中国神经再生研究(英文版) ›› 2018, Vol. 13 ›› Issue (5): 764-774.doi: 10.4103/1673-5374.232458

• 综述:周围神经损伤修复保护与再生 • 上一篇    下一篇

更新组织工程神经移植修复周围神经损伤

  

  • 收稿日期:2018-03-28 出版日期:2018-05-15 发布日期:2018-05-15

An update–tissue engineered nerve grafts for the repair of peripheral nerve injuries

Nitesh P. Patel1, Kristopher A. Lyon1, 2, Jason H. Huang1, 2   

  1. 1 Texas A&M College of Medicine, Temple, TX, USA
    2 Department of Neurosurgery, Baylor Scott & White Healthcare, Temple, TX, USA
  • Received:2018-03-28 Online:2018-05-15 Published:2018-05-15
  • Contact: Jason H. Huang, M.D., FAANS,FACS,Jason.Huang@BSWHealth.org or jasonhhuang@yahoo.com.
  • Supported by:

    This work was supported, in part, by a research grant from Baylor Scott & White Health Central Texas Foundation and NIH grant R01-NS067435 (JHH).

摘要:

orcid:0000-0002-4426-0168(Jason H. Huang)

Abstract:

Peripheral nerve injuries (PNI) are caused by a range of etiologies and result in a broad spectrum of disability. While nerve autografts are the current gold standard for the reconstruction of extensive nerve damage, the limited supply of autologous nerve and complications associated with harvesting nerve from a second surgical site has driven groups from multiple disciplines, including biomedical engineering, neurosurgery, plastic surgery, and orthopedic surgery, to develop a suitable or superior alternative to autografting. Over the last couple of decades, various types of scaffolds, such as acellular nerve grafts (ANGs), nerve guidance conduits, and non-nervous tissues, have been filled with Schwann cells, stem cells, and/or neurotrophic factors to develop tissue engineered nerve grafts (TENGs). Although these have shown promising effects on peripheral nerve regeneration in experimental models, the autograft has remained the gold standard for large nerve gaps. This review provides a discussion of recent advances in the development of TENGs and their efficacy in experimental models. Specifically, TENGs have been enhanced via incorporation of genetically engineered cells, methods to improve stem cell survival and differentiation, optimized delivery of neurotrophic factors via drug delivery systems (DDS), co-administration of platelet-rich plasma (PRP), and pretreatment with chondroitinase ABC (Ch-ABC). Other notable advancements include conduits that have been bioengineered to mimic native nerve structure via cell-derived extracellular matrix (ECM) deposition, and the development of transplantable living nervous tissue constructs from rat and human dorsal root ganglia (DRG) neurons. Grafts composed of non-nervous tissues, such as vein, artery, and muscle, will be briefly discussed.

Key words: peripheral nerve injury, peripheral nerve repair, tissue engineered nerve graft, nerve conduit, stem cells, Schwann cells, dorsal root ganglia neurons, axon stretch-growth, autologous tissue graft