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. 2024 Dec 11;7:0548. doi: 10.34133/research.0548

Fig. 5.

Fig. 5.

DAM appear in the spinal cord and brain stem after motor neuron death in SOD1G93A mice. (A and B) Representative microscopic images and quantification of NeuN+ and ChAT+ motor neurons at the ventral horn of the lumbar spinal cord in SOD1G93A and WT mice at different time points stained for NeuN. Nuclei are labeled with 4′,6-diamidino-2-phenylindole (DAPI). Scale bar: 20 μm. (C) Weekly rotarod performances of WT (n = 14) and SOD1 (n = 6) mice. Mean holding times on the rotating rod at indicated weeks were plotted. *P < 0.05 and **P < 0.01, Student t tests. Data are mean ± standard error of the mean (SEM). (D to I) Quantitative reverse transcription quantitative polymerase chain reaction (RT-qPCR) analysis of DAM signatures in the cerebrum, brain stem, and spinal cord at P60 and P110. Each result was normalized to Gapdh. Error bars denote SEM (n = 3 to 6). *P < 0.05, **P < 0.01, ***P < 0.001, and ****P < 0.0001, Student t tests. (J) A line chart showing the average fold change of the temporal evolution of each DAM marker. NeuN, neuronal nuclei; ChAT, choline acetyltransferase; ns, not significant.