Biphasic electrical targeting plays a significant role in schwann cell activation

Tissue Engineering - Part A

Volumn 17, Issue 9-10, 2011, Pages 1327-1340

  Kim, In Sook ^a   Song, Yun Mi ^a   Cho, Tae Hyung ^a   Pan, Hui ^a   Lee, Tae Hyung ^a   Kim, Sung June ^a   Hwang, Soon Jung ^a  

^a Seoul National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; NEURONS; PEPTIDES;

AXONAL OUTGROWTH; AXONAL REGENERATION; BIPHASIC; BRAIN-DERIVED NEUROTROPHIC FACTORS; COCULTURE; CONTROL GROUPS; CULTURE CONDITIONS; ELECTRICAL STIMULATIONS; ELECTRONIC DEVICE; FUNCTIONAL ACTIVITIES; GROWTH MEDIUM; IN-VIVO; MESENCHYMAL STROMAL CELLS; NERVE GROWTH FACTOR; NERVE REGENERATION; NEURAL CONDUITS; NEURITES; NEUROTROPHIC FACTORS; PC12 CELLS; PERIPHERAL NERVES; PHEOCHROMOCYTOMA CELLS; PROTEIN LEVEL; SCHWANN CELLS; SCIATIC NERVES; UP-REGULATION;

CELL CULTURE;

RATTUS;

ADULT; ANIMAL; ARTICLE; CELL DIFFERENTIATION; CELL STRAIN; CYTOLOGY; ELECTROSTIMULATION; ELECTROSTIMULATION THERAPY; FEMALE; HUMAN; INJURY; METABOLISM; METHODOLOGY; NERVE FIBER; NERVE REGENERATION; PERIPHERAL NERVE; RAT; SCHWANN CELL; SPRAGUE DAWLEY RAT; STROMA CELL; TISSUE REGENERATION; TRANSPLANTATION;

ADULT; ANIMALS; AXONS; CELL DIFFERENTIATION; ELECTRIC STIMULATION; ELECTRIC STIMULATION THERAPY; FEMALE; GUIDED TISSUE REGENERATION; HUMANS; NERVE REGENERATION; PC12 CELLS; PERIPHERAL NERVES; RATS; RATS, SPRAGUE-DAWLEY; SCHWANN CELLS; STROMAL CELLS;

EID: 79955029837     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2010.0519     Document Type: Article

References (63)

