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错颌畸形小鼠模型中颞下颌关节的变化和 semaphorin 4D/Plexin-B1 表达。

Changes of temporomandibular joint and semaphorin 4D/Plexin-B1 expression in a mouse model of incisor malocclusion.

出版信息

J Oral Facial Pain Headache. 2014 Winter;28(1):68-79. doi: 10.11607/jop.1082.

Abstract

AIMS

To investigate the changes in condylar cartilage and subchondral bone of the temporomandibular joint (TMJ) in a mouse model of incisor malocclusion.

METHODS

By bonding a single (single group) or a pair (pair group) of metal tube(s) to the left incisor(s), a crossbite-like relationship was created between left-side incisors in mice. The morphological changes in the TMJ condyles were examined by hematoxylin and eosin and toluidine blue staining. Indices of osteoclastic activity, including tartrate-resistant acid phosphatase (TRAP) staining and macrophage colony stimulating factor (M-CSF) were investigated by histochemistry or real-time polymerase chain reaction (PCR). The osteoblastic activity was indexed by osteocalcin expression. Expressions of semaphorin 4D and its receptor, Plexin-B1, were detected by real-time PCR. Two-way analysis of variance was used to assess the differences between groups.

RESULTS

One week and 3 weeks after bonding the metal tube(s), cartilage degradation and subchondral bone loss were evident histologically. Both indices of osteoclastic activity (TRAP and M-CSF) were significantly increased in cartilage and subchondral bone after bonding the metal tube(s). Osteocalcin expression in cartilage was significantly increased at week 3, while its expression in subchondral bone was significantly increased at week 1 but decreased at week 3. The semaphorin 4D expression in cartilage and subchondral bone was significantly decreased at week 1 but significantly increased at week 3. For Plexin-B1 expression, a significant increase was detected in subchondral bone at week 3.

CONCLUSION

Bonding a single or a pair of metal tube(s) to left incisor(s) is capable of inducing remodeling in the TMJ, which involved cartilage degradation and alteration of osteoclastic and osteoblastic activity.

摘要

目的

研究牙列不齐小鼠模型颞下颌关节(TMJ)髁突软骨和软骨下骨的变化。

方法

通过将单个(单组)或一对(双组)金属管粘合到左侧切牙上,在小鼠的左侧切牙之间建立类似反颌的关系。通过苏木精和伊红及甲苯胺蓝染色检查 TMJ 髁突的形态变化。通过组织化学或实时聚合酶链反应(PCR)研究破骨细胞活性指数,包括抗酒石酸酸性磷酸酶(TRAP)染色和巨噬细胞集落刺激因子(M-CSF)。通过骨钙素表达来评估成骨细胞活性。通过实时 PCR 检测信号素 4D 及其受体 Plexin-B1 的表达。采用双向方差分析评估组间差异。

结果

在粘合金属管后 1 周和 3 周,软骨降解和软骨下骨丢失在组织学上明显。粘合金属管后,软骨和软骨下骨的两种破骨细胞活性指数(TRAP 和 M-CSF)均显著增加。第 3 周时,软骨中的骨钙素表达明显增加,而第 1 周时,软骨下骨中的骨钙素表达明显增加,但第 3 周时减少。第 1 周时,软骨和软骨下骨中的信号素 4D 表达明显减少,但第 3 周时明显增加。对于 Plexin-B1 表达,第 3 周时在软骨下骨中检测到明显增加。

结论

将单个或一对金属管粘合到左侧切牙上能够诱导 TMJ 重塑,涉及软骨降解以及破骨细胞和成骨细胞活性的改变。

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