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[神经纤毛蛋白-1在创伤性脑损伤合并胫骨骨折愈合过程中的表达]

[Nrp-1 expression in healing process of traumatic brain injury combined with tibial fracture].

作者信息

Li Zhengzheng, Zhao Junwei, Luo Wei, Li Kang, Lei Shuanhu, Wang Yuliang

机构信息

Deparment of Orthopaedics, Second Hospital of Lanzhou University, Orthopaedics Key Laboratory of Gansu Province, Lanzhou 730030, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2017 Feb 28;42(2):154-160. doi: 10.11817/j.issn.1672-7347.2017.02.006.

Abstract

To examine the expression of neuropilin-1 (Nrp-1), semaphorin 3A (Sema3A) and vascular endothelial growth factor (VEGF) in the healing process of tibial fracture after traumatic brain injury and to explore the mechanism of Nrp-1 in the formation of pathological callus after nerve injury.
 Methods: A total of 192 Wister female rats, 8-10 weeks old and weighing 220-250 g, were randomly divided into a control group (Group C), a tibia fracture group (Group F), a traumatic brain injury group (Group TBI), a traumatic brain injury combined with the tibia fracture group (Group TBI+F) (n=48 in each group). Tissue samples were collected at 3, 5, 7, 14, 21 and 28 days, respectively (n=8 for each time point). The expression of Nrp-1 in callus tissues were examined by immunohistochemistry and Western blot, while the expression of Sema3A and VEGF were detected by Western blot.
 Results: Compared with the Group F , the expression of Nrp-1 in chondrocytes of bone formation area and cartilage area was higher in the Group TBI+F, particularly at the 7th , 14th and 21st day (P<0.05), while the expression of Nrp-1 in osteoblast cells of fresh bone trabecula region was lower in the Group TBI+F, particularly at the 14th and 21st day (both P<0.05). Western blot showed that the expression of Nrp-1, Sema 3A and VEGF had the same trends in the Group TBI+F and the Group F. However, at each time point, the expression of Nrp-1 in the Group TBI+F was significantly higher and slowly decreased, particularly at the 14th, 21st and 28th day (all P<0.05). Meanwhile, the ratio of Sema 3A/VEGF in the Group TBI+F was significantly higher than that in the Group F, with statistical difference (P<0.05).
 Conclusion: The Nrp-1 is expressed abnormally in the process of fracture healing after nerve injury. It may play a role in the formation of pathological callus after nerve injury by promoting the preliminary and proliferation of chondrocytes, and inhibiting the growth of nerve fibers in the soft callus as well as the differentiation of osteoblast cell.

摘要

观察创伤性脑损伤后胫骨骨折愈合过程中神经纤毛蛋白-1(Nrp-1)、3A 型信号素(Sema3A)和血管内皮生长因子(VEGF)的表达情况,探讨 Nrp-1 在神经损伤后病理性骨痂形成中的作用机制。方法:选取 192 只 8~10 周龄、体重 220~250 g 的雌性 Wister 大鼠,随机分为对照组(C 组)、胫骨骨折组(F 组)、创伤性脑损伤组(TBI 组)、创伤性脑损伤合并胫骨骨折组(TBI+F 组),每组 48 只。分别于术后 3、5、7、14、21 和 28 d 采集组织样本(每个时间点 n=8)。采用免疫组织化学和 Western blot 检测骨痂组织中 Nrp-1 的表达,Western blot 检测 Sema3A 和 VEGF 的表达。结果:与 F 组比较,TBI+F 组骨形成区和软骨区软骨细胞中 Nrp-1 的表达较高,尤其在术后 7、14 和 21 d(P<0.05);而 TBI+F 组新鲜骨小梁区成骨细胞中 Nrp-1 的表达较低,尤其在术后 14 和 21 d(均 P<0.05)。Western blot 结果显示,TBI+F 组与 F 组中 Nrp-1、Sema 3A 和 VEGF 的表达趋势一致。然而,在各时间点,TBI+F 组中 Nrp-1 的表达均显著升高且下降缓慢,尤其在术后第 14、21 和 28 天(均P<0.05)。同时,TBI+F 组中 Sema 3A/VEGF 的比值显著高于 F 组,差异有统计学意义(P<0.05)结论:Nrp-1 在神经损伤后骨折愈合过程中表达异常,可能通过促进软骨细胞早期增殖、抑制软痂中神经纤维生长和成骨细胞分化,在神经损伤后病理性骨痂形成中发挥作用。

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