The present protocol simulating central cord syndrome (CCS) in mice has improved repeatability and minimized operation damage to the experimental animals, avoiding disrupting the anatomical structure excessively. The strategy in this study is advantageous because it allows for research into injury mechanisms by producing consistent results.
Animal models of central cord syndrome (CCS) could substantially benefit preclinical research. Identifiable anatomical pathways can give minimally invasive exposure approaches and reduce extra injury to experimental animals during operation, enabling the maintenance of consistent and stable anatomical morphology during experiments to minimize behavioral and histological differences between individuals to improve the reproducibility of experiments. In this study, the C6 level spinal cord was exposed using a spinal cord injury coaxial platform (SCICP) and combination with a minimally invasive technique. With the assistance of a vertebral stabilizator, we fixed the vertebrae and compressed the spinal cords of C57BL/6J mice with 5 g/mm2 and 10 g/mm2 weights with SCICP to induce different degrees of C6 spinal cord injury. In line with the previous description of CCS, the results reveal that the lesion in this model is concentrated in the gray matter around the central cord, enabling further research into CCS. Finally, histological results are provided as a reference for the readers.
Recent years have witnessed a constantly rising incidence of spinal cord injury (SCI), with more injuries in older people from less violent tauma1. These injuries more frequently involve the cervical spine and more often lead to an incomplete neurologic dysfunction2.
In the twenty-first century, CCS is the most prevalent type of incomplete SCI, accounting for more than half of all SCI. Compared with conventional incomplete SCI, CCS is characterized by disproportionately more impairment of the upper than lower extremities3. It is characterized by predominantly upper extremity weakness with less significant sensory and bladder dysfunction. CCS is thought to be caused by post-traumatic central region hemorrhage and edema or, as recently proposed, by Wallerian degeneration from compression of the spinal cord in spinal canal stenosis. The management of CCS lacks high-level evidence to guide, which requires a comprehensive understanding of its pathophysiology4. However, models of CCS have not been reported. Suitable animal models are essential for the understanding of pathophysiology, which can provide a research base for clinical and preclinical studies5,6,7,8,9,10.
In this study, a CCS model in mice is established with a spinal cord injury coaxial platform (SCICP) and a minimally invasive operation plan, which allows for further research into and understanding of CCS. The model is proved valid in the course of the research process by histological, magnetic resonance imaging (MRI), and immunofluorescence analysis.
Of the numerous types of spinal cord injury, CCS is one of the most potentially treatable types of injury3,4. Due to the lack of laboratory research models, research on CCS from the 1950s focused on clinical studies and cadaveric dissection investigations3,16,17. The present study shows using compatible tools and minimally invasive procedures to establish mice's CCS model. From a technical perspective, this platform has strong operability and good reproducibility. Given that experiment results demonstrate the validity, our technique to establish the model closest to the standard previous studies have defined for CCS4.
Previous studies of compression injury have mainly employed aneurism clips, balloons, and calibrated forceps9,10,18. Moreover, most injuries occurred at the level of the thoracic spinal cord18. The spinal cord at the C6 level was chosen as the injured segment in this study to investigate the characteristics of CCS. It is worth the attention that the survival rate of the CCS model is also an essential factor in ensuring experimental consistency. The present study reports causing bilateral compression injury to the mouse cervical spinal cord, while high-level spinal cord traumatic injury, especially bilateral injury, could be fatal for experiment animals if too serious. According to El-Bohy, the C4/5 spinal cord is more likely to affect the descending bulbospinal tract and respiratory-related motoneurons, which leads experiment animals to respiratory depression and death18,19,20,21,22,23., In this study, mice with different degrees of compression on the C6 cervical spinal cord have significantly differentiated injury characteristics suggested by histological tests. Although there were significant behavioral and histological differences in the mouse cervical spinal cord clamping model reported by Forgione, disruption of the pedicles, articular processes, laminae, and even nerve roots were required in order to clamp the spinal cord with the modified clamps, which had a significant influence on the stability of the cervical structures24. Another study of cervical injuries reported using the transverse process as a fixation site5. Even though the articular processes were prevented from damage, over-muscular tissue breakdown could likewise lead to an impact on the stability of the spinal cord. In the present study, only the 6th cervical lamina was resected to maintain the stability of the cervical spinal cord, with the adjoining articular joints preserved and excessive muscular damage avoided. At the same time, compression from above the spinal cord prevents damage to the nerve roots.
