Different engagement of TLR 2 and TLR 4 in Porphyromonas gingivalis vs . ligature-induced periodontal bone loss

This study was conducted to investigate the roles of different Toll-like receptor (TLR) signaling in Porphyromonas gingivalis (P. gingivalis)-induced and ligature-induced experimental periodontal bone resorption in mice. Wild-type (WT), TLR2 knockout (KO), TLR4KO, and TLR2&4 KO mice with C57/BL6 background were divided into three groups: control, P. gingivalis infection, and ligation. Live P. gingivalis or silk ligatures were placed in the sulcus around maxillary second molars over a 2-week period. Images were captured by digital stereomicroscopy, and the bone resorption area was measured with ImageJ software. The protein expression level of gingival RANKL was measured by ELISA. The gingival mRNA levels of RANKL, IL-1β, TNF-α, and IL-10 were detected by RT-qPCR. The results showed that P. gingivalis induced significant periodontal bone resorption in WT mice and TLR2 KO mice but not in TLR4 KO mice or TLR2&4 KO mice. For all four types of mice, ligation induced significant bone loss compared with that in control groups, and this bone loss was significantly higher than that in the P. gingivalis infection group. RANKL protein expression was significantly increased in the ligation group compared with that in the control group for all four types of mice, and in the P. gingivalis infection group of WT, TLR2 KO, and TLR4 KO mice. Expression patterns of RANKL, IL-1β, TNF-α, and IL-10 mRNA were different in the P. gingivalis infection group and the ligation group in different types of mice. In summary, P. gingivalis-induced periodontal bone resorption is TLR4-dependent, whereas ligation-induced periodontal bone resorption is neither TLR2nor TLR4-dependent. Descriptors: Toll-Like Receptors; Bone Resorption; Periodontitis. Introduction Periodontal disease is one of the most common chronic diseases in humans and is induced by microbial pathogens that reside in the oral cavity.1,2 However, compelling evidence now indicates that periodontal disease is not only a conventional bacterial infectious disease but also an inflammatory disease triggered by the host immune response to microorganisms.3 In host immune response, innate immunity is considered to act as a sentinel for the immune system and is promptly activated after recognition of the diverse repertoire of microbial pathogens.4,5 Mei LIN(a) Yang HU(b) Yuhua WANG(c) Toshihisa KAWAI(b) Zuomin WANG(a) Xiaozhe HAN(b) (a) Beijing ChaoYang Hospital affiliated with Capital Medical University, Department of Stomatology, Beijing, China. (b) The Forsyth Institute, Department of Immunology and Infectious Diseases, Cambridge, MA, USA. (c) Ninth People’s Hospital, College of Stomatology, Shanghai JiaoTong University School of Medicine, Department of Prosthodontics, Shanghai Key Laboratory, Shanghai, China. Declaration of Interest: The authors certify that they have no commercial or associative interest that represents a conflict of interest in connection with the manuscript. Corresponding Author: Zuomin Wang E-mail: wzuomin@gmail.com https://doi.org/10.1590/1807-3107BOR-2017.vol31.0063 1 Braz. Oral Res. 2017;31:e63 Título resumido título resumido título resumido título resumido título resumido título resumido título resumido título resumido Toll-l ike receptors (TLRs) were the f i rst pat tern-recognit ion receptors (PRRs) to be identified and the best-characterized class of PRRs in mammalian species.6,7 Bacteria consist of various pathogen-associated molecular patterns (PAMP) that are detected by TLRs.7,8 Two members of the TLR family, TLR2 and TLR4, have been identified as the principal signaling receptors for bacterial cell wall components.9 TLR4 recognizes lipopolysaccharide (LPS) from Gram-negative bacteria.10,11 TLR2 recognizes a wide variety of PAMPs,12 such as lipoproteins13 and peptidoglycans (PGN),14 from both Gram-positive and -negative bacteria, as well as lipoteichoic acid from Gram-positive bacteria.15 Recently, the presence of TLR2 and TLR4 has been shown to be essential for the progression of periodontitis in animal models and human patients.16,17 However, the contributions of TLR2 and TLR4 to periodontitis induced by various antigens are still uncertain and complicated. Traditional methods of inducing experimental periodontitis include bacterial [Porphyromonas gingivalis (P. gingivalis) or Aggregatibacter actinomycetemcomitans (A.a.)] application, silk ligature, or a combination thereof.18,19 Animal models with both P. gingivalis-induced and ligature-induced experimental periodontitis are commonly used, but they have different mechanisms to induce periodontitis.20 P. gingivalis is a human-periodontitis-associated microbiome21,22 and ligatures will induce dysbiosis of the resident mouse microbiome to mimic dysbiosis of the human biofilm in periodontitis.18,23 Thus, the purpose of the present study was to compare the different roles of TLR2 and TLR4 in P. gingivalis-induced vs. ligature-induced experimental