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[拉伸对牛磺酸上调基因1介导的miR-545-3p/大麻素受体2通路调控大鼠牵张成骨的影响]

[Effect of stretch on taurine upregulated gene 1-mediated miR-545-3p/cannbinoida receptor 2 pathway regulating distraction osteogenesis in rats].

作者信息

Zhang Mengzhu, Wang Bin, Wang Zixin, Wu Yalong, Zheng Yongxin

机构信息

Department of Orthopedics, Affiliated Hospital of North China University of Science and Technology, Tangshan Hebei, 063000, P. R. China.

Department of Orthopedics, , the Second Hospital of Tangshan, Tangshan Hebei, 063000, P. R. China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2025 May 15;39(5):598-604. doi: 10.7507/1002-1892.202503010.

Abstract

OBJECTIVE

To investigate the effect of stretch on long non-coding RNA taurine upregulated gene 1 (TUG1)-mediated miR-545-3p/cannbinoida receptor 2 (CNR2) pathway regulating bone regeneration in the distraction area of rats during distraction osteogenesis.

METHODS

Thirty-six 10-week-old male Sprague Dawley rats were randomly divided into 3 groups ( =12 in each group): group A (femoral fracture+injection of interfering RNA), group B (distraction osteogenesis+injection of interfering RNA), and group C (distraction osteogenesis+injection of TUG1). Groups A and B were injected with 60 μg of interfering RNA at the beginning of incubation period (immediate after operation), the beginning of distraction phase (7 days after operation), and the end of distraction phase (21 days after operation), and group C was injected with 60 μg of synthetic TUG1 interfering sequence at the same time. The general situation of rats in each group was observed during the experiment. The mineralization of fracture space or distraction area was observed by X-ray films at 21, 35, and 49 days after operation. At 49 days after operation, the samples of the distraction area were taken for HE staining to observe the mineralization, and real-time fluorescence quantitative PCR (qRT-PCR) was used to detect the expressions of osteoblast-related genes such as TUG1, miR-545-3p, CNR2, alkaline phosphatase (ALP), osteocalcin (OCN), and osteopontin (OPN). Blood samples were collected from the abdominal aorta of the rats, and the expressions of ALP and C terminal telopeptide of type Ⅰ (CTX-Ⅰ) protein were detected by ELISA assay.

RESULTS

The results of X-ray film and HE staining observations showed that osteogenesis in group C was superior to groups A and B at the same time point. The results of qRT-PCR showed that the relative mRNA expressions of TUG1, CNR2, ALP, OCN, and OPN in group C were significantly higher than those in group A and group B, and the relative mRNA expression of miR-545-3p in group C was significantly lower than that in group A and group B ( <0.05). The relative mRNA expressions of TUG1 and ALP in group B were significantly higher than those in group A, and the relative mRNA expression of miR-545-3p in group B was significantly lower than that in group A ( <0.05). There was no significant difference in the relative mRNA expressions of CNR2, OCN, and OPN between group A and group B ( >0.05). The results of ELISA showed that the expressions of ALP and CTX-Ⅰ protein were significantly higher in group C than in group A and group B, and in group B than in group A ( <0.05).

CONCLUSION

Under the action of stretch, the expression of TUG1 in the femoral distraction area of rats increases, which promotes the expression of CNR2 by inhibiting the expression of miR-545-3P, which is helpful to the mineralization of the extension area and osteogenesis.

摘要

目的

探讨拉伸对长链非编码RNA牛磺酸上调基因1(TUG1)介导的miR-545-3p/大麻素受体2(CNR2)通路在大鼠牵张成骨过程中调控牵张区域骨再生的影响。

方法

将36只10周龄雄性Sprague Dawley大鼠随机分为3组(每组n = 12):A组(股骨骨折+注射干扰RNA)、B组(牵张成骨+注射干扰RNA)和C组(牵张成骨+注射TUG1)。A组和B组在孵育期开始时(术后即刻)、牵张期开始时(术后7天)和牵张期结束时(术后21天)注射60 μg干扰RNA,C组同时注射60 μg合成TUG1干扰序列。实验期间观察各组大鼠的一般情况。术后21、35和49天通过X线片观察骨折间隙或牵张区域的矿化情况。术后49天,取牵张区域样本进行HE染色观察矿化情况,并采用实时荧光定量PCR(qRT-PCR)检测TUG1、miR-545-3p、CNR2、碱性磷酸酶(ALP)、骨钙素(OCN)和骨桥蛋白(OPN)等成骨相关基因的表达。从大鼠腹主动脉采集血样,采用ELISA法检测ALP和Ⅰ型胶原C端肽(CTX-Ⅰ)蛋白的表达。

结果

X线片和HE染色观察结果显示,C组在同一时间点的成骨情况优于A组和B组。qRT-PCR结果显示C组TUG1、CNR2、ALP、OCN和OPN的相对mRNA表达显著高于A组和B组,C组miR-545-3p的相对mRNA表达显著低于A组和B组(P < 0.05)。B组TUG1和ALP的相对mRNA表达显著高于A组,B组miR-545-3p的相对mRNA表达显著低于A组(P < 0.05)。A组和B组之间CNR2、OCN和OPN的相对mRNA表达无显著差异(P > 0.05)。ELISA结果显示C组ALP和CTX-Ⅰ蛋白的表达显著高于A组和B组,B组高于A组(P < 0.05)。

结论

在拉伸作用下,大鼠股骨牵张区域TUG1表达增加,通过抑制miR-545-3P的表达促进CNR2的表达,有助于牵张区域的矿化和成骨。

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