可吞噬颗粒在骨形成和骨重塑中的不同作用。

S Goodman, P Aspenberg, Y Song, D Regula, L Lidgren
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引用次数: 9

摘要

先前,高密度聚乙烯(HDPE)的可吞噬小颗粒(而不是Ti6-Al4-V合金)在10(8)颗粒/mL浓度下抑制骨收获室(BHC)中3周后体内净骨形成。这些发现反映了颗粒在骨长入阶段的影响。在这项研究中,我们测试了这些影响在骨成熟和重塑阶段是否持续或不同。双侧植入成年雄性NZW家兔。经过6周的骨整合期后,收集并丢弃腔内的内容物。1%的透明质酸钠,载体,然后放置在双侧腔管中,三周后收集腔内的组织。HDPE颗粒单侧置入3周,随后Ti6-Al4-V置入3周,HDPE置入6周,Ti6-Al4-V置入6周。每次治疗选择的侧边连续切换;未植入的对侧腔作为对照。在3周时,对照治疗在纤维血管间质中产生编织骨小梁。6周时,外周小梁变厚,中央骨髓腔形成。与对照组相比,HDPE颗粒在3周和6周时骨长入较少。Ti6-Al4-V颗粒在3周时没有抑制骨长入,但在6周时有抑制趋势。颗粒的特性对间充质组织的分化、成熟和重塑有不同的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Different effects of phagocytosable particles during bone formation versus remodeling.

Previously, small phagocytosable particles of high density polyethylene (HDPE) but not Ti6-Al4-V alloy, at a concentration of 10(8) particles/mL inhibited net bone formation in vivo after 3 weeks in the bone harvest chamber (BHC). These findings reflected the effects of particles during the phase of bone ingrowth. In this study, we tested whether these effects persisted or were different during the phase of bone maturation and remodeling. BHCs were bilaterally implanted in mature male NZW rabbits. After a 6-week period for osseointegration, the contents of the chamber were harvested and discarded. One percent sodium hyaluronate, the carrier, was then placed within the canal of the chambers bilaterally and the tissue within the chambers was harvested 3 weeks later. HDPE particles were then inserted unilaterally for a 3-week period, followed by Ti6-Al4-V for 3 weeks, HDPE for 6 weeks, and Ti6-Al4-V for 6 weeks. The side chosen for each treatment was switched consecutively; the nonimplanted, contralateral chamber served as a control. At 3 weeks the control treatments yielded trabeculae of woven bone in a fibrovascular stroma. By 6 weeks, the peripheral trabeculae were thicker, and a central marrow cavity was developing. Bone ingrowth was less with HDPE particles at 3 and 6 weeks compared to controls. Ti6-Al4-V particles did not inhibit bone ingrowth at 3 weeks but showed a trend at 6 weeks. The characteristics of particles affect the differentiation, maturation, and remodeling of mesenchymal tissue differently.

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