periodontitis mouse models. Methodology Animals Wild-type (WT) C57BL/6J mice were purchased from the Jackson Laboratory (Bar Harbor, USA). TLR2 Knock-out (KO) mice, TLR4 KO mice, and TLR2&4 KO mice with a C57BL/6 background were a gift from Dr. Kawai (The Forsyth Institute). All the mice used in the study were 8–10 weeks old and maintained in specific pathogen-free (SPF) units. The mice were kept on a 12-hour light/dark cycle. The experimental protocols were approved by the Institutional Animal Care and Use Committee of The Forsyth Institute. Bacterial culture P. gingivalis (strain ATCC 33277) was grown on anaerobic blood agar plates (NHK agar, Northeast Laboratory Services, Winslow, USA) in an anaerobic chamber with 85% N2, 5% H2, and 10% CO2. Bacterial numbers in culture medium were determined from optical density values read by spectrophotometry and compared with a curve derived from a standard plate count. After incubation at 37°C for 5 days, bacteria were collected, washed three times with sterile phosphate-buffered saline (PBS), and re-suspended in PBS at the concentration of 1×1010/mL. Experimental periodontitis C57BL/6J wild-type (WT), TLR2KO, TLR4KO, and TLR2&4KO mice were used for P. gingivalis-induced experimental periodontitis or ligature-induced experimental periodontitis. Kanamycin and ampicillin were added to the drinking water for 4 days, and the oral cavity was swabbed with a 0.12% chlorhexidine gluconate mouthrinse to suppress the native oral microbiota on the 4th day. After 24 h, experimental periodontitis was induced by the application of 10 μL of live P. gingivalis (1 x 1010/mL in PBS) in the sulcus of the maxillary second molars or by the wrapping of silk ligatures (7-0, Fisher Scientific, Waltham, USA) around maxillary second molars on both sides over a 2-week period. To enhance reproducibility for the P. gingivalis infection group, P. gingivalis was applied around the tooth for 4 consecutive days after initial infection. Sample preparation Animals were euthanized by CO2 inhalation 2 weeks after P. gingivalis infection or ligation. The maxillary teeth were removed from each group, and gingival tissues were isolated under a surgical microscope for homogenate. The maxillary teeth were then de-fleshed by a Dermestid beetle colony. After being bleached with 3% hydrogen peroxide, the bone was stained with 1% toluidine blue and mounted on microscope slides for bone resorption measurement. For each gingival tissue, half of the collected gingival tissues were subjected to RNA isolation to determine 2 Braz. Oral Res. 2017;31:e63 Autores abreviados autores abreviados autores abreviados autores abreviados autores abreviados autores abreviados cytokine expression by RT-qPCR. The other half were used to measure RANKL expression by ELISA. Measurements of bone resorption Images were captured by digital stereomicroscopy on a custom-made stage-holder with maxillary teeth at a certain angle (15 degree) to enhance visualization of the cementoenamel junction (CEJ) and alveolar bone level. The bone resorption area was enclosed by the second molar CEJ, the lateral margins of the first molars distal to the exposed root and the third molars mesial to the exposed root, and the alveolar crest and ridge. The polygonal area was measured with ImageJ software (NIH, Bethesda, USA) on buccal and palatal surfaces for each segment, and a standard calibrator was used for calibration at the same magnification. All bone resorption measurements were performed without the operator having prior knowledge of the group designation of the mice, and the recordings were verified by a second examiner. The results were presented in mm2. Real-time PCR Gingival RNA was extracted with TRIzole reagent (Sigma, St. Louis, USA) reverse-transcribed with SuperScr ipt II Reverse Transcr iptase (Invitrogen, Carlsbad, USA). The primer (Sigma) sequences were as follows: RANKL, forward 5'GGGTGTGTACA AGACCC3’ a nd r ever s e 5’-CATGTGCCACTGAGAACCTTGAA-3’; IL-1β, forward 5’-CCAGCTTCAAATCTCACAGCAG-3’ and reverse 5’-CTTCTTTGGGTATTGCTTGGGATC-3’; TNFα, forward 5’-CACAGAAAGCATGATCCGCGACGT-3’ and reverse 5’-CGGCAGAGAGGAGGTTGACTTTCT-3’; IL-10, forward 5’-GACCAGCTGGACAACATACTGCTAA-3’ and reverse 5’-GATAAGGCTTGGCAACCCAAGTAA-3’; GAPDH, forward 5’-CCCCAGCAAGGACACTGAGCAA-3’ and reverse 5’GTGGGTGCAGCGAACTTTATTGATG-. Real-time PCR was conducted with the LightCycler® SYBR Green master solution and LightCycler® 480 system (Roche, Indianapolis, USA). mRNA expression levels were presented as fold changes relative to the GAPDH reference. ELISA assay The gingival tissues collected were homogenized with a Dounce glass homogenizer in RIPA buffer and proteinase inhibitor cocktail (Sigma). The secreted RANKL level in the gingival homogenate was detected by means of a murine RANKL ELISA development kit (PeproTech, Rocky Hill, USA) following the manufacturer’s instructions. The absorbance values were read by means of a Synergy HT Microplate Reader (BioTek, Winooski, USA) at 450 nm, and RANKL concentrations were calculated accord


