Literature DB >> 22246536

Magnetic field-based delivery of human CD133⁺ cells promotes functional recovery after rat spinal cord injury.

Yuki Fujioka1, Nobuhiro Tanaka, Kazuyoshi Nakanishi, Naosuke Kamei, Toshio Nakamae, Bunichiro Izumi, Ryo Ohta, Mitsuo Ochi.   

Abstract

STUDY
DESIGN: Experimental animal study of spinal cord injury (SCI), using a cell delivery system.
OBJECTIVE: To investigate the therapeutic effects of transplantation of peripheral blood-derived CD133 cells, with a magnetic delivery system in a rat SCI model. SUMMARY OF BACKGROUND DATA: There are no reports on intrathecal transplantation of peripheral blood-derived CD133 cells, with a magnetic cell delivery system to treat SCI.
METHODS: Magnetically isolated peripheral blood-derived CD133 cells were used as the cell source. Contusion SCI was induced by an Infinite Horizon impactor in athymic nude rats. CD133 cells or phosphate-buffered saline was administered via a lumbar puncture immediately after SCI, and a magnetic field was applied to rats for 30 minutes. Animals were analyzed at specific times after transplantation by several methods to examine cell tracking, functional recovery, and histological angiogenesis and neurogenesis.
RESULTS: A combination of cell transplantation and application of a magnetic field at the site of injury caused significant functional recovery. Transplantation of the cells alone in the absence of the magnetic field showed no effect beyond that observed in control rats.
CONCLUSION: The combination of intrathecal transplantation of CD133 cells and application of a magnetic field at the site of injury is a possible therapeutic strategy to treat rat SCI and may therefore find application in clinical settings.

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Year:  2012        PMID: 22246536     DOI: 10.1097/BRS.0b013e318246d59c

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  7 in total

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2.  Survival and migration of pre-induced adult human peripheral blood mononuclear cells in retinal degeneration slow (rds) mice three months after subretinal transplantation.

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3.  Magnet-Bead Based MicroRNA Delivery System to Modify CD133+ Stem Cells.

Authors:  Paula Müller; Natalia Voronina; Frauke Hausburg; Cornelia A Lux; Frank Wiekhorst; Gustav Steinhoff; Robert David
Journal:  Stem Cells Int       Date:  2016-10-04       Impact factor: 5.443

4.  Superparamagnetic Iron Oxide Nanoparticle-Mediated Forces Enhance the Migration of Schwann Cells Across the Astrocyte-Schwann Cell Boundary In vitro.

Authors:  Liangliang Huang; Bing Xia; Zhongyang Liu; Quanliang Cao; Jinghui Huang; Zhuojing Luo
Journal:  Front Cell Neurosci       Date:  2017-03-28       Impact factor: 5.505

Review 5.  Magnetic cell delivery for the regeneration of musculoskeletal and neural tissues.

Authors:  Naosuke Kamei; Nobuo Adachi; Mitsuo Ochi
Journal:  Regen Ther       Date:  2018-11-02       Impact factor: 3.419

Review 6.  Regenerative medicine in orthopedics using cells, scaffold, and microRNA.

Authors:  Mitsuo Ochi; Tomoyuki Nakasa; Goki Kamei; Muhammad Andry Usman; Elhussein Mahmoud; Hussein El Mahmoud
Journal:  J Orthop Sci       Date:  2014-05-13       Impact factor: 1.601

7.  Endothelial progenitor cell-conditioned medium promotes angiogenesis and is neuroprotective after spinal cord injury.

Authors:  Tao Wang; Xiao Fang; Zong-Sheng Yin
Journal:  Neural Regen Res       Date:  2018-05       Impact factor: 5.135

  7 in total

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