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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

In this study, nerve-mimetic composite hydrogels were developed and characterized that can be utilized to investigate and capitalize on the pro-regenerative behavior of adipose-derived stem cells for spinal cord injury repair.

Abstract

Traumatic spinal cord injury (SCI) induces permanent sensorimotor deficit below the site of injury. It affects approximately a quarter million people in the US, and it represents an immeasurable public health concern. Research has been conducted to provide effective therapy; however, SCI is still considered incurable due to the complex nature of the injury site. A variety of strategies, including drug delivery, cell transplantation, and injectable biomaterials, are investigated, but one strategy alone limits their efficacy for regeneration. As such, combinatorial therapies have recently gained attention that can target multifaceted features of the injury. It has been shown that extracellular matrices (ECM) may increase the efficacy of cell transplantation for SCI. To this end, 3D hydrogels consisting of decellularized spinal cords (dSCs) and sciatic nerves (dSNs) were developed at different ratios and characterized. Histological analysis of dSCs and dSNs confirmed the removal of cellular and nuclear components, and native tissue architectures were retained after decellularization. Afterward, composite hydrogels were created at different volumetric ratios and subjected to analyses of turbidity gelation kinetics, mechanical properties, and embedded human adipose-derived stem cell (hASC) viability. No significant differences in mechanical properties were found among the different ratios of hydrogels and decellularized spinal cord matrices. Human ASCs embedded in the gels remained viable throughout the 14-day culture. This study provides a means of generating tissue-engineered combinatorial hydrogels that present nerve-specific ECM and pro-regenerative mesenchymal stem cells. This platform can provide new insights into neuro-regenerative strategies after SCI with future investigations.

Introduction

Approximately 296,000 people are suffering from traumatic SCI, and every year there are about 18,000 new SCI cases occurring in the U.S.A.1. Traumatic SCI is commonly caused by falls, gunshot wounds, vehicle accidents, and sports activities and often causes permanent loss of sensorimotor function below the site of injury. The estimated lifetime expenses for SCI treatment range between one to five million dollars per individual with significantly lower life expectancies1. Yet, SCI is still poorly understood and largely incurable, mainly due to complex pathophysiological consequences after the injury....

Protocol

The porcine tissues were commercially obtained, so approval was not required by the animal ethics committee.

1. Decellularization of porcine spinal cords (Estimated time: 5 days)

NOTE: Perform the decellularization using previously established protocols with modifications25,26. All procedures should be done in a sterile biosafety cabinet at room temperature unless stated otherwise. All solutio.......

Representative Results

Decellularized tissues were prepared using previously established protocols with slight modifications26,27. After decellularization, lyophilization, and digestion, nerve composite hydrogels at ratios of SN:SC = 2:1, 1:1, 1:2, and spinal cord-only hydrogels were fabricated (Figure 1). Removal of nuclear components was confirmed by H&E staining (Figure 2A). To quantitatively assess the decellularizatio.......

Discussion

It is widely believed that the pathophysiology of SCI is complex and multifaceted. Even though single therapies such as cell transplantation, drug delivery, and biomaterials each have provided valuable insights into SCI, the complicated nature of SCI may limit their individual efficacy28,29,30,31. Therefore, efforts to develop effective combinatorial therapeutics have increased. The nerve compo.......

Acknowledgements

This work was supported by the PhRMA Foundation and the National Institutes of Health through the award number P20GM139768 and R15NS121884 awarded to YS. We want to thank Dr. Kartik Balachandran and Dr. Raj Rao in the Department of Biomedical Engineering at the University of Arkansas for letting us use their equipment. Also, we want to thank Dr. Jin-Woo Kim and Mr. Patrick Kuczwara from the Department of Biological and Agricultural Engineering at the University of Arkansas for providing training on rheometer.

....

