Control of myotube orientation using ultrasonication.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
28 10 2024
28 10 2024
Historique:
received:
20
03
2024
accepted:
21
10
2024
medline:
29
10
2024
pubmed:
29
10
2024
entrez:
29
10
2024
Statut:
epublish
Résumé
This study investigated a technique for controlling the orientation of C2C12-derived myotube cells using ultrasonication for future clinical applications of cultured skeletal muscle tissues. An ultrasonicating cell culture dish, comprising a plastic-bottomed culture dish and a circular glass plate (diameter, 35 mm; thickness, 1.1 mm) attached to an annular piezoelectric ultrasonic transducer (inner diameter, 10 mm; outer diameter, 20 mm; thickness, 1 mm), was constructed. A concentric resonant vibrational mode at 89 kHz was generated on the bottom of the dish, and the orientations of myotube cells were quantitatively evaluated using two-dimensional Fourier transform analysis of phase contrast microscopy images captured over a 14 × 10 mm
Identifiants
pubmed: 39468262
doi: 10.1038/s41598-024-77277-x
pii: 10.1038/s41598-024-77277-x
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
25737Informations de copyright
© 2024. The Author(s).
Références
Tsubata, T. et al. Axial transmission technique for screening bucked shin in a horse leg. Jpn J. Appl. Phys. 62 (SJ), SJ1026 (2023).
doi: 10.35848/1347-4065/acbaa4
Ma, C. et al. Preparation of oriented collagen fiber scaffolds and its application in bone tissue engineering. Appl. Mater. Today. 22, 100902 (2021).
doi: 10.1016/j.apmt.2020.100902
Bian, W. & Bursac, N. Engineered skeletal muscle tissue networks with controllable architecture. Biomaterials. 30 (7), 1401–1412 (2009).
doi: 10.1016/j.biomaterials.2008.11.015
pubmed: 19070360
Zhao, Y., Zeng, H., Nam, J. & Agarwal, S. Fabrication of skeletal muscle constructs by topographic activation of cell alignment. Biotechnol. Bioeng. 102 (2), 624–631 (2009).
doi: 10.1002/bit.22080
pubmed: 18958861
Altomare, L., Gadegaard, N., Visai, L., Tanzi, M. C. & Fare, S. Biodegradable microgrooved polymeric surfaces obtained by photolithography for skeletal muscle cell orientation and myotube development. Acta Biomater. 6 (6), 1948–1957 (2010).
doi: 10.1016/j.actbio.2009.12.040
pubmed: 20040385
Gutierrez, J., Gonzalez, D., Escalona-Rivano, R., Takahashi, C. & Brandan, E. Reduced RECK levels accelerate skeletal muscle differentiation, improve muscle regeneration, and decrease fibrosis. FASEB J. 35 (5), e21503 (2021).
doi: 10.1096/fj.202001646RR
pubmed: 33811686
Agarwal, M. et al. Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development. Development. 147 (7), dev184507 (2020).
doi: 10.1242/dev.184507
pubmed: 32094117
pmcid: 7157585
Bramson, M. T. K., Van Houten, S. K. & Corr, D. T. Mechanobiology in tendon, ligament, and skeletal muscle tissue engineering. ASME J. Biomech. Eng. 143 (7), 070801 (2021).
doi: 10.1115/1.4050035
Jang, Y., Kim, S. M., Spinks, G. M. & Kim, S. J. Carbon nanotube yarn for fiber-shaped electrical sensors, actuators, and energy storage for smart systems. Adv. Mater. 32 (5), e1902670 (2019).
doi: 10.1002/adma.201902670
pubmed: 31403227
Mu, J. et al. Sheath-run artificial muscles. Science. 365 (6449), 150–155 (2019).
doi: 10.1126/science.aaw2403
pubmed: 31296765
Lin, S., Liu, J., Liu, X. & Zhao, X. Muscle-like fatigue-resistant hydrogels by mechanical training. Proc. Natl. Acad. Sci. U S A. 116 (21), 10244–10249 (2019).
doi: 10.1073/pnas.1903019116
pubmed: 31068458
pmcid: 6535018
Shimizu, K., Fujita, H. & Nagamori, E. Evaluation systems of generated forces of skeletal muscle cell-based bio-actuators. J. Biosci. Bioeng. 115 (2), 115–121 (2013).
doi: 10.1016/j.jbiosc.2012.08.024
pubmed: 23026451
Fujita, H., Shimizu, K. & Nagamori, E. Fabrication of skeletal muscle tissue from C2C12 myoblast cell towards the use as bio-actuator. Animal cell. Technology: Basic Applied Aspects. 16, 177–183 (2010).
Yamasaki, K. et al. Control of myotube contraction using electrical pulse stimulation for bio-actuator. J. Artif. Organs. 12 (2), 131–137 (2009).
doi: 10.1007/s10047-009-0457-4
pubmed: 19536631
Chang, D., Fan, T., Gao, S. Y., Jin, M. & Zhang Ono. Application of mesenchymal stem cell sheet to treatment of ischemic heart disease. Stem Cell. Res. Ther. 12, 384 (2021).
doi: 10.1186/s13287-021-02451-1
pubmed: 34233729
pmcid: 8261909
Guo, R. et al. Stem cell-derived cell sheet transplantation for heart tissue repair in myocardial infarction. Stem Cell. Res. Ther. 11, 19 (2020).
doi: 10.1186/s13287-019-1536-y
pubmed: 31915074
pmcid: 6950817
Sawa, Y. et al. Tissue engineered myoblast sheets improved cardiac function sufficiently to discontinue LVAS in a patient with DCM: report of a case. Surg. Today. 42 (2), 181–184 (2012).
