Skip to main content
Top
Published in: Inflammation 5/2019

01-10-2019 | ORIGINAL ARTICLE

Cellular Inflammatory Response of the Spleen After Acute Spinal Cord Injury in Rat

Authors: Feng Wu, Xiao-Yan Ding, Xiao-Hui Li, Min-Jie Gong, Jia-Qi An, Jiang-Hua Lai, Sheng-Li Huang

Published in: Inflammation | Issue 5/2019

Login to get access

Abstract

Spinal cord injury (SCI) involves both primary and secondary damages. After the phase of primary injury, a series of inflammatory responses initiate, which belong to the secondary injury. There has been little investigation into the cellular inflammatory response of the spleen to SCI. To disclose the impact of SCI on the spleen, we examined the inflammatory reactions of the spleen during the acute phase of SCI in rat. Adult rats were used as experimental animals and divided into un-injured, sham, and SCI groups (n = 36). Contusion injuries were produced at the T3 vertebral level. Spinal cords were harvested 6 h, 24 h, 48 h, 72 h, 120 h, and 168 h after surgery and were prepared for immunohistochemistry. Spleen wet weight was measured. Blood and spleens were prepared for quantitative analyses. The spleen index was significantly decreased in the SCI groups. Immunohistochemical results showed an increase of the infiltrating cells in the spinal cord tissues from SCI rats at all time points, peaking in 72 h post injury. In the blood, T and B lymphocytes significantly decreased in the SCI group as compared with the sham group, while monocyte increased. Surprisingly, in the SCI group, neutrophil initially decreased and subsequently tended to return toward baseline levels, then remained elevated until the end of the study. Spleen analyses revealed a significant increase in monocyte and neutrophil but a minor (not statistically significant) reduction in T and B lymphocytes. Our data show that the four most prevalent inflammatory cells infiltrate the spinal cord after injury. Increased levels of inflammatory cells (monocyte and neutrophil) in the blood and spleen appear to be very sensitive to SCI. The spleen plays a critical role in the acute phase of SCI.
Literature
1.
go back to reference Moritz, C. 2018. A giant step for spinal cord injury research. Nature Neuroscience 21 (12): 1647–1648.CrossRefPubMed Moritz, C. 2018. A giant step for spinal cord injury research. Nature Neuroscience 21 (12): 1647–1648.CrossRefPubMed
2.
go back to reference Savic, G., M.J. DeVivo, H.L. Frankel, M.A. Jamous, B.M. Soni, and S. Charlifue. 2017. Causes of death after traumatic spinal cord injury—a 70-year British study. Spinal Cord 55 (10): 891–897.CrossRefPubMed Savic, G., M.J. DeVivo, H.L. Frankel, M.A. Jamous, B.M. Soni, and S. Charlifue. 2017. Causes of death after traumatic spinal cord injury—a 70-year British study. Spinal Cord 55 (10): 891–897.CrossRefPubMed
3.
go back to reference Zhao, F., X.Y. Ding, F. Wu, X.H. Li, Y.H. Li, M. Hu, and S.L. Huang. 2018. Relieving compression against injured spinal cord via non-suturing muscle layer in rat. Biomedical Research 29 (8): 1693–1696.CrossRef Zhao, F., X.Y. Ding, F. Wu, X.H. Li, Y.H. Li, M. Hu, and S.L. Huang. 2018. Relieving compression against injured spinal cord via non-suturing muscle layer in rat. Biomedical Research 29 (8): 1693–1696.CrossRef
4.
go back to reference Huang, S.L., L. Xiang, Y.J. Huang, F. Wang, L. Ji, J.L. Xue, and B.S. Lan. 2018. Electrophysiological monitoring techniques for spinal cord function in a canine model. International Journal of Clinical and Experimental Medicine 11 (6): 5986–5991. Huang, S.L., L. Xiang, Y.J. Huang, F. Wang, L. Ji, J.L. Xue, and B.S. Lan. 2018. Electrophysiological monitoring techniques for spinal cord function in a canine model. International Journal of Clinical and Experimental Medicine 11 (6): 5986–5991.
5.
