Combining Porous Se@SiO₂ Nanocomposites and dECM Enhances the Myogenic Differentiation of Adipose-Derived Stem Cells

References

• Patel KH, Talovic M, Dunn AJ, et al. Aligned nanofibers of decellularized muscle extracellular matrix for volumetric muscle loss. J Biomed Mater Res. 2020;108(6):2528–2537. doi:10.1002/jbm.b.34584
   Web of Science ®Google Scholar
• Gilbert-Honick J, Grayson W. Vascularized and Innervated Skeletal Muscle Tissue Engineering. Adv Healthc Mater. 2020;9(1):e1900626. doi:10.1002/adhm.201900626
   PubMed Web of Science ®Google Scholar
• McClure MJ, Cohen DJ, Ramey AN, et al. Decellularized Muscle Supports New Muscle Fibers and Improves Function Following Volumetric Injury. Tissue Eng Part A. 2018;24(15–16):1228–1241. doi:10.1089/ten.TEA.2017.0386
   PubMed Web of Science ®Google Scholar
• Zhang X, Chen X, Hong H, Hu R, Liu J, Liu C. Decellularized extracellular matrix scaffolds: recent trends and emerging strategies in tissue engineering. Bioact Mater. 2022;10:15–31. doi:10.1016/j.bioactmat.2021.09.014
   PubMed Web of Science ®Google Scholar
• Brown M, Li J, Moraes C, Tabrizian M, Li-Jessen NYK. Decellularized extracellular matrix: new promising and challenging biomaterials for regenerative medicine. Biomaterials. 2022;289:121786. doi:10.1016/j.biomaterials.2022.121786
   PubMed Web of Science ®Google Scholar
• Sicari BM, Dearth CL, Badylak SF. Tissue Engineering and Regenerative Medicine Approaches to Enhance the Functional Response to Skeletal Muscle Injury. Anatomical Record. 2014;297(1):51–64. doi:10.1002/ar.22794
   Google Scholar
• Clinical application of an acellular biologic scaffold for surgical repair of a large, traumatic quadriceps femoris muscle defect - PubMed. Available from: https://pubmed.ncbi.nlm.nih.gov/20608620/. Accessed November 1, 2023.
   Google Scholar
• Garg K, Ward CL, Rathbone CR, Corona BT. Transplantation of devitalized muscle scaffolds is insufficient for appreciable de novo muscle fiber regeneration after volumetric muscle loss injury. Cell Tissue Res. 2014;358(3):857–873. doi:10.1007/s00441-014-2006-6
   PubMed Web of Science ®Google Scholar
• Carnes ME, Pins GD. Skeletal Muscle Tissue Engineering: biomaterials-Based Strategies for the Treatment of Volumetric Muscle Loss. Bioengineering. 2020;7(3):85. doi:10.3390/bioengineering7030085
   PubMedGoogle Scholar
• Pinheiro CH, de Queiroz JCF, Guimarães-Ferreira L, et al. Local injections of adipose-derived mesenchymal stem cells modulate inflammation and increase angiogenesis ameliorating the dystrophic phenotype in dystrophin-deficient skeletal muscle. Stem Cell Rev Rep. 2012;8(2):363–374. doi:10.1007/s12015-011-9304-0
   PubMed Web of Science ®Google Scholar
• Montarras D, Morgan J, Collins C, et al. Direct isolation of satellite cells for skeletal muscle regeneration. Science. 2005;309(5743):2064–2067. doi:10.1126/science.1114758
   PubMed Web of Science ®Google Scholar
• Radak Z, Torma F, Berkes I, et al. Exercise effects on physiological function during aging. Free Radic Biol Med. 2019;132:33–41. doi:10.1016/j.freeradbiomed.2018.10.444
   PubMed Web of Science ®Google Scholar
• Jones RM, Mercante JW, Neish AS. Reactive oxygen production induced by the gut microbiota: pharmacotherapeutic implications. Curr Med Chem. 2012;19(10):1519–1529. doi:10.2174/092986712799828283
