Figure 5
Figure 5. tPA-binding to injured neurons is specific and occurs via the F, E, or K1 domains. (A) Increasing amounts of tPA633 were transiently perfused over neuronal cultures. Plotted is the binding of tPA633 to a single dead neuron over time (circled in the micrograph where tPA633 fluorescence is depicted in red). (B) tPA633 (1 nM) was perfused over neuronal cultures either alone (“no competitor”) or with various competitors. For a single experiment, the average relative amount of tPA633 binding was determined for all nonviable cells in a field. Shown are collated data from n = 3 to 7 independent experiments. Data represent average ± SEM. *P < .05 by 1-way ANOVA with Neumann-Keuls correction.

tPA-binding to injured neurons is specific and occurs via the F, E, or K1 domains. (A) Increasing amounts of tPA633 were transiently perfused over neuronal cultures. Plotted is the binding of tPA633 to a single dead neuron over time (circled in the micrograph where tPA633 fluorescence is depicted in red). (B) tPA633 (1 nM) was perfused over neuronal cultures either alone (“no competitor”) or with various competitors. For a single experiment, the average relative amount of tPA633 binding was determined for all nonviable cells in a field. Shown are collated data from n = 3 to 7 independent experiments. Data represent average ± SEM. *P < .05 by 1-way ANOVA with Neumann-Keuls correction.

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