Micro-patterned nanowire surfaces encourage directional neural progenitor cell adhesion and proliferation

Journal of Biomedical Nanotechnology

Volumn 9, Issue 10, 2013, Pages 1698-1706

  Bechara, Samuel ^a   Popat, Ketul C ^a  

^a Department of Mechanical Engineering   (United States)

Author keywords

Micropatterning; Nanowire surfaces; Neural progenitor cells; Neural tissue engineering

Indexed keywords

CELL ADHESION; CELL PROLIFERATION; CELLS; CYTOLOGY; HYDROPHOBICITY; MICROMACHINING; NANOWIRES; PATIENT MONITORING; PATIENT TREATMENT; SCAFFOLDS (BIOLOGY); SURFACE CHEMISTRY; SURFACE TOPOGRAPHY; TISSUE; TISSUE ENGINEERING; TOPOGRAPHY;

HYDROPHOBIC SURFACES; MICRO PATTERNING; NANOTOPOGRAPHIES; NANOWIRE SURFACE; NEURAL PROGENITOR CELLS; NEURAL TISSUE ENGINEERING; PERIPHERAL NERVES; TISSUE ENGINEERING SCAFFOLD;

CELL ENGINEERING;

NANOWIRE; POLYCAPROLACTONE; BIOMATERIAL; NANOTUBE;

ACTIN FILAMENT; ANIMAL CELL; ARTICLE; CELL ADHESION; CELL AGGREGATION; CELL DIFFERENTIATION; CELL DIVISION; CELL ELONGATION; CELL GROWTH; CELL PROLIFERATION; CELL SHAPE; CELL STRUCTURE; CONTROLLED STUDY; HYDROPHILICITY; HYDROPHOBICITY; IMMORTALIZED CELL LINE; IN VITRO STUDY; MOUSE; NERVE FIBER REGENERATION; NEURAL STEM CELL; NONHUMAN; PERIPHERAL NERVE INJURY; TISSUE ENGINEERING; TISSUE REGENERATION; ANIMAL; CELL LINE; CHEMISTRY; CYTOLOGY; DEVICE FAILURE ANALYSIS; DEVICES; EQUIPMENT DESIGN; MATERIALS TESTING; NERVE CELL; NERVE REGENERATION; PHYSIOLOGY; STEM CELL; SURFACE PROPERTY; SYNTHESIS; TISSUE SCAFFOLD;

ANIMALS; BIOCOMPATIBLE MATERIALS; CELL ADHESION; CELL DIFFERENTIATION; CELL LINE; CELL PROLIFERATION; EQUIPMENT DESIGN; EQUIPMENT FAILURE ANALYSIS; GUIDED TISSUE REGENERATION; MATERIALS TESTING; MICE; NANOTUBES; NERVE REGENERATION; NEURONS; STEM CELLS; SURFACE PROPERTIES; TISSUE SCAFFOLDS;

EID: 84922832576     PISSN: 15507033     EISSN: 15507041     Source Type: Journal    
DOI: 10.1166/jbn.2013.1667     Document Type: Article

References (34)

