Skip to main content Skip to main navigation menu Skip to site footer
Review
Published: 06-15-2023

Major considerations of the biological mechanisms of bone regeneration through mesenchymal stem cells, exosomes, and microRNAs in the scenario of bucco-maxillo-facial surgery: a systematic review

UNORTE - University Center of Northern São Paulo, Dentistry department, São José do Rio Preto, São Paulo, Brazil / UNIPOS - Post graduate and continuing education, Dentistry department, São José do Rio Preto, São Paulo, Brazil
UNORTE - University Center of Northern São Paulo, Dentistry department, São José do Rio Preto, São Paulo, Brazil / UNIPOS - Post graduate and continuing education, Dentistry department, São José do Rio Preto, São Paulo, Brazil
Bucco-maxillo-facial surgery Bone regeneration Exosomes MicroRNAs

Abstract

Introduction: In the context of bucco-maxillo facial surgery, the development of biomaterials for use in clinical dentistry in recent years has represented a powerful therapeutic instrument in the correction of bone defects. Adult tissue stem cells (mesenchymal stem cells) mediate homeostasis and regeneration of tissues and organs. Growing evidence suggests that metabolism during quiescence, activation, and differentiation may vary between tissues, integrating signaling cues and metabolic inputs with the release of exosomes and microRNAs as important metabolic messengers. Objective: It was to carry out a systematic review to present the main considerations and scientific evidence of the cellular and molecular mechanisms of bone formation or regeneration through mesenchymal stem cells, exosomes, and microRNAs in the scenario of bucco-maxillo-facial surgery with bone graft or biomaterials. Methods: The systematic review rules of the PRISMA Platform were followed. The search was carried out from March to May 2023 in the Scopus, PubMed, Science Direct, Scielo, and Google Scholar databases, with articles dated 2001 (gold standard) through 2022. The quality of the studies was based on the GRADE instrument and the risk of bias was analyzed accordingly, according to the Cochrane instrument. Results and Conclusion: A total of 145 articles were found, 45 articles were evaluated and 34 were included and developed in this systematic review study. Considering the Cochrane tool for risk of bias, the overall assessment resulted in 30 studies with a high risk of bias and 15 studies that did not meet GRADE. The greater potential of guided bone regeneration was associated with the graft material due to the higher grade of vital bone and the lower percentage of residual graft particles. Inorganic bovine bone and porcine bone minerals combined with autogenous maxillary cortical bone showed similar biological and radiological characteristics in terms of biomaterial resorption, osteoconduction, and osteogenesis when used for maxillary sinus floor augmentation. In this regard, three fundamental parameters in bone tissue engineering that determine the capacity for osteoinduction were evidenced, such as the presence of soluble osteoinductive signals, the viability of undifferentiated mesenchymal stem cells, having the ability to differentiate into bone-forming cells and production of adequate extracellular matrix. The exosomes that contain proteins, mRNAs, microRNAs, and DNAs stand out. Exosomes change the biochemical characteristics of recipient cells through the delivery of biomolecules and play a role in cell communication. Evidence suggests that exosomes derived from mesenchymal stem cells exhibit functions similar to mesenchymal stem cells with low immunogenicity and without tumorization.

Metrics

Metrics Loading ...

