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星形胶质细胞和周细胞与脑微血管内皮细胞毛细血管样结构的体外相互作用。

In vitro interaction of astrocytes and pericytes with capillary-like structures of brain microvessel endothelium.

作者信息

Minakawa T, Bready J, Berliner J, Fisher M, Cancilla P A

机构信息

Department of Pathology, UCLA School of Medicine.

出版信息

Lab Invest. 1991 Jul;65(1):32-40.

PMID:2072663
Abstract

A new method to study the interaction of astrocytes and pericytes with cerebral capillary endothelial cells in vitro is described. Endothelial cells derived from bovine brain were cultured on gelatin coated slides and covered with type 1 collagen. Endothelial cells aggregated and formed capillary-like structures (CS) within 3 days. The lining cells of the CS stained immunohistochemically for factor VIII-related antigen. Astrocytes isolated from neonatal mice or pericytes from bovine brain were added to the preparations after the formation of CS. After various periods of co-culture, the slides were fixed with methanol and examined with the immunohistochemical stain for glial fibrillary acidic protein or smooth muscle actin to demonstrate astrocytes or pericytes respectively. Five hours after addition, only 10% of astrocytes were associated with CS. However, by 24 hours, 70% of the astrocytes had assumed a position adjacent to the CS. The astrocytes then developed processes which were intimately apposed to the CS by 3 days, at which time they resembled the in vivo structural relationship between astrocytes and microvessels that occur in areas of central nervous system injury. Progressive elongation of the astrocytes or their processes at the CS was evident at 6 and 9 days of co-culture. The cross-section of CS co-cultured with astrocytes showed continuous cells surrounding a lumen, and the endothelial cells appeared to be connected by tight junctions. When pericytes were added to CS cultures they also preferentially associated with CS, but the contact occurred more rapidly than with astrocytes, 50% being associated with CS by 5 hours. The CS were almost completely covered with elongated pericytes by 24 hours. A chemotactic assay was developed that showed that there was a chemotactic attraction of pericytes to the CS. Thus an in vitro system is now available to study the interrelationships of these cell types and their interaction in development, regeneration and differentiation of the blood-brain barrier.

摘要

本文描述了一种体外研究星形胶质细胞、周细胞与脑毛细血管内皮细胞相互作用的新方法。从牛脑分离的内皮细胞培养在明胶包被的载玻片上,并覆盖Ⅰ型胶原。内皮细胞在3天内聚集并形成毛细血管样结构(CS)。CS的内衬细胞经免疫组织化学染色显示因子Ⅷ相关抗原阳性。在CS形成后,将新生小鼠分离的星形胶质细胞或牛脑周细胞加入培养物中。共培养不同时间后,用甲醇固定载玻片,并用免疫组织化学染色检测胶质纤维酸性蛋白或平滑肌肌动蛋白,分别显示星形胶质细胞或周细胞。加入后5小时,只有10%的星形胶质细胞与CS相关。然而,到24小时时,70%的星形胶质细胞已位于CS附近。然后星形胶质细胞伸出突起,到3天时与CS紧密相邻,此时它们类似于中枢神经系统损伤区域星形胶质细胞与微血管之间的体内结构关系。共培养6天和9天时,CS处的星形胶质细胞或其突起明显逐渐伸长。与星形胶质细胞共培养的CS横断面显示细胞围绕管腔连续排列,内皮细胞似乎通过紧密连接相连。当将周细胞加入CS培养物中时,它们也优先与CS相关,但与星形胶质细胞相比,接触发生得更快,5小时时50%与CS相关。到24小时时,CS几乎完全被伸长的周细胞覆盖。开发了一种趋化性分析方法,结果显示周细胞对CS有趋化性吸引。因此,现在有了一个体外系统来研究这些细胞类型之间的相互关系及其在血脑屏障发育、再生和分化中的相互作用。

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