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Caption | A and B, shown is accumulation of dystrophic subperiosteal (arrows) osteoblasts (*) along the trabecular bones (pink) in the nasal turbinates (A) and in the tibial growth plate (B) 3 weeks after castration in a male Akr1a1Gt(OST222400)Lex/Akr1a1Gt(OST222400)Lex (GR-/-) mouse fed regular chow (ascorbate (ASC) content = 0). These cell masses are never seen in castrated wild-type mice on regular chow or in castrated mutant mice fed an ASC diet. C-E, shown is the effects of castration (CX) on turbinate structure in male mutant mice. C shows few remnant fragments of trabecular bone (pink) and proliferation of dystrophic osteoblasts in mice fed a regular diet for 4 months after CX. D shows the effects of feeding ASC for 1 preterminal month after 3 months on a regular diet. Note the haphazard formation of new bone replacing the proliferating periosteal osteoblasts observed in C. E shows that ASC feeding after CX prevents the changes seen in C and preserves the normal turbinate structures. F and G, shown are higher magnification views of adjacent sections to C and D, respectively, immunostained with osterix antibody. F, not all cells are osterix-positive, possibly indicating different stages of osteoblast differentiation. G, ASC intake stimulates the formation of trabecular bone containing osteocytes and active plump subperiosteal mature elongated osteoblasts. | ||||
Copyright | This image is from Gabbay KH, J Biol Chem 2010 Jun 18;285(25):19510-20 and is displayed with the permission of the American Society for Biochemistry and Molecular Biology who owns the Copyright. Full text from JBC. J:164548 | ||||
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/12/2024 MGI 6.24 |
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