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. 2022 Apr 13;13:1989. doi: 10.1038/s41467-022-29633-6

Fig. 1. Deletion of Chd7 in MSCs leads to skeletal development disorder.

Fig. 1

a Representative images of the Chd7fl/fl and Prx1-cre;Chd7fl/fl mice at postnatal day 0, day 7, and day 28. b Alizarin red/Alcian blue whole-mount skeletal staining images of the Chd7fl/fl, Prx1-cre;Chd7fl/+, and Prx1-cre;Chd7fl/fl pups at postnatal day 2. Compared to the control littermates, The Prx1-cre;Chd7fl/fl pups had shorter forelimbs and hindlimbs and a lower degree of mineralization in the cranial and maxillofacial bone. Scale bar, 5 mm. c Quantification of (b), including the length of humeri, femurs, and tibiae of the mice at postnatal day 2 (n = 8). d Representative reconstructed microCT images of skulls of the 2-week-old and 4-week-old Chd7fl/fl and Prx1-cre;Chd7fl/fl mice. The skulls of Prx1-cre;Chd7fl/fl mice showed nonclosure of fontanels. Scale bar, 2 mm. e Quantification of (d), cranial defect area calculated by ImageJ (n = 8). Data are shown as the mean ± S.D.; p value by two-tailed for independent sample tests or one-way ANOVA with Tukey’s post hoc tests for multiple comparisons.