References

  1. Zhuang G, Mao J, Yang G, Wang H. Influence of different incision designs on bone increment of guided bone regeneration (Bio-Gide collagen membrane +BioOSS bone powder) during the same period of maxillary anterior tooth implantation. Bioengineered. 2021 Dec;12(1):2155-2163. doi: 10.1080/21655979.2021.1932209. PMID: 34057023.
  2. Abdel-Kader MA, Abdelazeem AF, Ahmed NEB, Khalil YM, Mostafa MI. Oral rehabilitation of a case with regional odontodysplasia using a regenerative approach-A case report and a review of literature. Spec Care Dentist. 2019, May;39(3):330-339. doi: 10.1111/scd.12378.
  3. Arab H, Shiezadeh F, Moeintaghavi A, Anbiaei N, Mohamadi S. Comparison of Two Regenerative Surgical Treatments for Peri-Implantitis Defect using Natix Alone or in Combination with Bio-Oss and Collagen Membrane. J Long Term Eff Med Implants. 2016;26(3):199-204. doi: 10.1615/JLongTermEffMedImplants.2016016396.
  4. Chiapasco M., Casentini P., Zaniboni M. Bone augmentation procedures in implant dentistry. Int J Oral Maxillofac Implants. 2009;24 Suppl: 237-59.
  5. Choukroun J, Diss A., Simonpieri A, Girard M.O. Schhoffler C., Dohan S.L., et al.Platelet-rich-fibrin (PRF): a second generation platelet concentrate. Part IV: clinical effects on tissue healing. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod 2006: 101 (3): e 56 – 60.
  6. Diana C, Mohanty S, Chaudhary Z, Kumari S, Dabas J, Bodh R. Does plateletrich fibrin have a role in osseointegration of immediate implants? A randomized, single-blind, controlled clinical trial. Int J Oral Maxillofac Surg. 2018 Sep;47(9):1178-1188. doi: 10.1016/j.ijom.2018.01.001. Epub 2018 May 7.
  7. Nícoli LG, Pigossi SC, Araújo RFdSB, Marcantonio C, Marcantonio E, Marcantonio JRE. Multidisciplinary approach to oral rehabilitation with dental implants after gunshot injury. A clinical report. The Journal of Prothestic Dentistry. 2018; 119 (3): 329 – 33.
  8. Locke M, Windsor J, Dunbar PR. Human adipose-derived stem cells: isolation, characterization and applications in surgery.ANZ J Surg, 2009, 79:235-244.
  9. Zotarelli Filho IJ, Frascino LF, Greco OT, Araujo JDD, Bilaqui A, Kassis EN, Ardito RV andBonilla-Rodriguez GO. Chitosan-collagen scaffolds can regulate the biologicalactivities of adipose mesenchymal stem cells for tissueengineering. J Regen Med Tissue Eng. 2013; 2:12. http://dx.doi.org/10.7243/2050-1218-2-12.
  10. Chacón-Martínez CA et al. Hair follicle stem cell cultures reveal self-organizing plasticity of stem cells and their progeny. EMBO J. 2017, 36, 151–164.
  11. Rodríguez-Colman, M.J. et al. Interplay between metabolic identities in the intestinal crypt supports stem cell function. Nature, 2017, 543, 424.
  12. Snoeck, H.W. Mitochondrial regulation of hematopoietic stem cells. Curr. Opin. Cell Biol. 2017, 49, 91–98.
  13. Zheng X. et al. Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation. Elife, 2016, 5, e13374.
  14. Shapira SN, Christofk HR. Metabolic Regulation of Tissue Stem Cells. Trends Cell Biol. 2020 Jul;30(7):566-576. doi: 10.1016/j.tcb.2020.04.004.
  15. Wu Z, Qiu X, Gao B, Lian C, Peng Y, Liang A, Xu C, Gao W, Zhang L, Su P, et al. Melatonin-mediated miR-526b-3p and miR-590-5p upregulation promotes chondrogenic differentiation of human mesenchymal stem cells. J Pineal Res. 2018;65:e12483. doi: 10.1111/jpi.12483.
  16. Nugent M. MicroRNAs: Exploring new horizons in osteoarthritis. Osteoarthritis Cartilage. 2016;24:573–580. doi: 10.1016/j.joca.2015.10.018.
  17. Miyaki S, Sato T, Inoue A, Otsuki S, Ito Y, Yokoyama S, Kato Y, Takemoto F, Nakasa T, Yamashita S, et al. MicroRNA-140 plays dual roles in both cartilage development and homeostasis. Genes Dev. 2010;24:1173–1185. doi: 10.1101/gad.1915510.
  18. Zampara E, Alshammari M, De Bortoli J, Mullings O, Gkisakis IG, Benalcázar Jalkh EB, Tovar N, Coelho PG, Witek L. A Histologic and Histomorphometric Evaluation of an Allograft, Xenograft, and Alloplast Graft for Alveolar Ridge Preservation in Humans: A Randomized Controlled Clinical Trial. J Oral Implantol. 2022 Dec 1;48(6):541-549. doi: 10.1563/aaid-joi-D-21-00012.
