Calcitonin gene-related peptide regulates periodontal tissue regeneration.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
16 Jan 2024
Historique:
received: 30 06 2023
accepted: 12 01 2024
medline: 17 1 2024
pubmed: 17 1 2024
entrez: 16 1 2024
Statut: epublish

Résumé

Calcitonin gene-related peptide (CGRP), a neuropeptide composed of 37 amino acids secreted from the sensory nerve endings, reportedly possesses various physiological effects, such as vasodilation and neurotransmission. Recently, there have been increasing reports of the involvement of CGRP in bone metabolism; however, its specific role in the pathogenesis of periodontitis, particularly in the repair and healing processes, remains to be elucidated. Therefore, this study aimed to investigate dynamic expression patterns of CGRP during the destruction and regeneration processes of periodontal tissues in a mouse model of experimental periodontitis. We also explored the effects of CGRP on periodontal ligament cells, which can differentiate to hard tissue-forming cells (cementoblasts or osteoblasts). Our findings demonstrated that CGRP stimulation promotes the differentiation of periodontal ligament cells into hard tissue-forming cells. Experimental results using a ligature-induced periodontitis mouse model also suggested fluctuations in CGRP expression during periodontal tissue healing, underscoring the vital role of CGRP signaling in alveolar bone recovery. The study results highlight the important role of nerves in the periodontal ligament not only in sensory reception in the periphery, as previously known, but also in periodontal tissue homeostasis and tissue repair processes.

Identifiants

pubmed: 38228723
doi: 10.1038/s41598-024-52029-z
pii: 10.1038/s41598-024-52029-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1344

Subventions

Organisme : Grants-in-Aid for Scientific Research by the Japan Society for the Promotion of Science
ID : 19K10127
Organisme : Grants-in-Aid for Scientific Research by the Japan Society for the Promotion of Science
ID : 22K21059

Informations de copyright

© 2024. The Author(s).

