Self-assembling peptides optimize the post-traumatic milieu and synergistically enhance the effects of neural stem cell therapy after cervical spinal cord injury

被引:83
作者
Zweckberger, Klaus [1 ]
Ahuja, Christopher S. [1 ]
Liu, Yang [1 ]
Wang, Jian [1 ]
Fehlings, Michael G. [1 ,2 ]
机构
[1] Toronto Western Hosp, Univ Hlth Network, Krembil Neurosci Ctr, Toronto, ON, Canada
[2] Univ Toronto, Univ Hlth Network, Inst Med Sci, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
Cervical spinal cord injury; Neural precursor cells; Self-assembling peptides; Functional recovery; Tissue-preservation; PRECURSOR CELLS; STEM/PROGENITOR CELLS; FUNCTIONAL RECOVERY; ADULT-RAT; NEUROLOGICAL RECOVERY; SCAR FORMATION; TRANSPLANTATION; REPAIR; GROWTH; REGENERATION;
D O I
10.1016/j.actbio.2016.06.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Introduction: The hostile environment after spinal cord injury (SCI) can compromise effects of regenerative therapies. We hypothesized that optimizing the post-traumatic environment with QL6 self assembling peptides (SAPs) before neural precursor cell (NPC) transplantation would improve cell survival, differentiation and functional recovery. Methods: A total of 90 Wistar rats received a clip-compression SCI at C7. Within each of two study arms, animals were randomized into 5 groups (NPC, SAP, NPC + SAP, vehicle, and sham). SAPs and NPCs were injected into the spinal cord 1 day and 14 days post-injury, respectively. Animals received growth factors over 7 days and were immunosuppressed. Rats were sacrificed at 4 weeks and sections of the cervical spinal cord prepared for immunohistochemistry (first study arm). Neurological function was assessed weekly for 8 weeks using a battery of behavioral tests. Nine weeks post-SCI, the corticospinal tract was assessed using fiber-tracking (second arm). Results: SAP-treated animals had significantly more surviving NPCs which showed increased differentiation to neurons and oligodendrocytes compared to controls. SAPs alone or in combination with NPCs resulted in smaller intramedullary cysts and larger volume of preserved tissue compared to other groups. The combined treatment group showed reduced astrogliosis and chondroitin sulfate proteoglycan deposition. Synaptic connectivity was increased in the NPC and combined treatment groups. Corticospinal tract preservation and behavioral outcomes improved with combinatorial treatment. Conclusion: Injecting SAPs after SCI enhances subsequent NPC survival, integration and differentiation and improves functional recovery. Statement of Significance The hostile environment after spinal cord injury (SCI) can compromise effects of regenerative therapies. We hypothesized that improving this environment with self-assembling peptides (SAPs) before neural precursor cell (NPC) transplantation would support their beneficial effects. SAPs assemble once injected, providing a supportive scaffold for repair and regeneration. We investigated this in a rat model of spinal cord injury. More NPCs survived in SAP-treated animals and these showed increased differentiation compared to controls. SAPS alone or in combination with NPCs resulted in smaller cysts and larger volume of preserved tissue with the combined treatment also reducing scarring and improving behavioral outcomes. Overall, injection of SAPs was shown to improve the efficacy of NPC treatment, a promising finding for those with SCIs. (C) 2016 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:77 / 89
页数:13
相关论文
共 63 条
[1]   Sonic hedgehog-induced neural precursor proliferation after adult rodent spinal cord injury [J].
Bambakidis, NC ;
Wang, RZ ;
Franic, L ;
Miller, RH .
JOURNAL OF NEUROSURGERY, 2003, 99 (01) :70-75
[2]   Update on the treatment of spinal cord injury [J].
Baptiste, Darryl C. ;
Fehlings, Michael G. .
NEUROTRAUMA: NEW INSIGHTS INTO PATHOLOGY AND TREATMENT, 2007, 161 :217-233
[3]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[4]   Microglia-mediated neurotoxicity: uncovering the molecular mechanisms [J].
Block, Michelle L. ;
Zecca, Luigi ;
Hong, Jau-Shyong .
NATURE REVIEWS NEUROSCIENCE, 2007, 8 (01) :57-69
[5]   METHYLPREDNISOLONE AND NEUROLOGICAL FUNCTION 1 YEAR AFTER SPINAL-CORD INJURY - RESULTS OF THE NATIONAL ACUTE SPINAL-CORD INJURY STUDY [J].
BRACKEN, MB ;
SHEPARD, MJ ;
HELLENBRAND, KG ;
COLLINS, WF ;
LEO, LS ;
FREEMAN, DF ;
WAGNER, FC ;
FLAMM, ES ;
EISENBERG, HM ;
GOODMAN, JH ;
PEROT, PL ;
GREEN, BA ;
GROSSMAN, RG ;
MEAGHER, JN ;
YOUNG, W ;
FISCHER, B ;
CLIFTON, GL ;
HUNT, WE ;
RIFKINSON, N .
JOURNAL OF NEUROSURGERY, 1985, 63 (05) :704-713
[6]  
Brook G., 2003, GLIA S2, p[1, P202]
[7]  
Carelli S., 2014, CELL TRANSPLANT
[8]   Evaluation of Early and Late Effects into the Acute Spinal Cord Injury of an Injectable Functionalized Self-Assembling Scaffold [J].
Cigognini, Daniela ;
Satta, Alessandro ;
Colleoni, Bianca ;
Silva, Diego ;
Donega, Matteo ;
Antonini, Stefania ;
Gelain, Fabrizio .
PLOS ONE, 2011, 6 (05)
[9]   Apoptosis and delayed degeneration after spinal cord injury in rats and monkeys [J].
Crowe, MJ ;
Bresnahan, JC ;
Shuman, SL ;
Masters, JN ;
Beattie, MS .
NATURE MEDICINE, 1997, 3 (01) :73-76
[10]   Human neural stem cell differentiation following transplantation into spinal cord injured mice: association with recovery of locomotor function [J].
Cummings, Brian J. ;
Uchida, Nobuko ;
Tamaki, Stan J. ;
Anderson, Aileen J. .
NEUROLOGICAL RESEARCH, 2006, 28 (05) :474-481