The modulation of myogenic cells differentiation using a semiconductor-muscle junction

Biomaterials

Volumn 32, Issue 18, 2011, Pages 4228-4237

  Quarta, Marco ^a,b   Scorzeto, Michele ^a   Canato, Marta ^a   Dal Maschio, Marco ^c   Conte, Davide ^d   Blaauw, Bert ^e   Vassanelli, Stefano ^a   Reggiani, Carlo ^a  

^a UNIVERSITY OF PADOVA   (Italy)

^b STANFORD UNIVERSITY   (United States)

^c ISTITUTO ITALIANO DI TECNOLOGIA   (Italy)

^d UNIVERSITY OF VERONA   (Italy)

^e VENETIAN INSTITUTE OF MOLECULAR MEDICINE   (Italy)

Author keywords

Calcium; Cell culture; Electrical Stimulation; Muscle; Plasticity; Silicon; Titanium

Indexed keywords

ACTION POTENTIALS; BIONIC SYSTEMS; CAPACITIVE CURRENTS; CHARGE ACCUMULATION; CYTOSOLIC CALCIUM; ELECTRICAL STIMULATIONS; ELECTROCHEMICAL REACTIONS; ELECTRONIC JUNCTIONS; HYBRID JUNCTION; HYBRID SILICON; IN-VITRO; MUSCLE CELL; MUSCLE CONTRACTIONS; MYOBLASTS; MYOGENIC CELLS; MYOTUBES; NEUROMUSCULAR JUNCTIONS; NON-INVASIVE; NUCLEAR TRANSLOCATIONS; REGENERATIVE MEDICINE; SINGLE CELLS; SYNAPTOGENESIS; VOLTAGE CHANGE; VOLTAGE GATED ION CHANNELS;

CALCIUM; CELL CULTURE; CELL MEMBRANES; DESIGN; MUSCLE; TITANIUM; TRANSIENTS;

SEMICONDUCTOR JUNCTIONS;

CHOLINERGIC RECEPTOR; ION CHANNEL; SILICON; TRANSCRIPTION FACTOR NFAT3;

ACTION POTENTIAL; ANIMAL CELL; ARTICLE; BIONICS; CELL DIFFERENTIATION; CELL JUNCTION; CELL STIMULATION; CONTROLLED STUDY; ELECTRIC CURRENT; IN VITRO STUDY; MODULATION; MOUSE; MUSCLE CELL; MUSCLE CONTRACTION; MYOBLAST; MYOTUBE; NEWBORN; NONHUMAN; NUCLEAR REPROGRAMMING; PLASTICITY; PRIORITY JOURNAL; SEMICONDUCTOR; SYNAPTOGENESIS;

ACTION POTENTIALS; ANIMALS; CALCIUM; CELL DIFFERENTIATION; CELLS, CULTURED; ELECTRIC CAPACITANCE; ELECTRIC STIMULATION; MICE; MUSCLE FIBERS, SKELETAL; MUSCLE, SKELETAL; MYOBLASTS; NFATC TRANSCRIPTION FACTORS; RECEPTORS, CHOLINERGIC; SEMICONDUCTORS; SILICON;

EID: 79955101204     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2011.02.024     Document Type: Article

References (54)