Références

Beertsen, W., McCulloch, C. A. & Sodek, J. The periodontal ligament: A unique, multifunctional connective tissue. Periodontology 13, 20–40 (1997).
doi: 10.1111/j.1600-0757.1997.tb00094.x
Seo, B. M. et al. Investigation of multipotent postnatal stem cells from human periodontal ligament. Lancet 364, 149–155 (2004).
pubmed: 15246727 doi: 10.1016/S0140-6736(04)16627-0
Lekic, P. & McCulloch, C. A. Periodontal ligament cell population: The central role of fibroblasts in creating a unique tissue. Anat. Rec. 245, 327–341 (1996).
pubmed: 8769671 doi: 10.1002/(SICI)1097-0185(199606)245:2<327::AID-AR15>3.0.CO;2-R
Lekic, P. C., Rajshankar, D., Chen, H., Tenenbaum, H. & McCulloch, C. A. Transplantation of labeled periodontal ligament cells promotes regeneration of alveolar bone. Anat. Rec. 262, 193–202 (2001).
pubmed: 11169914 doi: 10.1002/1097-0185(20010201)262:2<193::AID-AR1028>3.0.CO;2-7
Grant, D. & Bernick, S. The periodontium of aging humans. J. Periodontol. 43, 660–667 (1972).
pubmed: 4508345 doi: 10.1902/jop.1972.43.11.660
Severson, J. A., Moffett, B. C., Kokich, V. & Selipsky, H. A histologic study of age changes in the adult human periodontal joint (ligament). J. Periodontol. 49, 189–200 (1978).
pubmed: 276603 doi: 10.1902/jop.1978.49.4.189
Jung, H., Horiuchi, M. & Soma, K. Changes in the distribution of nerve fibers immunoreactive to calcitonin gene-related peptide according to growth and aging in rat molar periodontal ligament. Angle Orthod. 80, 309–315 (2010).
pubmed: 19905856 pmcid: 8973216 doi: 10.2319/040109-185.1
Maeda, T., Ochi, K., Nakakura-Ohshima, K., Youn, S. H. & Wakisaka, S. The Ruffini ending as the primary mechanoreceptor in the periodontal ligament: Its morphology, cytochemical features, regeneration, and development. Crit. Rev. Oral Biol. Med. 10, 307–327 (1999).
pubmed: 10759411 doi: 10.1177/10454411990100030401
Kato, J., Wakisaka, S. & Kurisu, K. Immunohistochemical changes in the distribution of nerve fibers in the periodontal ligament during an experimental tooth movement of the rat molar. Acta Anat. (Basel) 157, 53–62 (1996).
pubmed: 9096742 doi: 10.1159/000147866
Maggi, C. A. Tachykinins and calcitonin gene-related peptide (CGRP) as co-transmitters released from peripheral endings of sensory nerves. Prog. Neurobiol. 45, 1–98 (1995).
pubmed: 7716258 doi: 10.1016/0301-0082(94)E0017-B
Rosenfeld, M. G. et al. Production of a novel neuropeptide encoded by the calcitonin gene via tissue-specific RNA processing. Nature 304, 129–135 (1983).
pubmed: 6346105 doi: 10.1038/304129a0
Donnerer, J. & Stein, C. Evidence for an increase in the release of CGRP from sensory nerves during inflammation. Ann. N. Y. Acad. Sci. 657, 505–506 (1992).
pubmed: 1379022 doi: 10.1111/j.1749-6632.1992.tb22814.x
Kato, J. et al. Distribution of calcitonin gene-related peptide and substance P-immunoreactive nerve fibers and their correlation in the periodontal ligament of the mouse incisor. Acta Anat. (Basel) 145, 101–105 (1992).
pubmed: 1279925 doi: 10.1159/000147349
Kato, J. et al. The distribution of vasoactive intestinal polypeptides and calcitonin gene-related peptide in the periodontal ligament of mouse molar teeth. Arch. Oral Biol. 35, 63–66 (1990).
pubmed: 2202278 doi: 10.1016/0003-9969(90)90116-R
Kvinnsland, I. & Kvinnsland, S. Changes in CGRP-immunoreactive nerve fibres during experimental tooth movement in rats. Eur. J. Orthod. 12, 320–329 (1990).
pubmed: 2205509 doi: 10.1093/ejo/12.3.320
Norevall, L. I., Forsgren, S. & Matsson, L. Expression of neuropeptides (CGRP, substance P) during and after orthodontic tooth movement in the rat. Eur. J. Orthod. 17, 311–325 (1995).
pubmed: 8521925 doi: 10.1093/ejo/17.4.311
Zhang, Y. et al. Implant-derived magnesium induces local neuronal production of CGRP to improve bone-fracture healing in rats. Nat. Med. 22, 1160–1169 (2016).
pubmed: 27571347 pmcid: 5293535 doi: 10.1038/nm.4162
Appelt, J. et al. The neuropeptide calcitonin gene-related peptide alpha is essential for bone healing. EBiomedicine 59, 102970 (2020).
