Literature DB >> 16102813

Characterization of non-neuronal elements within fibronectin mats implanted into the damaged adult rat spinal cord.

V R King1, J B Phillips, H Hunt-Grubbe, R Brown, J V Priestley.   

Abstract

Previous studies have shown that mats made from fibronectin (FN) integrate well into spinal cord lesion sites and support extensive axonal growth. Using immunohistochemistry, we have investigated the non-neuronal factors that contribute to these properties. Extensive vascularization was observed in FN mats by 1 week along with heavy macrophage infiltration by 3 days post-implantation. By 1 week post-implantation, laminin tubules had formed and were associated with axons and p75 immunoreactive Schwann cells. By 4 weeks post-implantation, most axons were associated with Schwann cell derived myelin. Few oligodendrocytes were present within the mat, even with an increase in the number of oligodendrocyte precursors around the implant site by 7 days post-implantation. Astrocyte proliferation also occurred in the intact tissue, with a prominent glial scar forming around the implant within 4 weeks. However, by 2 months post-implantation astrocytes were present in the FN implant site and were intermingled with the axons. Axonal ingrowth and integration of the FN mats is probably due to the ability of FN mats to support and organize infiltration of Schwann cells and deposition of laminin. At later time points, myelinated axons remain in the implant site, even after other elements (e.g. macrophages and laminin) have disappeared. Both of these properties are likely to be important in the design of biomaterial bridges for CNS regeneration.

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Year:  2005        PMID: 16102813     DOI: 10.1016/j.biomaterials.2005.06.033

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  21 in total

Review 1.  Approaches to neural tissue engineering using scaffolds for drug delivery.

Authors:  Stephanie M Willerth; Shelly E Sakiyama-Elbert
Journal:  Adv Drug Deliv Rev       Date:  2007-04-10       Impact factor: 15.470

2.  Plasmid releasing multiple channel bridges for transgene expression after spinal cord injury.

Authors:  Laura De Laporte; Yang Yang; Marina L Zelivyanskaya; Brian J Cummings; Aileen J Anderson; Lonnie D Shea
Journal:  Mol Ther       Date:  2008-12-02       Impact factor: 11.454

3.  Multiple channel bridges for spinal cord injury: cellular characterization of host response.

Authors:  Yang Yang; Laura De Laporte; Marina L Zelivyanskaya; Kevin J Whittlesey; Aileen J Anderson; Brian J Cummings; Lonnie D Shea
Journal:  Tissue Eng Part A       Date:  2009-11       Impact factor: 3.845

4.  Host reaction to poly(2-hydroxyethyl methacrylate) scaffolds in a small spinal cord injury model.

Authors:  Hong Ying Li; Tobias Führmann; Yue Zhou; Paul D Dalton
Journal:  J Mater Sci Mater Med       Date:  2013-05-24       Impact factor: 3.896

5.  Long-term characterization of axon regeneration and matrix changes using multiple channel bridges for spinal cord regeneration.

Authors:  Hannah M Tuinstra; Daniel J Margul; Ashley G Goodman; Ryan M Boehler; Samantha J Holland; Marina L Zelivyanskaya; Brian J Cummings; Aileen J Anderson; Lonnie D Shea
Journal:  Tissue Eng Part A       Date:  2013-12-11       Impact factor: 3.845

6.  Transforming growth factor α transforms astrocytes to a growth-supportive phenotype after spinal cord injury.

Authors:  Robin E White; Meghan Rao; John C Gensel; Dana M McTigue; Brian K Kaspar; Lyn B Jakeman
Journal:  J Neurosci       Date:  2011-10-19       Impact factor: 6.167

Review 7.  Does the preclinical evidence for functional remyelination following myelinating cell engraftment into the injured spinal cord support progression to clinical trials?

Authors:  Scott A Myers; Andrew N Bankston; Darlene A Burke; Sujata Saraswat Ohri; Scott R Whittemore
Journal:  Exp Neurol       Date:  2016-04-13       Impact factor: 5.330

8.  Multifunctional, multichannel bridges that deliver neurotrophin encoding lentivirus for regeneration following spinal cord injury.

Authors:  Hannah M Tuinstra; Misael O Aviles; Seungjin Shin; Samantha J Holland; Marina L Zelivyanskaya; Alan G Fast; Sarah Y Ko; Daniel J Margul; Anne K Bartels; Ryan M Boehler; Brian J Cummings; Aileen J Anderson; Lonnie D Shea
Journal:  Biomaterials       Date:  2011-11-29       Impact factor: 12.479

9.  Local gene delivery from ECM-coated poly(lactide-co-glycolide) multiple channel bridges after spinal cord injury.

Authors:  Laura De Laporte; Anna Lei Yan; Lonnie D Shea
Journal:  Biomaterials       Date:  2009-01-13       Impact factor: 12.479

10.  Fibrin-based tissue engineering scaffolds enhance neural fiber sprouting and delay the accumulation of reactive astrocytes at the lesion in a subacute model of spinal cord injury.

Authors:  Philip J Johnson; Stanley R Parker; Shelly E Sakiyama-Elbert
Journal:  J Biomed Mater Res A       Date:  2010-01       Impact factor: 4.396

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