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The aim of this study was to establish a new animal model of demineralized implants of bone with osteogenic cells. These implants were obtained from the femoral head of rats, in which osteoprogenitor cells were transplanted in the marrow cavity of bones for approximately 10 days. When demineralized implants were placed in the implantation site, they were soaked in saline, BMSC and osteoprogenitor cells. Saline, BMSC and osteoprogenitor cells were implanted in femoral head of rats. After implantation, the samples were fixed and decalcified, and the decalcified samples were stained with Safranin-O/Fast Green for histologic analysis. In the osteoprogenitor cell group, osteogenic cells were found in the implant region from day 1 and osteoblasts were observed on the surface of the implant region. These results indicate that demineralized implants with osteogenic cells can be generated using this new animal model.In the past, both Australian (e.g. Lyons & Whitehead [1973](#jia225263-bib-0027){ref-type=”ref”}) and US (e.g. Melendez et al. [2003](#jia225263-bib-0030){ref-type=”ref”}) studies had observed much higher rates of HSV‐2 in men who have sex with men (MSM) than in women. There are a number of likely explanations for this divergence, including different rates of sexual‐risk taking, and higher rates of penetration in men [35](#jia225263-bib-0035){ref-type=”ref”}. Since many heterosexual‐MSM relationships also involve high‐risk heterosexual sex, rates of rectal infection may be similar between men and women.

In our study, the rate of HSV‐2 rectal detection in heterosexual‐MSM couples was similar to the rate in heterosexual‐MSM and heterosexual‐WF couples. This suggests that rates
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Rhamnogalacturonan II (RG-II) is a pectic epitope of the plant cell wall, but its defined structure has yet to be obtained. In this study, RG-II epitope sequences were found and cloned from Arabidopsis thaliana and tobacco via differential display and cDNA expression. The obtained sequences corresponded to RG-II epitopes, of which some were from the non-structural domain of RG-II while the other domains were unknown RG-II epitopes. Antibodies against the RG-II epitope sequences were produced and characterized in enzyme-linked immunosorbent assay, western blots, and immunohistochemical analyses. The results indicate that the RG-II epitope sequences identified in this study have been successfully expressed in bacteria, rabbits, mice, and Arabidopsis. The antibodies raised in the present study recognize RG-II in the mid-to-late elongation zone.[Current status of treatment of chronic obstructive pulmonary disease].
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