go back to reference Liu, J.J., X.Y. Ding, L. Xiang, F. Zhao, and S.L. Huang. 2017. A novel method for oxygen glucose deprivation model in organotypic spinal cord slices. Brain Research Bulletin 135: 163–169.CrossRefPubMed Liu, J.J., X.Y. Ding, L. Xiang, F. Zhao, and S.L. Huang. 2017. A novel method for oxygen glucose deprivation model in organotypic spinal cord slices. Brain Research Bulletin 135: 163–169.CrossRefPubMed
6.
go back to reference Liu, J.J., Y.J. Huang, L. Xiang, F. Zhao, and S.L. Huang. 2017. A novel method of organotypic spinal cord slice culture in rat. NeuroReport 28 (16): 1097–1102.CrossRefPubMed Liu, J.J., Y.J. Huang, L. Xiang, F. Zhao, and S.L. Huang. 2017. A novel method of organotypic spinal cord slice culture in rat. NeuroReport 28 (16): 1097–1102.CrossRefPubMed
7.
go back to reference Li, X.H., F. Wu, F. Zhao, and S.L. Huang. 2017. Fractional anisotropy is a marker in early-stage spinal cord injury. Brain Research 1672: 44–49.CrossRefPubMed Li, X.H., F. Wu, F. Zhao, and S.L. Huang. 2017. Fractional anisotropy is a marker in early-stage spinal cord injury. Brain Research 1672: 44–49.CrossRefPubMed
8.
go back to reference Huang, S.L., H.G. Qi, J.J. Liu, J.L. Li, Y.J. Huang, and L. Xiang. 2016. Alarm value of somatosensory-evoked potential in idiopathic scoliosis surgery. World Neurosurgery 92: 397–401.CrossRefPubMed Huang, S.L., H.G. Qi, J.J. Liu, J.L. Li, Y.J. Huang, and L. Xiang. 2016. Alarm value of somatosensory-evoked potential in idiopathic scoliosis surgery. World Neurosurgery 92: 397–401.CrossRefPubMed
9.
go back to reference Liu, J.J., Z. Guan, Z. Gao, L. Xiang, and S.L. Huang. 2016. Complications after spinal anesthesia in adult tethered cord syndrome. Medicine 95 (29): e4289.CrossRefPubMedPubMedCentral Liu, J.J., Z. Guan, Z. Gao, L. Xiang, and S.L. Huang. 2016. Complications after spinal anesthesia in adult tethered cord syndrome. Medicine 95 (29): e4289.CrossRefPubMedPubMedCentral
10.
go back to reference Huang, S.L., H.G. Qi, J.J. Liu, Y.J. Huang, and L. Xiang. 2015. A rare complication of spine surgery: Guillain–Barré syndrome. World Neurosurgery 84 (3): 697–701.CrossRefPubMed Huang, S.L., H.G. Qi, J.J. Liu, Y.J. Huang, and L. Xiang. 2015. A rare complication of spine surgery: Guillain–Barré syndrome. World Neurosurgery 84 (3): 697–701.CrossRefPubMed
11.
go back to reference Li, X.H., J.B. Li, X.J. He, F. Wang, S.L. Huang, and Z.L. Bai. 2015. Timing of diffusion tensor imaging in the acute spinal cord injury of rats. Scientific Reports 5: 12639.CrossRefPubMedPubMedCentral Li, X.H., J.B. Li, X.J. He, F. Wang, S.L. Huang, and Z.L. Bai. 2015. Timing of diffusion tensor imaging in the acute spinal cord injury of rats. Scientific Reports 5: 12639.CrossRefPubMedPubMedCentral
12.
go back to reference Huang, S.L., Y.X. Liu, G.L. Yuan, J. Zhang, and H.W. Yan. 2015. Characteristics of lumbar disc herniation with exacerbation of presentation due to spinal manipulative therapy. Medicine 94 (12): e661.CrossRefPubMedPubMedCentral Huang, S.L., Y.X. Liu, G.L. Yuan, J. Zhang, and H.W. Yan. 2015. Characteristics of lumbar disc herniation with exacerbation of presentation due to spinal manipulative therapy. Medicine 94 (12): e661.CrossRefPubMedPubMedCentral
13.
go back to reference Huang, S.L., J. Peng, G.L. Yuan, X.Y. Ding, and B.S. Lan. 2015. A new model of tethered cord syndrome produced by slow traction. Scientific Reports 5: 9116.CrossRefPubMedPubMedCentral Huang, S.L., J. Peng, G.L. Yuan, X.Y. Ding, and B.S. Lan. 2015. A new model of tethered cord syndrome produced by slow traction. Scientific Reports 5: 9116.CrossRefPubMedPubMedCentral
14.
go back to reference Huang, S.L., X.J. He, L. Xiang, G.L. Yuan, N. Ning, and B.S. Lan. 2014. CT and MRI features of patients with diastematomyelia. Spinal Cord 52 (9): 689–692.CrossRefPubMed Huang, S.L., X.J. He, L. Xiang, G.L. Yuan, N. Ning, and B.S. Lan. 2014. CT and MRI features of patients with diastematomyelia. Spinal Cord 52 (9): 689–692.CrossRefPubMed
15.