   PubMed Web of Science ®Google Scholar
• García-Redondo AB, Aguado A, Briones AM, Salaices M. NADPH oxidases and vascular remodeling in cardiovascular diseases. Pharmacol Res. 2016;114:110–120. doi:10.1016/j.phrs.2016.10.015
   PubMed Web of Science ®Google Scholar
• Cheng WH, Prabhu KS. Special Issue of “Optimal Selenium Status and Selenoproteins in Health. Biol Trace Elem Res. 2019;192(1):1–2. doi:10.1007/s12011-019-01898-x
   PubMed Web of Science ®Google Scholar
• Lee SC, Lee NH, Patel KD, et al. The Effect of Selenium Nanoparticles on the Osteogenic Differentiation of MC3T3-E1 Cells. Nanomaterials. 2021;11(2):557. doi:10.3390/nano11020557
   Web of Science ®Google Scholar
• Liu X, Deng G, Wang Y, et al. A novel and facile synthesis of porous SiO 2 -coated ultrasmall Se particles as a drug delivery nanoplatform for efficient synergistic treatment of cancer cells. Nanoscale. 2016;8(16):8536–8541. doi:10.1039/C6NR02298G
   PubMed Web of Science ®Google Scholar
• Zheng Z, Deng G, Qi C, et al. Porous Se@SiO2 nanospheres attenuate ischemia/reperfusion (I/R)-induced acute kidney injury (AKI) and inflammation by antioxidative stress. Int J Nanomed. 2019;14:215–229. doi:10.2147/IJN.S184804
   PubMed Web of Science ®Google Scholar
• Li C, Wang Q, Gu X, et al. Porous Se@SiO2 nanocomposite promotes migration and osteogenic differentiation of rat bone marrow mesenchymal stem cell to accelerate bone fracture healing in a rat model. Int J Nanomed. 2019;14:3845–3860. doi:10.2147/IJN.S202741
   PubMed Web of Science ®Google Scholar
• Porous Se@SiO2 nanoparticles improve oxidative injury to promote muscle regeneration via modulating mitochondria - PubMed. Available from: https://pubmed.ncbi.nlm.nih.gov/36331417/. Accessed November 12, 2023.
   Google Scholar
• Improved rotator cuff healing after surgical repair via suppression of reactive oxygen species by sustained release of Se | request PDF. Available from: https://www.researchgate.net/publication/350315662_Improved_rotator_cuff_healing_after_surgical_repair_via_suppression_of_reactive_oxygen_species_by_sustained_release_of_Se. Accessed October 31, 2023.
   Google Scholar
• Liu X, Zhou L, Chen X, et al. Culturing on decellularized extracellular matrix enhances antioxidant properties of human umbilical cord-derived mesenchymal stem cells. Mater Sci Eng C. 2016;61:437–448. doi:10.1016/j.msec.2015.12.090
   PubMed Web of Science ®Google Scholar
• Zhu Y, Deng G, Ji A, et al. Porous Se@SiO2 nanospheres treated paraquat-induced acute lung injury by resisting oxidative stress. IJN. 2017;12:7143–7152. doi:10.2147/IJN.S143192
   Web of Science ®Google Scholar
• Fei W, Pang E, Hou L, et al. Synergistic Effect of Hydrogen and 5-Aza on Myogenic Differentiation through the p38 MAPK Signaling Pathway in Adipose-Derived Mesenchymal Stem Cells. Int J Stem Cells. 2023;16(1):78–92. doi:10.15283/ijsc21238
   PubMed Web of Science ®Google Scholar
• Mitochondria-Modulating Porous Se@SiO2 Nanoparticles Provide Resistance to Oxidative Injury in Airway Epithelial Cells: implications for Acute Lung Injury - PubMed. Available from: https://pubmed.ncbi.nlm.nih.gov/32280221/. Accessed November 10, 2023.
