Investigative Ophthalmology & Visual Science Cover Image for Volume 61, Issue 7
June 2020
Volume 61, Issue 7
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ARVO Annual Meeting Abstract  |   June 2020
Wnt signaling crosstalk via Wnt16b improves human limbal epithelial stem/progenitor cell maintenance
Author Affiliations & Notes
  • Sarah Robertson
    Stein Eye Institute, Los Angeles, California, United States
  • Jakia Islam
    Stein Eye Institute, Los Angeles, California, United States
  • Sophie X. Deng
    Stein Eye Institute, Los Angeles, California, United States
  • Footnotes
    Commercial Relationships   Sarah Robertson, None; Jakia Islam, None; Sophie Deng, None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2020, Vol.61, 3283. doi:
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      Sarah Robertson, Jakia Islam, Sophie X. Deng; Wnt signaling crosstalk via Wnt16b improves human limbal epithelial stem/progenitor cell maintenance. Invest. Ophthalmol. Vis. Sci. 2020;61(7):3283.

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

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Abstract

Purpose : Understanding effective limbal epithelial stem cell maintenance is necessary to improve limbal stem cell deficiency (LSCD) treatment using ex vivo cultured limbal stem/progenitor cells (LSCs). We have previously demonstrated that canonical Wnt signaling is crucial for limbal stem cell maintenance and that Wnt2, Wnt6, Wnt11, and Wnt16b are upregulated in the limbus relative to the cornea. The purpose of this study is to investigate the effect and mechanism of supplementing Wnt16b in the LSC cultures on the expansion of the stem/progenitor cell population in vitro.

Methods : Wnt16b was overexpressed in 3T3 cells, which do not express Wnt16b, using a Wnt16b-IRES-GFP lentivirus vector. An IRES-GFP vector served as a control. Transduced 3T3 cells were sorted into low, medium, and high GFP expression groups, respectively. LSCs were isolated from five donors and cultured on low, medium, and high Wnt16b-expressing 3T3s compared to their respective GFP controls and an uninfected 3T3 control. After 12-14 days in culture, the cultivated LSCs were evaluated by quantifying cells expressing K12, K14, and high levels of p63. Canonical and non-canonical Wnt pathway markers expressed in the cultivated LSCs were evaluated by quantitative real-time PCR (qRT-PCR).

Results : LSCs cultured on low Wnt16b-3T3 cells contained higher percentages of p63-bright cells, higher proliferation rate, and higher colony forming efficiency than LSCs cultured on low GFP-3T3 cells, although these comparisons are not significant (p = 0.07, p = 0.07, p = 0.16, respectively). LSCs cultured on low Wnt16b-3T3 cells also expressed significantly higher levels of the canonical Wnt pathway markers Axin2 and Lrp5, and noncanonical Wnt coreceptor Ror2 compared to the low GFP-3T3 control (p < 0.05).

Conclusions : This study suggests that low levels of Wnt16b maintain a balance of Wnt canonical and non-canonical pathways to regulate limbal stem cell proliferation, differentiation, and self-renewal in vitro. Future studies will examine the interplay between the canonical and non-canonical pathways in LSCs, as well as the balance of the four Wnt ligands in the quiescence or proliferation of the LSCs.

This is a 2020 ARVO Annual Meeting abstract.

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