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. 2008 Oct 1;22(19):2645–2650. doi: 10.1101/gad.1711308

Figure 3.

Figure 3.

Defective ECM in Sumf1−/− growth plate. (A) Chondrocyte number in the growth plate proliferative zone. Values are the mean ± SD. Student’s test (*) P < 0.05. (B) Toluidin blue staining of chondrocostal cartilage of newborn Sumf1−/− and wild-type littermates. Note the presence of cytoplasmatic vacuolization in Sumf1−/− chondrocytes. (C) EM analysis of E14.5 Sumf1−/− and wild-type chondrocytes showing no evidence of lysosomal vacuolization in Sumf1−/− embryos. (D,E) Cytoplasmatic vacuoles in E16.5 (D) and newborn (E) Sumf1−/− chondrocytes filled with amorphous material (GAGs) and partially degraded collagen fiber (E, inset). (F) Sumf1−/− osteoblasts are less affected than chondrocytes by lysosomal vacuolization. (G) ECM proteoglycan produced by Sumf1−/− and wild-type primary chondrocytes labeled with 3H-glucosamine and Na35SO4. ECM amount was estimated by 3H and 35S incorporation and normalized for cells number. (H) Decreased alcian blue staining in P7 Sumf1−/− compared with wild-type growth plate.