   Google Scholar
• Grasman JM, Zayas MJ, Page RL, Pins GD. Biomimetic scaffolds for regeneration of volumetric muscle loss in skeletal muscle injuries. Acta Biomater. 2015;25:2–15. doi:10.1016/j.actbio.2015.07.038
   PubMed Web of Science ®Google Scholar
• Ostrovidov S, Hosseini V, Ahadian S, et al. Skeletal Muscle Tissue Engineering: methods to Form Skeletal Myotubes and Their Applications. Tissue Eng Part B, Rev. 2014;20(5):403–436. doi:10.1089/ten.teb.2013.0534
   PubMed Web of Science ®Google Scholar
• Aurora A, Roe JL, Corona BT, Walters TJ. An acellular biologic scaffold does not regenerate appreciable de novo muscle tissue in rat models of volumetric muscle loss injury. Biomaterials. 2015;67:393–407. doi:10.1016/j.biomaterials.2015.07.040
   PubMed Web of Science ®Google Scholar
• Garg K, Ward CL, Corona BT. Asynchronous inflammation and myogenic cell migration limit muscle tissue regeneration mediated by acellular scaffolds. Inflamm Cell Signal. 2014. doi:10.14800/ics.530
   PubMedGoogle Scholar
• Srivastava D, Subramanian R, Madamwar D, Flora S. Protective Effects of Selenium, Calcium, and Magnesium Against Arsenic-Induced Oxidative Stress in Male Rats. Archiv Indus Hygien Toxicol. 2010;61(2):153–159. doi:10.2478/10004-1254-61-2010-1993
   Google Scholar
• Kiełczykowska M, Kocot J, Paździor M, Musik I. Selenium – a fascinating antioxidant of protective properties. Adv Clin Exp Med. 2018;27(2):245–255. doi:10.17219/acem/67222
   PubMed Web of Science ®Google Scholar
• Khurana A, Tekula S, Saifi MA, Venkatesh P, Godugu C. Therapeutic applications of selenium nanoparticles. Biomed Pharmacother. 2019;111:802–812. doi:10.1016/j.biopha.2018.12.146
   PubMed Web of Science ®Google Scholar
• Fatima S, Alfrayh R, Alrashed M, Alsobaie S, Ahmad R, Mahmood A. Selenium Nanoparticles by Moderating Oxidative Stress Promote Differentiation of Mesenchymal Stem Cells to Osteoblasts. IJN. 2021;16:331–343. doi:10.2147/IJN.S285233
   Google Scholar
• Estevez H, Garcia-Lidon JC, Luque-Garcia JL, Camara C. Effects of chitosan-stabilized selenium nanoparticles on cell proliferation, apoptosis and cell cycle pattern in HepG2 cells: comparison with other selenospecies. Colloids Surf B Biointerfaces. 2014;122:184–193. doi:10.1016/j.colsurfb.2014.06.062
   PubMed Web of Science ®Google Scholar
• Chen H, Huang X, Fu C, et al. Recombinant Klotho Protects Human Periodontal Ligament Stem Cells by Regulating Mitochondrial Function and the Antioxidant System during H 2 O 2 -Induced Oxidative Stress. Oxidative Med Cell Longevity. 2019;2019:1–14. doi:10.1155/2019/9261565
   Web of Science ®Google Scholar
• Wagatsuma A, Sakuma K. Mitochondria as a Potential Regulator of Myogenesis. Sci World J. 2013;2013:1–9. doi:10.1155/2013/593267
   Google Scholar
• Bhattacharya D, Scimè A. Mitochondrial Function in Muscle Stem Cell Fates. Front Cell Dev Biol. 2020;8:480. doi:10.3389/fcell.2020.00480
   PubMed Web of Science ®Google Scholar
• Bahat A, Gross A. Mitochondrial plasticity in cell fate regulation. J Biol Chem. 2019;294(38):13852–13863. doi:10.1074/jbc.REV118.000828
   PubMed Web of Science ®Google Scholar
• Rosca AM, Burlacu A. Effect of 5-Azacytidine: evidence for Alteration of the Multipotent Ability of Mesenchymal Stem Cells. Stem Cells Dev. 2011;20(7):1213–1221. doi:10.1089/scd.2010.0433
   PubMed Web of Science ®Google Scholar
• Chabi B, Hennani H, Cortade F, Wrutniak‐Cabello C. Characterization of mitochondrial respiratory complexes involved in the regulation of myoblast differentiation. Cell Biol Int 2021;45(8):1676–1684. doi:10.1002/cbin.11602
   PubMed Web of Science ®Google Scholar
• Goncalves RLS, Watson MA, Wong HS, Orr AL, Brand MD. The use of site-specific suppressors to measure the relative contributions of different mitochondrial sites to skeletal muscle superoxide and hydrogen peroxide production. Redox Biol. 2020;28:101341. doi:10.1016/j.redox.2019.101341
   PubMed Web of Science ®Google Scholar