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ICAM-1和PECAM-1的免疫超微结构表达先于小鼠血脑屏障的结构成熟。

Immunoultrastructural expression of ICAM-1 and PECAM-1 occurs prior to structural maturity of the murine blood-brain barrier.

作者信息

Lossinsky A S, Wisniewski H M

机构信息

Huntington Medical Research Institutes, Department of Neurology, Pasadena, Calif. 91105, USA.

出版信息

Dev Neurosci. 1998;20(6):518-24. doi: 10.1159/000017352.

Abstract

This study investigated the time of expression of two endothelial cell adhesion molecules, ICAM-1/CD54 and PECAM-1/CD31 in the developing postpartum mouse blood-brain barrier (BBB). Immunoultrastructural studies demonstrated that both adhesion molecules are initially expressed primarily on the luminal endothelial cell surfaces at birth or shortly thereafter, they increase in an intensity at approximately 1 week postpartum and then decrease to a weak labeling of the luminal endothelial cell surfaces at 2 weeks after birth. In the adult animals, little or no adhesion molecule labeling was expressed on blood vessels. Our results present immunocytochemical evidence that upregulation of ICAM-1 and PECAM-1 occurs prior to structural maturity of the BBB. Moreover, these data support a notion that these adhesion molecules play an important role for angiogenesis in the developing murine BBB.

摘要

本研究调查了产后发育中的小鼠血脑屏障(BBB)中两种内皮细胞粘附分子,即细胞间粘附分子-1/CD54和血小板内皮细胞粘附分子-1/CD31的表达时间。免疫超微结构研究表明,这两种粘附分子最初主要在出生时或出生后不久表达于管腔内的内皮细胞表面,产后约1周时其表达强度增加,然后在出生后2周时降至管腔内内皮细胞表面的弱标记。在成年动物中,血管上几乎没有或没有粘附分子标记表达。我们的结果提供了免疫细胞化学证据,表明ICAM-1和PECAM-1的上调发生在血脑屏障结构成熟之前。此外,这些数据支持这样一种观点,即这些粘附分子在发育中的小鼠血脑屏障血管生成中起重要作用。

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