Characterization of the F-box Proteins FBXW2 and FBXL14 in the Initiation of Bone Regeneration in Transplants given to Nude Mice.

Q3 Medicine Open Biomedical Engineering Journal Pub Date : 2018-10-18 eCollection Date: 2018-01-01 DOI:10.2174/1874120701812010075
Mari Akiyama
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引用次数: 4

Abstract

Background: Cultured bovine-periosteum-derived cells can form three-dimensional structures on tissue culture dishes without artificial scaffolding material, can induce bone regeneration in vivo. The utility of cultured bovine-periosteum-derived cells for bone tissue regeneration after their transplantation into nude mice has been reported, the precise F-box molecular mechanism was unclear.

Objective: The aim of this study was to investigate the specific F-box proteins required for bone regeneration by cultured bovine-periosteum-derived cells in vitro.

Methods: In the present study, periosteum tissue and cultured periosteum-derived cells were cultured for 5 weeks in vitro and then embedded in collagen gel with a green tissue-marking dye. Electrophoresis and immunohistochemistry were used to identify the specific F-box proteins required for tissue bone regeneration.

Results: The bovine-periosteum-derived cells were observed to form bone shortly after the expression of F-box proteins. After the initial phase of bone formation, the expression of the F-box proteins ceased. FBXW2 was shown to be expressed in the periosteum, but not in cultured periosteum-derived cells. Furthermore, FBXL14 disappeared during bone formation.

Conclusions: Bone regeneration requires progenitor cells, such as bovine-periosteum-derived cells and the activation of the F-box Proteins FBXW2 and FBXL14, over time the expression of these proteins ceases. Further scientific and clinical trials are needed to investigate how the F-box Proteins can be used therapeutically to treat osteoporosis and osteonecrosis.

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F-box蛋白FBXW2和FBXL14在裸鼠移植骨再生启动中的特性
背景:培养的牛骨膜源性细胞无需人工支架材料即可在组织培养皿上形成三维结构,在体内可诱导骨再生。培养的牛骨膜来源细胞移植到裸鼠体内后用于骨组织再生已有报道,但确切的F-box分子机制尚不清楚。目的:研究体外培养的牛骨膜源性细胞骨再生所需的特异性F-box蛋白。方法:体外培养骨膜组织和培养的骨膜来源细胞5周后,用绿色组织标记染料包埋于胶原凝胶中。利用电泳和免疫组织化学鉴定组织骨再生所需的特异性F-box蛋白。结果:F-box蛋白表达后,牛骨膜源性细胞很快形成骨。骨形成初期,F-box蛋白停止表达。FBXW2在骨膜中表达,但在培养的骨膜来源细胞中不表达。此外,FBXL14在骨形成过程中消失。结论:骨再生需要祖细胞,如牛骨膜来源的细胞和F-box蛋白FBXW2和FBXL14的激活,随着时间的推移,这些蛋白的表达停止。需要进一步的科学和临床试验来研究F-box蛋白如何用于治疗骨质疏松症和骨坏死。
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来源期刊
Open Biomedical Engineering Journal
Open Biomedical Engineering Journal Medicine-Medicine (miscellaneous)
CiteScore
1.60
自引率
0.00%
发文量
4
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