1. Fromherz P., Offenhausser A., Vetter T., Weis J. A neuron-silicon junction:a Retzius cell of the leech on an insulated-gate field-effect transistor. Science 1991, 31:1290-1293.
2. Boussaad S., Diner B.-A., Fan J. Influence of redox molecules on the electronic conductance of single-walled carbon nanotube field-effect transistors: application to chemical and biological sensing. J Am Chem Soc 2008, 130:3780-3787.
3. Stengel M., Spaldin N.A. Origin of the dielectric dead layer in nanoscale capacitors. Nature 2006, 443:679-682.
4. Patolsky F., Timko B.-P., Yu G., Fang Y., Greytak A.-B., Zheng G., et al. Detection, stimulation, and inhibition of neuronal signals with high-density nanowire transistor arrays. Science 2006, 313:1100-1104.
5. Cooper S.T., Maxwell A.L., Kizana E., Ghoddusi M., Hardeman E.C., Alexander E.I., et al. C2C12 co-culture on a fibroblast substratum enables sustained survival of contractile, highly differentiated myotubes with peripheral nuclei and adult fast myosin expression. Cell Motil Cytoskeleton 2004, 58:200-211.
6. Fromherz P. Neuroelectronic interfacing: semiconductor chips with ion channels, nerve cells, and brain. Nanoelectronics and information technology 2003, 781-810. Willey-VCH Verlag, Berlin. R. Wasser (Ed.).
7. Schoen I., Fromherz P. The mechanism of extracellular stimulation of nerve cells on an electrolyte-oxide-semiconductor capacitor. Biophys J 2007, 92:1096-1111.
8. Gleixner R., Fromherz P. The extracellular electrical resistivity in cell adhesion. Biophys J 2006, 90:2600-2611.
9. Straub B., Meyer E., Fromherz P. Recombinant maxi-K channels on transistor, a prototype of iono-electronic interfacing. Nat Biotechnol 2001, 19:121-124.
10. Vassanelli S., Fromherz P. Transistor probes local potassium conductances in the adhesion region of cultured rat hippocampal neurons. J Neurosci 1999, 19:6767-6773.
11. Zeck G., Fromherz Z. Noninvasive neuroelectronic interfacing with synaptically connected snail neurons immobilized on a semiconductor chip. Proc Natl Acad Sci 2001, 98:10457-10462.
12. Ingerbrandt S., Yeung C.K., Krause M. A Offenhausser. Cardiomyocyte-transistor-hybrids for sensor application. Biosens Bioelectron 2001, 16:565-570.
13. Rios E., Pizzarro G. Voltage sensor of excitation-contraction coupling in skeletal muscle. Physiol Rev 1991, 71:849-908.
14. Wallrapp F., Fromherz P. TiO2 and HfO2 in electrolyte-oxide-silicon confi{ligature}guration for applications in bioelectronics. J Appl Phys 2006, 99:114103-114110.
15. Braun D., Fromherz P. Fast voltage transients in capacitive silicon-to- cell stimulation detected with a lumininescent molecular electronic probe. Phys Rev Lett 2001, 86:2905-2908.
16. Cognard C., Constantin B., River-Bastide M., Imbert N., Besse C., Raymond G. Appearance and evolution of calcium currents and contraction during the early post-fusional stages of rat skeletal muscle cells developing in primary culture. Development 1993, 117:1153-1161.
17. Fujita H., Nedachi T., Kanzaki M. Accelerated de novo sarcomere assembly by electric pulse stimulation in C2C12 myotubes. Exp Cell Res 2007, 15:1853-1865.
18. Valdes J.A., Hidalgo J., Galaz J.L., Puentes N., Silva M., Jaimovich E., et al. NF-kappaB activation by depolarization of skeletal muscle cells depends on ryanodine and IP3 receptor-mediated calcium signals. Am J Physiol Cell Physiol 2007, 292:C1960-C1970.
19. Molgò J., Colasantei C., Adams D.S., Jaimovich E. IP3 receptors and Ca2+ signals in adult skeletal muscle satellite cells in situ. Biol Res 2004, 37:635-639.
20. Estrada M., Cardenas C., Liberona J.L., Carasco M.A., Mignery G.A., Allen P.D., et al. Calcium transients in 1B5 myotubes lacking ryanodine receptors are related to inositol trisphosphate receptors. J Biol Chem 2001, 276:22868-22874.
21. Tarroni P., Rossi D., Conti A., Sorrentino V. Expression of the ryanodine receptor type 3 calcium release channel during development and differentiation of mammalian skeletal muscle cells. J Biol Chem 1997, 272:19808-19813.
22. Lorenzon P., Grohovaz F., Ruzier F. Voltage- and ligand-gated ryanodine receptors are functionally separated in developing C2C12 mouse myotubes. J Physiol 2000, 2:499-507.
23. Stern-Straeter J., Bach A.D., Stangenberg L., Foerster V.T., Horch R.E., Stark G.B., et al. Impact of electrical stimulation on three-dimensional myoblast cultures - a real-time RT-PCR study. J Cell Mol Med 2005, 9:883-892.
24. Dennis R.G., Kosnik P.E., Gilbert M.E., Faulkner J.A. Excitability and contractility of skeletal muscle engineered from primary cultures and cell lines. Am J Physiol Cell Physiol 2001, 280:C288-C295.
25. Huang Y., Dennis R.G., Baar K. Cultured slow vs. fast skeletal muscle cells differ in physiology and responsiveness to stimulation. Am J Physiol Cell Physiol 2006, 291:C11-C17.
