Samples were decalcified

in a heat-controlled microwave in 19% EDTA for two weeks and after complete demineralization, the implant was gently removed from the samples. Specimens were selleck dehydrated through an ascending ethanol series prior to paraffin embedding. Eight-micron-thick longitudinal sections were cut and collected on SuperFrost-plus slides for histology including Movat’s pentachrome, aniline blue, and Picrosirius red staining. Alkaline phosphatase (ALP) activity was detected by incubation in nitro blue tetrazolium chloride (NBT; Roche), 5-bromo-4-chloro-3-indolyl phosphate (BCIP; Roche), and NTM buffer (100 mM NaCl, 100 mM Tris pH 9.5, 5 mM MgCl). Tartrate-resistant acid phosphatase (TRAP) activity was observed using a leukocyte

acid phosphatase staining kit (Sigma). After its development, the slides were dehydrated in a series of ethanol and xylene OSI-906 research buy and subsequently cover-slipped with Permount mounting media. For TUNEL staining, sections were incubated in proteinase K buffer (20 μg/mL in 10 mM Tris pH 7.5), applied to a TUNEL reaction mixture (In Situ Cell Death Detection Kit, Roche), and mounted with DAPI mounting medium (Vector Laboratories). Slides were viewed under an epifluorescence microscope. Tissue sections were deparaffinized following standard procedures. Endogenous peroxidase activity was quenched by 3% hydrogen peroxide for 5 min, and then washed in PBS. Slides were blocked with 5% goat serum (Vector S-1000) for 1 h at room temperature. The appropriate primary antibody was added and incubated overnight at 4 °C, then washed in PBS. Samples were Montelukast Sodium incubated with appropriate biotinylated secondary antibodies (Vector BA-x) for 30 min, then washed in PBS. An avidin/biotinylated enzyme complex (Kit ABC Peroxidase Standard Vectastain PK-4000) was added and incubated for 30 min and a DAB substrate kit (Kit Vector Peroxidase substrate DAB SK-4100) was used to develop the color reaction. Antibodies used include proliferating cell nuclear antigen (PCNA, Invitrogen) Osteocalcin (Abcam ab93876), Decorin (NIH LF 113), Osteopontin

(NIH LF 175), Fibromodulin (NIH LF 149), and Procollagen 1(NIH LF42). Each immunostaining reaction was accompanied by a negative control, where the primary antibody was not included. Maxillas were collected on postsurgical days 7, 14, 21, and 28 to quantify the amount of new bone generated in response to the implant. All maxilla were embedded in paraffin and sectioned longitudinally. The 0.6-mm implant was represented across ∼ 20 tissue sections, each of which was 8 μm thick. Of those 20 sections, we used a minimum of 4 sections to quantify the amount of new bone. All the tissue sections were stained with aniline blue, which labels osteoid matrix. The sections were photographed using a Leica digital imaging system at the same magnification (× 10 objective).