Introduction
Periodontal disease is one of the most common chronic diseases in humans and is induced by microbial pathogens that reside in the oral cavity. 1,2However, compelling evidence now indicates that periodontal disease is not only a conventional bacterial infectious disease but also an inflammatory disease triggered by the host immune response to microorganisms. 3In host immune response, innate immunity is considered to act as a sentinel for the immune system and is promptly activated after recognition of the diverse repertoire of microbial pathogens. 4,5i LIN (a) Yang HU (b) Yuhua WANG (c) Toshihisa KAWAI (b) Zuomin WANG (a) Xiaozhe HAN (b) (a) Beijing ChaoYang Hospital affiliated with Capital Medical University, Department of Stomatology, Beijing, China.
(b) The Forsyth Institute, Department of Immunology and Infectious Diseases, Cambridge, MA, USA.
(c) Ninth People's Hospital, College of Stomatology, Shanghai JiaoTong University School of Medicine, Department of Prosthodontics, Shanghai Key Laboratory, Shanghai, China.

Declaration of Interest:
The authors certify that they have no commercial or associative interest that represents a conflict of interest in connection with the manuscript.
Toll-like receptors (TLRs) were the first pat ter n-recog n it ion receptors (PRRs) to be identified and the best-characterized class of PRRs in mammalian species. 6,7Bacteria consist of various pathogen-associated molecular patterns (PAMP) that are detected by TLRs. 7,8Two members of the TLR family, TLR2 and TLR4, have been identified as the principal signaling receptors for bacterial cell wall components. 9TLR4 recognizes lipopolysaccharide (LPS) from Gram-negative bacteria. 10,11TLR2 recognizes a wide variety of PAMPs, 12 such as lipoproteins 13 and peptidoglycans (PGN), 14 from both Gram-positive and -negative bacteria, as well as lipoteichoic acid from Gram-positive bacteria. 15Recently, the presence of TLR2 and TLR4 has been shown to be essential for the progression of periodontitis in animal models and human patients. 16,17However, the contributions of TLR2 and TLR4 to periodontitis induced by various antigens are still uncertain and complicated.
Traditional methods of inducing experimental periodontitis include bacterial [Porphyromonas gingivalis (P.gingivalis) or Aggregatibacter actinomycetemcomitans (A.a.)] application, silk ligature, or a combination thereof. 18,19Animal models with both P. gingivalis-induced and ligature-induced experimental periodontitis are commonly used, but they have different mechanisms to induce periodontitis. 20P. gingivalis is a human-periodontitis-associated microbiome 21,22 and ligatures will induce dysbiosis of the resident mouse microbiome to mimic dysbiosis of the human biofilm in periodontitis. 18,23Thus, the purpose of the present study was to compare the different roles of TLR2 and TLR4 in P. gingivalis-induced vs. ligature-induced experimental periodontitis mouse models.

Methodology Animals
Wild-type (WT) C57BL/6J mice were purchased from the Jackson Laboratory (Bar Harbor, USA).TLR2 Knock-out (KO) mice, TLR4 KO mice, and TLR2&4 KO mice with a C57BL/6 background were a gift from Dr. Kawai (The Forsyth Institute).All the mice used in the study were 8-10 weeks old and maintained in specific pathogen-free (SPF) units.The mice were kept on a 12-hour light/dark cycle.The experimental protocols were approved by the Institutional Animal Care and Use Committee of The Forsyth Institute.

