In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Kirsten Haastert-Talini
  • Janett Schaper-Rinkel
  • Ruth Schmitte
  • Rode Bastian
  • Martina Mühlenhoff
  • David Schwarzer
  • Gerald Draeger
  • Yi Su
  • Thomas Scheper
  • Rita Gerardy-Schahn
  • Claudia Grothe

Externe Organisationen

  • Medizinische Hochschule Hannover (MHH)
  • Stiftung Tierärztliche Hochschule Hannover
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)3085-3098
Seitenumfang14
FachzeitschriftTissue Engineering - Part A
Jahrgang16
Ausgabenummer10
PublikationsstatusVeröffentlicht - 16 Juni 2010

Abstract

With the aim to develop new biomaterials for peripheral nerve grafts, the current study used bioidentical polysialic acid (polySia) as complement in synthetic conduits. polySia provides an important guidance cue during nervous system development and regeneration. First in vivo results on the use of cell-free and Schwann cell-containing synthetic peripheral nerve grafts complemented with soluble exogenous K1-polySia are presented. Reconstructing 10mm rat sciatic nerve gaps, K1-polySia complementation significantly improved structural nerve regeneration in comparison to cell-free and K1-polySia-free grafts. Subsequently, long nerve gaps (13mm) were reconstructed by Schwann cell transplants plus K1-polySia and compared to nerve autotransplantation. Structural but also functional regeneration could be observed using K1-polySia transplants; however, autotransplantation was still significantly more successful. Overall, the current study demonstrates that exogenous K1-polySia has no negative but rather regeneration promoting effects. This is important novel evidence on the applicability of exogenous polySia in vivo. Further studies are required to develop solid three-dimensional polySia-based scaffolds for nerve tissue engineering. Biocompatible and assessable biodegrading materials will ensure long-lasting presence of polySia to allow its applicability and prolonged efficacy in the slow regenerating scenario of human peripheral nerve reconstruction.

ASJC Scopus Sachgebiete

Zitieren

In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants. / Haastert-Talini, Kirsten; Schaper-Rinkel, Janett; Schmitte, Ruth et al.
in: Tissue Engineering - Part A, Jahrgang 16, Nr. 10, 16.06.2010, S. 3085-3098.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Haastert-Talini, K, Schaper-Rinkel, J, Schmitte, R, Bastian, R, Mühlenhoff, M, Schwarzer, D, Draeger, G, Su, Y, Scheper, T, Gerardy-Schahn, R & Grothe, C 2010, 'In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants', Tissue Engineering - Part A, Jg. 16, Nr. 10, S. 3085-3098. https://doi.org/10.1089/ten.tea.2010.0180
Haastert-Talini, K., Schaper-Rinkel, J., Schmitte, R., Bastian, R., Mühlenhoff, M., Schwarzer, D., Draeger, G., Su, Y., Scheper, T., Gerardy-Schahn, R., & Grothe, C. (2010). In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants. Tissue Engineering - Part A, 16(10), 3085-3098. https://doi.org/10.1089/ten.tea.2010.0180
Haastert-Talini K, Schaper-Rinkel J, Schmitte R, Bastian R, Mühlenhoff M, Schwarzer D et al. In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants. Tissue Engineering - Part A. 2010 Jun 16;16(10):3085-3098. doi: 10.1089/ten.tea.2010.0180
Haastert-Talini, Kirsten ; Schaper-Rinkel, Janett ; Schmitte, Ruth et al. / In Vivo Evaluation of Polysialic Acid as Part of Tissue-Engineered Nerve Transplants. in: Tissue Engineering - Part A. 2010 ; Jahrgang 16, Nr. 10. S. 3085-3098.
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abstract = "With the aim to develop new biomaterials for peripheral nerve grafts, the current study used bioidentical polysialic acid (polySia) as complement in synthetic conduits. polySia provides an important guidance cue during nervous system development and regeneration. First in vivo results on the use of cell-free and Schwann cell-containing synthetic peripheral nerve grafts complemented with soluble exogenous K1-polySia are presented. Reconstructing 10mm rat sciatic nerve gaps, K1-polySia complementation significantly improved structural nerve regeneration in comparison to cell-free and K1-polySia-free grafts. Subsequently, long nerve gaps (13mm) were reconstructed by Schwann cell transplants plus K1-polySia and compared to nerve autotransplantation. Structural but also functional regeneration could be observed using K1-polySia transplants; however, autotransplantation was still significantly more successful. Overall, the current study demonstrates that exogenous K1-polySia has no negative but rather regeneration promoting effects. This is important novel evidence on the applicability of exogenous polySia in vivo. Further studies are required to develop solid three-dimensional polySia-based scaffolds for nerve tissue engineering. Biocompatible and assessable biodegrading materials will ensure long-lasting presence of polySia to allow its applicability and prolonged efficacy in the slow regenerating scenario of human peripheral nerve reconstruction.",
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AU - Haastert-Talini, Kirsten