  19. Galindo-Moreno P, Abril-García D, Carrillo-Galvez AB, Zurita F, MartínMorales N, O'Valle F, Padial-Molina M. Maxillary sinus floor augmentation comparing bovine versus porcine bone xenografts mixed with autogenous bone graft. A split-mouth randomized controlled trial. Clin Oral Implants Res. 2022 May;33(5):524-536. doi: 10.1111/clr.13912.
  20. Meschi N, EzEldeen M, Garcia AET, Lahoud P, Van Gorp G, Coucke W, Jacobs R, Vandamme K, Teughels W, Lambrechts P. Regenerative Endodontic Procedure of Immature Permanent Teeth with Leukocyte and Platelet-rich Fibrin: A Multicenter Controlled Clinical Trial. J Endod. 2021 Nov;47(11):1729-1750. doi: 10.1016/j.joen.2021.08.003.
  21. Gimble JM, Katz AJ, Bunnell BA. Adipose-Derived Stem Cells for Regenerative Medicine. Circ Res; 2013, 100:1249-1260.
  22. Dai Z, Shu Y, Wan C, Wu C. Effects of pH and thermally sensitive hybrid gels on osteogenic differentiation of mesenchymal stem cells. J Biomater Appl. 2015;29:1272-83.
  23. Zuk PA, Zhu M, Ashjian P. Human adipose tissue is a source of multipotent stem cells. Mol Biol Cell; 2002, 13: 4279–4295.
  24. Thery C, Boussac M, Veron P, Ricciardi-Castagnoli P, Raposo G, Garin J, et al., Proteomic analysis of dendritic cell-derived exosomes: a secreted subcellular compartment distinct from apoptotic vesicles, J. Immunol. 2001, 166:7309–7318.
  25. Baharlooi H, Nouraei Z, Azimi M, Moghadasi AN, Tavassolifar MJ, Moradi B, Sahraian MA, Izad M. Umbilical cord mesenchymal stem cells as well as their released exosomes suppress proliferation of activated PBMCs in multiple sclerosis. Scand J Immunol. 2020 Dec 18:e13013. doi: 10.1111/sji.13013.
  26. Mears R, Craven RA, Hanrahan S, Totty N, Upton C, Young SL, et al., Proteomic analysis of melanoma-derived exosomes by two-dimensional polyacrylamide gel electrophoresis and mass spectrometry, Proteomics, 2004, 4:4019–4031, https://doi.org/10.1002/pmic.200400876.
  27. Gastpar R, Gehrmann M, Bausero MA, Asea A, Gross C, Schroeder JA, et al., Heat shock protein 70 surface-positive tumor exosomes stimulate migratory and cytolytic activity of natural killer cells, Cancer Res. 2005, 65:5238–5247, https://doi.org/10.1158/0008-5472.can-04-3804.
  28. W. Xu, Z. Yang, N. Lu, From pathogenesis to clinical application: insights into exosomes as transfer vectors in cancer, J. Exp. Clin. Cancer Res. 2016, 35 :156,https://doi.org/10.1186/s13046-016-0429-5.
  29. H. Valadi, K. Ekstrom, A. Bossios, M. Sjostrand, J.J. Lee, J.O. Lotvall, Exosomemediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells, Nat. Cell Biol. 2007, 9:654–659, https://doi.org/10.1038/ncb1596.
  30. B. Zhang, L. Shen, H. Shi, Z. Pan, L. Wu, Y. Yan, et al., Exosomes from Human Umbilical Cord Mesenchymal Stem Cells: Identification, Purification, and Biological Characteristics, 2016, p. 1929536, https://doi.org/10.1155/2016/1929536.
  31. Mesimäki K, Lindroos B, Törnwall J, Mauno J, Lindqvist C, Kontio R, Miettinen S, Suuronen R: Novel maxillary reconstruction with ectopic bone formation by GMP adipose stem cells. Int J Oral Maxillofac Surg 2009, 38 : 201-209.
  32. Zotarelli Filho IJ, Frascino LF, Greco OT, Araujo JDD, Bilaqui A, Kassis EN, Ardito RV and Bonilla-Rodriguez GO. Chitosan-collagen scaffolds can regulate the biological activities of adipose mesenchymal stem cells for tissue engineering. J Regen Med Tissue Eng. 2013; 2:12. http://dx.doi.org/10.7243/2050-1218-2-12.
  33. Egido-Moreno S, Valls-Roca-Umbert J, Céspedes-Sánchez JM, López-López J, Velasco-Ortega E. Clinical Efficacy of Mesenchymal Stem Cells in Bone Regeneration in Oral Implantology. Systematic Review and Meta-Analysis. Int J Environ Res Public Health. 2021 Jan 21;18(3):894. doi: 10.3390/ijerph18030894.
  34. Liang W, Han B, Hai Y, Sun D, Yin P. Mechanism of Action of Mesenchymal Stem Cell-Derived Exosomes in the Intervertebral Disc Degeneration Treatment and Bone Repair and Regeneration. Front Cell Dev Biol. 2022 Jan 14;9:833840. doi: 10.3389/fcell.2021.833840.

How to Cite

Mello, Álvaro A. de, & Kassis, E. N. (2023). Major considerations of the biological mechanisms of bone regeneration through mesenchymal stem cells, exosomes, and microRNAs in the scenario of bucco-maxillo-facial surgery: a systematic review. MedNEXT Journal of Medical and Health Sciences, 4(S2). https://doi.org/10.54448/mdnt23S217