Table of Contents Author Guidelines Submit a Manuscript
BioMed Research International
Volume 2018, Article ID 5746525, 6 pages
https://doi.org/10.1155/2018/5746525
Research Article

Effects of Cyclic Tensile Strain on Oxidative Stress and the Function of Schwann Cells

Tianjin Hospital, Jiefang Nan Road 406, Tianjin 300211, China

Correspondence should be addressed to Xinlong Ma; moc.361@102gnolnixaM

Received 1 March 2018; Accepted 16 May 2018; Published 10 June 2018

Academic Editor: Yan Huang

Copyright © 2018 Shuang Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. A. Gruart, M. Streppel, O. Guntinas-Lichius, D. N. Angelov, W. F. Neiss, and J. M. Delgado-García, “Motoneuron adaptability to new motor tasks following two types of facial-facial anastomosis in cats,” Brain, vol. 126, no. 1, pp. 115–133, 2003. View at Publisher · View at Google Scholar · View at Scopus
  2. A. Brosius Lutz and B. A. Barres, “Contrasting the glial response to axon injury in the central and peripheral nervous systems,” Developmental Cell, vol. 28, no. 1, pp. 7–17, 2014. View at Publisher · View at Google Scholar
  3. C. Zheng, Q. Zhu, X. Liu et al., “Effect of platelet-rich plasma (PRP) concentration on proliferation, neurotrophic function and migration of Schwann cells in vitro,” Journal of Tissue Engineering and Regenerative Medicine, vol. 10, no. 5, pp. 428–436, 2016. View at Publisher · View at Google Scholar · View at Scopus
  4. L.-X. Deng, P. Deng, Y. Ruan et al., “A novel growth-promoting pathway formed by GDNF-overexpressing Schwann cells promotes propriospinal axonal regeneration, synapse formation, and partial recovery of function after spinal cord injury,” The Journal of Neuroscience, vol. 33, no. 13, pp. 5655–5667, 2013. View at Publisher · View at Google Scholar · View at Scopus
  5. B. He, S.-Q. Liu, Q. Chen, H.-H. Li, W.-J. Ding, and M. Deng, “Carboxymethylated chitosan stimulates proliferation of Schwann cells in vitro via the activation of the ERK and Akt signaling pathways,” European Journal of Pharmacology, vol. 667, no. 1-3, pp. 195–201, 2011. View at Publisher · View at Google Scholar · View at Scopus
  6. S. O. Yazdani, A. F. Golestaneh, A. Shafiee, M. Hafizi, H.-A. G. Omrani, and M. Soleimani, “Effects of low level laser therapy on proliferation and neurotrophic factor gene expression of human schwann cells in vitro,” Journal of Photochemistry and Photobiology B: Biology, vol. 107, no. 1, pp. 9–13, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. E. F. Morgan, K. T. Salisbury Palomares, R. E. Gleason et al., “Correlations between local strains and tissue phenotypes in an experimental model of skeletal healing,” Journal of Biomechanics, vol. 43, no. 12, pp. 2418–2424, 2010. View at Publisher · View at Google Scholar · View at Scopus
  8. C. E. Sarraf, W. R. Otto, and M. Eastwood, “In vitro mesenchymal stem cell differentiation after mechanical stimulation,” Cell Proliferation, vol. 44, no. 1, pp. 99–108, 2011. View at Publisher · View at Google Scholar · View at Scopus
  9. C. Schwarz, D. Wulsten, A. Ellinghaus, J. Lienau, B. M. Willie, and G. N. Duda, “Mechanical load modulates the stimulatory effect of BMP2 in a rat nonunion model,” Tissue Engineering Part: A, vol. 19, no. 1-2, pp. 247–254, 2013. View at Publisher · View at Google Scholar · View at Scopus
  10. A. Areti, V. G. Yerra, V. Naidu, and A. Kumar, “Oxidative stress and nerve damage: Role in chemotherapy induced peripheral neuropathy,” Redox Biology, vol. 2, no. 1, pp. 289–295, 2014. View at Publisher · View at Google Scholar · View at Scopus