Bacterial culture
P. gingivalis (strain ATCC 33277) was grown on anaerobic blood agar plates (NHK agar, Northeast Laboratory Services, Winslow, USA) in an anaerobic chamber with 85% N 2 , 5% H 2 , and 10% CO 2 .Bacterial numbers in culture medium were determined from optical density values read by spectrophotometry and compared with a curve derived from a standard plate count.After incubation at 37°C for 5 days, bacteria were collected, washed three times with sterile phosphate-buffered saline (PBS), and re-suspended in PBS at the concentration of 1×10 10 /mL.

Experimental periodontitis
C57BL/6J wild-type (WT), TLR2KO, TLR4KO, and TLR2&4KO mice were used for P. gingivalis-induced experimental periodontitis or ligature-induced experimental periodontitis.Kanamycin and ampicillin were added to the drinking water for 4 days, and the oral cavity was swabbed with a 0.12% chlorhexidine gluconate mouthrinse to suppress the native oral microbiota on the 4th day.After 24 h, experimental periodontitis was induced by the application of 10 μL of live P. gingivalis (1 x 10 10 /mL in PBS) in the sulcus of the maxillary second molars or by the wrapping of silk ligatures (7-0, Fisher Scientific, Waltham, USA) around maxillary second molars on both sides over a 2-week period.To enhance reproducibility for the P. gingivalis infection group, P. gingivalis was applied around the tooth for 4 consecutive days after initial infection.

Sample preparation
Animals were euthanized by CO 2 inhalation 2 weeks after P. gingivalis infection or ligation.The maxillary teeth were removed from each group, and gingival tissues were isolated under a surgical microscope for homogenate.The maxillary teeth were then de-fleshed by a Dermestid beetle colony.After being bleached with 3% hydrogen peroxide, the bone was stained with 1% toluidine blue and mounted on microscope slides for bone resorption measurement.For each gingival tissue, half of the collected gingival tissues were subjected to RNA isolation to determine cytokine expression by RT-qPCR.The other half were used to measure RANKL expression by ELISA.

Measurements of bone resorption
Images were captured by digital stereomicroscopy on a custom-made stage-holder with maxillary teeth at a certain angle (15 degree) to enhance visualization of the cementoenamel junction (CEJ) and alveolar bone level.The bone resorption area was enclosed by the second molar CEJ, the lateral margins of the first molars distal to the exposed root and the third molars mesial to the exposed root, and the alveolar crest and ridge.The polygonal area was measured with ImageJ software (NIH, Bethesda, USA) on buccal and palatal surfaces for each segment, and a standard calibrator was used for calibration at the same magnification.All bone resorption measurements were performed without the operator having prior knowledge of the group designation of the mice, and the recordings were verified by a second examiner.The results were presented in mm 2 .

ELISA assay
The gingival tissues collected were homogenized with a Dounce glass homogenizer in RIPA buffer and proteinase inhibitor cocktail (Sigma).The secreted RANKL level in the gingival homogenate was detected by means of a murine RANKL ELISA development kit (PeproTech, Rocky Hill, USA) following the manufacturer's instructions.The absorbance values were read by means of a Synergy HT Microplate Reader (BioTek, Winooski, USA) at 450 nm, and RANKL concentrations were calculated according to the standard curve.

Statistical analysis
All the quantitative data were expressed as means ± standard error.Statistical analysis was performed by Student's t-test for comparisons of two groups and by nonparametric ANOVA (Kruskal-Wallis test) with post hoc adjustments for multiple comparisons.Statistical significance was set at p < 0.05.

