Exfoliated Human Deciduous Tooth Stem Cells Incorporating Carbonate Apatite Scaffold Enhance BMP-2, BMP-7 and Attenuate MMP-8 Expression During Initial Alveolar Bone Remodeling in Wistar Rats (Rattusnorvegicus)

References

• United Nations, Department of Economic and Social Affairs, Population Division. World population prospects 2019: highlights (ST/ESA/SER.A/423); 2019. Available from: https://population.un.org/wpp/Publications/Files/WPP2019_Highlights.pdf. Accessed November 26, 2019.
   Google Scholar
• Ministry of Health Republic of Indonesia. The Republic of Indonesia health system review. Health Syst Transit. 2017;7(1):1–291.
   Google Scholar
• Ministry of Health Republic of Indonesia. Basic health research in oral health result; 2018. Available from: https://www.depkes.go.id/resources/download/info-terkini/hasil-riskesdas-2018.pdf. Accessed November 26, 2019.
   Google Scholar
• Nugraha AP, Narmada IB, Ernawati DS, et al. Osteogenic potential of gingival stromal progenitor cells cultured in platelet rich fibrin is predicted by core-binding factor subunit-α1/Sox9 expression ratio (in vitro). F1000Res. 2018;7:1134.
   Google Scholar
• Ministry of Health Republic of Indonesia: Health Profile in Indonesia 2014. Ministry of health Republic of Indonesia. Sekretaris Jenderal. Jakarta; 2015.
   Google Scholar
• Lande R, Kepel BJ, Siagian KV. Profile of risk factor and complication of tooth extraction at RSGM PSPDG-FK unsrat. J E Gigi (Eg). 2015;3(2):1–6.
   Google Scholar
• Agarwal G, Thomas R, Mehta D. Postextraction maintenance of the alveolar ridge: rationale and review. Compend Cont Educ Dent. 2012;33(5):320–324;quiz 327, 336.
   Google Scholar
• Hansson S, Halldin S. Alveolar ridge resorption after tooth extraction: a consequence of a fundamental principle of bone physiology. J Dent Biomech. 2012;3:1758736012456543.
   Google Scholar
• Schropp L, Wenzel A, Kostopoulos L, Karring T. Bone healing and soft tissue contour changes following single-tooth extraction: a clinical and radiographic 12-month prospective study. Int J Periodontics Restorative Dent. 2003;23(4):313–323.
   PubMed Web of Science ®Google Scholar
• Sari DS, Maduratna E, Latief FDE, Nugraha AP, Sudiana K, Rantam FA. Osteogenic differentiation and biocompatibility of bovine teeth scaffold with rat adipose-derived mesenchymal stem cells. Eur J Dent. 2019;13(02):206–212.
   Google Scholar
• Nugraha AP, Narmada IB, Ernawati DS, et al. Bone alkaline phosphatase and osteocalcin expression of rat’s gingival mesenchymal stem cells cultured in platelet-rich fibrin for bone remodeling (in vitro). study). Eur J Dent. 2018;12(4):566–573.
   Google Scholar
• Nugraha AP, Rantam FA, Ernawati DS, et al. Gingival mesenchymal stem cells from Wistar rat’s gingiva (Rattus norvegicus) isolation and characterization (in vitro study). J Int Dent Med Res. 2018;11(2):694–699.
   Google Scholar
• Nugraha AP, Narmada IB, Ernawati DS, et al. Somatic cells acceleration by platelet rich fibrin. Indian Vet J. 2019;96(04):30–34.
   Google Scholar
• Nugraha AP, Narmada IB, Ernawati DS, et al. In vitro bone sialoprotein-I expression in combined gingival stromal cells and platelet rich fibrin during osteogenic differentiation. Trop J Pharm Res. 2018;17(12):2341–2345.
   Web of Science ®Google Scholar
• Nugraha AP, Narmada IB, Ernawati DS, et al. The Aggrecan expression post platelet rich fibrin administration in gingival medicinal signaling cells in Wistar rats (Rattus norvegicus) during the early osteogenic differentiation (in vitro) Kafkas. Univ Vet Fak Derg. 2019;25(3):421–425.
   Web of Science ®Google Scholar
• Narmada IB, Laksono V, Nugraha AP, et al. Regeneration of salivary gland defects of diabetic wistar rats post human dental pulp stem cells intraglandular transplantation on acinar cell vacuolization and interleukin-10. Pesqui Bras Odontopediatria Clin Integr. 2019;19(1):1–10.
   Web of Science ®Google Scholar
• Suciadi SP, Nugraha AP, Ernawati DS, et al. The efficacy of human dental pulp stem cells in regenerating submandibular gland defects in diabetic wistar rats (Rattus novergicus). Res J Pharm Technol. 2019;12(4):1573–1579.
   Google Scholar
• Saskianti T, Ramadhani R, Budipramana ES, Pradopo S, Suardita K. Potential proliferation of stem cell from human exfoliated deciduous teeth (SHED) in carbonate apatite and hydroxyapatite scaffold. J Int Dent Med Res. 2017;10(2):350–353.
   Google Scholar
• Egusa H, Sonoyama W, Nishimura M, Atsuta I, Akiyama K. Stem cells in dentistry – part I: stem cell sources. J Prosthodont Res. 2012;56:151‑65.
   Web of Science ®Google Scholar
• Miura M, Gronthos S, Zhao M, et al. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci U S A. 2003;100(10):5807–5812.
   PubMed Web of Science ®Google Scholar
• Gronthos S, Mankani M, Brahim J, Robey PG, Shi S. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci U S A. 2000;97(25):13625–13630.
