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. 2020 Nov 25;9:e59489. doi: 10.7554/eLife.59489

Table 1. Influence of heparan sulfate proteoglycans on the dynamics of Wnt3EGFP, LynEGFP, and secretedEGFP at 48 hpf. Data are mean ± SD.

Table 1—source data 1. Tg(−4.0wnt3:Wnt3EGFP) embryos treated by heparinase and surfen.
(A) The expression of Wnt3EGFP after heparinase treatment. (B) Distribution of Dextran-TRITC coinjected with heparinase in the BV of Tg(−4.0wnt3:Wnt3EGFP) embryo. (C) Expression of Wnt3EGFP after surfen treatment. BV, brain ventricle; Ce, cerebellum. Images orientation: anterior to the left. Scale bar 50 μm.
Table 1—source data 2. Individual fluorescence correlation spectroscopy measurements of Wnt3EGFP, LynEGFP, and secEGFP embryos before and after heparan sulfate proteoglycan disruption.
Sample Dfast (µm2/s) Dslow (µm2/s) Fslow No. of measurements
Wnt3EGFP 24.7 ± 4.8 0.6 ± 0.3 0.6 ± 0.02 47
Wnt3EGFP + heparinase 43.4 ± 7.6 0.4 ± 0.2 0.6 ± 0.04 63
Wnt3EGFP + surfen 42.0 ± 6.9 0.5 ± 0.3 0.6 ± 0.08 30
LynEGFP 39.1 ± 11.2 2.2 ± 0.6 0.7 ± 0.04 29
LynEGFP + heparinase 40.1 ± 9.5 2.7 ± 0.7 0.6 ± 0.04 35
LynEGFP + surfen 41.4 ± 6.9 3.1 ± 0.9 0.7 ± 0.06 18
SecEGFP 59.4 ± 9.4 - - 30
SecEGFP + heparinase 56.9 ± 9.7 - - 30
SecEGFP + surfen 53.5 ± 8.5 - - 18