Role of cathepsin S In periodontal wound healing–an in vitro study on human PDL cells
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Cathepsin S is a cysteine protease, which is expressed in human periodontal ligament (PDL) cells under inflammatory and infectious conditions. This in vitro study was established to investigate the effect of cathepsin S on PDL cell wound closure.
An in vitro wound healing assay was used to monitor wound closure in wounded PDL cell monolayers for 72 h in the presence and absence of cathepsin S. In addition, the effects of cathepsin S on specific markers for apoptosis and proliferation were studied at transcriptional level. Changes in the proliferation rate due to cathepsin S stimulation were analyzed by an XTT assay, and the actions of cathepsin S on cell migration were investigated via live cell tracking. Additionally, PDL cell monolayers were treated with a toll-like receptor 2 agonist in the presence and absence of a cathepsin inhibitor to examine if periodontal bacteria can alter wound closure via cathepsins.
Cathepsin S enhanced significantly the in vitro wound healing rate by inducing proliferation and by increasing the speed of cell migration, but had no effect on apoptosis. Moreover, the toll-like receptor 2 agonist enhanced significantly the wound closure and this stimulatory effect was dependent on cathepsins.
Our findings provide original evidence that cathepsin S stimulates PDL cell proliferation and migration and, thereby, wound closure, suggesting that this cysteine protease might play a critical role in periodontal remodeling and healing. In addition, cathepsins might be exploited by periodontal bacteria to regulate critical PDL cell functions.
Keywordscathepsin S periodontal ligament cells wound closure migration
Dulbecco’s minimal essential medium
Fetal bovine serum
Proliferating cell nuclear antigen
Standard errors of the mean
Periodontitis is a highly-prevalent chronic inflammatory disease characterized by bone, attachment and even tooth loss . Oral periodontopathogens are a prerequisite for the disease but not sufficient to induce periodontitis. Additional risk factors, such as smoking, genetic predisposition and certain systemic diseases contribute to the initiation and progression of periodontitis . The periodontal microorganisms such as Fusobacterium nucleatum induce an inflammatory host response through binding to special receptors such as toll-like receptor (TLR) 2, which can ultimately result in the destruction of periodontal structures .
Periodontal ligament (PDL) cells are resident cells of the periodontium and have a critical role in tissue homeostasis, destruction and regeneration by their ability to synthesize and degrade collagen and other matrix molecules . However, these cells can also participate in the immunoinflammatory processes of periodontitis . Periodontal healing is determined by the type of cells that repopulate the root. By the application of regenerative treatment methods, which promote PDL cell proliferation, migration and attachment, the re-establishment of the initial periodontal tissue architecture is possible . However, the outcomes of currently available regenerative treatment approaches are sometimes compromised by a number of factors and are not predictable [7, 8]. Therefore, the search for new molecules with a regenerative potential are a major goal in periodontology .
Cathepsin S (CTSS) is a lysosomal cysteine protease and has the ability to remain stable and active under neutral pH [10, 11, 12]. Therefore, it can evoke both intra- and extracellular activities. Intracellularly, CTSS functions as a processing enzyme and is critical for protein trafficking and secretion, while extracellularly it has a pivotal role in tissue remodeling . This protease has the capacity to degrade multiple components of the extracellular matrix, such as collagen, elastin, fibronectin, laminin and proteolglycans [11, 13, 14]. Moreover, substrates of CTSS not only comprise antigenic as well as antimicrobial peptides but also play a fundamental role in antigen processing and presentation [11, 15, 16]. Additionally, it has been shown that CTSS promotes cell migration . Hence, these functions of CTSS suggest a complex role in immunoinflammatory diseases and healing processes [14, 18, 19].
