J Korean Ophthalmol Soc.  2009 Apr;50(4):588-593. 10.3341/jkos.2009.50.4.588.

The Effects of Wnt Protein on Proliferation and Stemness Maintenance of Corneal Limbal Stem Cells (CLSCs)

• Jin HJ
• Joo CK

• KMID: 2212261
• DOI: http://doi.org/10.3341/jkos.2009.50.4.588

Abstract

PURPOSE: To evaluate the effects of the Wnt protein on proliferation and stemness maintenance of cultured corneal limbal stem cells.
METHODS
We examined the expression of Wnt proteins by Western blot analysis. We then evaluated the effects of Wnt on cell proliferation by colony forming efficiency. beta-catenin activation using Wnt proteins was examined by immunocytochemistry. We also examined the effects of Wnt on proliferation and stemness maintenance by reverse transcriptase polymerase chain reaction of p63 and connexin43.
RESULTS
Wnt has a different effect on corneal epithelial stem cells. Colony forming efficiency was also significantly higher in treated Wnt2 and Wnt4 cells compared with controls. The Wnt2 and Wnt4 treated cells showed nuclear accumulation of beta-catenin. In addition, the limbal stem cell marker p63 was strongly expressed in Wnt2, Wnt4 Wnt5a, and Wnt5b. Connexin43 mRNA was also strongly expressed in Wnt5a, Wnt5b and Wnt7b cells.
CONCLUSIONS
We suggest that Wnt2 and Wnt4 could lead to more effective proliferation and stemness maintenance for human corneal epithelial stem cells.

Keyword

Limbal stem cell; Proliferation; Stemness; Wnt protein

MeSH Terms

beta Catenin
Blotting, Western
Cell Proliferation
Connexin 43
Humans
Immunohistochemistry
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger
Stem Cells
Wnt Proteins
Connexin 43
RNA, Messenger
Wnt Proteins
beta Catenin

Figure

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  Figure 1. Wnt gene expression in NIH3T3 cells. HA‐Wnt protein expression was determined by western blot analysis. The protein was extracted from cytoplasm and media. HA was expressed Wnt trasnfected. Cnt as an empty vector‐transfected control.

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  Figure 2. Proliferation of limbal stem cells by Wnt. (A) Proliferation capacity of Wnt was evaluated by 0.1% crystal violet staining at 13 days. (B) The colony formed in Wnt2 and Wnt4 higher in treated Wnt2 and Wnt4 compared with control. In addition, CFE was calculated as the number of colonies/number of inoculated cells. Colony counting (holoclone): diameter of colony>1 mm. Values represent the mean± S.E.M of three independent experiments. Significant difference (* p<0.05) compared with vector‐transfected control are represented by* for Wnt-treated. Control as a vector-transfected control. Abbreviation: CFE, colony‐forming efficiency.

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  Figure 3. Nuclear translocation of β‐catenin in the colony induced by Wnt2 and Wnt4. The localization of β‐catenin was examined by immunocytochemistry at 11 days. (A) β‐catenin is observed in the cytoplasm and plasma membrane. (B)(C) Wnt2 and Wnt4 treated cells show nuclear accumulation of β‐catenin. β‐catenin proteins were detected as a red color using anti‐rabbit alexa 546. Cell nuclei were stained with Hoechst 33342 Scale bar=10 μm.

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  Figure 4. Expression of limbal stem cells and differentiation marker in cultured limbal stem cells. RT‐PCR profiles showing mRNA expression of Connexin43 and p63 with GAPDH as an internal control. Limbal stem cell marker p63 mRNA was strongly expressed in Wnt4 and Wnt5a. Otherwise, Differentiation marker Connexin43 mRNA strongly expressed in Wnt5a, Wnt5b, Wnt7b.

Reference

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