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Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) <t>ELISA</t> analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic <t>VEGF</t> release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.
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Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) <t>ELISA</t> analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic <t>VEGF</t> release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.
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Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) <t>ELISA</t> analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic <t>VEGF</t> release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.
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Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) <t>ELISA</t> analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic <t>VEGF</t> release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.
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Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) ELISA analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic VEGF release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.

Journal: Journal of Anatomy

Article Title: Neurotrophic extracellular matrix proteins promote neuronal and iPSC astrocyte progenitor cell‐ and nano‐scale process extension for neural repair applications

doi: 10.1111/joa.14163

Figure Lengend Snippet: Extracellular matrix proteins do not impact astrocyte progenitor physiological function. (a) IPSC‐derived astrocyte progenitors were cultured on different ECM proteins of interest. (b) Analysis of metabolic activity demonstrated significantly enhanced metabolic activity of astrocyte progenitors cultured on fibronectin compared to control substrate poly L‐lysine (PLL) following 7 days of culture. (c) ECM substrates did not significantly affect astrocyte progenitor LDH release at day 7. (d, e) ELISA analysis revealed no significant differences in pro‐inflammatory IL‐6 or pro‐angiogenic VEGF release from astrocyte progenitors at day 7. All statistical analysis was performed using a one‐way ANOVA with a Tukey post‐hoc test. N = 3 for all experiments. Data expressed as mean ± SEM.

Article Snippet: To investigate cytokine release from astrocyte progenitors in response to each ECM, ELISAs were performed on collected media using human interleukin‐6 (IL‐6) and vascular endothelial growth factor (VEGF) ELISA kits (R&D Systems, USA).

Techniques: Derivative Assay, Cell Culture, Activity Assay, Control, Enzyme-linked Immunosorbent Assay