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Fig. 3 | Molecular Brain

Fig. 3

From: Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs

Fig. 3

Differentiation of SBMA disease specific iPSCs into motor neurons. a Schematic presentation of the culture protocol for the differentiation of iPSCs. LSC, LDN-193189 (L), SB4315342 (S), CHIR99021 (C); RA, retinoic acid; PM, purmorphamine. b Immunocytochemical analysis of HB9, ISL-1, and βIII-Tubulin after 1 week of monolayer differentiation with 10 nM DHT. Scale bar, 100 μm. c Quantitative RT-PCR analysis of HB9, ISL-1, ChAT, and AR expressions at 4 weeks (n = 4, mean ± SEM). HB9 and ISL-1 expressions were higher in SBMA than controls in the presence of 10 nM DHT (*p < 0.05; Student’s t-test)

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