Literature DB >> 28112028

Introduction of neurosupportive cells into processed acellular nerve allografts results in greater number and more even distribution when injected compared to soaking techniques.

Matthew J Thompson1, Gaurangkumar Patel1, Jonathan Isaacs1, John McMurtry1, Nathan Richards1, William Daner1.   

Abstract

OBJECTIVES: Processing necessary to remove immunogenic components of nerve allograft renders it acellular. Seeding with supportive cells may improve axon regeneration. We aim to identify the method associated with implantation of the greatest volume and most even distribution of cells.
METHODS: Hypodermic needle injection was compared to soaking in solution under both normal and pressurized conditions after micropuncture of the allograft. Distribution within the allograft was measured using an in vitro model of fluorescent beads, as well as cultured Schwann cells.
RESULTS: Injection treatment resulted in larger volumes and a more uniform cross-sectional distribution of implanted cells. Beads and cells behaved similarly relative to the measured outcomes.
CONCLUSIONS: Injection instills more cells in a more uniform distribution. In vivo testing may evaluate whether these techniques vary relative to cell survival, cell migration, and clinical outcomes. Size- and concentration-matched fluorescent beads may represent a viable model for analyzing cell implantation.

Entities:  

Keywords:  Cold-preserved processed acellular human nerve allograft; cell delivery; in vitro model; microneedle; neuro-supportive cells

Mesh:

Year:  2017        PMID: 28112028      PMCID: PMC5596505          DOI: 10.1080/01616412.2017.1282336

Source DB:  PubMed          Journal:  Neurol Res        ISSN: 0161-6412            Impact factor:   2.448


  21 in total

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6.  Automated microscopy as a quantitative method to measure differences in adipogenic differentiation in preparations of human mesenchymal stromal cells.

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7.  A systematic evaluation of Schwann cell injection into acellular cold-preserved nerve grafts.

Authors:  Nithya J Jesuraj; Katherine B Santosa; Piyaraj Newton; Z Liu; Daniel A Hunter; Susan E Mackinnon; Shelly E Sakiyama-Elbert; Philip J Johnson
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8.  Repair of extended peripheral nerve lesions in rhesus monkeys using acellular allogenic nerve grafts implanted with autologous mesenchymal stem cells.

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10.  Limited regeneration in long acellular nerve allografts is associated with increased Schwann cell senescence.

Authors:  Maryam Saheb-Al-Zamani; Ying Yan; Scott J Farber; Daniel A Hunter; Piyaraj Newton; Matthew D Wood; Sheila A Stewart; Philip J Johnson; Susan E Mackinnon
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  4 in total

1.  Adhesion, distribution, and migration of differentiated and undifferentiated mesenchymal stem cells (MSCs) seeded on nerve allografts.

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Review 2.  Targeted stimulation of MSCs in peripheral nerve repair.

Authors:  Femke Mathot; Alexander Y Shin; Andre J Van Wijnen
Journal:  Gene       Date:  2019-03-05       Impact factor: 3.688

3.  Introducing human adipose-derived mesenchymal stem cells to Avance nerve grafts and NeuraGen nerve guides.

Authors:  Femke Mathot; Nadia Rbia; Roman Thaler; Allen T Bishop; Andre J van Wijnen; Alexander Y Shin
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4.  An update-tissue engineered nerve grafts for the repair of peripheral nerve injuries.

Authors:  Nitesh P Patel; Kristopher A Lyon; Jason H Huang
Journal:  Neural Regen Res       Date:  2018-05       Impact factor: 5.135

  4 in total

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