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Gene therapy using macrophage transplantation for spinal cord injury

Research Project

Project/Area Number 15591584
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthopaedic surgery
Research InstitutionEhime University

Principal Investigator

YAMAMOTO Haruyasu  Ehime University, School of Medicines, Professor, 医学部, 教授 (10092446)

Co-Investigator(Kenkyū-buntansha) OGATA Tadanori  Ehime University, School of Medicine, Instructor, 医学部, 助手 (30291503)
Project Period (FY) 2003 – 2004
Project Status Completed (Fiscal Year 2004)
Budget Amount *help
¥2,400,000 (Direct Cost: ¥2,400,000)
Fiscal Year 2004: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2003: ¥1,200,000 (Direct Cost: ¥1,200,000)
Keywordsmacrophage / electroporation / gene transfer / spinal cord injury / neurotrophic factor / green fluorescent protein / Spinal cord / Macrophage / Rat / Gene / Motor function
Research Abstract

Spinal cord injury is one of the most serious condition in the field of orthopedic surgery. Several pharmacological trials have been performed for the treatment of traumatic spinal cord injury. However, only high-dose steroid therapy was established for this condition. In the injured spinal cord, blood flow of neuronal tissue remarkably decreased. Therefore, when we add neuroprotective substances intravenously, only few substances will reach the injured tissue. To develop novel drug delivery system to ischemic tissue, we notice the tissue-migration activity of macrophages. In the rat, itraperitoneal macrophage were easily harvested. Using electroporation, a non-viral DNA transfection method, we added a vecter including green fluorescent protein (GFP) to the macrophage. Then the vector-incorporated autogenous macrophage was injected into subarachnoid space of the rat after the spinal cord injury. Injected macrophage were migrated and concentrated into the injured part of the spinal cord. Using this system, we transfer the target compound into the damaged neuronal tissue. This method maybe useful drug-delivery system for the spinal cord injury.

Report

(3 results)
  • 2004 Annual Research Report   Final Research Report Summary
  • 2003 Annual Research Report

URL: 

Published: 2003-04-01   Modified: 2016-04-21  

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