
Temporal and spatial expression analysis of periostin in mice periodontitis model
Li Yue, Xu Chunmei, Xie Xudong, Shi Peilei, Wang Jun, Ding Yi
Temporal and spatial expression analysis of periostin in mice periodontitis model
Objective This study aimed to investigate the temporal and spatial changes in the expression of periostin during periodontal inflammation in mice. Methods A periodontitis model was constructed using silk thread ligation. Mice were randomly divided into five groups including control group, 4-day ligation group, 7-day ligation group, 14-day ligation group, and self-healing group (thread removal for 14 days after 14-day ligation). Micro-CT and histological staining were performed to characterize the dynamic changes in the mouse periodontal tissue in each group. RNAscope and immunohistochemical staining were used to analyze the pattern of changes in periostin at various stages of periodontitis. The cell experiment was divided into three groups: control group, lipopolysaccharide (LPS) stimulation group (treated with LPS for 12 h), and LPS stimulation removal group (treated with LPS for 3 h followed by incubation with medium for 9 h). Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the expression of periostin, transforming growth factor-β1 (TGF-β1), and matrix metalloproteinase 2 (MMP2). Results Significant alveolar bone resorption was observed 7 days after ligation. With increasing duration of ligation, the damage to the mouse periodontal tissue was aggravated, which manifested as increased osteoclasts, widening of the periodontal membrane space, and decreased alveolar bone height. Some degree of periodontal tissue repair was observed in the self-healing group. Periostin expression decreased at 4 and 7 days compared with the control group and increased at 14 days compared with 4 and 7 days. A significant recovery was found in the self-healing group. The qRT-PCR results showed that the expression of periostin and TGF-β1 in the LPS stimulation group decreased compared with that in the control group but significantly recovered in the LPS removal group. Conclusion Periostin expression in the PDL of mice showed a downward and upward trend with inflammation progression. The significant recovery of periostin expression after removing inflammatory stimuli may be related to TGF-β1, which is crucial to maintain the integrity of the PDL.
periodontitis / periostin / periodontal regeneration / alveolar bone / animal model
R781.4
1 | Slots J. Periodontitis: facts, fallacies and the future[J]. Periodontol 2000, 2017, 75(1): 7-23. |
2 | Chien WC, Fu E, Chung CH, et al. Type 2 diabetes mellitus and periodontitis: bidirectional association in population-based 15-year retrospective cohorts[J]. J Clin Endocrinol Metab, 2023, 108(11): e1289-e1297. |
3 | Sun J, Guo G. Association between atherogenic index of plasma and periodontitis among US adults[J]. BMC Oral Health, 2023, 23(1): 166. |
4 | Lazar L, Dako T, Bortoc R, et al. Periostin as a marker of periodontal status. A narrative review[J]. Romanian J Oral Rehabil, 2022, 14(4): 228-238. |
5 | Sophia K, Suresh S, Sudhakar U, et al. Comparative eva-luation of serum and gingival crevicular fluid periostin levels in periodontal health and disease: a biochemical study[J]. Cureus, 2020, 12(3): e7218. |
6 | Arslan R, Karsiyaka Hendek M, Kisa U, et al. The effect of non-surgical periodontal treatment on gingival crevicular fluid periostin levels in patients with gingivitis and periodontitis[J]. Oral Dis, 2021, 27(6): 1478-1486. |
7 | Kii I, Ito H. Periostin and its interacting proteins in the construction of extracellular architectures[J]. Cell Mol Life Sci, 2017, 74(23): 4269-4277. |
8 | Du J, Li M. Functions of Periostin in dental tissues and its role in periodontal tissues’ regeneration[J]. Cell Mol Life Sci, 2017, 74(23): 4279-4286. |
9 | Padial-Molina M, Volk SL, Rios HF. Periostin increases migration and proliferation of human periodontal ligament fibroblasts challenged by tumor necrosis factor-α and Porphyromonas gingivalis lipopolysaccharides[J]. J Periodontal Res, 2014, 49(3): 405-414. |
