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Development of Self-assembled Muscle-powered Microdevices

Published online by Cambridge University Press:  15 March 2011

Jianzhong Xi ,
Jacob J. Schmidt  and
Carlo D. Montemagno
Jianzhong Xi
Affiliation:
Department of Bioengineering, University of California, Los Angeles, 7523 Boelter Hall, 420 Westwood Plaza, Los Angeles, CA, 90095
Jacob J. Schmidt
Affiliation:
Department of Bioengineering, University of California, Los Angeles, 7523 Boelter Hall, 420 Westwood Plaza, Los Angeles, CA, 90095
Carlo D. Montemagno
Affiliation:
Department of Bioengineering, University of California, Los Angeles, 7523 Boelter Hall, 420 Westwood Plaza, Los Angeles, CA, 90095
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Abstrat

As microcomponents in engineered systems, biological muscles have unique advantages such as large force transduction, utilization of biochemical fuel, and self-assembly from single cells, over other inorganic actuators for biomedical engineering applications. Successful integration of muscles with inorganic fabricated structures and electronics promises the capability of precisely characterizing muscles' mechanical properties and fabricating self-assembled controllable autonomous structures powered by ubiquitous glucose. However, the use of extracted muscle tissue from animals on these devices is impractical and inefficient, as the tissues must be dissected and incorporated into each device by hand with crude interfaces between the biological tissue and inorganic materials. Integration of muscle with fabricated structures would be optimally achieved through self-assembling muscle cells on MEMS. The construction of self-assembled muscle-powered MEMS structures is complicated by the stringent requirements to spatially direct the cell growth, control the tight connection of these differentiated structures with MEMS structures, and enable the cells and the integrated hybrid freedom to move. Conventional and soft photolithography techniques have been extensively employed to pattern the growth of a variety of cell types and investigate their interaction with substrate in the micrometer level. However, all studies are only suitable for patterning static cells on an immobile surface, so a novel system of spatially patterning the contractible cells must be developed to enable the cells and the integrated hybrid devices to be free to move.

We present a novel system of self-assembling myocytes on MEMS devices. This system has shown its capability of spatially and selectively directed growth and differentiation of myocytes into single muscle bundles, attachment of these functional bundles to MEMS structures, and the controlled partial release of the resultant hybrid devices. Two groups of self-assembled muscle-MEMS devices, force-measuring cantilevers and muscle-powered microrobots have been created. Here the further detailed studies of this system are discussed, especially the concept of the self-assembly and the material interfacial problems in this system.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 820: Symposia O/R – Nanoengineered Assemblies and Advanced Micro/Nanosystems , 2004 , O5.8/W9.8
Copyright
Copyright © Materials Research Society 2004

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References

[1] Brady, A. J., “Mechanical properties of isolated cardiac myocytes,” Physiol Rev, vol. 71, pp. 413–28, 1991.Google Scholar
[2] Fauver, M. E., Dunaway, D. L., Lilienfeld, D. H., Craighead, H. G., and Pollack, G.H., “Microfabricated cantilevers for measurement of subcellular and molecular force,” IEEE transactions on Biomedical Engineering, vol. 45, pp. 891–898, 1998.Google Scholar
[3] Herzog, W., Skeletal muscle mechanics: John Wiley & Sons, LTD, 2000.Google Scholar
[4] Lin, G., Palmer, R. E., Pister, K. S. J., and Roos, K. P., “Miniature heart cell force transducer system implemented in MEMS technology,” IEEE Transactions on Biomedical Engineering, vol. 48, pp. 996–1006, 2001.Google Scholar
[5] Xi, J. Z., Schmidt, J., and Montemagno, C., “A Novel System for the Self-Assembly of Muscle on Microdevices,” In Preparation, 2003.Google Scholar
[6] Okano, T., Yamada, N., Sakai, H., and Sakurai, Y., “A novel recovery system for cultured cells using plasma-treated polystyrene dishes grafted with poly(N-isopropylacrylamide),” Journal of Biomedical Materials Research, vol. 27, pp. 1243–1251, 1993.Google Scholar
[7] Shimizu, T., Yamato, M., Kikuchi, A., and Okano, T., “Two-dimensional manipulation of cardiac myocytes sheets utilizing temperature-responsive culture dishes augments the pulsatile Amplitude,” Tissue Engineering, vol. 7, pp. 141–151, 2001.Google Scholar
[8] McMahon, D., Anderson, P., Nassar, R., Bunting, J. B., Saba, Z., Oakeley, A., and Malouf, N., “C2C12 cells: biophysical, biochemical, and immunocytochemical properties,” the American Physiological Society, vol. 35, pp. C1795–C1802, 1994.Google Scholar
[9] Ross, R. S., Pham, C., Shai, S. Y., Goldhaber, J. I., Fenczik, C., Glembotski, C. C., Ginsberg, M. H., and Loftus, J. C., “ß1 integrins participate in the hypertrophic response of rat ventricular myocytes,” Circulation Research, vol. 82, pp. 1160–1172, 1998.Google Scholar
[10] Sen, A., Dunnmon, P., Henderson, S. A., Gerard, R. D., and Chien, K. R., “Terminally differentiated neonatal rat myocardial cells proliferate and maintain specific differentiated functions following expression of SV40 large T antigen,” Journal of Biological Chemistry, vol. 263, pp. 19132–19136, 1988.Google Scholar
[11] Folch, A. and Toner, M., “Microengeering of Cellular Interactions,” Annu. Rev. Biomed. Eng., vol. 02, pp. 227–56, 2000.Google Scholar
[12] Kane, R. S., Takayama, S., Ostuni, E., Ingber, D. E., and Whitesides, G. M., “Patterning proteins and cells using soft lithography,” Biomaterials, vol. 20, pp. 2363–2376, 1999.Google Scholar
[13] Fromherz, P., “Electrical interfacing of nerve cells and semiconductor chips,” Chemphyschem, vol. 3, pp. 276–284, 2002.Google Scholar
[14] Ito, Y., “Surface micropatterning to regulate cell functions,” Biomaterials, vol. 20, pp. 2333–2342, 1999.Google Scholar
[15] Yamato, M., Konno, C., Utsumi, M., Kikuchi, A., and Okano, T., “Thermally responsive polymer-grafted surfaces facilitate patterned cell seeding and co-culture,” Biomaterials, vol. 23, pp. 561–567, 2002.Google Scholar
[16] Yamato, M., Utsumi, M., Kushida, A., Konno, C., Kikuchi, A., and Okano, T., “Thermo-responsive culture dishes allow the intact harvest of multilayered keratinocyte sheets without dispase by reducing temperature,” Tissue Engineering, vol. 7, pp. 473–480, 2001.Google Scholar
[17] Chen, G., Ito, Y., and Imanishi, Y., “Regulation of growth and adhesion of cultured cells by insulin conjugated with thermoresponsive polymers,” Biotechnology and Bioengineering, vol. 53, pp. 339–344, 1997.Google Scholar
[18] Hu, Z., Chen, Y., Wang, C., Zheng, Y., and Li, Y., “Polymer gels with engineered environmentally responsive surface patterns,” Nature, vol. 393, pp. 149–152, 1998.Google Scholar