Trono Ruben, Bossart Mattie I., Milam John D., Norman John C.
Cardiovascular Research Laboratories, Texas Heart Institute of St. Luke's Episcopal and Texas Children's Hospitals, Houston, Texas.
Cardiovasc Dis. 1979 Jun;6(2):153-172.
Following each of 21 clinical trials with the partial artificial heart or abdominal left ventricular assist device (ALVAD), we have examined the blood-interfacing human pseudoneointimal (PNI) linings formed on the fibril-flocked pumping surface by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The salient results of these ultrastructural analyses can be summarized: (1) early PNI accretion kinetics (< 24 hrs) involve plasma protein adsorption, entrapment of erythrocytes, platelets, lymphocytes, numerous neutrophils and macrophages, and the deposition of fibrin within fibril flock interstices (TEM); (2) the surface (< 24 hrs) consists of interconnected fibrin strands (SEM); (3) later PNI accretion kinetics (1-6 days) involve the formation of alternating cellular and fibrin layers (TEM); (4) the surface (1-6 days) consists of cellular aggregates (inter-membrane distances of 340 A) simulating an endothelial interface (SEM, TEM). Based on these analyses, a plausible sequence of events for human PNI accretion kinetics can be advanced, i.e., 0-24 hrs: (a) maximal foreign body response of blood in contact with Dacron fibrils, (b) cellular lysis and fibrin compaction; 1-6 days: (c) accretion and lysis of cellular aggregates (neutrophils, macrophages) 3-4micro thick, (d) accretion of linear fibrin aggregates, 8-10micro thick, and (e) cyclic replication (up to six) of phases c and d.
在使用部分人工心脏或腹部左心室辅助装置(ALVAD)进行的21项临床试验中的每一项之后,我们通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)检查了在纤维植绒泵送表面上形成的与人血接触的假性内膜(PNI)衬里。这些超微结构分析的主要结果可以总结如下:(1)早期PNI增生动力学(<24小时)涉及血浆蛋白吸附、红细胞、血小板、淋巴细胞、大量中性粒细胞和巨噬细胞的截留,以及纤维蛋白在纤维束间隙内的沉积(TEM);(2)表面(<24小时)由相互连接的纤维蛋白链组成(SEM);(3)后期PNI增生动力学(1 - 6天)涉及交替的细胞层和纤维蛋白层的形成(TEM);(4)表面(1 - 6天)由模拟内皮界面的细胞聚集体组成(膜间距离为340埃)(SEM,TEM)。基于这些分析,可以提出人类PNI增生动力学的一个合理事件序列,即0 - 24小时:(a)与涤纶纤维接触的血液的最大异物反应,(b)细胞溶解和纤维蛋白压实;1 - 6天:(c)3 - 4微米厚的细胞聚集体(中性粒细胞、巨噬细胞)的增生和溶解,(d)8 - 10微米厚的线性纤维蛋白聚集体的增生,以及(e)阶段c和d的循环复制(最多六次)。