The HE results suggest that the area of damage to the cervical spinal cord of the mice in each group was mainly in the gray matter near the central cord, which characterized CCS, with significant differences in the scope of injury between the different groups. Notably, the pathological sections we displayed may have alleviated injury manifestation because the specimens were collected at a few days post-injury. Immunofluorescence (NF-200) showed less damage to the neural tracts in the white matter region of the spinal cord, which also confirmed that the damage in CCS was mainly concentrated around the central cord. Immunofluorescence result was compounded by previous histological results of pathology. Previous studies have shown that CCS leads to edema near the central cord, leading to hematoma and, ultimately, dysfunction in the medial portion of the lateral corticospinal tract3. Hemorrhage has been reported as a typical component of CCS but is rarely seen in subsequent imaging and autopsy studies17. In this study, HE results at 7 days post-injury suggested signs of tissue edema in all groups; however, no residual red blood cells were found in the injury area. Therefore, Prussian blue was used to examine the injury area for hemorrhage, and the results corresponded with hemosiderosis observed in the injury area of the severe injury group at 7 days post-injury, whereas the mild group did not. MRI T2 images showed that both mild and severe injuries had low signal areas in the damaged area of the injury at 7 days post-injury, indicating the deposition of reticulocyte lysate here. These results provide circumstantial evidence that the discrepancy between the previously reported findings is probably due to the MRI test being potentially more sensitive than the histological test14, in addition to the severity of the injury, which may also influence the amount of hemorrhage in the area of injury. GFAP was also expressed extensively in the damaged area. At the same time, Iba-1 expression was also seen in intact areas, suggesting the persistence of an inflammatory response, consistent with the MRI results, where a ring of hyperintense signal around the hypointense signal area in the lesion suggests the presence of an inflammatory response. Ultimately, based on the results of the present study, the area of injury in the model was focused on the gray matter around the central cord, which is generally consistent with the descriptions previously reported13. Unfortunately, we did not perform MRI repetitively in every experiment animal to show how the injury site dynamically changes with time. Future researchers can include this in their work for better investigation into CCS. Also, Immunolabeling with neuronal markers like NeuN, which define the gray matter can be included in the study.
In conclusion, the characteristics of the findings on pathology and MRI scans have close similarities with those described for CCS in previous studies4. The present protocol feasibly modeling CCS enables further research into and understanding of CCS.
The authors have nothing to disclose.
This study was supported by the National Key Research and Development Project of Stem Cell and Transformation Research (2019YFA0112100) and the State Key Program of National Natural Science of China (81930070).
4% fixative solution | Solarbio | P1110 | 4% |
Anti-Neurofilament heavy polypeptide antibody | Abcam | ab8135 | Dilution ratio (1:2000) |
Eosin Staining Solution (water soluble) | Biosharp | BL727B | |
Ethanol | Fuyu Reagent | ||
Fluorescent microscope | KEYENCE | BZ-X800 | |
Frozen Slicer | Leica | ||
GFAP (GA5) Mouse mAb | Cell Signaling TECHNOLOGY | #3670 | Dilution ratio (1:600) |
Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 488 | ThermoFisher SCIENTIFIC | A32723TR | Dilution ratio (1:1000) |
Goat anti-Rabbit IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 594 | ThermoFisher SCIENTIFIC | A32740 | Dilution ratio (1:1000) |
Hematoxylin Staining Solution | Biosharp | BL702A | |
Mice | Jinan Pengyue Experimental AnimalCompany | C57BL/6J | |
Microsurgery apparatus | Shandong ULT Biotechnology Co., Ltd | All the surgey instruments are custom-made | Ophthalmic scissors, micro mosquito forceps, microsurgery forceps, micro scissors |
Normal sheep serum for blocking (working solution) | Zhong Shan Jin Qiao | ZLI-9022 | working solution |
O.C.T. Compound | SAKURA | 4583 | |
Phosphate buffered solution (PBS) | Solarbio | P1020 | pH 7.2–7.4 |
Prussian Blue Iron Stain Kit (With Eosin) | Solarbio | G1424 | |
RWD Laboratory inhalation anesthetic station | RWD Life Science Co., Ltd | R550 | |
Small animal in vivo microCT imaging system | PerkinElmer | Quantum GX2 | |
Spinal cord injury coaxial platform | Shandong ULT Biotechnology Co., Ltd | Custom-made(Feng's standard) | https://shop43957633.m.youzan.com/wscgoods/detail/367x5ovgn69q18g?banner_id=f.81386274~goods.7~ 1~b0yRFKOq&alg_id= 0&slg=tagGoodList-default%2COpBottom%2Cuuid% 2CabTraceId&components_ style_layout =1&reft=1659409105184&spm= g.930111970_f.81386274&alias= 367x5ovgn69q18g&from_uuid= 1362cc46-ffe0-6886-2c65-01903 dbacbba&sf=qq_sm&is_share= 1&shopAutoEnter=1&share_cmpt =native_wechat&is_silence_auth=1 |
Surgery microscope | Zumax Medical Co., Ltd. | zumax, OMS2355 | |
Tris Buffered Saline+Tween (TBST) | Solarbio | T1082 | Dilution ratio (1:19) |
Xylene | Fuyu Reagent |