  11. I. R. Kashani, Z. Golipoor, M. Akbari et al., “Schwann-like cell differentiation from rat bone marrow stem cells,” Archives of Medical Science, vol. 7, no. 1, pp. 45–52, 2011. View at Publisher · View at Google Scholar · View at Scopus
  12. Y. Wei, K. Gong, Z. Zheng et al., “Schwann-like cell differentiation of rat adipose-derived stem cells by indirect co-culture with Schwann cells in vitro,” Cell Proliferation, vol. 43, no. 6, pp. 606–616, 2010. View at Publisher · View at Google Scholar · View at Scopus
  13. M. B. Murphy, D. Blashki, R. M. Buchanan et al., “Adult and umbilical cord blood-derived platelet-rich plasma for mesenchymal stem cell proliferation, chemotaxis, and cryo-preservation,” Biomaterials, vol. 33, no. 21, pp. 5308–5316, 2012. View at Publisher · View at Google Scholar · View at Scopus
  14. T. Lahlali, M.-L. Plissonnier, C. Romero-López et al., “Netrin-1 Protects Hepatocytes Against Cell Death Through Sustained Translation During the Unfolded Protein Response,” Cellular and Molecular Gastroenterology and Hepatology, vol. 2, no. 3, pp. 281–301.e9, 2016. View at Publisher · View at Google Scholar · View at Scopus
  15. L. Carr, D. B. Parkinson, and X.-P. Dun, “Expression patterns of Slit and Robo family members in adult mouse spinal cord and peripheral nervous system,” PLoS ONE, vol. 12, no. 2, Article ID e0172736, 2017. View at Publisher · View at Google Scholar · View at Scopus
  16. G. Liu, G. Guan, and J. Fang, “Macleaya cordata extract decreased diarrhea score and enhanced intestinal barrier function in growing piglets,” BioMed Research International, vol. 2016, Article ID 1069585, 7 pages, 2016. View at Publisher · View at Google Scholar
  17. K.-A. Nave and H. B. Werner, “Myelination of the nervous system: mechanisms and functions,” Annual Review of Cell and Developmental Biology, vol. 30, pp. 503–533, 2014. View at Publisher · View at Google Scholar · View at Scopus
  18. K. Xu, Z. Wu, N. Renier et al., “Structures of netrin-1 bound to two receptors provide insight into its axon guidance mechanism,” Science, vol. 344, no. 6189, pp. 1275–1279, 2014. View at Publisher · View at Google Scholar · View at Scopus
  19. J. B. Bongo and D. Q. Peng, “The neuroimmune guidance cue netrin-1: A new therapeutic target in cardiovascular disease,” Journal of Cardiology, vol. 63, no. 2, pp. 95–98, 2014. View at Publisher · View at Google Scholar · View at Scopus
  20. M. Kim, W. T. Farmer, B. Bjorke et al., “Pioneer midbrain longitudinal axons navigate using a balance of Netrin attraction and Slit repulsion,” Neural Development, vol. 9, no. 1, article no. 17, 2014. View at Publisher · View at Google Scholar · View at Scopus
  21. S. Li, X. Wang, Y. Gu et al., “Let-7 microRNAs regenerate peripheral nerve regeneration by targeting nerve growth factor,” Molecular Therapy, vol. 23, no. 3, pp. 423–433, 2015. View at Publisher · View at Google Scholar · View at Scopus
  22. H. B. Henninger, W. R. Valdez, S. A. Scott, and J. A. Weiss, “Elastin governs the mechanical response of medial collateral ligament under shear and transverse tensile loading,” Acta Biomaterialia, vol. 25, pp. 304–312, 2015. View at Publisher · View at Google Scholar · View at Scopus
  23. L. Zhang, X. Yang, Y. Yue et al., “Cyclic mechanical stress modulates neurotrophic and myelinating gene expression of Schwann cells,” Cell Proliferation, vol. 48, no. 1, pp. 59–66, 2015. View at Publisher · View at Google Scholar · View at Scopus
  24. I. Allodi, E. Udina, and X. Navarro, “Specificity of peripheral nerve regeneration: interactions at the axon level,” Progress in Neurobiology, vol. 98, no. 1, pp. 16–37, 2012. View at Publisher · View at Google Scholar · View at Scopus