For the second antibody, combination of Alexa Fluor donkey anti-goat 488 and donkey anti-rabbit 555 (Invitrogen, Grand Island, NY, USA) were incubated for 60 min

at room temperature at a dilution of 1:600 for the anti goat and 1:800 for the anti-rabbit. For the combination of polyclonal goat and monoclonal mouse, both Alexa Fluor donkey anti-goat 488 and donkey anti-mouse 555 were incubated for 60 min at room temperature at a dilution of 1:600. Finally for nuclear staining, sections were incubated 30 min with DAPI (Sigma-Aldrich, Oakville, Ontario, Canada) then mounted with permanent aqueous mounting media. Before taking the pictures for immunofluorescence, the tissues

were first examined Gemcitabine purchase under “phase contrast” in order to visualize the various types of cells, then the pictures were acquired with different fluorochromes; DAPI (UV), Alexa Fluor 488 (green) and the Alexa Fluor 555 (red). Images were captured with a fluorescent selleck products microscope (Leica model with software ACDSee, magnification 630 ×). Superposition of images was performed with Adobe Photoshop software. The following were analyzed BMP2, BMP7, BMP3, BAMBI, noggin, gremlin, pSmad 1/5/8, chordin, Smad-6 and Smad-7. Similar to our previous work, standard light microscopy of H&E-stained histological sections revealed callus formation at various stages of development in all fracture cases [7]. Most specimens contained a mixture of endochondral and intramembranous ossification. There were also interspersed areas of stroma formed by fibroblast-like cells and areas of new blood vessel formation. We did not

attempt to correlate the maturity of the callus with the time since fracture. For ethical reasons we could only remove callus tissue that was interfering with operative repair of the bone and we could not obtain control tissue from the same patient. Non-unions revealed a mixture of different tissue types. There were foci of woven bone interspersed by areas of fibrous tissue with presence of blood vessels. In general, our results showed that expression of BMP-inhibitors was stronger than Fossariinae BMP ligands. In addition, active BMP signaling as exemplified by presence of pSmad 1/5/8 was present in osteoblasts of all specimens, fracture callus and non-union. The main differences were found to be in the chondrocytes and fibroblasts. Overall, our results showed decreased or no expression of BMPs in cartilaginous cells (hypertrophic and non-hypertrophic) of non-unions compared to fracture callus. The expression of BMP2 was decreased in cartilaginous cells (hypertrophic and non-hypertrophic chondrocytes) of non-unions while it was increased in osteoblasts and osteoclasts of non-unions.