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Rap1蛋白在非创伤性股骨头坏死骨组织血管内皮中的表达

Expression of Ras-Associated Protein 1 in the Vascular Endothelium of Bone Tissue with Non-Traumatic Osteonecrosis of Femoral Head

  • 摘要:
      目的  分析Ras相关蛋白1(Ras-associated protein 1,Rap1)在非创伤性股骨头坏死(non-traumatic osteonecrosis of the femoral head,NONFH)患者骨组织坏死与正常区域的表达差异。
      方法  分别收集NONFH和创伤性股骨头坏死(traumatic osteonecrosis of the femoral head,TONFH)患者经髋关节置换术后的股骨头组织各30例。NONFH组男19例,女11例;年龄26~69岁,平均49.6岁,国际骨循环协会(ARCO)Ⅲb期8例,Ⅳ期10例,Ⅴ期12例;TONFH组男16例,女14例;年龄37~68岁,平均54.2岁,ARCO Ⅲb期11例,Ⅳ期9例,Ⅴ期10例。两组间性别及年龄差异无统计学意义(P>0.05),ARCO分期构成比差异亦无统计学意义(Z=−0.769,P=0.442)。取NONFH骨标本坏死区(A区)和正常区(B区),TONFH骨标本正常区域(B’区)(对照组)。采用Western blot、实时荧光定量PCR分析3个区域骨组织中Rap1、血管内皮生长因子(VEGF)、磷脂酰肌醇3-激酶(PI3K)、Akt蛋白及相应mRNA表达差异,HE和免疫组化染色观察各区域的形态学改变。
      结果  Western blot检测结果显示,B区、B’区间Rap1、VEGF、PI3K及Akt蛋白相对表达量差异均无统计学意义(P>0.05)。而A区Rap1、VEGF、PI3K及Ak蛋白相对表达量均较B区减少,差异有统计学意义(P<0.05)。实时荧光定量PCR检测结果显示,与B区比较,A区Rap1、VEGFPI3KAkt mRNA相对表达量均较B区降低,差异有统计学意义(P<0.05);B区、B’区两组间Rap1、VEGFPI3KAkt mRNA相对表达量差异均无统计学意义(P>0.05)。HE和免疫组化染色:NONFH坏死区域(A区)软骨细胞减少、细胞核消失,软骨下骨小梁断裂,骨小梁増厚,出现空骨陷窝;坏死区周围新生毛细血管和纤维组织构成的肉芽组织增生爬行,但Rap1、VEGF、PI3K和Akt在此区域阳性表达较正常区域弱。同时Rap1、PI3K、Akt在A、B两区域的骨小梁中均有阳性表达,表达强度相似。B区域微动脉、微静脉内膜及周围间质细胞膜上可见Rap1、VEGF、PI3K及Akt均有强阳性表达,但A区较B区阳性表达明显减少;而B’与B区各指标的阳性表达部位与强度相似。
      结论  NONFH的坏死可能与Rap1-PI3K/Akt信号通路受到抑制导致其表达下降所引起的血管内皮损伤有关。

     

    Abstract:
      Objective  To investigate the difference in the expression of Ras-associated protein 1 (Rap1) in necrotic and healthy areas of non-traumatic osteonecrosis of femoral head (NONFH) patients.
      Methods  Femoral head tissue samples from 30 cases of NONFH and 30 cases of traumatic osteonecrosis of the femoral head (TONFH) were collected after hip replacement surgery, respectively. No significant difference of Association Research Circulation Osseous (ARCO) staging was found between the NONFH and the TONFH groups (Z=−0.769, P=0.442). In the NONFH group, 8 patients were ARCO stage IIIb, 10 were stage IV, and 12 were stage V, while in the TONFH ground, 11 patients were ARCO stage IIIb, 9 were stage IV, and 10 were stage V. There were 19 males and 11 females in the NONFH group, with an average age of 49.6 yr. (26-69 yr.), and 16 males and 14 females in the TONFH group, with an average age of 54.2 yr. (37-68 yr.). There was no significant difference in gender or age between the two groups (P>0.05). Specimens were collected from different bone areas, including those from the necrotic areas (area A) and the healthy areas (area B) of the NONFH group, and those from the healthy areas (area B') of the TONFH group, i.e., the control group. Western blot and quantitative real-time reverse transcription PCR (qRT-PCR) were used to analyze the different expression of Rap1, vascular endothelial growth factor (VEGF) protein, phosphoinositide 3-kinase (PI3K), and Akt protein and their corresponding mRNA in the three areas of bone tissue. HE staining and immunohistochemisty staining were done in order to observe the morphological changes of each area.
      Results  Western blot results indicated that there was no statistical difference in the relative expression of Rap1, VEGF, PI3K, and Akt proteins (P>0.05). The relative expressions of Rap1, VEGF, PI3K, and Akt proteins in the area A were lower than those in the area B and the difference was statistically significant (P<0.05). qRT-PCR results showed that the relative expressions of Rap1, VEGF, PI3K and Akt mRNA in area A were lower than those of area B, and a statistical difference was found (P<0.05). The relative expression of the mRNA of Rap1, VEGF , PI3K and Akt in area B and area B' were not significantly different (P>0.05). HE staining and immunohistochemisty staining showed that chondrocytes decreased in the necrotic area (area A) of NONFH, chondrocytes nucleus disappeared, subchondral bone trabeculae were broken, bone trabeculae thickened, and empty bone lacunae appeared. Granulation tissues composed of new capillaries and fibrous cells have proliferated and crawled around the necrotic area. Positive expressions of the Rap1, VEGF, PI3K and Akt proteins in area A were weaker than those of the normal area. In addition, there were positive expressions of Rap1, PI3K and Akt on the trabecular bone of both area A and area B at similar intensity of expression. There were strong positive expressions of Rap1, VEGF, PI3K and Akt on the intima of arterioles and venules, and on the peripheral stromal cell membrane, but the positive expression in area A was significantly lower than that in area B. However, the positive expression positions and intensity of all indicators were similar in area B and area B'.
      Conclusion  The necrosis in NONFH may be related to vascular endothelial damages caused by the inhibition of the Rap1-PI3K/Akt signaling pathways and the subsequent decline in the protein expression.

     

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