April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Evaluation of B7-1 expression in the murine retina
Author Affiliations & Notes
  • Wei Wang
    Ophthalmology, JSEI, Jules Stein Eye Institute, UCLA, Los Angeles, CA
    Eye and ENT Hospital, Fudan University, Shanghai, China
  • Negin Ashki
    Ophthalmology, JSEI, Jules Stein Eye Institute, UCLA, Los Angeles, CA
  • Ann M Chan
    Ophthalmology, JSEI, Jules Stein Eye Institute, UCLA, Los Angeles, CA
  • Ling Chen
    Eye and ENT Hospital, Fudan University, Shanghai, China
  • Lynn K Gordon
    Ophthalmology, JSEI, Jules Stein Eye Institute, UCLA, Los Angeles, CA
  • Footnotes
    Commercial Relationships Wei Wang, None; Negin Ashki, None; Ann Chan, None; Ling Chen, None; Lynn Gordon, Paganini BioPharma (P)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 1340. doi:https://doi.org/
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    • Get Citation

      Wei Wang, Negin Ashki, Ann M Chan, Ling Chen, Lynn K Gordon; Evaluation of B7-1 expression in the murine retina. Invest. Ophthalmol. Vis. Sci. 2014;55(13):1340. doi: https://doi.org/.

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

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Abstract

Purpose: During the course of murine postnatal retinal maturation, many retinal ganglion cells (RGC) undergo programmed cell death. The immunoregulatory receptor, programmed cell death-1 (PD-1) is expressed in RGCs and contributes to RGC culling early in postnatal life. In contrast, absence of the PD-1 ligands, PD-L1 and PD-L2, in double ligand knockout mice, is associated with increased RGC numbers into adulthood. This observation supports an additional binding partner for PD-ligands in the retina. B7-1 is known to also bind PD-L1 in cells of lymphoid origin. In this study we tested whether B7-1 is expressed in the murine retina in the adult and early postnatal period.

Methods: Expression of B7-1 protein in neonatal and adult retinas was examined by Western blot analysis and immunofluorescence staining of vertical retina sections. The following retinal cell markers were co-stained with B7-1 to determine colocalization and identify specific cell types-- Brn3a, protein kinase C (PKC) α, Goα,AP2α,calbindin D28K and glutamine synthetase. B7-1 gene expression was detected by RT-PCR and normalized using the housekeeping gene GAPDH.

Results: RT-PCR results demonstrate that B7-1 gene expression is found throughout the neonatal and adult retina, peaking in the mature retina. Protein expression via Western blot analysis indicates that B7-1 gene expression undergoes translational regulation, wherein B7-1 expression is higher in neonatal retinas. B7-1 is expressed in the RGCs and bipolar interneurons of the mature mouse retina, but not in amacrine cells, horizontal cells, and Müller cells.

Conclusions: B7-1 is expressed in RGCs and bipolar cells during murine postnatal retina maturation. Similar to that of PD-1 and PD-Ligands, B7-1 expression in the retina undergoes dynamic regulation during development, raising the possibility that B7-1 engagement through PD-ligand may play a role in RGC cell survival. These findings may lead to a greater understanding of the role of PD-1/PD-ligand in retinal development and health.

Keywords: 691 retina: proximal (bipolar, amacrine, and ganglion cells) • 698 retinal development • 615 neuroprotection  
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