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Local tissue geometry determines contractile force generation of engineered muscle networks.

Publication ,  Journal Article
Bian, W; Juhas, M; Pfeiler, TW; Bursac, N
Published in: Tissue engineering. Part A
May 2012

The field of skeletal muscle tissue engineering is currently hampered by the lack of methods to form large muscle constructs composed of dense, aligned, and mature myofibers and limited understanding of structure-function relationships in developing muscle tissues. In our previous studies, engineered muscle sheets with elliptical pores ("muscle networks") were fabricated by casting cells and fibrin gel inside elastomeric tissue molds with staggered hexagonal posts. In these networks, alignment of cells around the elliptical pores followed the local distribution of tissue strains that were generated by cell-mediated compaction of fibrin gel against the hexagonal posts. The goal of this study was to assess how systematic variations in pore elongation affect the morphology and contractile function of muscle networks. We found that in muscle networks with more elongated pores the force production of individual myofibers was not altered, but the myofiber alignment and efficiency of myofiber formation were significantly increased yielding an increase in the total contractile force despite a decrease in the total tissue volume. Beyond a certain pore length, increase in generated contractile force was mainly contributed by more efficient myofiber formation rather than enhanced myofiber alignment. Collectively, these studies show that changes in local tissue geometry can exert both direct structural and indirect myogenic effects on the functional output of engineered muscle. Different hydrogel formulations and pore geometries will be explored in the future to further augment contractile function of engineered muscle networks and promote their use for basic structure-function studies in vitro and, eventually, for efficient muscle repair in vivo.

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Published In

Tissue engineering. Part A

DOI

EISSN

1937-335X

ISSN

1937-3341

Publication Date

May 2012

Volume

18

Issue

9-10

Start / End Page

957 / 967

Related Subject Headings

  • Tissue Engineering
  • Rats, Sprague-Dawley
  • Rats
  • Myoblasts
  • Dimethylpolysiloxanes
  • Cells, Cultured
  • Biomedical Engineering
  • Animals
  • 4003 Biomedical engineering
  • 0912 Materials Engineering
 

Citation

APA
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ICMJE
MLA
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Bian, W., Juhas, M., Pfeiler, T. W., & Bursac, N. (2012). Local tissue geometry determines contractile force generation of engineered muscle networks. Tissue Engineering. Part A, 18(9–10), 957–967. https://doi.org/10.1089/ten.tea.2011.0313
Bian, Weining, Mark Juhas, Terry W. Pfeiler, and Nenad Bursac. “Local tissue geometry determines contractile force generation of engineered muscle networks.Tissue Engineering. Part A 18, no. 9–10 (May 2012): 957–67. https://doi.org/10.1089/ten.tea.2011.0313.
Bian W, Juhas M, Pfeiler TW, Bursac N. Local tissue geometry determines contractile force generation of engineered muscle networks. Tissue engineering Part A. 2012 May;18(9–10):957–67.
Bian, Weining, et al. “Local tissue geometry determines contractile force generation of engineered muscle networks.Tissue Engineering. Part A, vol. 18, no. 9–10, May 2012, pp. 957–67. Epmc, doi:10.1089/ten.tea.2011.0313.
Bian W, Juhas M, Pfeiler TW, Bursac N. Local tissue geometry determines contractile force generation of engineered muscle networks. Tissue engineering Part A. 2012 May;18(9–10):957–967.

Published In

Tissue engineering. Part A

DOI

EISSN

1937-335X

ISSN

1937-3341

Publication Date

May 2012

Volume

18

Issue

9-10

Start / End Page

957 / 967

Related Subject Headings

  • Tissue Engineering
  • Rats, Sprague-Dawley
  • Rats
  • Myoblasts
  • Dimethylpolysiloxanes
  • Cells, Cultured
  • Biomedical Engineering
  • Animals
  • 4003 Biomedical engineering
  • 0912 Materials Engineering