Abstract |
Ischemic cerebral infarction is a leading cause of death and disability, but the key inflammatory cytokines were not fully understood and no successful therapy has been established. We have used the methods of reverse transcriptase-polymerase chain reaction (RT-PCR), enzyme-linked immunosorbent assay (ELISA), western blot, and immunohistochemical staining to detect the dynamic changes of IL-23/IL-17 axis in brain infarction and BMSC treatment on the sixth day. BMSC transplantation could reduce the infarct size (P<0.05) and improve functional deficits (P<0.001) in brain infarction. The level of IL-23/IL-17 axis expression is higher (P<0.05) in pMCAO-operated group than that in sham operated group. BMSC treatment could reduce IL-23 expression (P<0.05) and attenuate IL-17 expression (P<0.01) both in serum and around infarct lesion. So we have drawn the conclusion that IL-23/IL-17 axis induces inflammation in the pathophysiological process of cerebral infarction. BMSC treatment plays therapeutic role by immunomodulating the expression of IL-23/IL-17 axis. These findings may help to understand the cytokines in cerebral infarction and open up a possible new way of immunological treatment.
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Authors | Shuainan Ma, Di Zhong, Hongping Chen, Yi Zheng, Yanyan Sun, Jian Luo, Hulun Li, Guozhong Li, Yanhong Yin |
Journal | Journal of neuroimmunology
(J Neuroimmunol)
Vol. 257
Issue 1-2
Pg. 28-35
(Apr 15 2013)
ISSN: 1872-8421 [Electronic] Netherlands |
PMID | 23415922
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier B.V. All rights reserved. |
Chemical References |
- Interleukin-17
- Interleukin-23
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Topics |
- Animals
- Bone Marrow Transplantation
(methods)
- Brain Ischemia
(immunology, metabolism, surgery)
- Immunomodulation
(physiology)
- Interleukin-17
(antagonists & inhibitors, biosynthesis)
- Interleukin-23
(antagonists & inhibitors, biosynthesis)
- Male
- Mesenchymal Stem Cells
(immunology, metabolism)
- Mice
- Mice, Inbred C57BL
- Random Allocation
- Stroke
(immunology, metabolism, surgery)
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