gCTRP3 inhibits oophorectomy-induced osteoporosis by activating the AMPK/SIRT1/Nrf2 signaling pathway in mice

被引:7
作者
Zhang, Xiaojuan [1 ]
Zhang, Di [2 ]
Zhao, Huan [3 ]
Qin, Jing [1 ]
Qi, Hao [2 ]
Zu, Feiyu [2 ]
Zhou, Yaru [1 ]
Zhang, Yingze [4 ,5 ]
机构
[1] Hebei Med Univ, Hosp 3, Dept Endocrinol, Shijiazhuang 050051, Hebei, Peoples R China
[2] Hebei Med Univ, Hosp 3, Dept Spinal Surg, Shijiazhuang 050051, Hebei, Peoples R China
[3] Hebei Med Univ, Hosp 3, Dept Obstet & Gynecol, Shijiazhuang 050051, Hebei, Peoples R China
[4] Hebei Med Univ, Hosp 3, Natl Hlth Commiss Key Lab Intelligent Orthopaed Eq, Shijiazhuang 050051, Hebei, Peoples R China
[5] Hebei Med Univ, Hosp 3, Dept Orthoped, 139 Ziqiang Rd, Shijiazhuang 050051, Hebei, Peoples R China
关键词
gCTRP3; osteoporosis; oophorectomy; AMPK/SIRT1/Nrf2 signaling pathway; EPITHELIAL-CELLS; IN-VITRO; CTRP3; DIFFERENTIATION; EXPRESSION; APOPTOSIS; NRF2; OSTEOCLASTOGENESIS; OVEREXPRESSION; CALCIFICATION;
D O I
10.3892/mmr.2024.13257
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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页数:11
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