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. 2021 Aug 5;12:4730. doi: 10.1038/s41467-021-24775-5

Fig. 4. The tissue-specific effects of 3D ECM hydrogels on brain organoid development.

Fig. 4

a Bright-field images of brain organoids encapsulated in ECM hydrogels derived from different decellularized organs [brain (BEM), intestine (IEM), liver (LEM), and heart (HEM)] at day 30 (scale bars = 500 μm). b Immunostaining of brain organoids on day 30 for Tuj1 and SOX2 (scale bars = 500 μm). c Image-based quantification of the longest diameter of brain organoid at day 30 (n = 10 per group, BEM versus Mat p = 0.0069, BEM versus IEM p = 0.0013, BEM versus LEM p = 0.0002, BEM versus HEM p = 0.0301). d The gene expression analysis of brain organoids at day 30 by qPCR for transcriptional factors (REST, DNMT3B) and neuronal markers (TUBB3, MAP2) (n = 4 per group, Mat versus LEM p = 0.025, Mat versus BEM p = 0.0009 for REST; Mat versus BEM p = 0.0498 for DNMT3B; Mat versus LEM p = 0.031, Mat versus HEM p = 0.0085, Mat versus BEM p = 0.0004 for TUBB3; Mat versus LEM p = 0.0017, Mat versus HEM p = 0.0128, Mat versus BEM p = 0.0003 for MAP2). Mat and BEM organoids were cultured in a dish on an orbital shaker. All quantitative data are expressed as mean ± SD. Statistical differences between the groups were determined by unpaired two-tailed t-test (*p < 0.05, **p < 0.01, ***p < 0.001). Independent replicates for all data in (ad) = 4. Source data are provided as a Source Data file.