学術雑誌論文 Cells transplanted onto the surface of the glial scar reveal hidden potential for functional neural regeneration

Sekiya, Tetsuji  ,  Holley, Matthew C.  ,  Hashido, Kento  ,  Ono, Kazuya  ,  Shimomura, Koichiro  ,  Horie, Rie T.  ,  Hamaguchi, Kiyomi  ,  Yoshida, Atsuhiro  ,  Sakamoto, Tatsunori  ,  Ito, Juichi

112 ( 26 )  , pp.E3431 - E3440 , 2015-06-15 , National Academy of Sciences
ISSN:0027-8424
NII書誌ID(NCID):AA00786025
内容記述
新しい細胞移植法によって、聴神経の機能再生に成功. 京都大学プレスリリース. 2015-06-16.
Cell transplantation therapy has long been investigated as a therapeutic intervention for neurodegenerative disorders, including spinal cord injury, Parkinson’s disease, and amyotrophic lateral sclerosis. Indeed, patients have high hopes for a cell-based therapy. However, there are numerous practical challenges for clinical translation. One major problem is that only very low numbers of donor cells survive and achieve functional integration into the host. Glial scar tissue in chronic neurodegenerative disorders strongly inhibits regeneration, and this inhibition must be overcome to accomplish successful cell transplantation. Intraneural cell transplantation is considered to be the best way to deliver cells to the host. We questioned this view with experiments in vivo on a rat glial scar model of the auditory system. Our results show that intraneural transplantation to the auditory nerve, preceded by chondroitinase ABC (ChABC)-treatment, is ineffective. There is no functional recovery, and almost all transplanted cells die within a few weeks. However, when donor cells are placed on the surface of a ChABC-treated gliotic auditory nerve, they autonomously migrate into it and recapitulate glia- and neuron-guided cell migration modes to repair the auditory pathway and recover auditory function. Surface transplantation may thus pave the way for improved functional integration of donor cells into host tissue, providing a less invasive approach to rescue clinically important neural tracts.
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http://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/198455/1/pnas.1501835112.pdf

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