   PubMed Web of Science ®Google Scholar
• Alhasyimi AA, Pudyani PP, Asmara W, Ana ID. Enhancement of post-orthodontic tooth stability by carbonated hydroxyapatite-incorporated advanced platelet-rich fibrin in rabbits. Orthod Craniofac Res. 2018;21(2):112–118.
   Web of Science ®Google Scholar
• Khoswanto C. A new technique for research on wound healing through extraction of mandibular lower incisors in wistar rats. Euro Dent J. 2019;9:1–3.
   Google Scholar
• Prahasanti C, Subrata LH, Saskianti T, Suardita K, Ernawati DS. Combined hydroxyapatite scaffold and stem cell from human exfoliated deciduous teeth modulating alveolar bone regeneration via regulating receptor activator of nuclear factor-Κb and osteoprotegerin system. Iran J Med Sci. 2019;44(5):415.
   PubMed Web of Science ®Google Scholar
• Narmada IB, Husodo KRD, Ardani IGAW, Rahmawati D, Nugraha AP, Iskandar RPD. Effect of vitamin D during orthodontic tooth movement on receptor activator of nuclear factor Kappa-B ligand expression and osteoclast number in pregnant wistar rat (Rattus novergicus). Krishna Inst Med Sci Univ. 2019;8(1):37–42.
   Web of Science ®Google Scholar
• Nareswari RAAR, Narmada IB, Djaharu’ddin I, Rahmawati D, Putranti NAR, Nugraha AP. Effect of vitamin D administration on vascular endothelial growth factor expression and angiogenesis number in orthodontic tooth movement of pregnant Wistar rats. J Postgrad Med Inst. 2019;33(3):182–188.
   Google Scholar
• Sheikh Z, Javaid MA, Hamdan N, Hashmi R. Bone regeneration using bone morphogenetic proteins and various biomaterial carriers. Materials (Basel). 2015;8(4):1778–1816.
   Web of Science ®Google Scholar
• Termaat MF, Den Boer FC, Bakker FC, Patka P, Haarman HJ. Bone morphogenetic proteins. Development and clinical efficacy in the treatment of fractures and bone defects. J Bone Joint Surg Am. 2005;87(6):1367–1378.
   PubMed Web of Science ®Google Scholar
• Bibbo C, Nelson J, Ehrlich D, Rougeux B. Bone morphogenetic proteins: indications and uses. Clin Podiatr Med Surg. 2015;32(1):35–43.
   Web of Science ®Google Scholar
• Gautschi OP, Frey SP, Zellweger R. Bone morphogenetic proteins in clinical applications. ANZ J Surg. 2007;77(8):626–631.
   PubMed Web of Science ®Google Scholar
• Beederman M, Lamplot JD, Nan G, et al. BMP signaling in mesenchymal stem cell differentiation and bone formation. J Biomed Sci Eng. 2013;6(8A):32–52.
   PubMedGoogle Scholar
• Lo KWH, Ulery BD, Ashe KM, Laurencin CT. Studies of bone morphogenetic protein-based surgical repair. Adv Drug Deliv Rev. 2012;64(12):1277–1291.
   PubMed Web of Science ®Google Scholar
• Bandyopadhyay A, Tsuji K, Cox K, Harfe BD, Rosen V, Tabin CJ. Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis. PLoS Genet. 2006;2(12):e216.
   PubMed Web of Science ®Google Scholar
• Wu Y, Zhang C, Wu J, Han Y, Wu C. Angiogenesis and bone regeneration by mesenchymal stem cell transplantation with danshen in a rabbit model of avascular necrotic femoral head. Exp Ther Med. 2019;18(1):163–171.
   Web of Science ®Google Scholar
• Liu J, Li Z, Zhu Y, Luo C, Yang D. Bone morphogenetic protein-7 promoted the differentiation of bone marrow-derived mesenchymal stromal cells towards chondrocytes. Int J Clin Exp Med. 2018;11(3):1835–1844.
   Web of Science ®Google Scholar
• Savonius O, Roine I, Alassiri S, et al. The potential role of matrix metalloproteinases 8 and 9 and myeloperoxidase in predicting outcomes of bacterial meningitis of childhood. Mediators Inflamm. 2019;7436932:1–8.
   Web of Science ®Google Scholar
• de Morais EF, Pinheiro JC, Leite RB, Santos PPA, Barboza CAG, Freitas RA. Matrix metalloproteinase-8 levels in periodontal disease patients: a systematic review. J Periodontal Res. 2018;53(2):156–163.
   PubMed Web of Science ®Google Scholar
• Paiva KBS, Granjeiro JM. Matrix metalloproteinases in bone resorption, remodeling, and repair. Prog Mol Biol Transl Sci. 2017;148:203–303.
   PubMed Web of Science ®Google Scholar
• Arakawa H, Uehara J, Hara ES, et al. Matrix metalloproteinase-8 is the major potential collagenase in active peri-implantitis. J Prosthodont Res. 2012;56(4):249–255.
   Web of Science ®Google Scholar
• Mauney J, Volloch V. Adult human bone marrow stromal cells regulate expression of their MMPs and TIMPs in differentiation type-specific manner. Matrix Biol. 2010;29(1):3–8.
   Web of Science ®Google Scholar
• Almalki SG, Agrawal DK. Effects of matrix metalloproteinases on the fate of mesenchymal stem cells. Stem Cell Res Ther. 2016;7(1):129.
   PubMed Web of Science ®Google Scholar
• Kunimatsu R, Nakajima K, Awada T, et al. Comparative characterization of stem cells from human exfoliated deciduous teeth, dental pulp, and bone marrow-derived mesenchymal stem cells. Biochem Biophys Res Commun. 2018;501(1):193–198.
   Web of Science ®Google Scholar