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. 2022 Oct 10;13:5859. doi: 10.1038/s41467-022-33605-1

Fig. 1. Lens-induced myopia induces axial elongation and endoplasmic reticulum stress in the sclera.

Fig. 1

a Changes in axial length during 3-week lens-induced myopia (LIM) in C57BL6J mice (n = 4). NL: No Lens control, −30D: minus 30 D lens-wearing eye. ***p = 0.00062; Student’s two-tailed t-test. b Changes in refraction during 3-week LIM in C57BL6J mice (n = 4); ***p = 0.00029; Student’s two-tailed t-test. c Transmission electron microscopy images of no lens (NL)-wearing (left panels) and minus 30 D lens-wearing (right panels) sclerae. Representative images of three biologically independent samples; N indicates nucleus and allow heads indicate rough endoplasmic reticulum. Scale bars: 1.0 µm. d Immunoblots showing ER sensor protein activation evaluated by phosphorylation levels of IRE1, PERK, eIF2α (downstream of PERK), and the ATF6 precursor (ATF6-P) and cleaved form of ATF6 (ATF6-N). Representative blots from four independent experiments are shown. Age-match: age-matched non-treated control, NL: No Lens-wearing eye, −30D: minus 30 D lens-wearing eye. e Densitometric quantification of blots in Fig. 1d using ImageJ. NL group was assigned a value of 1.0. Each group were n = 4 (each sample pooled 3 sclerae). The p values were determined by one-way ANOVA with Tukey HSD (two-tailed). NS: Not Significant. f UPR target gene expression level determined by quantitative PCR in age-matched control (right gray), No-Lens control (white) and LIM (gray) sclerae for 3-week LIM (n = 7 or 8). NL group was assigned a value of 1.0. The p values were determined by one-way ANOVA with Tukey HSD (two-tailed). Source data are provided as a Source Data file.