CTSS is not produced ubiquitously and its synthesis seemed to be restricted to immunocompetent cells, such as macrophages, lymphocytes and dendritic cells [14, 19]. Previously, we have found that CTSS is also secreted by PDL cells and that its synthesis is regulated by inflammatory and microbial stimuli, suggesting strongly a role of this protease in oral inflammatory diseases . Moreover, in gingival biopsies from sites of periodontitis, CTSS was identified as a hub protein in the protein-protein interaction network of differentially expressed genes, also suggesting an involvement of CTSS in periodontitis . Therefore, the aim of this in vitro study was to investigate the effects of CTSS on PDL cell wound closure.
Isolation and characterization of PDL cells
Written informed consent and approval of the Ethics Committee of the University of Bonn were obtained (#117/15). Human PDL cells were taken from caries-free and periodontally healthy teeth of 5 donors (mean age: 14.6 years, min/max: 13/19 years; 3 males/2 females), who had to undergo tooth extractions for orthodontic reasons [22, 23]. Cells were harvested from the medial part of the tooth root and grown in Dulbecco’s minimal essential medium (DMEM, Invitrogen, Karlsruhe, Germany) supplemented with 10% fetal bovine serum (FBS, Invitrogen), 100 units penicillin and 100 μg/mL streptomycin (Invitrogen) in a humidified atmosphere of 5% CO2 at 37 °C. Cells between passages 3 to 5 were phenotyped according to Basdra and Komposch and used for experiments at 60%-100% confluence, depending on the individual protocol of each experiment .
One day prior to the experiments, the FBS concentration was reduced to 1%. PDL cells were incubated with the active form of CTSS (1 ng/μl; activity 143.4 U/mL; Calbiochem, San Diego, CA, USA) for up to 72 h . In a subset of experiments, PDL cells were incubated with a TLR2 agonist (1 μg/ml; Pam3CSK4; Invivogen, San Diego, CA, USA) in the presence and absence of a cathepsin inhibitor (50 μM; Z-FA-FMK; Santa Cruz Biotechnology, Dallas, TX, USA) for 24 h [25, 26].
In vitro wound healing assay
To analyze the in vitro wound healing, a well-established in vitro wound healing model was applied as in our previous studies [27, 28, 29]. Briefly, PDL cells were cultured on 35 mm plastic culture dishes and grown to 100% confluence. One day after reduction of FBS concentration, a 3–4 mm-wide wound was inflicted in a standardized manner so that cell free areas were created in the cell monolayers. Afterwards, all non-adherent cells were removed through multiple washing steps with DMEM. The wounded monolayers were then cultured in the presence and absence of CTSS for 72 h or the TLR2 agonist in combination with or without the cathepsin inhibitor for 24 h, as described above. By using a JuLI™ Br and the JuLI™ Br PC software (both NanoEnTek, Seoul, Korea), the wound closure was monitored over time and, subsequently, the wound healing rates were calculated.
Live cell imaging was applied to monitor cell migration over a period of 24 h. Cells were grown to 100% confluence, and cell free areas were created in a standardized manner. Subsequently, cells were treated as described above. The live cell tracker JuLI™ Br device and the JuLI™ Br PC software were used to capture images and to monitor the migration of individual cells. In each group and donor, 6 cells which had moved the farthest into the cell-free area after 24 h, were marked and traced. Images were transferred to and analyzed by the freely available image-processing software Image J 1.43 .
PDL cell monolayers were cultured in the presence and absence of CTSS for 24 h. Afterwards, RNA extraction was performed with a commercially available RNA extraction kit (RNeasy Protect Minikit, Qiagen, Hilden, Germany) and 1 μg of RNA was converted into cDNA by reverse-transcription with the IScript Select cDNA Synthesis Kit (Bio-Rad Laboratories, Munich, Germany). Expressions of Proliferating Cell Nuclear Antigen (PCNA) and p53, which are markers for cell proliferation and cell death, respectively, were determined by real-time PCR by using the iCyler iQ detection system (Bio-Rad Laboratories) [31, 32]. cDNA expression of 1 μl of cDNA was detected via real-time PCR in a 25 μl reaction mixture containing 2.5 μl respective QuantiTect Primer assay (Qiagen), 12.5 μl QuantiTect SYBR Green Master Mix (Qiagen) and 9 μl of nuclease free water, as recommended by the manufacturer. The protocol comprised a heating phase at 95 °C for 5 min to activate the enzyme, followed by 40 cycles of a denaturation step at 95 °C for 10 s and a combined annealing/extension step at 60 °C for 30 s. Melting point analysis was performed after each run. For normalization, the housekeeping gene GAPDH was used.
