Investigation of gloom-targeted cell therapy using imbroglio
| Project/Area Number |
14571343
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Cerebral neurosurgery
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| Research Institution | Fujita Health University |
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Principal Investigator |
IMAI Fumihiro Fujita Health University, School of Medicine, Assistant professor, 医学部, 講師 (20288476)
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| Co-Investigator(Kenkyū-buntansha) |
SAWADA Makoto Fujita Health University, Institute Comprehensive Medical Science, professor, 総合医科学研究所, 教授 (10187297)
井水 秀栄 藤田保健衛生大学, 医学部, 助手
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| Project Period (FY) |
2002 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2003: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2002: ¥1,800,000 (Direct Cost: ¥1,800,000)
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| Keywords | microglia / Cerebral ischemia / glioma / Cell therapy / Blood brain barriar / 血液能関門 / 血管脳関門 |
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| Research Abstract |
We have reported that exogenous microglia enter the brain parenchyma through blood brain barrier and migrate to ischemic hippocampal lesions when they are injected into the circulation. When we develop this therapy, we must investigate the effect of microglia to the cerebral ischemia, because most of the glioma patients were middle or old age and have silent cerebral infarction. At first, we investigated the effect of the exogenous microglia on the ischemic pyramidal neurons. To this end, we isolated microglia from the neonatal mixed brain cultures, labeled them with the fluorescent dye PKH26, and injected into the artery of Mongolian gerbils subjected to ischemia reperfusion neuronal injury. PKH26-labeled microglia migrated to the ischemic hippocampal lesion and increased the survival neurons, even when the cells were injected at 24h after the ischemic insult. Stimulation of isolatede microglia with interferon gamma (IFNγ) enhanced the neuroprotective effect on the ischemic neurons. Microglia also protected ischaemia-induced learning disability.
Next, we produced mouse glioma model by inoculation of GL2Gl mouse glioma cells to the brain. Then, we injected PKH26-labeled microglia to the circulation of the glioma model. We confirmed that microglia had high migration activity to glioma and that the injection of microgliaprolonged the survival statistically. It is possible to develop glioma-targeted cell therapy using microglia.
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Report
(3 results)
Research Products
(1 results)
