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死亡受体 3(TNFRSF25)可增加成骨细胞的矿化沉积并促进雄性 DBA/1 小鼠轴骨的特定区域新骨形成。

Death Receptor 3 (TNFRSF25) Increases Mineral Apposition by Osteoblasts and Region Specific New Bone Formation in the Axial Skeleton of Male DBA/1 Mice.

机构信息

Institute of Infection and Immunity, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.

University Hospital Llandough, Cardiff & Vale University Health Board, Cardiff CF64 2XX, UK.

出版信息

J Immunol Res. 2015;2015:901679. doi: 10.1155/2015/901679. Epub 2015 May 3.

Abstract

Objectives. Genome wide association studies identified TNFSF member TNF-like protein 1A (TL1A, TNFSF15) as a potential modulator of ankylosing spondylitis (AS). TL1A is the only confirmed TNFSF ligand of death receptor 3 (DR3, TNFRSF25); however, its role in disease pathology is not characterised. We evaluated DR3's role in controlling osteoblast- (OB-) dependent bone formation in vitro and in vivo. Methods. Osteoprogenitor cells and OB were cultured from male DR3-deficient (DR3(ko)) and wild-type (DR3(wt)) DBA/1 mice. DR3 and RANKL expression were tested by flow cytometry. Alkaline phosphatase and mineralization were quantified. Osteopontin, osteoprotegerin, and pro MMP-9 were measured by ELISA. A fluorescent probe (BoneTag) was used to measure in vivo mineralization in 10-month-old mice. Results. DR3 was expressed on osteoprogenitors and OB from DR3(wt) mice. Alkaline phosphatase, osteopontin, and mineral apposition were significantly elevated in DR3(wt) cultures. Levels of RANKL were comparable whilst osteoprotegerin was significantly increased in DR3(wt) cultures. In vivo incorporation of BoneTag was significantly lower in the thoracic vertebrae of 10-month-old DR3(ko) mice. Conclusions. These data identify new roles for DR3 in regulating OB-dependent bone mineral apposition. They potentially begin to explain the atypical pattern of new bone formation observed in the axial skeleton of grouped, aging DBA/1 mice.

摘要

目的。全基因组关联研究鉴定出 TNF 样蛋白 1A(TL1A,TNFSF15)是强直性脊柱炎(AS)的潜在调节因子。TL1A 是唯一被确认的死亡受体 3(DR3,TNFRSF25)的 TNF 超家族配体;然而,其在疾病发病机制中的作用尚未确定。我们评估了 DR3 在体外和体内控制成骨细胞(OB)依赖性骨形成中的作用。

方法。从小鼠的雄性 DR3 缺陷型(DR3(ko))和野生型(DR3(wt))DBA/1 中培养成骨祖细胞和 OB。通过流式细胞术检测 DR3 和 RANKL 的表达。定量碱性磷酸酶和矿化。通过 ELISA 测量骨桥蛋白、骨保护素和 pro MMP-9。使用荧光探针(BoneTag)测量 10 个月大的小鼠体内的矿化情况。

结果。DR3 在 DR3(wt)小鼠的成骨祖细胞和 OB 上表达。DR3(wt) 培养物中的碱性磷酸酶、骨桥蛋白和矿化明显升高。RANKL 水平相当,而骨保护素在 DR3(wt) 培养物中显著增加。10 个月大的 DR3(ko)小鼠的胸椎中 BoneTag 的掺入明显降低。

结论。这些数据确定了 DR3 在调节 OB 依赖性骨矿化中的新作用。它们可能开始解释在成群、衰老的 DBA/1 小鼠的轴骨中观察到的新骨形成的异常模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e74c/4433704/12b7f30c9848/JIR2015-901679.001.jpg

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