Three-dimensional nanofibrillar surfaces covalently modified with tenascin-C-derived peptides enhance neuronal growth in vitro

Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐L‐lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin‐1). However, these 2D surfaces represent a poor topological approxima...

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Published in:	Journal of biomedical materials research. Part A Vol. 76A; no. 4; pp. 851 - 860
Main Authors:	Ahmed, Ijaz, Liu, Hsing-Yin, Mamiya, Ping C., Ponery, Abdul S., Babu, Ashwin N., Weik, Thom, Schindler, Melvin, Meiners, Sally
Format:	Journal Article
Language:	English
Published:	Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.03.2006
Subjects:	Amino Acid Sequence Animals Biocompatible Materials extracellular matrix Molecular Sequence Data nanofiber Nanotechnology neuron Neurons - cytology Neurons - drug effects peptide Peptides - chemistry Peptides - pharmacology Rats Surface Properties Tenascin - chemistry Tenascin - pharmacology tenascin-C
ISSN:	1549-3296, 1552-4965
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Abstract	Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐L‐lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin‐1). However, these 2D surfaces represent a poor topological approximation of the three‐dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL‐coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin‐C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide‐modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
AbstractList	Current methods to promote growth of cultured neurons use two-dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly-L-lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin-1). However, these 2D surfaces represent a poor topological approximation of the three-dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL-coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin-C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide-modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury. Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐ L ‐lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin‐1). However, these 2D surfaces represent a poor topological approximation of the three‐dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo . Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL‐coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin‐C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro . Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide‐modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006 Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐L‐lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin‐1). However, these 2D surfaces represent a poor topological approximation of the three‐dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL‐coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin‐C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide‐modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res, 2006 Current methods to promote growth of cultured neurons use two-dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly-L-lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin-1). However, these 2D surfaces represent a poor topological approximation of the three-dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL-coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin-C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide-modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury.Current methods to promote growth of cultured neurons use two-dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly-L-lysine (PLL)) or an isolated extracellular matrix (ECM) protein (e.g. laminin-1). However, these 2D surfaces represent a poor topological approximation of the three-dimensional (3D) architecture of the assembled ECM that regulates neuronal growth in vivo. Here we report on the development of a new 3D synthetic nanofibrillar surface for the culture of neurons. This nanofibrillar surface is composed of polyamide nanofibers whose organization mimics the porosity and geometry of the ECM. Neuronal adhesion and neurite outgrowth from cerebellar granule, cerebral cortical, hippocampal, motor, and dorsal root ganglion neurons were similar on nanofibers and PLL-coated glass coverslips; however, neurite generation was increased. Moreover, covalent modification of the nanofibers with neuroactive peptides derived from human tenascin-C significantly enhanced the ability of the nanofibers to facilitate neuronal attachment, neurite generation, and neurite extension in vitro. Hence the 3D nanofibrillar surface provides a physically and chemically stabile cell culture surface for neurons and, potentially, an exciting new opportunity for the development of peptide-modified matrices for use in strategies designed to encourage axonal regrowth following central nervous system injury.
Author	Liu, Hsing-Yin Meiners, Sally Schindler, Melvin Ahmed, Ijaz Ponery, Abdul S. Mamiya, Ping C. Weik, Thom Babu, Ashwin N.
Author_xml	– sequence: 1 givenname: Ijaz surname: Ahmed fullname: Ahmed, Ijaz organization: Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854 – sequence: 2 givenname: Hsing-Yin surname: Liu fullname: Liu, Hsing-Yin organization: Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854 – sequence: 3 givenname: Ping C. surname: Mamiya fullname: Mamiya, Ping C. organization: Department of Psychology, Busch Campus, Rutgers University, New Brunswick, New Jersey 08903 – sequence: 4 givenname: Abdul S. surname: Ponery fullname: Ponery, Abdul S. organization: Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854 – sequence: 5 givenname: Ashwin N. surname: Babu fullname: Babu, Ashwin N. organization: Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854 – sequence: 6 givenname: Thom surname: Weik fullname: Weik, Thom organization: Donaldson Company, Inc., P.O. Box 1299, Minneapolis, Minnesota 55440 – sequence: 7 givenname: Melvin surname: Schindler fullname: Schindler, Melvin organization: Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824 – sequence: 8 givenname: Sally surname: Meiners fullname: Meiners, Sally email: meiners@umdnj.edu organization: Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854
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Snippet	Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐L‐lysine... Current methods to promote growth of cultured neurons use two‐dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly‐ L... Current methods to promote growth of cultured neurons use two-dimensional (2D) glass or polystyrene surfaces coated with a charged molecule (e.g. poly-L-lysine...
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SubjectTerms	Amino Acid Sequence Animals Biocompatible Materials extracellular matrix Molecular Sequence Data nanofiber Nanotechnology neuron Neurons - cytology Neurons - drug effects peptide Peptides - chemistry Peptides - pharmacology Rats Surface Properties Tenascin - chemistry Tenascin - pharmacology tenascin-C
Title	Three-dimensional nanofibrillar surfaces covalently modified with tenascin-C-derived peptides enhance neuronal growth in vitro
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