go back to reference Huang, S.L., X.J. He, L. Lin, and B. Cheng. 2014. Neuroprotective effect of ginsenoside Rg1 against spinal cord ischemia and reperfusion in rats. Neurochemical Journal 8 (3): 199–204.CrossRef Huang, S.L., X.J. He, L. Lin, and B. Cheng. 2014. Neuroprotective effect of ginsenoside Rg1 against spinal cord ischemia and reperfusion in rats. Neurochemical Journal 8 (3): 199–204.CrossRef
16.
go back to reference Huang, S.L., X.J. He, Z.F. Li, L. Lin, and B. Cheng. 2014. Neuroprotective effects of ginsenoside Rg1 on oxygen-glucose deprivation reperfusion in PC12 cells. Pharmazie 69 (3): 208–211.PubMed Huang, S.L., X.J. He, Z.F. Li, L. Lin, and B. Cheng. 2014. Neuroprotective effects of ginsenoside Rg1 on oxygen-glucose deprivation reperfusion in PC12 cells. Pharmazie 69 (3): 208–211.PubMed
17.
go back to reference Huang, S.L., H.X. Jiang, B. Cheng, N. Ning, and X.J. He. 2013. Characteristics and management of occult intrasacral extradural cyst in children. British Journal of Neurosurgery 27 (4): 509–512.CrossRefPubMed Huang, S.L., H.X. Jiang, B. Cheng, N. Ning, and X.J. He. 2013. Characteristics and management of occult intrasacral extradural cyst in children. British Journal of Neurosurgery 27 (4): 509–512.CrossRefPubMed
18.
go back to reference Huang, S.L., H.W. Yan, and K.Z. Wang. 2013. Use of Fidji cervical cage in the treatment of cervical spinal cord injury without radiographic abnormality. BioMed Research International 2013: 810172.PubMedPubMedCentral Huang, S.L., H.W. Yan, and K.Z. Wang. 2013. Use of Fidji cervical cage in the treatment of cervical spinal cord injury without radiographic abnormality. BioMed Research International 2013: 810172.PubMedPubMedCentral
19.
go back to reference Huang, S.L., X.J. He, K.Z. Wang, and B.S. Lan. 2013. Diastematomyelia: A 35-year experience. Spine 38 (6): E344–E349.CrossRefPubMed Huang, S.L., X.J. He, K.Z. Wang, and B.S. Lan. 2013. Diastematomyelia: A 35-year experience. Spine 38 (6): E344–E349.CrossRefPubMed
20.
go back to reference Huang, S.L., W. Shi, and L.G. Zhang. 2012. Congenital dermal sinus of the cervical spine: Clinical characteristics and management. Journal of Neurosurgical Sciences 56 (1): 61–66.PubMed Huang, S.L., W. Shi, and L.G. Zhang. 2012. Congenital dermal sinus of the cervical spine: Clinical characteristics and management. Journal of Neurosurgical Sciences 56 (1): 61–66.PubMed
21.
go back to reference Huang, S.L., W. Shi, and L.G. Zhang. 2010. Characteristics and surgery of cervical myelomeningocele. Child’s Nervous System 26 (1): 87–91.CrossRefPubMed Huang, S.L., W. Shi, and L.G. Zhang. 2010. Characteristics and surgery of cervical myelomeningocele. Child’s Nervous System 26 (1): 87–91.CrossRefPubMed
22.
go back to reference Huang, S.L., W. Shi, and L.G. Zhang. 2010. Surgical treatment for lipomyelomeningocele in children. World Journal of Pediatrics 6 (4): 361–365.CrossRefPubMed Huang, S.L., W. Shi, and L.G. Zhang. 2010. Surgical treatment for lipomyelomeningocele in children. World Journal of Pediatrics 6 (4): 361–365.CrossRefPubMed
23.
go back to reference Hilton, B.J., A.J. Moulson, and W. Tetzlaff. 2017. Neuroprotection and secondary damage following spinal cord injury: Concepts and methods. Neuroscience Letters 652: 3–10.CrossRefPubMed Hilton, B.J., A.J. Moulson, and W. Tetzlaff. 2017. Neuroprotection and secondary damage following spinal cord injury: Concepts and methods. Neuroscience Letters 652: 3–10.CrossRefPubMed
24.
go back to reference Dantzer, R. 2018. Neuroimmune interactions: From the brain to the immune system and vice versa. Physiological Reviews 98 (1): 477–504.CrossRefPubMed Dantzer, R. 2018. Neuroimmune interactions: From the brain to the immune system and vice versa. Physiological Reviews 98 (1): 477–504.CrossRefPubMed
25.