1. Mycielska, M.E., and Djamgoz, M.B. Cellular mechanisms of direct-current electric field effects: galvanotaxis and metastatic disease. J Cell Sci 117, 1631, 2004.
2. Markov, M.S. Expanding use of pulsed electromagnetic field therapies. Electromagn Biol Med 26, 257, 2007.
3. Catterall, W.A., Perez-Reyes, E., Snutch, T.P., and Striessnig, J. International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels. Pharmacol Rev 57, 411, 2005.
4. Moore, T., and Fallah, M. Control of eye movements and spatial attention. Proc Natl Acad Sci USA 98, 1273, 2001.
5. Williams, Z.M., and Eskandar, E.N. Selective enhancement of associative learning by microstimulation of the anterior caudate. Nat Neurosci 9, 562, 2006.
6. Sommer, M.A., and Wurtz, R.H. A pathway in primate brain for internal monitoring of movements. Science 296, 1480, 2002.
7. Histed, M.H., Bonin, V., and Reid, R.C. Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation. Neuron 63, 508, 2009.
8. Al-Majed, A.A., Neumann, C.M., Brushart, T.M., and Gordon, T. Brief electrical stimulation promotes the speed and accuracy of motor axonal regeneration. J Neurosci 20, 2602, 2000.
9. Brushart, T.M., Hoffman, P.N., Royall, R.M., Murinson, B.B., Witzel, C., and Gordon, T. Electrical stimulation promotes motoneuron regeneration without increasing its speed or conditioning the neuron. J Neurosci 22, 6631, 2002.
10. Mendonca, A.C., Barbieri, C.H., and Mazzer, N. Directly applied low intensity direct electric current enhances peripheral nerve regeneration in rats. J Neurosci Methods 129, 183, 2003.
11. Gordon, T., Brushart, T.M., Amirjani, N., and Chan, K.M. The potential of electrical stimulation to promote functional recovery after peripheral nerve injury-comparisons between rats and humans. Acta Neurochir 100, 3, 2007.
12. Nix, W.A., and Hopf, H.C. Electrical stimulation of regenerating nerve and its effect on motor recovery. Brain Res 272, 21, 1983.
13. Moon, A.K., Zwolan, T.A. and Pfingst, B.E. Effects of phase duration on detection of electrical stimulation of the human cochlea. Hear Res 67, 166, 1993.
14. Humayun, M.S., de Juan, E., Jr., Weiland, J.D., Dagnelie, G., Katona, S., Greenberg, R., and Suzuki, S. Pattern electrical stimulation of the human retina. Vision Res 39, 2569, 1999.
15. Dostrovsky, J.O., Levy, R., Wu, J.P., Hutchison, W.D., Tasker, R.R., and Lozano, A.M. Microstimulation-induced inhibition of neuronal firing in human globus pallidus. J Neurophysiol 84, 570, 2000.
16. Gordon, T., Sulaiman, O.A., and Ladak, A. Electrical stimulation for improving nerve regeneration: where do we stand? Int Rev Neurobiol 87, 433, 2009.
17. Fawcett, J.W., and Keynes, R.J. Peripheral nerve regeneration. Annu Rev Neurosci 13, 43, 1990.
18. Torigoe, K., Tanaka, H.F., Takahashi, A., Awaya, A., and Hashimoto, K. Basic behavior of migratory Schwann cells in peripheral nerve regeneration. Exp Neurol 137, 301, 1996.
19. Sulaiman, O., Boyd, J.G., and Gordon, T. Axonal Regeneration in the Peripheral System of Mammals. Oxford: Oxford University Press, 2005.
20. Frostick, S.P., Yin, Q., and Kemp, G.J. Schwann cells, neurotrophic factors, and peripheral nerve regeneration. Microsurgery 18, 397, 1998.
21. Hall, S. The response to injury in the peripheral nervous system. J Bone Joint Surg Br 87, 1309, 2005.
22. Heumann, R., Korsching, S., Bandtlow, C., and Thoenen, H. Changes of nerve growth factor synthesis in nonneuronal cells in response to sciatic nerve transection. J Cell Biol 104, 1623, 1987.
23. Acheson, A., Barker, P.A., Alderson, R.F., Miller, F.D., and Murphy, R.A. Detection of brain-derived neurotrophic factor-like activity in fibroblasts and Schwann cells: inhibition by antibodies to NGF. Neuron 7, 265, 1991.
24. Boyd, J.G., and Gordon, T. Neurotrophic factors and their receptors in axonal regeneration and functional recovery after peripheral nerve injury. Mol Neurobiol 27, 277, 2003.
