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参与低强度脉冲超声诱导金鱼鳞片成骨分化的基因。

Genes involved in osteogenic differentiation induced by low‑intensity pulsed ultrasound in goldfish scales.

作者信息

Tabuchi Yoshiaki, Kuroda Kouhei, Furusawa Yukihiro, Hirano Tetsushi, Nagaoka Ryo, Omura Masaaki, Hasegawa Hideyuki, Hirayama Jun, Suzuki Nobuo

机构信息

Division of Molecular Genetics Research, Life Science Research Center, University of Toyama, Toyama 930-0194, Japan.

Noto Marine Laboratory, Institute of Nature and Environmental Technology, Kanazawa University, Ishikawa 927-0553, Japan.

出版信息

Biomed Rep. 2024 Nov 22;22(2):18. doi: 10.3892/br.2024.1896. eCollection 2025 Feb.

Abstract

The teleost scale is a unique calcified tissue that contains osteoclasts, osteoblasts, osteocytes and the bone matrix, similar to mammalian bone. Here, the effects of low-intensity pulsed ultrasound (LIPUS) on osteoblasts and osteoclasts in goldfish scales were investigated. Scales were treated with LIPUS, which is equivalent to use under clinical conditions (30 mW/cm for 20 min), then cultured at 15˚C. Alkaline phosphatase activity, a marker of osteoblasts, or tartrate-resistant acid phosphatase (TRAP) activity, a marker of osteoclasts was measured. The gene expression profile was examined using RNA-sequencing. Gene network and biological function analyses were performed using the Ingenuity Pathways Knowledge Base. A single exposure of LIPUS significantly increased ALP activity but did not affect TRAP activity. These data indicated that LIPUS induced osteoblastic activation in goldfish scales. Using RNA-sequencing, numerous genes that were significantly and differentially expressed 3, 6, and 24 h after LIPUS exposure were observed. Ingenuity pathway analysis demonstrated that three gene networks, GN-3h, GN-6h, and GN-24h, were obtained from upregulated genes at 3, 6 and 24 h culture, respectively, and included several genes associated with osteoblast differentiation, such as protein kinase D1, prostaglandin-endoperoxide synthase 2, TNFRSF11B (tumor necrosis factor receptor superfamily, member 11b) and WNT3A (Wnt family member 3A). A significant upregulation of expression levels of these genes in scales treated with LIPUS was confirmed by reverse transcription-quantitative polymerase chain reaction. These results contribute to elucidating the molecular mechanisms of osteoblast activation induced by LIPUS.

摘要

硬骨鱼的鳞片是一种独特的钙化组织,含有破骨细胞、成骨细胞、骨细胞和骨基质,类似于哺乳动物的骨骼。在此,研究了低强度脉冲超声(LIPUS)对金鱼鳞片中成骨细胞和破骨细胞的影响。将鳞片用LIPUS处理(相当于临床条件下使用,30 mW/cm,持续20分钟),然后在15˚C下培养。测量了作为成骨细胞标志物的碱性磷酸酶活性或作为破骨细胞标志物的抗酒石酸酸性磷酸酶(TRAP)活性。使用RNA测序检查基因表达谱。使用Ingenuity Pathways Knowledge Base进行基因网络和生物学功能分析。单次LIPUS暴露显著增加了碱性磷酸酶活性,但不影响TRAP活性。这些数据表明LIPUS诱导了金鱼鳞片中的成骨细胞活化。通过RNA测序,观察到LIPUS暴露后3、6和24小时有大量基因显著差异表达。Ingenuity通路分析表明,分别从培养3、6和24小时的上调基因中获得了三个基因网络,即GN-3h、GN-6h和GN-24h,其中包括几个与成骨细胞分化相关的基因,如蛋白激酶D1、前列腺素内过氧化物合酶2、TNFRSF11B(肿瘤坏死因子受体超家族成员11b)和WNT3A(Wnt家族成员3A)。通过逆转录定量聚合酶链反应证实了LIPUS处理的鳞片中这些基因的表达水平显著上调。这些结果有助于阐明LIPUS诱导成骨细胞活化的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd55/11621920/f8e63365e4b6/br-22-02-01896-g00.jpg

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