells were collected in 400 μL lysis buffer from the MagnaPure mRNA Isolation Kit I containing 1 % DTT (v/w) (ROCHE Applied Sciences - RAS, Mannheim). mRNA was isolated with the MagnaPure-LC device using the mRNA-I standard protocol. An aliquot was reversely transcribed using AMV-RT and oligo-(dT) as primer (First Strand cDNA synthesis kit, Roche) according to the manufactures protocol in a thermocycler. Primer sets optimized for the LightCycler® (RAS, Mannheim Germany) were developed and purchased from SEARCH-LC GmbH (www.Search-LC.com). The PCR was performed with the LightCycler® FastStart DNA Sybr GreenI kit (RAS) according to the protocol provided in the parameter specific kits. To control for specificity of the amplification products, a melting curve analysis was performed. The copy number was calculated from a standard curve, obtained by plotting known input concentrations of four different plasmids at log dilutions to the PCR-cycle number (CP) at which the detected fluorescence intensity reaches a fixed value. To correct for differences in the content of mRNA, the calculated transcript numbers were normalized according to the expression of the housekeeping gene peptidylprolyl isomerase B (PPIB). Values were thus given as transcripts per 1000 transcripts of PPIB.
IL-8, IL-6 and CCL2 in cell culture supernatants were determined using commercially available ELISA kits according to the protocol provided by the manufacturer. The human Elisa kits were purchased from R& D Systems (Minneapolis, USA).
Differences between groups were calculated using ANOVA one-way or Mann–Whitney test using Origin 9.0 software. Significance level was determined as P < 0.05.
Osteoblasts in culture
Phagocytosis of bacteria and release of cytokines
Phagocytosis of live bacteria
bacteria associated with cells (% of input) (mean of n = 4)
colonies counted after 24 h
osteoblasts + S. epidermidis
47 ± 15
51 ± 21
osteoblasts + heparin + S.epidermidis
39 ± 21
34 ± 12
Effects of extracellular biofilm substance on osteoblasts
Implant-associated infections are a feared complication in the field of orthopaedics, since these infections are difficult to diagnose and usually require prolonged treatment [29–31]. The reason for these difficulties is ascribed to the fact that bacteria attach to an implant surface, produce and embed themselves in an extracellular polymeric substance and are thus capable of forming biofilm-colonies that are resistant to antibiotic treatment (reviewed in [17–19, 32, 33]). Moreover, it has been proposed that bacteria in biofilms are protected from the immune system; the latter even being incapable of recognising biofilms [34–36].
However, given the fact that biofilm-formation is actually the preferred and thus probably predominant living-form of bacteria, makes it unlikely that the immune system does not respond to these infections. In support of this theory it has been shown that immune cells infiltrate areas of biofilm formation and attack biofilms [22, 37]. Of note, phagocytic cells recognize biofilms even without opsonisation; a process which is required for recognition and phagocytosis of free-swimming bacteria [38, 39]. Indeed, neutrophils were activated by the eluted extracellular matrix, and more recently, we identified lipoteichoic acid (LTA) and the bacterial heat shock protein GroEL as activating entities within the biofilm matrix . In neutrophils, GroEL leads to an up-regulation of activation-associated markers on the cell surface and increased oxygen radical production .
Since neutrophils are not necessarily the first cells to encounter a biofilm infection, we now evaluated the effects of the extracellular polymeric substance, LTA, and GroEL on local tissue cells, namely osteoblasts. We were able to demonstrate that osteoblasts responded by an increased production of pro-inflammatory cytokines which in turn can attract immuno-competent cells, and might thus initiate or perpetuate the defence against biofilm infections. That osteoblasts produce cytokines in response to inflammatory stimuli has been reported before by others ; the novel aspect of our study is, that bacteria-derived entities and by implication bacterial biofilms activate the inflammatory potential of osteoblasts, most likely as the first reaction to an infection.
Another interesting aspect of osteoblast-bacteria interaction is the uptake of bacteria by osteoblasts and the intracellular survival of bacteria. In extension of previous studies by others [3, 28, 40] we found that the contact of bacteria with the osteoblast is sufficient to induce cytokine induction. Moreover, in line with data by others, this effect could be inhibited by heparin, which interacts with fibronectin-binding; the latter being essential for internalization of bacteria [28, 41]. We also demonstrated that bacteria are capable of intracellular survival in osteoblasts which might offer a feasible explanation of persisting and recurring bone infections. These findings are in line with our previous findings on enhanced cytokine expression in the tissue surrounding an infected implant which might be generated not merely by infiltrating leukocytes, but also local tissue cells [24, 42, 43].
In conclusion, we were able to show that aside from the obvious role of osteoblasts in bone formation, they also respond to bacterial infections. Osteoblasts are capable of increased expression and release of pro-inflammatory cytokines when challenged with free-swimming bacteria. Furthermore, we demonstrated internalization of bacteria and intracellular survival as a method of bacterial persistence leading to chronic infectious disease.
Osteoblasts not only respond to free-swimming bacteria, but also to components of the extracellular polymeric substance, among them the bacterial heat shock protein GroEL, and may therefore be critically involved in defence mechanisms against biofilm infections.
CCL2, monocyte chemotactic protein 1 (MCP1α); EPS, extracellular polymeric substance; IL-6, Interleukin-6; IL-8, Interleukin-8; LTA, lipoteichoic acid; qRT-PCR, quantitative real-time polymerase chain reaction.
The authors declare no conflict of interest.
Dr. Ulrike Dapunt was supported by the Olympia-Morata-Scholarship of the Faculty of Medicine of Heidelberg University.
All authors have made substantial contributions to conception and design, acquisition of data, analysis and interpretation of data and have been involved in drafting the manuscript or revising it critically for important intellectual content. All authors have given final approval of the version to be published and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
Informed and written consent was obtained from the patients, and the study was approved by the local ethic committee of Heidelberg University.
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