1. I. K. Cohen, R. F. Die-gelmann, W. J. Lindblad, and N. E. Hugo, Wound Healing: Biochemical and Clinical Aspects. Plast. Reconstr. Surg. 90, 926 (1992).
2. T. Kretschmer, G. Antoniadis, V. Braun, S. A. Rath, and H. P. Richter, Evaluation of iatrogenic lesions in 722 surgically treated cases of peripheral nerve trauma. J. Neurosurg. 94, 905 (2001).
3. S. E. Mackinnon, V. B. Doolabh, C. B. Novak, and E. P. Trulock, Clinical outcome following nerve allograft transplantation. Plast. Reconstr. Surg. 107, 1419 (2001).
4. H. Millesi, Nerve transplantation for reconstruction of peripheral nerves injured by the use of the microsurgical technic, Minerva Chir. 22, 950 (1967).
5. D. G. Kline, Surgical repair of peripheral nerve injury. Muscle Nerve Delivered by Publishing Technology IP: 203.56.241.128 On: Sat,Copyright: American 13, 843 (1990).
6. A. Moradzadeh, G. H. Borschel, J. P. Luciano, E. L. Whitlock, A. Hayashi, D. A. Hunter, and S. E. Mackinnon, The impact of motor and sensory nerve architecture on nerve regeneration. Exp. Neurol. 212, 370 (2008).
7. J. Ryu, C. F. Beimesch, and T. J. Lalli, (iii) Peripheral nerve repair. Orthopaedics and Trauma 25, 174 (2011).
8. S. Yoshii, M. Oka, N. Ikeda, M. Akagi, Y. Matsusue, and T. Nakamura, Bridging a peripheral nerve defect using collagen filaments. J. Hand Surg Am. 26, 52 (2001).
9. M. J. Bertleff, M. F. Meek, and J. P. Nicolai, A prospective clinical evaluation of biodegradable neurolac nerve guides for sensory nerve repair in the hand. J. Hand Surg. Am. 30, 513 (2005).
10. S. Morelli, S. Salerno, A. Piscioneri, B. J. Papenburg, A. Di Vito, G. Giusi, M. Canonaco, D. Stamatialis, E. Drioli, and L. De Bartolo, Influence of micro-patterned PLLA membranes on outgrowth and orientation of hippocampal neurites. Biomaterials 31, 7000 (2010).
11. A. Ruiz, L. Buzanska, D. Gilliland, H. Rauscher, L. Sirghi, T. Sobanski, M. Zychowicz, L. Ceriotti, F. Bretagnol, S. Coecke, P. Colpo, and F. Rossi, Micro-stamped surfaces for the patterned growth of neural stem cells. Biomaterials 29, 4766 (2008).
12. F. Meng, V. Hlady, and P. A. Tresco, Inducing alignment in astrocyte tissue constructs by surface ligands patterned on biomaterials. Biomaterials 33, 1323 (2012).
13. S. Kelly, E. M. Regan, J. B. Uney, A. D. Dick, J. P. McGeehan, E. J. Mayer, and F. Claeyssens, Patterned growth of neuronal cells on modified diamond-like carbon substrates. Biomaterials 29, 2573 (2008).
14. J. B. Recknor, D. S. Sakaguchi and S. K. Mallapragada, Directed growth and selective differentiation of neural progenitor cells on micropatterned polymer substrates. Biomaterials 27, 4098 (2006).
15. A. Tsuruma, M. Tanaka, S. Yamamoto, and M. Shimomura, Control of neural stem cell differentiation on honeycomb films. Colloids and Surfaces A Physicochemical and Engineering Aspects 313-314, 536 (2008).
16. C. Luo, L. Liu, X. Ni, L. Wang, S. M. Nomura, Q. Ouyang, and Y. Chen, Differentiating stem cells on patterned substrates for neural network formation. Microelectronic Engineering 88, 1707 (2011).
17. J. Lee, M. M. Miró, C. K. Akkan, A. Haidar, W. Metzger, L. K. Schwarz, V. Zaporojtchenko, K. H. Schäfer, H. Abdul-Khaliq, M. Veith, and C. Aktas, Development of Multi Scale Structured Al/Al2O3 Nanowires for Controlled Cell Guidance. Journal of biomedical nanotechnology 9, 295 (2013).
18. D. R. Nisbet, A. E. Rodda, M. K. Horne, J. S. Forsythe, and D. I. Finkelstein, Neurite infiltration and cellular response to electrospun polycaprolactone scaffolds implanted into the brain. Biomaterials 30, 4573 (2009).