25. Hoke, A., Redett, R., Hameed, H., Jari, R., Zhou, C., Li, Z.B., Griffin, J.W., and Brushart, T.M. Schwann cells express motor and sensory phenotypes that regulate axon regeneration. J Neurosci 26, 9646, 2006.
26. Boyd, J.G., and Gordon, T. Glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor sustain the axonal regeneration of chronically axotomized motoneurons in vivo. Exp Neurol 183, 610, 2003.
27. Anton, E.S., Weskamp, G., Reichardt, L.F., and Matthew, W.D. Nerve growth factor and its low-affinity receptor promote Schwann cell migration. Proc Natl Acad Sci USA 91, 2795, 1994.
28. Li, Q., Ping, P., Jiang, H., and Liu, K. Nerve conduit filled with GDNF gene-modified Schwann cells enhances regeneration of the peripheral nerve. Microsurgery 26, 116, 2006.
29. Gordon, T. The physiology of neural injury and regeneration: the role of neurotrophic factors. J Commun Disord 43, 265, 2010.
30. Madduri, S., Feldman, K., Tervoort, T., Papaloizos, M., and Gander, B. Collagen nerve conduits releasing the neurotrophic factors GDNF and NGF. J Control Release 143, 168, 2010.
31. Al-Majed, A.A., Brushart, T.M., and Gordon, T. Electrical stimulation accelerates and increases expression of BDNF and trkB mRNA in regenerating rat femoral motoneurons. Eur J Neurosci 12, 4381, 2000.
32. English, A.W., Schwartz, G., Meador, W., Sabatier, M.J., and Mulligan, A. Electrical stimulation promotes peripheral axon regeneration by enhanced neuronal neurotrophin signaling. Dev Neurobiol 67, 158, 2007.
33. Kim, I.S., Song, J.K., Song, Y.M., Cho, T.H., Lee, T.H., Lim, S.S., Kim, S.J., and Hwang, S.J. Novel effect of biphasic electric current on in vitro osteogenesis and cytokine production in human mesenchymal stromal cells. Tissue Eng Part A 15, 2411, 2009.
34. Kim, I.S., Song, Y.M., Cho, T.H., Park, Y.D., Lee, K.B., Noh, I., Weber, F., and Hwang, S.J. In vitro response of primary human bone marrow stromal cells to recombinant human bone morphogenic protein-2 in the early and late stages of osteoblast differentiation. Dev Growth Differ 50, 553, 2008.
35. Pittenger, M.F., Mackay, A.M., Beck, S.C., Jaiswal, R.K., Douglas, R., Mosca, J.D., Moorman, M.A., Simonetti, D.W., Craig, S., and Marshak, D.R. Multilineage potential of adult human mesenchymal stem cells. Science 284, 143, 1999.
36. Noth, U., Osyczka, A.M., Tuli, R., Hickok, N.J., Danielson, K.G., and Tuan, R.S. Multilineage mesenchymal differentiation potential of human trabecular bone-derived cells. J Orthop Res 20, 1060, 2002.
37. Caddick, J., Kingham, P.J., Gardiner, N.J., Wiberg, M., and Terenghi, G. Phenotypic and functional characteristics of mesenchymal stem cells differentiated along a Schwann cell lineage. Glia 54, 840, 2006.
38. Dezawa, M., Takahashi, I., Esaki, M., Takano, M., and Sawada, H. Sciatic nerve regeneration in rats induced by transplantation of in vitro differentiated bone-marrow stromal cells. Eur J Neurosci 14, 1771, 2001.
39. Brohlin, M., Mahay, D., Novikov, L.N., Terenghi, G., Wiberg, M., Shawcross, S.G., and Novikova, L. N. Characterisation of human mesenchymal stem cells following differentiation into Schwann cell-like cells. Neurosci Res 64, 41, 2009.
40. Lee, T.H., Pan, H., Kim, I.S., Kim, J.K., Cho, T.H., Oh, J.H., Yoon, Y.B., Lee, J.H., Hwang, S.J., and Kim, S.J. Functional regeneration of a severed peripheral nerve with a 7mm gap in rats through the use of an implantable electrical stimulator and a conduit electrode with collagen coating. Neuromodulation Technol Neural Interface 13, 299, 2010.
41. Geremia, N.M., Gordon, T., Brushart, T.M., Al-Majed, A.A., and Verge, V.M. Electrical stimulation promotes sensory neuron regeneration and growth-associated gene expression. Exp Neurol 205, 347, 2007.
42. Baptista, A.F., Gomes, J.R., Oliveira, J.T., Santos, S.M., Vannier-Santos, M.A., and Martinez, A. M. High- and lowfrequency transcutaneous electrical nerve stimulation delay sciatic nerve regeneration after crush lesion in the mouse. J Peripher Nerv Syst 13, 71, 2008.
