March 2012
Volume 53, Issue 14
Free
ARVO Annual Meeting Abstract  |   March 2012
Differentiation of Bone-Marrow Derived Cells into Non-Immunocompetent Corneal Cells
Author Affiliations & Notes
  • Yosuke Harada
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Osamu Taguchi
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Waka Ishida
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Mina Kajisako
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Ken Fukuda
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Yoshiaki Kiuchi
    Ophthalmology & Visual Science, Hiroshima University, Minami-Ku, Japan
  • Atsuki Fukushima
    Ophthalmology, Kochi Medical School, Nankoku, Japan
  • Footnotes
    Commercial Relationships  Yosuke Harada, None; Osamu Taguchi, None; Waka Ishida, None; Mina Kajisako, None; Ken Fukuda, None; Yoshiaki Kiuchi, None; Atsuki Fukushima, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science March 2012, Vol.53, 1080. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Yosuke Harada, Osamu Taguchi, Waka Ishida, Mina Kajisako, Ken Fukuda, Yoshiaki Kiuchi, Atsuki Fukushima; Differentiation of Bone-Marrow Derived Cells into Non-Immunocompetent Corneal Cells. Invest. Ophthalmol. Vis. Sci. 2012;53(14):1080.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose: : Bone marrow (BM)-derived stem cells are able to differentiate into various types of tissue resident cells. Previous studies revealed that BM-derived cells exist in mouse cornea and the majority of these cells were CD11b+ or CD11c+ immunocompetent cells. Although some of BM-derived cells in the cornea were negative for CD11b and CD11c, it remains elusive whether these cells are actually non-immunocompetent cells. The aim of this study is to clarify whether BM-derived cells can differentiate into non-immunocompetent cells in the cornea.

Methods: : BM cells from C57BL/6 green fluorescent protein (GFP)-transgenic mice were intravenously injected into C57BL/6 wild type (WT) recipient mice that had been lethally x ray-irradiated (BMT mice). Four months after BM transplantation, the BMT mice were again lethally x ray-irradiated and received BM cells from C57BL/6 WT mice (2nd BMT mice). Three weeks later, the 2nd BMT mice were sacrificed and corneas and spleens were harvested for immunofluorescent microscopic and flow cytometric analyses, respectively.

Results: : The percentage of GFP+ cells out of whole splenocytes was less than 1% in 2nd BMT mice. In contrast, many GFP+ cells were detected in the cornea of the 2nd BMT mice. These cells distributed abundantly in the limbus and less in the peripheral and central cornea. These cells existed in the stroma but not in the epithelial and endothelial layers.

Conclusions: : Because most of GFP+ immunocompetent cells were depleted by the second x ray-irradiation, GFP+ cells in the cornea are considered to be non-immunocompetent cells. Thus, it appears that BM-derived cells differentiate into non-immunocompetent cells in the cornea.

Keywords: cornea: stroma and keratocytes • cornea: basic science 
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×