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. 2022 Jan 13;11:e71256. doi: 10.7554/eLife.71256

Figure 5. Characterization of vacuoles in pikfyveΔ8 mutants.

(A) Time-lapse imaging indicating the dynamic changes of vacuole formation in the lens of 4-dpf pikfyveΔ8 mutants. White arrows indicate the fusion process of two small vacuoles. (B) Representative images showing the lens of 3.5-dpf siblings and pikfyveΔ8 mutants injected with gfp-rab5c mRNA. (C) Representative images showing lens of 3.5-dpf siblings and pikfyveΔ8 mutants injected with gfp-rab7 mRNA. (D) Representative images showing lens of 3.5-dpf siblings and pikfyveΔ8 mutants injected with gfp-rab11a mRNA. (E) Representative images showing lens of 3.5-dpf siblings and pikfyveΔ8 mutants injected with mcherry-lc3b mRNA. All experiments were repeated three times. All the scale bars represent 10 μm.

Figure 5.

Figure 5—figure supplement 1. Characterization of lysosomes in microglia and lens of pikfyveΔ8 mutant zebrafish.

Figure 5—figure supplement 1.

Confocal images of the lens and microglia of 4-dpf pikfyveΔ8 mutants in Tg(mpeg1:dsredx) background after LysoSensor staining. The results were confirmed in more than three different individuals. The scale bars represent 20 μm.