AU - Schaper-Rinkel, Janett

AU - Schmitte, Ruth

AU - Bastian, Rode

AU - Mühlenhoff, Martina

AU - Schwarzer, David

AU - Draeger, Gerald

AU - Su, Yi

AU - Scheper, Thomas

AU - Gerardy-Schahn, Rita

AU - Grothe, Claudia

PY - 2010/6/16

Y1 - 2010/6/16

N2 - With the aim to develop new biomaterials for peripheral nerve grafts, the current study used bioidentical polysialic acid (polySia) as complement in synthetic conduits. polySia provides an important guidance cue during nervous system development and regeneration. First in vivo results on the use of cell-free and Schwann cell-containing synthetic peripheral nerve grafts complemented with soluble exogenous K1-polySia are presented. Reconstructing 10mm rat sciatic nerve gaps, K1-polySia complementation significantly improved structural nerve regeneration in comparison to cell-free and K1-polySia-free grafts. Subsequently, long nerve gaps (13mm) were reconstructed by Schwann cell transplants plus K1-polySia and compared to nerve autotransplantation. Structural but also functional regeneration could be observed using K1-polySia transplants; however, autotransplantation was still significantly more successful. Overall, the current study demonstrates that exogenous K1-polySia has no negative but rather regeneration promoting effects. This is important novel evidence on the applicability of exogenous polySia in vivo. Further studies are required to develop solid three-dimensional polySia-based scaffolds for nerve tissue engineering. Biocompatible and assessable biodegrading materials will ensure long-lasting presence of polySia to allow its applicability and prolonged efficacy in the slow regenerating scenario of human peripheral nerve reconstruction.

AB - With the aim to develop new biomaterials for peripheral nerve grafts, the current study used bioidentical polysialic acid (polySia) as complement in synthetic conduits. polySia provides an important guidance cue during nervous system development and regeneration. First in vivo results on the use of cell-free and Schwann cell-containing synthetic peripheral nerve grafts complemented with soluble exogenous K1-polySia are presented. Reconstructing 10mm rat sciatic nerve gaps, K1-polySia complementation significantly improved structural nerve regeneration in comparison to cell-free and K1-polySia-free grafts. Subsequently, long nerve gaps (13mm) were reconstructed by Schwann cell transplants plus K1-polySia and compared to nerve autotransplantation. Structural but also functional regeneration could be observed using K1-polySia transplants; however, autotransplantation was still significantly more successful. Overall, the current study demonstrates that exogenous K1-polySia has no negative but rather regeneration promoting effects. This is important novel evidence on the applicability of exogenous polySia in vivo. Further studies are required to develop solid three-dimensional polySia-based scaffolds for nerve tissue engineering. Biocompatible and assessable biodegrading materials will ensure long-lasting presence of polySia to allow its applicability and prolonged efficacy in the slow regenerating scenario of human peripheral nerve reconstruction.

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