19. M. B. Runge, M. Dadsetan, J. Baltrusaitis, A. M. Knight, T. Ruesink, E. A. Lazcano, L. Lu, A. J. Windebank, and M. J. Yaszemski, The development of electrically conductive polycaprolactone fumaratepolypyrrole composite materials for nerve regeneration. Biomaterials 31, 5916 (2010).
20. X. Kang, Y. Xie, H. M. Powell, L. James Lee, M. A. Belury, J. J. Lannutti, and D. A. Kniss, Adipogenesis of murine embryonic stem cells in a three-dimensional culture system using electrospun polymer scaffolds. Biomaterials 28, 450 (2007).
21. L. He, S. Liao, D. Quan, M. Ngiam, C. K. Chan, S. Ramakrishna, and J. Lu, The influence of laminin-derived peptides conjugated to Lys-capped PLLA on neonatal mouse cerebellum C17.2 stem cells. Biomaterials 30, 1578 (2009).
22. B. Li, Y. Ma, S. Wang, and P. M. Moran, Influence of carboxyl group density on neuron cell attachment and differentiation behavior: gradient-guided neurite outgrowth. Biomaterials 26, 4956 (2005).
23. L. Ghasemi-Mobarakeh, M. P. Prabhakaran, M. Morshed, M. H. Nasr-Esfahani, and S. Ramakrishna, Electrospun poly(epsiloncaprolactone)/ gelatin nanofibrous scaffolds for nerve tissue engineering. Biomaterials 29, 4532 (2008).
24. E. Y. Snyder, D. L. Deitcher, C. Walsh, S. Arnold-Aldea, E. A. Hartwieg, and C. L. Cepko, Multipotent neural cell lines can engraft and participate in development of mouse cerebellum. Cell 68, 33 (1992).
25. L. P. Niles, K. J. Armstrong, L. M. Rincon Castro, C. V. Dao, R. Sharma, C. R. McMillan, L. C. Doering, and D. L. Kirkham, Neural stem cells express melatonin receptors and neurotrophic factors: colocalization of the MT1 receptor with neuronal and glial markers. BMC Neurosci 5, 41 (2004).
26. S. L. Bechara, A. Judson, and K. C. Popat, Template synthesized poly(epsilon-caprolactone) nanowire surfaces for neural tissue engineering. Biomaterials 31, 3492 (2010).
27. S. L. Bechara, L. Wadman, and K. C. Popat, Electroconductive polymeric nanowire templates facilitates in vitro C17.2 neural stem cell line adhesion, proliferation and differentiation. Acta Biomater. 7, 2892 (2011).
28. D. Berger, K. Popat, and A. Prasad, PCL Nanopillars Versus Nanofibers: A Contrast in Progenitor Cell Morphology, Proliferation, and Fate Determination. Adv. Eng. Mater. 14, B351 (2012).
29. S. M. Frisch and H. Francis, Disruption of epithelial cell-matrix interactions induces apoptosis. J. Cell Biol. 124, 619 (1994).
30. L. K. Hansen, D. J. Mooney, J. P. Vacanti, and D. E. Ingber, Integrin binding and cell spreading on extracellular matrix act at different points in the cell cycle to promote hepatocyte growth. Mol. Biol. Cell 5, 967 (1994).
31. J. E. Davies, C. Huang, C. Proschel, M. Noble, M. Mayer-Proschel, and S. J. Davies, Astrocytes derived from glial-restricted precursors promote spinal cord repair. J. Biol. 5, 7 (2006).
32. J. M. Schakenraad, H. J. Busscher, C. R. Wildevuur, and J. Arends, The influence of substratum surface free energy on growth and spreading of human fibroblasts in the presence and absence of serum proteins. J. Biomed. Mater. Res. 20, 773 (1986).
33. A. P. Balgude, X. Yu, A. Szymanski, and R. V. Bellamkonda, Agarose gel stiffness determines rate of DRG neurite extension in 3D cultures. Biomaterials 22, 1077 (2001).
34. G. H. Borschel, K. F. Kia, W. M. Kuzon, Jr, and R. G. Dennis, Mechanical properties of acellular peripheral nerve. J. Surg. Res. 114, 133 (2003).