小鼠骨调质蛋白缺乏症会导致横向皮质骨体积缩小。

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2024-08-05 DOI:10.1093/jbmr/zjae072
Wenbo Zhao, Simon von Kroge, Jelena Jadzic, Petar Milovanovic, Praveer Sihota, Julia Luther, Laura Brylka, Felix N von Brackel, Ernesto Bockamp, Björn Busse, Michael Amling, Thorsten Schinke, Timur A Yorgan
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引用次数: 0

摘要

骨骼的生长、建模和重塑受多种分子的调控,最近发现的骨合成代谢因子 WNT1 就是其中之一。我们以前曾报道过,WNT1 能转录激活小鼠间充质细胞系中编码骨调制蛋白(OMD)的 Omd 的表达,这可能解释了 WNT1 突变失活小鼠骨骼脆弱的原因,因为 OMD 已被证明能在体外调节 I 型胶原纤维的形成。在本研究中,我们通过对转染细胞进行全基因组表达分析,证实了 Omd 的强诱导表达,并进一步证明了 Omd 是 WNT1 的直接靶基因。为了评估这种调控在体内的相关性,我们将 Omd 缺陷小鼠与携带诱导性成骨细胞特异性 Wnt1 转基因的小鼠品系杂交。在诱导 Wnt1 表达 1 周或 3 周后,尽管小鼠缺乏 Omd,但 WNT1 的骨合成代谢能力并未受损。由于目前对 OMD 体内生理功能的了解有限,我们接下来重点研究了在没有 Wnt1 转基因的情况下,野生型和 Omd 缺失型同胎仔鼠的骨骼表型。在这里,我们通过组织形态测量和μCT也没有观察到Omd缺陷对小梁骨参数的影响。但重要的是,12周龄和24周龄的雄性和雌性Omd缺陷小鼠表现出骨骼细长的表型,长骨横向尺寸明显较小,而纵向骨骼生长不受影响。虽然力学测试没有发现骨材料性能受损所导致的明显变化,但原子力显微镜观察 Omd 基因缺陷小鼠的股骨表面发现了纳米结构水平的适度变化,表明胶原纤维形成和聚集的调控发生了改变。综上所述,我们的数据表明,虽然 OMD 对于 WNT1 的骨合成作用是不可或缺的,但小鼠缺乏 OMD 会特异性地调节横向皮质骨形态。
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Osteomodulin deficiency in mice causes a specific reduction of transversal cortical bone size.

Skeletal growth, modeling, and remodeling are regulated by various molecules, one of them being the recently identified osteoanabolic factor WNT1. We have previously reported that WNT1 transcriptionally activates the expression of Omd, encoding Osteomodulin (OMD), in a murine mesenchymal cell line, which potentially explained the skeletal fragility of mice with mutational WNT1 inactivation, since OMD has been shown to regulate type I collagen fibril formation in vitro. In this study we confirmed the strong induction of Omd expression in a genome-wide expression analysis of transfected cells, and we obtained further evidence for Omd being a direct target gene of WNT1. To assess the in vivo relevance of this regulation, we crossed Omd-deficient mice with a mouse line harboring an inducible, osteoblast-specific Wnt1 transgene. After induction of Wnt1 expression for 1 or 3 weeks, the osteoanabolic potency of WNT1 was not impaired despite the Omd deficiency. Since current knowledge regarding the in vivo physiological function of OMD is limited, we next focused on skeletal phenotyping of wild-type and Omd-deficient littermates, in the absence of a Wnt1 transgene. Here we did not observe an impact of Omd deficiency on trabecular bone parameters by histomorphometry and μCT either. Importantly, however, male and female Omd-deficient mice at the ages of 12 and 24 weeks displayed a slender bone phenotype with significantly smaller long bones in the transversal dimension, while the longitudinal bone growth remained unaffected. Although mechanical testing revealed no significant changes explained by impaired bone material properties, atomic force microscopy of the femoral bone surface of Omd-deficient mice revealed moderate changes at the nanostructural level, indicating altered regulation of collagen fibril formation and aggregation. Taken together, our data demonstrate that, although OMD is dispensable for the osteoanabolic effect of WNT1, its deficiency in mice specifically modulates transversal cortical bone morphology.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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