May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Effect of Dendritic Cells on the Retinal Progenitor Cells in vitro and in Co–Culture With Retinal Explant
Author Affiliations & Notes
  • M. Mandai
    Kyoto University, Sakyo–Ku, Japan
    Translational,
  • A. Oishi
    Kyoto University, Sakyo–Ku, Japan
    Department of Ophthalmology and Visual Sciences,
  • M. Akimoto
    Kyoto University, Sakyo–Ku, Japan
    Translational,
  • t. suzuki
    Kyoto University, Sakyo–Ku, Japan
    Department of Ophthalmology and Visual Sciences,
  • H. Ikeda
    Kyoto University, Sakyo–Ku, Japan
    Translational,
  • N. Kawagoe
    Kyoto University, Sakyo–Ku, Japan
    Department of Ophthalmology and Visual Sciences,
  • Y. Hirami
    Kyoto University, Sakyo–Ku, Japan
    Department of Ophthalmology and Visual Sciences,
  • F. Osakada
    Kyoto University, Sakyo–Ku, Japan
    Translational,
  • M. Takahashi
    Kyoto University, Sakyo–Ku, Japan
    Translational,
  • N. Yoshimura
    Kyoto University, Sakyo–Ku, Japan
    Department of Ophthalmology and Visual Sciences,
  • Footnotes
    Commercial Relationships  M. Mandai, None; A. Oishi, None; M. Akimoto, None; T. suzuki, None; H. Ikeda, None; N. Kawagoe, None; Y. Hirami, None; F. Osakada, None; M. Takahashi, None; N. Yoshimura, None.
  • Footnotes
    Support  Grant–in–Aid from the Ministry of Education, Science, Sports and Culture of Japan
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 1401. doi:
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      M. Mandai, A. Oishi, M. Akimoto, t. suzuki, H. Ikeda, N. Kawagoe, Y. Hirami, F. Osakada, M. Takahashi, N. Yoshimura; Effect of Dendritic Cells on the Retinal Progenitor Cells in vitro and in Co–Culture With Retinal Explant . Invest. Ophthalmol. Vis. Sci. 2006;47(13):1401.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To examine the effect of bone marrow cell (BMC) derived immature dendritic cells (iDCs) on the retinal progenitor cells (RPCs) in vitro and ex vivo transplantation (co–culture with retinal explant).

Methods: : RPCs were collected from green fluorescent protein (GFP) transgenic mice. BMC were collected from 6 week rd1 mice. 1) We studied the effects of iDCs or BMCs on RPCs in vitro. 2) We co–cultured RPCs, iDCs, RPCs+iDCs, or none (control) with explanted retinas from 6 week rd1 mice. The explants were kept for 2 weeks and were processed for histological study. 3) We also examined the effect of iDCs on T cell activation induced by RPCs from a different mouse strain by evluating CD107a expression by CD8 T cells.

Results: : In vitro, iDCs but not BMCs enhanced the survival and proliferation of RPCs in DMEM/F12 with no supplement. With N2 supplement and bFGF, iDCs or its supernatant induced prominent differentiation in the RPCs but this effect was not observed with BMCs. 2) Retinal explants cultured with RPCs+iDCs or with iDCs better retained the thickness and organized structure of retina compared to the controls. Some of the RPCs extended neurites into the explanted retina when co–cultured with iDCs. 3) iDC reduced the activation of CD8 T cells induced by RPCs to the background level.

Conclusions: : These results suggested the preferable effects of the use of iDCs in RPC transplantation in retinal degenerative diseases.

Keywords: regeneration • transplantation 
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