The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Rapid formation of functional muscle in vitro using fibrin gels
Abstract
The transition of a muscle cell from a differentiated myotube into an adult myofiber is largely unstudied. This is primarily due to the difficulty of isolating specific developmental stimuli in vivo and the inability to maintain viable myotubes in culture for sufficient lengths of time. To address these limitations, a novel method for rapidly generating three-dimensional engineered muscles using fibrin gel casting has been developed. Myoblasts were seeded and differentiated on top of a fibrin gel. Cell-mediated contraction of the gel around artificial anchors placed 12 mm apart culminates 10 days after plating in a tubular structure of small myotubes (10-μm diameter) surrounded by a fibrin gel matrix. These tissues can be connected to a force transducer and electrically stimulated between parallel platinum electrodes to monitor physiological function. Three weeks after plating, the three-dimensional engineered muscle generated a maximum twitch force of 329 ± 26.3 μN and a maximal tetanic force of 805.8 ± 55 μN. The engineered muscles demonstrated normal physiological function including length-tension and force-frequency relationships. Treatment with IGF-I resulted in a 50% increase in force production, demonstrating that these muscles responded to hormonal interventions. Although the force production was maximal at 3 wk, constructs can be maintained in culture for up to 6 wk with no intervention. We conclude that fibrin-based gels provide a novel method to engineer three-dimensional functional muscle tissue and that these tissues may be used to model the development of skeletal muscle in vitro.
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Rommel, C., Bodine, S. C., Clarke, B. A., Rossman, R., Nunez, L., Stitt, T. N., Yancopoulos, G. D., & Glass, D. J. (2001) · Nature Cell Biology · doi:10.1038/ncb1101-1009 · Cited by 1,583
Musarò, A., McCullagh, K., Paul, A., Houghton, L., Dobrowolny, G., Molinaro, M., Barton, E. R., L Sweeney, H., & Rosenthal, N. (2001) · Nature Genetics · doi:10.1038/84839 · Cited by 1,137 · cited 1×
“The importance of IGF-I in muscle growth is most strikingly demonstrated by the twofold increase in muscle size in mice carrying a transgene for muscle-specific overexpression of IGF-I (6, 19).”
Background
Cited by
Fibrin: A versatile scaffold for tissue engineering applications
Ahmed, T. A. E., Dare, E. V., & Hincke, M. (2008) · Tissue Engineering Part B: Reviews · doi:10.1089/ten.teb.2007.0435 · Cited by 994
Guo, B., Qu, J., Zhao, X., & Zhang, M. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.12.008 · Cited by 339
Organ-on-a-chip platforms: a convergence of advanced materials, cells, and microscale technologies
Ahadian, S., Civitarese, R., Bannerman, D., Mohammadi, M. H., Lu, R., Wang, E., Davenport‐Huyer, L., Lai, B., Zhang, B., Zhao, Y., et al. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201700506 · Cited by 315
Formation and optogenetic control of engineered 3D skeletal muscle bioactuators
Sakar, M. S., Neal, D., Boudou, T., Borochin, M. A., Li, Y., Weiss, R., Kamm, R. D., Chen, C. S., & Asada, H. H. (2012) · Lab on a Chip · doi:10.1039/c2lc40338b · Cited by 288
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Bian, W., & Bursac, N. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2008.11.015 · Cited by 287
Metadata
- Authors
- Huang, Y.-C., Dennis, R. G., Larkin, L., & Baar, K.
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 2005-02
- Volume
- 98
- Issue
- 2
- Pages
- 706-713
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2044291159
- Cited by
- 316
- References
- 2
- FWCI
- 6.06
- Type
- journal article
- Language
- en
- Open access
- closed
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- Huang, Y.-C., Dennis, R. G., Larkin, L., & Baar, K. (2005). Rapid formation of functional muscle in vitro using fibrin gels. Journal of Applied Physiology. https://doi.org/10.1152/japplphysiol.00273.2004
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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