Cell proliferation was analyzed by using the AppliChem Cell Proliferation Kit XTT (AppliChem, Darmstadt, Germany). In a 96-well-plate, PDL cells (5.000/well) were grown to 60% confluence and stimulated with CTSS for up to 24 h. XTT reaction solution was added to the medium 4 h before measurements. Finally, the absorbance was determined with a microplate reader (PowerWave x, BioTek Instruments, Winooski, VT, USA) at 475 nm.
The IBM SPSS Statistics software (Version 22, IBM SPSS, Chicago, IL, USA) was used for statistical analysis. Mean values and standard errors of the mean (SEM) were calculated for quantitative data. All experiments were performed in triplicate and repeated at least twice. For statistical comparison of the groups, the t- and Mann-Whitney-U tests were applied. Differences between groups were considered significant at p < 0.05.
Effect of CTSS on wound healing
Influence of CTSS on migration
Actions of CTSS on proliferation and apoptosis
Involvement of cathepsins in TLR2 effects on wound closure
The present study investigated the effects of CTSS on PDL cell wound closure. Our findings provide original evidence that CTSS stimulates PDL cell proliferation and migration and, thereby, wound closure, suggesting that this cysteine protease might play a critical role in periodontal remodeling and healing. Moreover, TLR2 activation also accelerates the PDL cell wound closure and this stimulatory effect depends on cathepsins, suggesting that cathepsins might be exploited by periodontal bacteria to regulate critical PDL cell functions.
CTSS has been broadly implicated in health and pathology including autoimmune diseases, allergic inflammation and asthma, diabetes and obesity, cardiovascular and pulmonary diseases as well as cancer . CTSS is a lysosomal cysteine protease capable of degrading components of the extracellular matrix, such as collagen, elastin, fibronectin, laminin and proteoglycans, suggesting a pivotal role in tissue homeostasis and repair [11, 13, 14]. This assumption is further supported by the observation that CTSS promotes cell migration and, additionally, regulates osteoblast differentiation and bone remodeling [17, 18, 34]. The synthesis of CTSS by periodontal cells and its role in periodontal tissues has been neglected so far. Our previous experiments have provided novel evidence that PDL cells can produce this cysteine protease . Periodontal therapy results in wounding of the periodontal tissues and, subsequently, wound healing is initiated. Ideally, the healing is characterized by the restoration of the original tissue structure, form and function. However, periodontal regeneration requires appropriate PDL cell proliferation and migration. Therefore, in the present study, we sought to investigate possible actions of CTSS on PDL cells with a special focus on proliferation, migration and wound healing in vitro. The present experiments revealed that these cell functions are regulated by CTSS. The cysteine protease caused a significant upregulation of PCNA, a specific marker of proliferation, and proliferation, as assessed by an XTT assay. Moreover, our experiments showed that CTSS also increased the speed of PDL cell migration. Since both proliferation and migration determine the would fill rate, our observation that CTSS promotes wound healing is supported by these findings.
Gonzales et al. studied the gene expression in gingival biopsies from Rhesus monkeys and advocated a role for CTSS in periodontitis . Furthermore, CTSS was identified as a hub protein in the protein-protein interaction network of differentially expressed genes, also indicating an involvement of this protease in periodontal diseases . The results of our previous study which showed an increased production of CTSS by periodontal cells in response to inflammatory and infectious stimuli concur very well with these reports . However, the findings of the present study demonstrate that CTSS might not only play a role in periodontal tissue destruction but also healing.
