Human Motor Neurons Elicit Pathological Hallmarks of ALS and Reveal Potential Biomarkers of the Disease in Response to Prolonged IFNγ Exposure

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.
Figure 2.

IFNγ triggers the p21 upregulation and TDP-43 proteinopathy in iPSC-derived motor neurons. A, qRT-PCR analysis for each experimental group quantifying the time-dependent expression of p21, the early transcriptional target of p53 signaling. UT, untreated control group; IFNγ, 5 ng/ml IFNγ-treated group. Flow of hypothesis for this study (right panel). B, Immunocytochemistry assay of WT and Q331K+/− mutant cultures at Days 25, 32, and 40, showing a significant cytoplasmic translocation and aggregation of the TDP-43 protein in response to the IFNγ stimulation at the later phases of both cultures. C, Quantitative analysis of the cytoplasmic TDP-43 translocation for each experimental condition (error bars indicate SD, n = 5 biological replicates; *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; ns, not significant).

  1. The Journal of Neuroscience vol. 44 no. 16
Responses to This Article
Be the first to respond to this article
Advertisement