doi: 10.1007/s00595-011-0106-4
pubmed: 22200756
Heher, P. et al. A novel bioreactor for the generation of highly aligned 3D skeletal muscle-like constructs through orientation of fibrin via application of static strain. Acta Biomater. 24 (89), 251–265 (2015).
doi: 10.1016/j.actbio.2015.06.033
pubmed: 26141153
Chen, X. et al. Uniaxial stretching of cell-laden microfibers for promoting C2C12 myoblasts alignment and myofibers formation. ACS Appl. Mater. Interfaces. 12 (2), 2162–2170 (2020).
doi: 10.1021/acsami.9b22103
pubmed: 31856565
Riboldi, S. A. et al. Skeletal myogenesis on highly orientated microfibrous polyesterurethane scaffolds. J. Biomed. Mater. Res. A. 84 (4), 1094–1101 (2008).
doi: 10.1002/jbm.a.31534
pubmed: 17685407
Connon, C. J. & Gouveia, R. M. Milliscale substrate curvature promotes myoblast self-organization and differentiation. Adv. Biol. 5 (4), 2000280 (2021).
doi: 10.1002/adbi.202000280
Balint, R., Cassidy, N. J. & Cartmell, S. H. Electrical stimulation: a novel tool for tissue engineering. Tissue Eng. Part. B Rev. 19 (1), 48–57 (2013).
doi: 10.1089/ten.teb.2012.0183
pubmed: 22873689
Siebner, H. R. et al. Transcranial magnetic stimulation of the brain: What is stimulated? – A consensus and critical position paper. Clin. Neurophysiol. 140, 59–97 (2022).
doi: 10.1016/j.clinph.2022.04.022
pubmed: 35738037
pmcid: 9753778
Mansouri, N. & Bagheri, S. The influence of topography on tissue engineering perspective. Mater. Sci. Eng. C Mater. Biol. Appl. 61, 906–921 (2016).
doi: 10.1016/j.msec.2015.12.094
pubmed: 26838922
Salgarella, A. R. et al. Optimal ultrasound exposure conditions for maximizing C2C12 muscle cell proliferation and differentiation. Ultrasound Med. Biol. 43 (7), 1452–1265 (2017).
doi: 10.1016/j.ultrasmedbio.2017.03.003
pubmed: 28433437
Ibata, N. & Terentjev, E. M. Why exercise builds muscles: titin mechanosensing controls skeletal muscle growth under load. Biophys. J. 120 (7), 3649–3663 (2021).
doi: 10.1016/j.bpj.2021.07.023
pubmed: 34389312
pmcid: 8456289
Lam, M. T., Sim, S., Zhu, X. & Takyama, S. The effect of continuous wavy micropatterns on silicone substrates on the alignment of skeletal muscle myoblasts and myotubes. Biomaterials. 27 (24), 4340–4347 (2006).
doi: 10.1016/j.biomaterials.2006.04.012
pubmed: 16650470
Choi, J. S., Lee, S. J., Christ, G. J., Atala, A. & Yoo, J. J. The influence of electrospun aligned poly(epsilon-caprolactone)/collagen nanofiber meshes on the formation of self-aligned skeletal muscle myotubes. Biomaterials. 29 (19), 2899–2906 (2008).
doi: 10.1016/j.biomaterials.2008.03.031
pubmed: 18400295
Yin, Q. et al. Acoustic cell patterning for structured cell-laden hydrogel fibers/tubules. Adv. Sci. 11 (14), 2308396 (2024).
doi: 10.1002/advs.202308396
Wu, D. et al. Biomolecular actuators for genetically selective acoustic manipulation of cells. Sci. Adv. 9 (8), eadd9186 (2023).
doi: 10.1126/sciadv.add9186
pubmed: 36812320
pmcid: 9946353
Gao, X. et al. Acoustic quasi-periodic bioassembly based diverse stem cell arrangements for differentiation guidance. Lab. Chip. 23 (20), 4413–4421 (2023).
doi: 10.1039/D3LC00448A
pubmed: 37772435
Tani, K., Fujiwara, K. & Koyama, D. Adhesive cell patterning technique using ultrasound vibrations. Ultrasonics. 96, 18–23 (2019).
doi: 10.1016/j.ultras.2019.03.018
pubmed: 30939389
Maruyama, H., Fujiwara, K., Kumeta, M. & Koyama, D. Ultrasonic control of neurite outgrowth direction. Sci. Rep. 11 (1), 20099 (2021).
doi: 10.1038/s41598-021-99711-0
pubmed: 34635756
pmcid: 8505449
van den Eijnde, S. M. et al. Transient expression of phosphatidylserine at cell-cell contact areas is required for myotube formation. J. Cell. Sci. 114 (20), 3631–3642 (2001).
doi: 10.1242/jcs.114.20.3631
pubmed: 11707515
Cao, N. et al. Conversion of human fibroblasts into functional cardiomyocytes by small molecules. Science. 352 (6290), 1216–1220 (2016).
doi: 10.1126/science.aaf1502
pubmed: 27127239
Bansal, V. et al. Chemical induced conversion of mouse fibroblasts and human adipose-derived stem cells into skeletal muscle-like cells. Biomaterials. 193, 30–46 (2019).
doi: 10.1016/j.biomaterials.2018.11.037
pubmed: 30554025
Iezzi, S., Cossu, G., Nervi, C., Sartorelli, V. & Puri, P. L. Stage-specific modulation of skeletal myogenesis by inhibitors of nuclear deacetylases. Proc. Natl. Acad. Sci. U S A. 99 (11), 7757–7762 (2002).
doi: 10.1073/pnas.112218599
pubmed: 12032356
pmcid: 124343