go back to reference Li, B., K. Concepcion, X. Meng, and L. Zhang. 2017. Brain-immune interactions in perinatal hypoxic-ischemic brain injury. Progress in Neurobiology 159: 50–68.CrossRefPubMedPubMedCentral Li, B., K. Concepcion, X. Meng, and L. Zhang. 2017. Brain-immune interactions in perinatal hypoxic-ischemic brain injury. Progress in Neurobiology 159: 50–68.CrossRefPubMedPubMedCentral
26.
go back to reference Rust, R., and J. Kaiser. 2017. Insights into the dual role of inflammation after spinal cord injury. Journal of Neuroscience 37 (18): 4658–4660.CrossRefPubMed Rust, R., and J. Kaiser. 2017. Insights into the dual role of inflammation after spinal cord injury. Journal of Neuroscience 37 (18): 4658–4660.CrossRefPubMed
27.
go back to reference Orr, M.B., and J.C. Gensel. 2018. Spinal cord injury scarring and inflammation: Therapies targeting glial and inflammatory responses. Neurotherapeutics 15 (3): 541–553.CrossRefPubMedPubMedCentral Orr, M.B., and J.C. Gensel. 2018. Spinal cord injury scarring and inflammation: Therapies targeting glial and inflammatory responses. Neurotherapeutics 15 (3): 541–553.CrossRefPubMedPubMedCentral
28.
go back to reference Hausmann, O.N. 2003. Post-traumatic inflammation following spinal cord injury. Spinal Cord 41 (7): 369–378.CrossRefPubMed Hausmann, O.N. 2003. Post-traumatic inflammation following spinal cord injury. Spinal Cord 41 (7): 369–378.CrossRefPubMed
29.
go back to reference Donnelly, D.J., and P.G. Popovich. 2008. Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury. Experimental Neurology 209 (2): 378–388.CrossRefPubMed Donnelly, D.J., and P.G. Popovich. 2008. Inflammation and its role in neuroprotection, axonal regeneration and functional recovery after spinal cord injury. Experimental Neurology 209 (2): 378–388.CrossRefPubMed
30.
go back to reference de Menezes, M.F., F. Nicola, I.R.V. da Silva, A. Vizuete, V.R. Elsner, L.L. Xavier, C.A.S. Gonçalves, C.A. Netto, and R.G. Mestriner. 2018. Glial fibrillary acidic protein levels are associated with global histone H4 acetylation after spinal cord injury in rats. Neural Regeneration Research 13 (11): 1945–1952.CrossRefPubMedPubMedCentral de Menezes, M.F., F. Nicola, I.R.V. da Silva, A. Vizuete, V.R. Elsner, L.L. Xavier, C.A.S. Gonçalves, C.A. Netto, and R.G. Mestriner. 2018. Glial fibrillary acidic protein levels are associated with global histone H4 acetylation after spinal cord injury in rats. Neural Regeneration Research 13 (11): 1945–1952.CrossRefPubMedPubMedCentral
31.
go back to reference Seifert, H.A., A.A. Hall, C.B. Chapman, L.A. Collier, A.E. Willing, and K.R. Pennypacker. 2012. A transient decrease in spleen size following stroke corresponds to splenocyte release into systemic circulation. Journal of Neuroimmune Pharmacology 7 (4): 1017–1024.CrossRefPubMedPubMedCentral Seifert, H.A., A.A. Hall, C.B. Chapman, L.A. Collier, A.E. Willing, and K.R. Pennypacker. 2012. A transient decrease in spleen size following stroke corresponds to splenocyte release into systemic circulation. Journal of Neuroimmune Pharmacology 7 (4): 1017–1024.CrossRefPubMedPubMedCentral
33.
go back to reference Zhang, B., and J.C. Gensel. 2014. Is neuroinflammation in the injured spinal cord different than in the brain? Examining intrinsic differences between the brain and spinal cord. Experimental Neurology 258: 112–120.CrossRefPubMed Zhang, B., and J.C. Gensel. 2014. Is neuroinflammation in the injured spinal cord different than in the brain? Examining intrinsic differences between the brain and spinal cord. Experimental Neurology 258: 112–120.CrossRefPubMed
Metadata
Title
Cellular Inflammatory Response of the Spleen After Acute Spinal Cord Injury in Rat
Authors
Feng Wu
Xiao-Yan Ding
Xiao-Hui Li
Min-Jie Gong
Jia-Qi An
Jiang-Hua Lai
Sheng-Li Huang
Publication date
01-10-2019
Publisher
Springer US
Published in
Inflammation / Issue 5/2019
Print ISSN: 0360-3997
Electronic ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-019-01024-y

Other articles of this Issue 5/2019

Inflammation 5/2019 Go to the issue