Fig. 3 Vertebral columns of sqstm1tmΔUBA zebrafish are characterized by structural defects and ectopic mineralization. a Representative µCT images at 6 and 12 mpf. Vertebral malformations, including fused vertebrae, are evident in carriers of one or two mutant sqstm1 alleles, mainly in the precaudal to caudal vertebral junction and/or the tail region (red squares). b Close-up of the red squares shown in (a), labeled by 1–3. c Quantification of animals with certain number of vertebral defects. For 6 mpf, n = 4 (WT) or 6 (HET/HOM) zebrafish/genotype and for 12 mpf, n = 10 zebrafish/genotype. d Alizarin Red staining of a wild-type and homozygous zebrafish, including a magnification box. Ectopic mineralization and osteophytes affecting the whole vertebral column are shown by green arrows. WT wild type (sqstm1+/+), HET heterozygous mutant (sqstm1tmΔUBA/+), HOM homozygous mutant (sqstm1.tmΔUBA/tmΔUBA)
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Full text @ Calcif. Tissue Int.