pubmed: 32853990 pmcid: 7452713 doi: 10.1016/j.ebiom.2020.102970
He, H. et al. CGRP may regulate bone metabolism through stimulating osteoblast differentiation and inhibiting osteoclast formation. Mol. Med. Rep. 13, 3977–3984 (2016).
pubmed: 27035229 doi: 10.3892/mmr.2016.5023
Wang, L. et al. Calcitonin-gene-related peptide stimulates stromal cell osteogenic differentiation and inhibits RANKL induced NF-kappaB activation, osteoclastogenesis and bone resorption. Bone 46, 1369–1379 (2010).
pubmed: 19962460 doi: 10.1016/j.bone.2009.11.029
Zhou, R., Yuan, Z., Liu, J. & Liu, J. Calcitonin gene-related peptide promotes the expression of osteoblastic genes and activates the WNT signal transduction pathway in bone marrow stromal stem cells. Mol. Med. Rep. 13, 4689–4696 (2016).
pubmed: 27082317 pmcid: 4878536 doi: 10.3892/mmr.2016.5117
Hendrikse, E. R. et al. Characterization of antibodies against receptor activity-modifying protein 1 (RAMP1): A cautionary tale. Int. J. Mol. Sci. 23, 16035 (2022).
pubmed: 36555690 pmcid: 9787598 doi: 10.3390/ijms232416035
Nishio, Y. et al. Runx2-mediated regulation of the zinc finger Osterix/Sp7 gene. Gene 372, 62–70 (2006).
pubmed: 16574347 doi: 10.1016/j.gene.2005.12.022
Koga, T. et al. NFAT and Osterix cooperatively regulate bone formation. Nat. Med. 11, 880–885 (2005).
pubmed: 16041384 doi: 10.1038/nm1270
Komori, T. Signaling networks in RUNX2-dependent bone development. J. Cell. Biochem. 112, 750–755 (2011).
pubmed: 21328448 doi: 10.1002/jcb.22994
Mayr, B. & Montminy, M. Transcriptional regulation by the phosphorylation-dependent factor CREB. Nat. Rev. Mol. Cell Biol. 2, 599–609 (2001).
pubmed: 11483993 doi: 10.1038/35085068
Tian, G., Zhang, G. & Tan, Y. H. Calcitonin gene-related peptide stimulates BMP-2 expression and the differentiation of human osteoblast-like cells in vitro. Acta Pharmacol. Sin. 34, 1467–1474 (2013).
pubmed: 23708553 pmcid: 4006471 doi: 10.1038/aps.2013.41
Mrak, E. et al. Calcitonin gene-related peptide (CGRP) inhibits apoptosis in human osteoblasts by β-catenin stabilization. J. Cell. Physiol. 225, 701–708 (2010).
pubmed: 20533307 doi: 10.1002/jcp.22266
Schifter, S. Circulating concentrations of calcitonin gene-related peptide (CGRP) in normal man determined with a new, highly sensitive radioimmunoassay. Peptides 12, 365–369 (1991).
pubmed: 2067988 doi: 10.1016/0196-9781(91)90027-M
Brain, S. D., Williams, T. J., Tippins, J. R., Morris, H. R. & MacIntyre, I. Calcitonin gene-related peptide is a potent vasodilator. Nature 313, 54–56 (1985).
pubmed: 3917554 doi: 10.1038/313054a0
Brain, S. D., Tippins, J. R., Morris, H. R., MacIntyre, I. & Williams, T. J. Potent vasodilator activity of calcitonin gene-related peptide in human skin. J. Investig. Dermatol. 87, 533–536 (1986).
pubmed: 2428885 doi: 10.1111/1523-1747.ep12455620
Jiang, Z. G. & Smith, R. A. Regulation by nerve growth factor of neuropeptide phenotypes in primary cultured sensory neurons prepared from aged as well as adult mice. Brain Res. Dev. Brain Res. 90, 190–193 (1995).
pubmed: 8719344 doi: 10.1016/0165-3806(96)83501-2
Nagao, S. et al. Expression of neuropeptide receptor mRNA during osteoblastic differentiation of mouse iPS cells. Neuropeptides 48, 399–406 (2014).
pubmed: 25464890 doi: 10.1016/j.npep.2014.10.004
Tsujikawa, K. et al. Hypertension and dysregulated proinflammatory cytokine production in receptor activity-modifying protein 1-deficient mice. Proc. Natl Acad. Sci. USA 104, 16702–16707 (2007).
pubmed: 17923674 pmcid: 2034234 doi: 10.1073/pnas.0705974104
Mikami, N. et al. Calcitonin gene-related peptide regulates type IV hypersensitivity through dendritic cell functions. PLoS One 9, e86367 (2014).
pubmed: 24466057 pmcid: 3897726 doi: 10.1371/journal.pone.0086367
Schinke, T. et al. Decreased bone formation and osteopenia in mice lacking alpha-calcitonin gene-related peptide. J. Bone Miner. Res. 19, 2049–2056 (2004).
pubmed: 15537449 doi: 10.1359/jbmr.040915