Materials

NameCompanyCatalog NumberComments
3-(Decyldimethylammonio)propane sulfonate inner saltSigma-AldrichD4266Used during sciatic nerve decellularization, SB-10
3-(N,N-Dimethylpalmitylammonio)propane sulfonateSigma-AldrichH6883Used during sciatic nerve decellularization, SB-16
AlamarBlue reagentFisher ScientificDAL1100Used during AlamaBlue cell viabiiltiy test
Chondroitinase ABCSigma-AldrichC3667Used during sciatic nerve decellularization
CryostatLeicaCM1860
DeoxyribonuclaseSigma-AldrichD4263Used during sciatic nerve decellularization
Disodium hydrogen phosphate heptahydrateVWRBDH9296Chemical for 100 mM Na/50 mM phos and 50 mM Na/10 mM phos buffer
DNeasy Blood & Tissue kitQiagen69506Used during DNA analysis
Dpx Mountant for histology,slide mounting mediumSigma-Aldrich6522Used during H&E staining
EosinSigma-AldrichHT110216Used during H&E staining
EthanolVWR89125-172
FormaldehydeSigma-Aldrich252549Used during H&E staining
Glutaraldehyde (GA)Sigma-AldrichG6257Used during PDMS surface functionalization
hASC growth mediaLonzaPT-4505Used to culture hASCs, containing of fetal bovine serum and penicilin/streptomycin
HematoxylinVWR26041-06Used during H&E staining
human adipose-derived stem cellLonzaPT-5006
Hydrochloric acid (HCl)Sigma-Aldrich320331Used to digest decellularizied tissues and adjust pregels solutions
M199 mediaSigma-AldrichM0650Used to dilute pregels to desired concentration
Optimal cutting temperatue compoundTissue-Tek4583
PepsinSigma-AldrichP7000Used to digest decellularized tissues
Peracetic acidLab AlleyPAA1001Used during spinal cord decellularization
Phosphate buffered saline (PBS)VWR97062-948
Plate readerBioTek InstrumentsSynergy Mx
Polyethyleneimine (PEI)Sigma-Aldrich181978Used during PDMS surface functionalization
Porcine sciatic nerveTissue Source LLCLive pigs, with no identifiable information and no traceability details
Porcine spinal cordTissue Source LLCLive pigs, with no identifiable information and no traceability details
QuantiFluor dsDNA systemPromegaE2670Used to analyze DNA contents
RheometerTA InstrumentsDHR 2
Rugged rotatorGlas-co099A RD4512Used during spinal cord decellularization
Sodium chloride (NaCl)VWRBDH9286Chemical for 100 mM Na/50 mM phos and 50 mM Na/10 mM phos buffer
sodium deoxycholateSigma-AldrichD6750
Sodium dihydrogen phosphate monohydrateVWRBDH9298Chemical for 100 mM Na/50 mM phos and 50 mM Na/10 mM phos buffer
Sodium hydroxide solution (NaOH)Sigma-Aldrich415443Used to adjust pregels solutions
SU-8Kayaku advnaced materialsSU8-100Used to coat silicon wafer
SucroseSigma-AldrichS8501Used during spinal cord decellularization
Sylgard 184 silicone elastomer kitDOW1317318Polydimethylxiloxane (PDMS) base and curing agent
Triton X-100Sigma-AldrichX100Used during spinal cord decellularization
Trypsin-EDTA (0.05%), phenol redThermo Fisher25300062Used during hASC work and during spinal cord decellularization
Tube revolver rotatorThermo Fisher88881001Used during sciatic nerve decellularization
XyleneVWRMK866816Used during H&E staining

References

  1. National Spinal Cord Injury Statistical Center. . Spinal Cord Injury Facts and Figures at a Glance. , (2017).
  2. Anjum, A., et al. Spinal cord injury: Pathophysiology, multimolecular interactions, and underlying recovery mechanisms.

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Spinal Cord InjuryCombinatorial TherapyStem Cell DeliveryExtracellular MatrixDecellularized Spinal CordDecellularized Sciatic NerveHydrogelHuman Adipose derived Stem CellsRegeneration

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