生物矿化
钙化
病理
组织学
免疫组织化学
异位钙化
微量分析
病态的
主动脉
透射电子显微镜
解剖
扫描电子显微镜
化学
生物
医学
材料科学
内科学
纳米技术
古生物学
有机化学
复合材料
作者
I.-M. Radomychelski,Artem Piddubnyi,Sergey Danilchenko,O. S. Maksymova,Yuliia Moskalenko,Roman Moskalenko
标识
DOI:10.1017/s1431927621012721
摘要
Abstract Ectopic calcification or pathological biomineralization correlates with morbidity and mortality from cardiovascular diseases. Aortas with atherosclerotic lesions and biomineralization were selected for the study. Thirty samples of mineralized abdominal aortas (group M) were examined by histology. Depending on the calcifications size, samples were separated into group M1 (macroscopic calcifications) and M2 (microscopic calcifications). Each group consists of 15 samples. Calcification 2 mm or less were considered as microscopic, >2 mm—macroscopic. Thirty samples of aortic tissue without biomineralization (group C) were used as a control group. Aortic tissue was examined by macroscopic description, histology, histochemistry, immunohistochemistry (IHC), scanning electron microscopy (SEM) with microanalysis, and transmission electron microscopy (TEM). The results of IHC showed the involvement of OPN in the formation and development of pathological biomineralization, but the obvious role of OPN in the differentiation of macro- and microcalcifications of atherosclerotic aorta was not revealed. SEM with X-ray microanalysis confirmed that the biomineral part of the aortic samples of the M1 group consisted mainly of apatites, which correspond to previous studies. The Ca/P ratio was less in the M2 group than in the M1 group. It means that microcalcifications can be formed by more defective (immature) hydroxyapatite.
科研通智能强力驱动
Strongly Powered by AbleSci AI