Cell transplantation therapy for spinal cord injury

被引:743
作者
Assinck, Peggy [1 ,2 ]
Duncan, Greg J. [1 ,3 ]
Hilton, Brett J. [1 ,3 ]
Plemel, Jason R. [4 ,5 ]
Tetzlaff, Wolfram [1 ,3 ,6 ]
机构
[1] Univ British Columbia, Int Collaborat Repair Discoveries, Vancouver, BC, Canada
[2] Univ British Columbia, Grad Program Neurosci, Vancouver, BC, Canada
[3] Univ British Columbia, Dept Zool, Vancouver, BC, Canada
[4] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[5] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[6] Univ British Columbia, Dept Surg, Vancouver, BC, Canada
关键词
CENTRAL-NERVOUS-SYSTEM; OLFACTORY ENSHEATHING CELLS; NEURAL STEM-CELLS; IMMUNE-DEFICIENCY SYNDROME; SKIN-DERIVED PRECURSORS; FUNCTIONAL RECOVERY; SCHWANN-CELL; AXONAL REGENERATION; MACROPHAGE ACTIVATION; LOCOMOTOR RECOVERY;
D O I
10.1038/nn.4541
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Spinal cord injury can lead to severe motor, sensory and autonomic dysfunction. Currently, there is no effective treatment for the injured spinal cord. The transplantation of Schwann cells, neural stem cells or progenitor cells, olfactory ensheathing cells, oligodendrocyte precursor cells and mesenchymal stem cells has been investigated as potential therapies for spinal cord injury. However, little is known about the mechanisms through which these individual cell types promote repair and functional improvements. The five most commonly proposed mechanisms include neuroprotection, immunomodulation, axon regeneration, neuronal relay formation and myelin regeneration. A better understanding of the mechanisms whereby these cells promote functional improvements, as well as an appreciation of the obstacles in implementing these therapies and effectively modeling spinal cord injury, will be important to make cell transplantation a viable clinical option and may lead to the development of more targeted therapies.
引用
收藏
页码:637 / 647
页数:11
相关论文
共 150 条
[41]   Nociceptor sensitization in pain pathogenesis [J].
Gold, Michael S. ;
Gebhart, Gerald F. .
NATURE MEDICINE, 2010, 16 (11) :1248-1257
[42]   A Pericyte Origin of Spinal Cord Scar Tissue [J].
Goritz, Christian ;
Dias, David O. ;
Tomilin, Nikolay ;
Barbacid, Mariano ;
Shupliakov, Oleg ;
Frisen, Jonas .
SCIENCE, 2011, 333 (6039) :238-242
[43]   Transplantation of bone marrow mesenchymal stem cells reduces lesion volume and induces axonal regrowth of injured spinal cord [J].
Gu, Weidong ;
Zhang, Fujun ;
Xue, Qingsheng ;
Ma, Zhengwen ;
Lu, Peihua ;
Yu, Buwei .
NEUROPATHOLOGY, 2010, 30 (03) :205-217
[44]   Demyelination and Schwann cell responses adjacent to injury epicenter cavities following chronic human spinal cord injury [J].
Guest, JD ;
Hiester, ED ;
Bunge, RP .
EXPERIMENTAL NEUROLOGY, 2005, 192 (02) :384-393
[45]   An Examination of the Mechanisms by Which Neural Precursors Augment Recovery Following Spinal Cord Injury: A Key Role for Remyelination [J].
Hawryluk, Gregory W. J. ;
Spano, Stefania ;
Chew, Derek ;
Wang, Shelly ;
Erwin, Mark ;
Chamankhah, Mahmood ;
Forgione, Nicole ;
Fehlings, Michael G. .
CELL TRANSPLANTATION, 2014, 23 (03) :365-380
[46]   An In Vivo Characterization of Trophic Factor Production Following Neural Precursor Cell or Bone Marrow Stromal Cell Transplantation for Spinal Cord Injury [J].
Hawryluk, Gregory W. J. ;
Mothe, Andrea ;
Wang, Jian ;
Wang, Shelly ;
Tator, Charles ;
Fehlings, Michael G. .
STEM CELLS AND DEVELOPMENT, 2012, 21 (12) :2222-2238
[47]   Intrinsic Control of Axon Regeneration [J].
He, Zhigang ;
Jin, Yishi .
NEURON, 2016, 90 (03) :437-451
[48]   LONG LIVES FOR HOMOZYGOUS TREMBLER MUTANT MICE DESPITE VIRTUAL ABSENCE OF PERIPHERAL-NERVE MYELIN [J].
HENRY, EW ;
SIDMAN, RL .
SCIENCE, 1988, 241 (4863) :344-346
[49]   Chronic Oligodendrogenesis and Remyelination after Spinal Cord Injury in Mice and Rats [J].
Hesp, Zoe C. ;
Goldstein, Evan A. ;
Miranda, Carlos J. ;
Kaspar, Brain K. ;
McTigue, Dana M. .
JOURNAL OF NEUROSCIENCE, 2015, 35 (03) :1274-1290
[50]   Labeled Schwann cell transplantation: Cell loss, host Schwann cell replacement, and strategies to enhance survival [J].
Hill, CE ;
Moon, LDF ;
Wood, PM ;
Bunge, MB .
GLIA, 2006, 53 (03) :338-343