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小鼠松果体中蛋白质和肽的血管通透性。

Vascular permeability to proteins and peptides in the mouse pineal gland.

作者信息

Møller M, van Deurs B, Westergaard E

出版信息

Cell Tissue Res. 1978 Dec 14;195(1):1-15. doi: 10.1007/BF00233673.

Abstract

The permeability of fenestrated capillaries in the mouse pineal gland to proteins and peptides was demonstrated by means of ultrastructural tracers. Horseradish peroxidase (HRP) and microperoxidase (MP) were injected intravenously and allowed to circulate for approximately 30 s, 1 min, 5 min, 1 or 2 h. The tissue was then fixed by vascular perfusion or by immersion with aldehydes. In all experiments a pronounced extravasation of HRP and MP occurred. Transendothelial vesicular transport seemed to have occurred across the fenestrated capillaries. The most pronounced tracer labeling of vesicles was found after 1 min of MP- or HRP-circulation. The vesicles were uncoated and more than 70% of the HRP- and MP-containing vesicles exhibited diameters between 50 and 110 nm. Furthermore, three other transcapillary pathways taken by the tracers are suggested: 1) via intercellular junctions, 2) through fenestrae and 3) via channels formed by fusion of vesicles with the luminal and abluminal cell membranes. Based on these results, it is assumed that the capillaries in the mouse pineal gland also permeable to peptides synthesized and secreted by the pineal gland.

摘要

通过超微结构示踪剂证明了小鼠松果体中窗孔毛细血管对蛋白质和肽的通透性。将辣根过氧化物酶(HRP)和微过氧化物酶(MP)静脉注射,并使其循环约30秒、1分钟、5分钟、1或2小时。然后通过血管灌注或用醛类浸泡固定组织。在所有实验中,HRP和MP均出现明显的外渗。跨内皮囊泡运输似乎发生在窗孔毛细血管上。在MP或HRP循环1分钟后,发现囊泡的示踪剂标记最为明显。这些囊泡无被膜,超过70%含有HRP和MP的囊泡直径在50至110纳米之间。此外,还提出了示踪剂所采用的其他三种跨毛细血管途径:1)通过细胞间连接,2)通过窗孔,3)通过囊泡与管腔和管腔外细胞膜融合形成的通道。基于这些结果,推测小鼠松果体中的毛细血管对松果体合成和分泌的肽也具有通透性。

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