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The immunomodulatory effect of bone marrow stromal cells (BMSCs) on interleukin (IL)-23/IL-17-mediated ischemic stroke in mice.

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.
AuthorsShuainan Ma, Di Zhong, Hongping Chen, Yi Zheng, Yanyan Sun, Jian Luo, Hulun Li, Guozhong Li, Yanhong Yin
JournalJournal of neuroimmunology (J Neuroimmunol) Vol. 257 Issue 1-2 Pg. 28-35 (Apr 15 2013) ISSN: 1872-8421 [Electronic] Netherlands
PMID23415922 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Elsevier B.V. All rights reserved.
Chemical References
  • Interleukin-17
  • Interleukin-23
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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