Cellular stress or neuronal excitotoxic stress increases DPR levels for all C9orf72 NRE ORFs in rat cortical neurons and in patient‐derived iPS spinal.

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Cellular stress or neuronal excitotoxic stress increases DPR levels for all C9orf72 NRE ORFs in rat cortical neurons and in patient‐derived iPS spinal motor neurons Cellular stress or neuronal excitotoxic stress increases DPR levels for all C9orf72 NRE ORFs in rat cortical neurons and in patient‐derived iPS spinal motor neurons AQuantitative fluorescent microscopy imaging shows a dose‐dependent increase in the number of C9 DPR reporter‐positive cells with increasing concentrations of an apoptotic stimulator, staurosporine (SSP). The C9 DPR reporter in the GP frame was utilized for these experiments. n = 4.BFilter‐trap binding assays using DPR‐specific antibodies show all DPR levels are increased for the sense‐coding C9 DPR reporter when NSC34 cells are challenged with stress‐inducing compounds. These stress‐inducing compounds broadly cover distinct or overlapping cellular pathways (see Table EV2). Antibodies specific for the C9orf72 NRE DPRs, poly‐GA, ‐GP, or ‐GR, were used to quantify DPR levels normalized to GAPDH 24 h post‐transient transfection of the C9 DPR reporter constructs. n = 4.CQuantitative fluorescent microscopy imaging shows that NSC34, rat primary cortical neurons, have increased relative DPR fluorescent intensity levels following compound induced cellular stress. In NES‐mIFP cotransfection‐positive NSC34 and rat primary cortical neurons, there is a significant increase in C9 DPR reporter fluorescent intensity levels 24 post‐treatment with most stress‐inducing compounds. Fluorescent intensity was not normalized to NES‐mIFP fluorescent levels. NSC34: n = 10 with m > 500 cells analyzed per n. Cortical neuron: n = 6 with m > 40 cells per n.DEndogenously expression of DPRs in iPS spinal motor neurons (iPS sMN) derived from C9orf72 NRE patients increases following induction of cellular stress. DPR fluorescent intensity in iPS sMN was measured using the DPR‐specific antibodies described above. IPS sMN: n = 4 with m > 20 cells per n. Statistical comparisons were performed using an uncorrected Fisher's exact test.Data information: All changes in DPR levels are shown relative to non‐stressed or DMSO‐only (vehicle) treated CTRL cells unless otherwise noted. Control (CTRL), thapsigargin (TG), menadione (Mena), staurosporine (SSP), diamide (Daim), cytochalasin D (Cyto D), etoposide (Etop), leptomycin B (Lepto), homocystine (HC), sodium arsenite (NaArs), tunicamycin (TM), glutamate (Glut). Statistical comparisons in (A) were calculated using t‐tests per concentration, and (B) and (C) were calculated using an uncorrected Fisher LSD two‐way ANOVA for CTRL versus treatment (****P < 0.0001, ***P < 0.001, **P < 0.01, *P < 0.05). See also Table EV2 and Figs EV2 and EV3.Source data are available online for this figure. Error bars represent the mean ± SEM. Thomas Westergard et al. EMBO Mol Med. 2019;emmm.201809423 © as stated in the article, figure or figure legend