gCTRP3 通过激活小鼠的 AMPK/SIRT1/Nrf2 信号通路,抑制输卵管切除术诱发的骨质疏松症。

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular medicine reports Pub Date : 2024-08-01 Epub Date: 2024-05-31 DOI:10.3892/mmr.2024.13257
Xiaojuan Zhang, Di Zhang, Huan Zhao, Jing Qin, Hao Qi, Feiyu Zu, Yaru Zhou, Yingze Zhang
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引用次数: 0

摘要

骨质疏松症患者血清中C1q/肿瘤坏死因子相关蛋白3(CTRP3)的表达明显减少。本研究旨在探讨CTRP3是否能通过AMP激活蛋白激酶(AMPK)/sirtuin 1(SIRT1)/核因子E2相关因子2(Nrf2)信号通路减少输卵管切除术(OVX)诱导小鼠的骨质流失。雌性 C57BL/6J 小鼠和 MC3T3-E1 细胞分别被用来构建骨质疏松症的体内和体外模型。使用微型计算机断层扫描检查了小鼠的左股骨,并进行了与骨相关的定量形态学评估。使用苏木精、伊红和耐酒石酸磷酸酶(TRAP)染色法检测小鼠左股骨的病理变化和破骨细胞数量。通过免疫荧光分析检测了左侧股骨中 Runt 相关转录因子-2(RUNX2)的表达,并检测了血清中骨吸收标记物(I 型胶原的 C-十肽和 TRAP)和骨形成标记物(骨钙素(OCN)和 1 型胶原 N-端前肽)的水平。此外,还分别使用碱性磷酸酶(ALP)和茜素红染色法检测了 MC3T3-E1 细胞的成骨细胞分化和钙沉积情况。此外,还利用反转录定量 PCR 检测了 RUNX2、ALP 和 OCN 的表达水平,并利用 Western 印迹分析检测了与 AMPK/SIRT1/Nrf2 信号通路相关的蛋白质的表达水平。结果发现,球状 CTRP3(gCTRP3)能缓解 OVX 诱导的小鼠骨质流失并促进骨形成。加入 AMPK 抑制剂(化合物 C)、SIRT1 抑制剂(EX527)或 Nrf2 抑制剂(ML385)可通过抑制 gCTRP3 减少 MC3T3-E1 细胞的成骨分化。总之,gCTRP3通过激活AMPK/SIRT1/Nrf2信号通路来抑制OVX诱导的骨质疏松症。
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gCTRP3 inhibits oophorectomy‑induced osteoporosis by activating the AMPK/SIRT1/Nrf2 signaling pathway in mice.

C1q/tumor necrosis factor‑related protein 3 (CTRP3) expression is markedly reduced in the serum of patients with osteoporosis. The present study aimed to investigate whether CTRP3 reduces bone loss in oophorectomy (OVX)‑induced mice via the AMP‑activated protein kinase (AMPK)/sirtuin 1 (SIRT1)/nuclear factor E2‑related factor 2 (Nrf2) signaling pathway. Female C57BL/6J mice and MC3T3‑E1 cells were used to construct in vivo and in vitro models of osteoporosis, respectively. The left femurs of mice were examined using micro‑computed tomography scans and bone‑related quantitative morphological evaluation was performed. Pathological changes and the number of osteoclasts in the left femurs of mice were detected using hematoxylin and eosin, and tartrate‑resistant acid phosphatase (TRAP) staining. Runt‑related transcription factor‑2 (RUNX2) expression in the left femurs was detected using immunofluorescence analysis, and the serum levels of bone resorption markers (C‑telopeptide of type I collagen and TRAP) and bone formation markers [osteocalcin (OCN) and procollagen type 1 N‑terminal propeptide] were detected. In addition, osteoblast differentiation and calcium deposits were examined in MC3T3‑E1 cells using alkaline phosphatase (ALP) and Alizarin red staining, respectively. Moreover, RUNX2, ALP and OCN expression levels were detected using reverse transcription‑quantitative PCR, and the expression levels of proteins associated with the AMPK/SIRT1/Nrf2 signaling pathway were detected using western blot analysis. The results revealed that globular CTRP3 (gCTRP3) alleviated bone loss and promoted bone formation in OVX‑induced mice. gCTRP3 also facilitated the osteogenic differentiation of MC3T3‑E1 cells through the AMPK/SIRT1/Nrf2 signaling pathway. The addition of an AMPK inhibitor (Compound C), SIRT1 inhibitor (EX527) or Nrf2 inhibitor (ML385) reduced the osteogenic differentiation of MC3T3‑E1 cells via inhibition of gCTRP3. In conclusion, gCTRP3 inhibits OVX‑induced osteoporosis by activating the AMPK/SIRT1/Nrf2 signaling pathway.

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来源期刊
Molecular medicine reports
Molecular medicine reports 医学-病理学
CiteScore
7.60
自引率
0.00%
发文量
321
审稿时长
1.5 months
期刊介绍: Molecular Medicine Reports is a monthly, peer-reviewed journal available in print and online, that includes studies devoted to molecular medicine, underscoring aspects including pharmacology, pathology, genetics, neurosciences, infectious diseases, molecular cardiology and molecular surgery. In vitro and in vivo studies of experimental model systems pertaining to the mechanisms of a variety of diseases offer researchers the necessary tools and knowledge with which to aid the diagnosis and treatment of human diseases.
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