Results
Bone resorption differences of P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice Experimental periodontitis was induced by the application of P. gingivalis in the sulcus of the maxillary second molars or by silk ligatures wrapped around maxillary second molars on both sides for 14 days in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.Images of the palatal surfaces of maxillae were captured (Figure 1), and bone loss in the polygonal area around maxillary second molars was measured with ImageJ software.The P. gingivalis infection group showed significantly higher bone loss compared with the control group for WT mice (Figure 2A) and TLR2 KO mice (Figure 2B), but there were no significant differences in TLR4 KO mice (Figure 2C) and TLR2&4 KO mice (Figure 2D).However, the ligation group revealed significantly higher bone loss in all four types of mice compared with the control group (Figure 2A-D).Taken together, bone loss induced by P. gingivalis showed a TLR4-dependence, and bone loss induced by ligation was TLR2-and TLR4-independent and significantly higher than in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO control mice.
RANKL mRNA and protein expression differences of P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice For investigation of the molecular mechanism of bone resorption in P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice, gingival RANKL mRNA levels and protein expression levels were measured by RT-qPCR and ELISA, respectively.For RANKL mRNA, the P. gingivalis infection group showed significantly higher levels compared with the control group for TLR4  KO mice (Figure 3C), with no significant differences in WT mice (Figure 3A), TLR2 KO mice (Figure 3B), and TLR2&4 KO mice (Figure 3D).The ligation group showed significantly higher levels compared with the control group for WT mice (Figure 3A) and TLR4 KO mice (Figure 3C), with no significant differences in TLR2 KO mice (Figure 3B) and TLR2&4 KO mice (Figure 3D).For gingivally secreted RANKL, the P. gingivalis infection group showed significantly higher expression compared with the control group for WT mice (Figure 3E), TLR2 KO mice (Figure 3F), and TLR4 KO mice (Figure 3G), with no significant differences in TLR2&4 KO mice (Figure 3H).However, the ligation group showed significantly higher expression compared with the control group in all four types of mice (Figure 3E-H).These results indicated that increased RANKL mRNA and protein expression induced by P. gingivalis was diminished when both TLR2 and TLR4 were lacking, suggesting that TLR2 was also involved in the regulation of RANKL-mediated bone loss in the P. gingivalis-induced experimental periodontitis model.Moreover, the ligation-induced increase of RANKL protein expression was TLR2-and TLR4-independent.
IL-1β, TNF-α, and IL-10 mRNA differences in P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice For comparison of the effects of TLR2 and TLR4 on inflammation in P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice, mRNA levels of the pro-inflammatory cytokines IL-1β and TNF-α and the anti-inflammatory cytokine IL-10 were measured by RT-qPCR.For IL-1β mRNA, the P. gingivalis infection group showed no significant differences compared with the control group for WT mice (Figure 4A), TLR2 KO mice (Figure 4B), TLR4 KO mice (Figure 4C), and TLR2&4 KO mice (Figure 4D).The ligation group showed significantly higher levels of IL-1β expression compared with the control group in all four types of mice (Figure 4A-D).For TNF-α mRNA, both the P. gingivalis infection group and the ligation group showed no significant differences compared with the control group for WT mice (Figure 4E), TLR2 KO mice (Figure 4F), TLR4 KO   4G), and TLR2&4 KO mice (Figure 4H).For IL-10 mRNA, the P. gingivalis infection group showed significantly higher levels compared with the control group for WT mice (Figure 4I), and no differences for TLR2 KO mice (Figure 4J), TLR4 KO mice (Figure 4K), and TLR2&4 KO mice (Figure 4L).The ligation group showed no significant differences compared with the control group for WT, TLR2 KO, and TLR4 KO mice (Figure 4I-K) but showed significantly lower levels in TLR2&4 KO mice (Figure 4L).These results indicated that P. gingivalis infection-induced and ligation-induced experimental periodontitis showed differential regulation of gingival IL-1β and IL-10 expression through TLR2/4 signaling.

