Journal: JBMR Plus
Article Title: An inducible knock-in mouse model of fibrodysplasia ossificans progressiva shows spontaneous formation of heterotopic ossification
doi: 10.1093/jbmrpl/ziaf123
Figure Lengend Snippet: Acvr1 ARC-R206H/+ ;R26 creERT2/creERT2 mice. (A) Genetic construct of Acvr1 ARC-R206H/+ knock-in allele (see text for additional description). (B) Experimental design showing the dosing and timing of Tamoxifen administration and assay time points. (C) Representative microCT images (VivaCT80) to detect mineralized bone at indicated days post-injury (dpi) by CTX injection. Arrow points to HO. n = 3 per time point. Scale bar = 5 mm. (D) Quantification of HO bone volume. Mean ± SEM displayed. n = 3. (E) Representative images of hind limb sections stained with H&E, Alcian Blue, and Orange G at indicated time points show immune cell infiltration (I) at 3 dpi, fibroproliferation (FP) at 7 dpi, and hypertrophic chondrocytes (C) with adjacent regions of (B) maturing heterotopic bone at 21 dpi. Scale bar = 50 μm for low magnification images (4×, top panel); 10 μm for high magnification images (40×, lower panel) (i-iii). Abbreviations: F, fibula; G, gastrocnemius; FP, fibroproliferation; C, chondrocytes; B, bone.
Article Snippet: A total of 3 doses were given via intraperitoneal (i.p.) injections every 2 d. Acvr1 ARC-R206H/+ mice were crossed with mice double transgenic for Rosa26-rtTA and tetO-Cre (Gt(ROSA)26Sortm1(rtTA*M2)Jae and Tg(tetO-Cre)1Jaw; Jackson Laboratories 006965 and 006224) that express Cre recombinase in response to doxycycline.
Techniques: Construct, Knock-In, Injection, Staining