Notably, exposure of PDL cell monolayers to the TLR2 agonist resulted in a significantly accelerated wound closure in our study. Further experiments revealed that the stimulation of the in vitro wound healing by the TLR2 agonist was dependent on cathepsins. Interestingly, inhibition of TLR2 has been shown to reduce the CTSS gene expression in human endothelial cells, supporting our data . Our observation is of major importance, because it links the experiments of this study with our previous findings . Moreover, since we used a TLR2 agonist and an unspecific cathepsin inhibitor, this result may have an even broader significance for the understanding of periodontal diseases, because periodontitis is not only caused by a single bacterium or mediated by a single member of the cathepsin family. Whether the increased wound closure in the presence of the TLR2 agonist, as observed in our experiments, might be an attempt of the cells to maintain tissue homeostasis, has to be clarified in further studies.
Cathepsin K (CTSK), another member of the cathepsin family, has also been associated with periodontal diseases [37, 38, 39]. Interestingly, CTSS has the ability to degrade CTSK, indicating complex interactions between both cathepsins . Further research should also focus on the role of CTSK in PDL cell proliferation, migration and wound closure.
Although not investigated in our study, the stimulatory effects of CTSS on cell migration and proliferation might involve TLR2-mediated p38/Akt signaling activation and histone deacetylase 6, as it has been disclosed in vascular smooth muscle cells by Wu and colleagues . Another study on macrophages suggests that CTSS promotes cell migration through degradation of elastic fiber integrity . Furthermore, CTSS might influence proliferation of PDL cells via peroxisome proliferator-activated receptor-gamma, as revealed in human umbilical vein endothelial cells . Further studies should focus on the mechanisms underlying the stimulatory effects of CTSS on wound healing in periodontal cells.
In the present study, CTSS was used at concentrations of 1 ng/μl, as used in our previous experiments and in studies by other investigators . Furthermore, we applied an established vitro wound healing model which is commonly used [27, 28, 29, 42, 43]. Nonetheless, the limitation of any in vitro model, including this one, is that it cannot fully mimic the plethora of actions and interactions of different cell and tissue types that take place in vivo . Our experiments focussed on PDL cells, which constitute a heterogenous cell population, because they are critical for both periodontal destruction and regeneration. By phenotyping the cells before our experiments, we confirmed their ability to differentiate into osteoblastic cells. But as no osteogenic medium was applied in the experiments, the cells acquired a fibroblastic phenotype. Future studies should also examine the actions of CTSS on other periodontal cells involved in periodontal homeostasis and repair. Moreover, in order to further explore the role of CTSS in a more complex environment, an experimental periodontitis model in CTSS knock-out mice might be helpful.
In summary, our study investigated the actions of CTSS on PDL cell wound closure. Our findings provide original evidence that cathepsin S stimulates PDL cell proliferation and migration and, thereby, wound closure, suggesting that this cysteine protease might play a critical role in periodontal remodeling and healing. In addition, cathepsins might be exploited by periodontal bacteria to regulate critical PDL cell functions.
The authors would like to thank Ms. Ramona Menden, Ms. Silke van Dyck, Ms. Inka Bay and Prof. Heiko Spallek for their valuable support.
This study was supported by the Medical Faculty of the University of Bonn, the University of Sydney, the German Orthodontic Society (DGKFO) and the German Research Foundation (DFG, ME 4798/1–1).
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
SM, CP, EB, WG, JC, AJ and JD made substantial contributions to conception and design. SM, MN, AN and JD substantially contributed to the acquisition of data. SM, AD, AP, BRD and JD substantially contributed to interpretation of data and analysis. SM, MN, AD, AN, AP, CP, EB, BRD, WG, JC, AJ and JD have been involved in drafting the manuscript or revising it critically for important intellectual content. SM, MN, AD, AN, AP, CP, EB, BRD, WG, JC, AJ and JD have given final approval of the version to be published. SM, MN, AD, AN, AP, CP, EB, BRD, WG, JC, AJ and JD agreed 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. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Approval of the Ethics Committee of the University of Bonn was obtained (#117/15). All donors of the PDL cells or their parents gave written informed consent.
Consent for publication
The authors declare that they have no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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