Discussion
The Toll-like receptor (TLR) family of innate immune recognition receptors plays a fundamental role in the induction of innate immunity, inflammation, cell survival, and proliferation. 24,25The presence of TLR2 and TLR4 has been shown to be essential for the progression of inflammation and related bone metabolism in periodontitis. 16,26However, little is known about the specific contributions of TLR2 and TLR4 signaling in different models of experimental periodontitis in mice.In the present study, we investigated the changes in bone resorption, RANKL (bone resorption marker) mRNA and protein levels, IL-1β, TNF-α (pro-inflammatory marker), and IL-10 (anti-inflammatory marker) mRNA levels in P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.The results showed that P. gingivalis-induced periodontal bone resorption is TLR4-dependent, whereas ligation-induced periodontal bone resorption is neither TLR2-nor TLR4-dependent.Also, TLR2 and TLR4 signaling plays different roles in gingival IL-1β, TNF-α, and IL-10 expression in P. gingivalis-induced and ligation-induced experimental periodontitis.
P. gingivalis-induced periodontitis is mediated by the disruption of the host tissue homeostasis and adaptive immune response. 27,28In the present study, P. gingivalis infection showed significant increases in periodontal bone resorption in WT mice and TLR2 KO mice but not in TLR4 KO mice and TLR2&4 KO mice (Figure 2A-D), suggesting that TLR4 is essential for bone loss associated with P. gingivalis infection.However, RANKL protein levels were significantly higher in the P. gingivalis infection group in TLR4 KO mice (Figure 3G) and showed no significant change in TLR2&4 KO mice (Figure 3H), indicating that not only TLR4 signaling but also TLR2 signaling is involved in the RANKL-mediated bone loss.Moreover, there could be cross-talk between TLR4 and TLR2 signaling to fully regulate periodontal bone resorption in P. gingivalis-induced periodontitis.These possible mechanisms need to be investigated in the future.
Ligature-induced periodontitis disrupts the resident mouse microbiome and mimics dysbiosis of the human biofilm in periodontitis. 18,23,29,30Analysis of our data showed that ligation-induced bone loss was observed in all types of mice tested, including WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice (Figure 2A-D).Analysis further suggested that ligation-induced periodontal bone loss is neither TLR2-nor TLR4-dependent.Other TLRor non-TLR-related pathways are also involved in the pathogenesis of ligation-induced bone loss.Moreover, IL-1β mRNA levels were consistently elevated in the ligation groups compared with the control groups in all types of mice (Figure 4A-D), suggesting that the TLR-independent pathways activated in ligation-induced bone loss are mediated through the up-regulation of IL-1β.Also, analysis of our data showed that, in the presence of both TLR2 and TLR4 deficiency, the ligation group still demonstrated significantly increased bone loss and in f lammatory cytokine expression compared with the control group (Figures 2D,  3H, 4D), further suggesting that TLR-independent pathways may be involved in the ligation-induced experimental periodontitis that regulates bone loss and inflammation.Taken together, for investigations focused on periodontal bone loss and inflammation, the ligation-induced experimental periodontitis mouse model may represent a broader spectrum of pathogenesis than the P. gingivalis infection mouse model, and results derived from these two models should be compared and interpreted with caution.

Conclusion
In summary, TLR2 and TLR4 signaling contributes differently to mouse models of P. gingivalis-induced and ligature-induced experimental periodontitis.P. gingivalis-induced periodontal bone resorption is TLR4-dependent, whereas ligation-induced periodontal bone resorption is neither TLR2-nor TLR4-dependent.

Figure 1 .
Figure1.Maxillary images of P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.Experimental periodontitis was induced by the application of live P. gingivalis in the sulcus of maxillary second molars or by silk ligatures wrapped around maxillary second molars on both sides over a 14-day period in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.Maxillae were collected on day 14 and de-fleshed by a Dermestid beetle colony.After being bleached with 3% hydrogen peroxide, the bone was stained with 1% toluidine blue.The alveolar bone resorption areas around maxillary secondary molars were viewed by microscopy (30X) for the control group, the P. gingivalis infection group, and the ligation group of WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice, respectively (scale bar, 1 mm).

Figure 2 .
Figure 2. Bone resorption analysis of P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.The bone resorption area of P. gingivalis-induced and ligation-induced experimental periodontitis was measured and analyzed with ImageJ software on buccal and palatal surfaces in WT mice (A), TLR2 KO mice (B), TLR4 KO mice (C), and TLR2&4 KO mice (D) (means ± SE, n = 5 mice per group, **p < 0.01, N.S. = no significant difference).For each segment, a standard calibrator was used for calibration at the same magnification for all images.

Figure 3 .Figure 4 .
Figure 3. Gingival RANKL mRNA and protein expression levels of P. gingivalis-induced and ligation-induced experimental periodontitis in WT, TLR2 KO, TLR4 KO, and TLR2&4 KO mice.Gingival tissues on the palatal side were collected under a surgical microscope from maxillae and then homogenized for RNA extraction or protein measurement.Gingival RANKL mRNA levels were determined by real-time PCR in the control group, the P. gingivalis infection group, and the ligation group of WT mice (A), TLR2 KO mice (B), TLR4 KO mice (C), and TLR2&4 KO mice (D) (means ± SE, n = 5 mice per group, *p < 0.05, **p < 0.01).Gingival RANKL protein expression levels were measured by ELISA in the control group, the P. gingivalis infection group, and the ligation group of WT mice (E), TLR2 KO mice (F), TLR4 KO mice (G), and TLR2&4 KO mice (H) (means ± SE, n = 5 mice per group, *p < 0.05, **p < 0.01).