43. Greene, L.A., and Tischler, A.S. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci USA 73, 2424, 1976.
44. Yang, J., Lou, Q., Huang, R., Shen, L., and Chen, Z. Dorsal root ganglion neurons induce transdifferentiation of mesenchymal stem cells along a Schwann cell lineage. Neurosci Lett 445, 246, 2008.
45. Luduena, R.F. Are tubulin isotypes functionally significant. Mol Biol Cell 4, 445, 1993.
46. Garbay, B., Heape, A.M., Sargueil, F., and Cassagne, C. Myelin synthesis in the peripheral nervous system. Prog Neurobiol 61, 267, 2000.
47. Gordon, T., Sulaiman, O., and Boyd, J.G. Experimental strategies to promote functional recovery after peripheral nerve injuries. J Peripher Nerv Syst 8, 236, 2003.
48. Courtine, G., Gerasimenko, Y., van den Brand, R., Yew, A., Musienko, P., Zhong, H., Song, B., Ao, Y., Ichiyama, R.M., Lavrov, I., Roy, R.R., Sofroniew, M.V., and Edgerton, V. R. Transformation of nonfunctional spinal circuits into functional states after the loss of brain input. Nat Neurosci 12, 1333, 2009.
49. Gordon, T., Udina, E., Verge, V.M., and de Chaves, E.I. Brief electrical stimulation accelerates axon regeneration in the peripheral nervous system and promotes sensory axon regeneration in the central nervous system. Motor Control 13, 412, 2009.
50. Rutten, W.L. Selective electrical interfaces with the nervous system. Annu Rev Biomed Eng 4, 407, 2002.
51. Assouline, J.G., Bosch, P., Lim, R., Kim, I.S., Jensen, R., and Pantazis, N.J. Rat astrocytes and Schwann cells in culture synthesize nerve growth factor-like neurite-promoting factors. Brain Res 428, 103, 1987.
52. Villegas, R., Villegas, G.M., Nunez, J., Hernandez, M., and Castillo, C. Neuron-like differentiation of PC12 cells treated with media conditioned by either sciatic nerves, optic nerves, or Schwann cells. Cell Mol Neurobiol 25, 451, 2005.
53. Bampton, E.T., and Taylor, J.S. Effects of Schwann cell secreted factors on PC12 cell neuritogenesis and survival. J Neurobiol 63, 29, 2005.
54. Huang, J., Ye, Z., Hu, X., Lu, L., and Luo, Z. Electrical stimulation induces calcium-dependent release of NGF from cultured Schwann cells. Glia 58, 622, 2010.
55. Huang, E.J., and Reichardt, L.F. Neurotrophins: roles in neuronal development and function. Annu Rev Neurosci 24, 677, 2001.
56. Althaus, H.H., Kloppner, S., Schmidt-Schultz, T., and Schwartz, P. Nerve growth factor induces proliferation and enhances fiber regeneration in oligodendrocytes isolated from adult pig brain. Neurosci Lett 135, 219, 1992.
57. Lin, L.F., Doherty, D.H., Lile, J.D., Bektesh, S., and Collins, F. GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons. Science 260, 1130, 1993.
58. Henderson, C.E., Phillips, H.S., Pollock, R.A., Davies, A.M., Lemeulle, C., Armanini, M., Simmons, L., Moffet, B., Vandlen, R.A., Simpson, L.C., et al. GDNF: a potent survival factor for motoneurons present in peripheral nerve and muscle. Science 266, 1062, 1994.
59. McCaig, C.D., Rajnicek, A.M., Song, B., and Zhao, M. Controlling cell behavior electrically: current views and future potential. Physiol Rev 85, 943, 2005.
60. Li, L., El-Hayek, Y.H., Liu, B., Chen, Y., Gomez, E., Wu, X., Ning, K., Chang, N., Zhang, L., Wang, Z., Hu, X., and Wan, Q. Direct-current electrical field guides neuronal stem/progenitor cell migration. Stem Cells 26, 2193, 2008.
61. Huang, C., Shepherd, R.K., and Carter, P.M. Electrical stimulation of the auditory nerve: pH changes in vivo and in vitro. Proc 20th Aust Neurosci Soc 11, 216, 1990.
62. Snipes, G.J., Suter, U., Welcher, A.A., and Shooter, E.M. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13). J Cell Biol 117, 225, 1992.
63. Benninger, Y., Thurnherr, T., Pereira, J.A., Krause, S., Wu, X., Chrostek-Grashoff, A., Herzog, D., Nave, K.A., Franklin, R.J., Meijer, D., Brakebusch, C., Suter, U., and Relvas, J.B. Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development. J Cell Biol 177, 1051, 2007.