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Macroporous nanofiber wraps promote axonal regeneration and functional recovery in nerve repair by limiting fibrosis.
Sarhane, Karim A; Ibrahim, Zuhaib; Martin, Russell; Krick, Kellin; Cashman, Christopher R; Tuffaha, Sami H; Broyles, Justin M; Prasad, Nijaguna; Yao, Zhi-Cheng; Cooney, Damon S; Mi, Ruifa; Lee, Wp Andrew; Hoke, Ahmet; Mao, Hai-Quan; Brandacher, Gerald.
Afiliación
  • Sarhane KA; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Surgery, University of Toledo College of Medicine, Toledo, OH, United States.
  • Ibrahim Z; Institute for Advanced Reconstruction, Shrewsbury, NJ, United States.
  • Martin R; Institute for NanoBioTechnology, Johns Hopkins University, Baltimore, MD, United States; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins U
  • Krick K; Institute for NanoBioTechnology, Johns Hopkins University, Baltimore, MD, United States; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, M
  • Cashman CR; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Tuffaha SH; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Broyles JM; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Prasad N; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Yao ZC; Institute for NanoBioTechnology, Johns Hopkins University, Baltimore, MD, United States; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins U
  • Cooney DS; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Mi R; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Lee WA; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Hoke A; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Mao HQ; Institute for NanoBioTechnology, Johns Hopkins University, Baltimore, MD, United States; Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, United States; Department of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins U
  • Brandacher G; Department of Plastic and Reconstructive Surgery, Vascularized Composite Allotransplantation (VCA) Laboratory, Johns Hopkins University School of Medicine, Baltimore, MD, United States. Electronic address: brandacher@jhmi.edu.
Acta Biomater ; 88: 332-345, 2019 04 01.
Article en En | MEDLINE | ID: mdl-30807875
ABSTRACT
Functional outcomes following nerve repair remain suboptimal. Scarring at the repair site is a major impediment to regeneration. A biomaterial scaffold applied around the coaptation site that decreases inflammation holds great potential in reducing scarring, enhancing axonal growth, and improving functional recovery. In this study, we evaluated the effect of a macroporous nanofiber wrap, comprised of nonwoven electrospun poly-ε-caprolactone (PCL), in improving axonal regeneration in a rat sciatic nerve cut and direct repair model. Controls consisted of conventional epineurial repair. We also evaluated our wrap against the commercially available AxoGuard wrap. At five weeks following repair, the nanofiber wrap group showed a significantly decreased intraneural macrophage invasion and collagen deposition at the repair site. This was associated with increased expression of the anti-inflammatory cytokine (IL-10), decreased expression of the pro-inflammatory cytokine (TNF-α), and a decrease in the M1M2 macrophage phenotype ratio. These findings suggest that this nanofiber wrap, with its unique macroporosity, is modulating the inflammatory response at the repair site by polarizing macrophages towards a pro-regenerative M2 phenotype. Concomitantly, a higher number of regenerated axons was noted. At sixteen weeks, the nanofiber wrap resulted in enhanced functional recovery as demonstrated by electrophysiology, neuromuscular re-innervation, and muscle histology. When compared to the AxoGuard wrap, the nanofiber wrap showed similar inflammation at the repair site and similar nerve morphometric findings, but there was a trend towards a lower overall number of macrophages invading the wrap wall. These results demonstrate favorable outcomes of the macroporous nanofiber wrap in promoting neuroregeneration and functional recovery following nerve repair. STATEMENT OF

SIGNIFICANCE:

Electrospun nanofiber scaffolds, with specific fiber and pore sizes, were shown to modulate the immune response and create a regenerative environment. In this paper, we present a macroporous nanofiber wrap, made of poly-ε-caprolactone, to be applied at the coaptation site in primary nerve repair. We show that it regulates the inflammatory response at the repair site and decreases scarring/fibrosis. This results in enhanced axonal regeneration, allowing a higher number of axons to cross the suture line and reach the target muscle in a timely fashion. Functional outcomes are thus improved.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Axones / Recuperación de la Función / Nanofibras / Regeneración Nerviosa Tipo de estudio: Prognostic_studies Idioma: En Revista: Acta Biomater Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Axones / Recuperación de la Función / Nanofibras / Regeneración Nerviosa Tipo de estudio: Prognostic_studies Idioma: En Revista: Acta Biomater Año: 2019 Tipo del documento: Article