26. Jamovich E., Reyes R., Liberona J.L., Powel J.A. IP3 receptors, IP3 transients, and nucleus-associated Ca2+ signals in cultured skeletal muscle. Am J Physiol Cell Physiol 2000, 278:998-1010.
27. Timmerman L.A., Clipstone N.A., Ho S.N., Northrop J.P., Crabtree G.R. Rapid shuttling of NF-AT in discrimination of Ca2+ signals and immunosuppression. Nature 1996, 383:837-840.
28. Dolmetsch R.E., Lewis R.S., Goodnow C.C., Healy J.I. Differential activation of transcription factors induced by Ca2+ response amplitude and duration. Nature 1997, 386:855-858.
29. Cardenas C., Liberona J.L., Molgo J., Colasante C., Mignery G.A., Jaimovich E. Nuclear inositol 1,4,5-trisphosphate receptors regulate local Ca2+ transients and modulate cAMP response element binding protein phosphorylation. J Cell Sci 2005, 118:3131-3140.
30. Olson E.N., Williams R.S. Calcineurin signaling and muscle remodeling. Cell 2000, 101:689-692.
31. Crabtree G., Olson E. NFAT signaling:choreographing the social lives of cells. Cell 2002, 109:67-79.
32. Crabtree G.R. Generic signals and specific outcomes:signaling through Ca2+, calcineurin, and NF-AT. Cell 1999, 96:611-614.
33. Delling U., Tureckova J., Lim H.W., De Windt L.J., Rotwein P., Molkentin J.D. A calcineurin-NFATc3-dependent pathway regulates skeletal muscle differentiation and slow myosin heavy-chain expression. Mol Cell Biol 2000, 20:6600-6611.
34. Krause R.M., Hamann M., Bader C.R., Liu J.H., Baroffio A., Bernheim L. Activation of nicotinic acetylcholine receptors increases the rate of fusion of cultured human myoblasts. J Physiol 1995, 489:779-790.
35. Bandi E., Bernareggi A., Grandolfo M., Mozzetta C., Augusti-Tocco G., Ruzzier F., et al. Autocrine activation of nicotinic acetylcholine receptors contributes to Ca2+ spikes in mouse myotubes during myogenesis. J Physiol 2005, 568:171-180. 171.
36. McMahan U.J., Wallace B.G. Molecules in basal lamina that direct the formation of synaptic specializations at neuromuscular junctions. Dev Neurosci 1989, 11:227-247.
37. Glass D.J., Bowen D.C., Stitt T.N., Radziejewski C., Bruno J., Ryan T.E., et al. Agrin acts via a MuSK receptor complex. Cell 1996, 85:513-523.
38. Borges L.S., Lee Y., Ferns M. Dual role for calcium in agrin signaling and acetylcholine receptor clustering. J Neurobiol 2002, 50:69-79.
39. Megeath L.J., Fallon J.R. Intracellular calcium regulates agrin-induced acetylcholine receptor clustering. J Neurosci 1998, 18:672-678.
40. Megeath L.J., Kirber M.T., Hopf C., Hoch W., Fallon J.R. Calcium-dependent maintenance of agrin-induced postsynaptic specializations. Neuroscience 2003, 122:659-668.
41. Li X., Zhou W., Zeng S., Liu M., Luo Q. Characterization of synchronized bursts in cultured hippocampal neuronal networks with learning training on microelectrode arrays. Biosens Bioelectron 2007, 22:2976-2982.
42. Suzuki I., Sugio Y., Jimbo Y., Yasuda K. Stepwise pattern modification of neuronal network in photo-thermally-etched agarose architecture on multi-electrode array chip for individual-cell-based electrophysiological measurement. Lab Chip 2005, 5:241-247.
43. Ravel-Chapuis A., Vandromme M., Thomas J., Schaeffer L. Postsynaptic chromatin is under neural control at the neuromuscular junction. EMBO J 2007, 26:1117-1128.
44. Vogel E. Technology and metrology of new electronic materials and devices. Nat Nanotechnol 2007, 2:25-32.
45. Stengel M., Spaldin N.A. Origin of the dielectric dead layer in nanoscale capacitors. Nature 2006, 443:679-682.
46. Kosar T.F., Tourovskaia A., Figueroa-Masot X., Adams M.E., Folch A. A nanofabricated planar aperture as a mimic of the nerve-muscle contact during synaptogenesis. Lab Chip 2006, 6:632-638.
47. Pfeifer R., Lungarella M., Iida F. Self-organization, embodiment, and biologically inspired robotics. Science 2007, 318:1088-1093.
48. Rudrauf D., Lutz A., Cosmelli D., Lachaux J.P., Le Van Quyen M. From autopoiesis to neurophenomenology:Francisco Varela's exploration of the biophysics of being. Biol Res 2003, 36:27-65.
49. Chien H.J., Beer R.D. The brain has a body:adaptive behavior emerges from interactions of nervous system, body and environment. Trend Neurosci 1997, 20:553-557.
50. Brezina V., Horn C.C., Weiss K.R. Modeling neuromuscular modulation in Aplysia. III. Interaction of central motor commands and peripheral modulatory state for optimal behavior. J Neurophysiol 2005, 93:1523-1556.
51. Richard A.N. Technology insight: future neuroprosthetic therapies for disorders of the nervous system. Nat Clin Pract Neurol 2007, 3:444-452.
52. Chapin J.K. Using multi-neuron population recordings for neural prosthetics. Nat Neurosci 2004, 7:452-455.
53. Ziemke T. On the role of emotion in biological and robotic autonomy. Biosystems 2008, 91(2):401-408.
54. Beer R.D., Chiel H.J., Quinn R.D., Ritzmann R.E. Biorobotic approaches to the study of motor systems. Curr Opin Neurobiol 1998, 8:777-782.