Vandevska-Radunovic, V., Kvinnsland, S. & Kvinnsland, I. H. Effect of experimental tooth movement on nerve fibres immunoreactive to calcitonin gene-related peptide, protein gene product 9.5, and blood vessel density and distribution in rats. Eur. J. Orthod. 19, 517–529 (1997).
pubmed: 9386338 doi: 10.1093/ejo/19.5.517
Nagayama, T. et al. Increase of CGRP-containing nerve fibers in the rat periodontal ligament after luxation. Cell. Mol. Neurobiol. 32, 391–397 (2012).
pubmed: 22038237 doi: 10.1007/s10571-011-9767-1
Takahashi, N. et al. Neuronal TRPV1 activation regulates alveolar bone resorption by suppressing osteoclastogenesis via CGRP. Sci. Rep. 6, 29294 (2016).
pubmed: 27388773 pmcid: 4937344 doi: 10.1038/srep29294
Sample, S. J., Hao, Z., Wilson, A. P. & Muir, P. Role of calcitonin gene-related peptide in bone repair after cyclic fatigue loading. PLoS One 6, e20386 (2011).
pubmed: 21694766 pmcid: 3111413 doi: 10.1371/journal.pone.0020386
Wakisaka, S., Atsumi, Y., Youn, S. H. & Maeda, T. Morphological and cytochemical characteristics of periodontal Ruffini ending under normal and regeneration processes. Arch. Histol. Cytol. 63, 91–113 (2000).
pubmed: 10885447 doi: 10.1679/aohc.63.91
Sato, O. Responses of pulpal nerves to cavity preparation in rat molars: An immunohistochemical study using neurofilament protein (NFP) antiserum. Arch. Histol. Cytol. 52, 433–446 (1989).
pubmed: 2513855 doi: 10.1679/aohc.52.433
Mukouyama, Y. S., Shin, D., Britsch, S., Taniguchi, M. & Anderson, D. J. Sensory nerves determine the pattern of arterial differentiation and blood vessel branching in the skin. Cell 109, 693–705 (2002).
pubmed: 12086669 doi: 10.1016/S0092-8674(02)00757-2
Khalil, Z. & Helme, R. Sensory peptides as neuromodulators of wound healing in aged rats. J. Gerontol. A Biol. Sci. Med. Sci. 51, B354–B361 (1996).
pubmed: 8808984 doi: 10.1093/gerona/51A.5.B354
Brain, S. D. & Grant, A. D. Vascular actions of calcitonin gene-related peptide and adrenomedullin. Physiol. Rev. 84, 903–934 (2004).
pubmed: 15269340 doi: 10.1152/physrev.00037.2003
Mishima, T. et al. Calcitonin gene-related peptide facilitates revascularization during hindlimb ischemia in mice. Am. J. Physiol. Heart Circ. Physiol. 300, H431–H439 (2011).
pubmed: 21131474 doi: 10.1152/ajpheart.00466.2010
Nagayasu-Tanaka, T. et al. Action mechanism of fibroblast growth Factor-2 (FGF-2) in the promotion of periodontal regeneration in beagle dogs. PLoS One 10, e0131870 (2015).
pubmed: 26120833 pmcid: 4488280 doi: 10.1371/journal.pone.0131870
Murakami, S. Periodontal tissue regeneration by signaling molecule(s): What role does basic fibroblast growth factor (FGF-2) have in periodontal therapy?. Periodontology 56, 188–208 (2011).
doi: 10.1111/j.1600-0757.2010.00365.x
Yanagita, M. et al. Cooperative effects of FGF-2 and VEGF-A in periodontal ligament cells. J. Dent. Res. 93, 89–95 (2014).
pubmed: 24186558 pmcid: 3872850 doi: 10.1177/0022034513511640
Yamada, S. et al. PLAP-1/asporin, a novel negative regulator of periodontal ligament mineralization. J. Biol. Chem. 282, 23070–23080 (2007).
pubmed: 17522060 doi: 10.1074/jbc.M611181200
McLatchie, L. M. et al. RAMPs regulate the transport and ligand specificity of the calcitonin-receptor-like receptor. Nature 393, 333–339 (1998).
pubmed: 9620797 doi: 10.1038/30666
Abe, T. & Hajishengallis, G. Optimization of the ligature-induced periodontitis model in mice. J. Immunol. Methods 394, 49–54 (2013).
pubmed: 23672778 pmcid: 3707981 doi: 10.1016/j.jim.2013.05.002

Auteurs

Koji Miki (K)

Department of Periodontology and Regenerative Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan. miki.koji.dent@osaka-u.ac.jp.

Noboru Takeshita (N)

Department of Periodontology and Regenerative Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Motozo Yamashita (M)

Department of Periodontology and Regenerative Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Masahiro Kitamura (M)

Department of Periodontology and Regenerative Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Shinya Murakami (S)

Department of Periodontology and Regenerative Dentistry, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka, 565-0871, Japan.

Classifications MeSH