Cardio Vascular Diseases and Diabetes Biology Program, Rajiv Gandhi Centre for Biotechnology, Poojapura, Thycaud, Thiruvananthapuram, Kerala, India.
Manipal Academy of Higher Education, Manipal, Karnataka, India.
PLoS One. 2018 Jun 13;13(6):e0198617. doi: 10.1371/journal.pone.0198617. eCollection 2018.
Arteriovenous malformations (AVMs) are characterised by tangles of dysplastic blood vessels which shunt blood from arteries to veins with no intervening capillary bed. It is not known at what stage of development and differentiation, AVM vessels became aberrant. To address this, we have analysed the expression of vascular differentiation, vascular maturation and brain capillary specific genes in AVM nidus.
We performed immunohistochemistry and western blot analysis of vascular differentiation (HEY2, DLL4, EFNB2, and COUP-TFII), vascular maturation (ENG and KLF2) and brain capillary specific genes (GGTP and GLUT1) on ten surgically excised human brain AVMs and ten normal human brain tissues.
Immunohistochemical analysis revealed that AVM vessels co-express both artery and vein differentiation genes. H-score analysis revealed that there is statistically significant (P < 0.0001) increase in expression of these proteins in AVM vessels compared to control vessels. These findings were further confirmed by western blot analysis and found to be statistically significant (P < 0.0001 and P < 0.001) for all proteins except Hey2. Both immunostaining and western blot analysis revealed that AVM vessels express GGTP and GLUT1, markers specific to brain capillaries. Immunofluorescent staining demonstrated that expression of KLF2, a vascular maturation marker is significantly (P <0.001) decreased in AVM vessels and was further confirmed by western blot analysis (P < 0.001). Immunohistochemical and western blot analysis demonstrated that another vascular maturation protein Endoglin had high expression in AVM vessels compared to control vessels. The results were found to be statistically significant (P < 0.0001).
Our findings suggest that vascular structures of AVMs co-express markers specific for arteries, veins and capillaries. We conclude that AVM nidus constitutes of aberrant vessels which are not terminally differentiated and inadequately matured.
动静脉畸形(AVM)的特征是血管结构紊乱,血液从动脉直接分流到静脉,中间没有毛细血管床。目前尚不清楚 AVM 血管在哪个发育和分化阶段发生了异常。为了解决这个问题,我们分析了 AVM 病灶中血管分化、血管成熟和脑毛细血管特异性基因的表达。
我们对 10 例手术切除的人脑 AVM 和 10 例正常脑组织进行了血管分化(HEY2、DLL4、EFNB2 和 COUP-TFII)、血管成熟(ENG 和 KLF2)和脑毛细血管特异性基因(GGTP 和 GLUT1)的免疫组织化学和 Western blot 分析。
免疫组织化学分析显示,AVM 血管共同表达动脉和静脉分化基因。H 评分分析显示,与对照血管相比,AVM 血管中这些蛋白的表达有统计学意义的(P < 0.0001)增加。Western blot 分析进一步证实了这一点,除了 HEY2 外,所有蛋白的表达均有统计学意义(P < 0.0001 和 P < 0.001)。免疫染色和 Western blot 分析显示,AVM 血管表达 GGTP 和 GLUT1,这是脑毛细血管的特异性标志物。免疫荧光染色显示,血管成熟标志物 KLF2 的表达在 AVM 血管中显著降低(P <0.001),Western blot 分析进一步证实了这一点(P < 0.001)。免疫组织化学和 Western blot 分析显示,另一种血管成熟蛋白 Endoglin 在 AVM 血管中的表达明显高于对照血管(P < 0.0001)。
我们的研究结果表明,AVM 的血管结构共同表达动脉、静脉和毛细血管的标志物。我们得出结论,AVM 病灶由异常的血管组成,这些血管没有终末分化,成熟度不足。