10 | Wu Z, Dai W, Wang P, et al. Periostin promotes migration, proliferation, and differentiation of human perio-dontal ligament mesenchymal stem cells[J]. Connect Tissue Res, 2018, 59(2): 108-119. |
11 | Yan Y, Zhang H, Liu L, et al. Periostin reverses high glucose-inhibited osteogenesis of periodontal ligament stem cells via AKT pathway[J]. Life Sci, 2020, 242: 117184. |
12 | Ma D, Zhang R, Sun Y, et al. A novel role of periostin in postnatal tooth formation and mineralization[J]. J Biol Chem, 2011, 286(6): 4302-4309. |
13 | Rios H, Koushik SV, Wang H, et al. Periostin null mice exhibit dwarfism, incisor enamel defects, and an early-onset periodontal disease-like phenotype[J]. Mol Cell Biol, 2005, 25(24): 11131-11144. |
14 | Rios HF, Ma D, Xie Y, et al. Periostin is essential for the integrity and function of the periodontal ligament during occlusal loading in mice[J]. J Periodontol, 2008, 79(8): 1480-1490. |
15 | Rangiani A, Jing Y, Ren YS, et al. Critical roles of periostin in the process of orthodontic tooth movement[J]. Eur J Orthod, 2015, 38(4): 373-378. |
16 | Balli U, Keles ZP, Avci B, et al. Assessment of periostin levels in serum and gingival crevicular fluid of patients with periodontal disease[J]. J Periodontal Res, 2015, 50(6): 707-713. |
17 | Padial-Molina M, Volk SL, Taut AD, et al. Periostin is down-regulated during periodontal inflammation[J]. J Dent Res, 2012, 91(11): 1078-1084. |
18 | Tang HN, Xia Y, Yu Y, et al. Stem cells derived from “inflamed” and healthy periodontal ligament tissues and their sheet functionalities: a patient-matched comparison[J]. J Clin Periodontol, 2016, 43(1): 72-84. |
19 | Jolly S, Lang V, Koelzer VH, et al. Single-cell quantification of mRNA expression in the human brain[J]. Sci Rep, 2019, 9(1): 12353. |
20 | Socransky SS, Haffajee AD, Goodson JM, et al. New concepts of destructive periodontal disease[J]. J Clin Pe-riodontol, 1984, 11(1): 21-32. |
21 | Daines SM, Wang Y, Orlandi RR. Periostin and osteopontin are overexpressed in chronically inflamed sinuses[J]. Int Forum Allergy Rhinol, 2011, 1(2): 101-105. |
22 | Uchida M, Shiraishi H, Ohta S, et al. Periostin, a matricellular protein, plays a role in the induction of chemokines in pulmonary fibrosis[J]. Am J Respir Cell Mol Biol, 2012, 46(5): 677-686. |
23 | Kii I, Amizuka N, Minqi L, et al. Periostin is an extracellular matrix protein required for eruption of incisors in mice[J]. Biochem Biophys Res Commun, 2006, 342(3): 766-772. |
24 | Tabata C, Hongo H, Sasaki M, et al. Altered distribution of extracellular matrix proteins in the periodontal ligament of periostin-deficient mice[J]. Histol Histopathol, 2014, 29(6): 731-742. |
25 | Suzuki H, Amizuka N, Kii I, et al. Immunohistochemical localization of periostin in tooth and its surrounding tissues in mouse mandibles during development[J]. Anat Rec A Discov Mol Cell Evol Biol, 2004, 281(2): 1264-1275. |
26 | Afanador E, Yokozeki M, Oba Y, et al. Messenger RNA expression of periostin and Twist transiently decrease by occlusal hypofunction in mouse periodontal ligament[J]. Arch Oral Biol, 2005, 50(12): 1023-1031. |
27 | Park CH, Rios HF, Jin Q, et al. Tissue engineering bone-ligament complexes using fiber-guiding scaffolds[J]. Bio-materials, 2012, 33(1): 137-145. |
28 | Jiang Y, Yang P, Li C, et al. Periostin regulates LPS-induced apoptosis via Nrf2/HO-1 pathway in periodontal li-gament fibroblasts[J]. Oral Dis, 2023, 29(5): 2188-2204. |
29 | Lodyga M, Hinz B. TGF?β1—A truly transforming grow-th factor in fibrosis and immunity[J]. Semin Cell Dev Biol, 2020, 101: 123-139. |
30 | Moreau JM, Velegraki M, Bolyard C, et al. Transforming growth factor-β1 in regulatory T cell biology[J]. Sci Immunol, 2022, 7(69): eabi4613. |
31 | Wei Q, Liu D, Chu G, et al. TGF-β1-supplemented decellularized annulus fibrosus matrix hydrogels promote annulus fibrosus repair[J]. Bioact Mater, 2022, 19: 581-593. |
32 | Khurshid Z, Mali M, Adanir N, et al. Periostin: immunomodulatory effects on oral diseases[J]. Eur J Dent, 2020, 14(3): 462-466. |
33 | Yin SL, Qin ZL, Yang X. Role of periostin in skin wound healing and pathologic scar formation[J]. Chin Med J (Engl), 2020, 133(18): 2236-2238. |
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