Cai W Q, Terenghi G, Bodin P, Burnstock G, Polak J M
Department of Anatomy and Developmental Biology, University College London, UK.
Histochemistry. 1993 Oct;100(4):277-83. doi: 10.1007/BF00270047.
The localization of mRNA encoding preproatrial natriuretic peptide (ANP) was investigated in cultured human umbilical vein endothelial cells (HUVEC) and tissue preparations of umbilical vein and artery. The techniques used were in situ hybridization and in situ hybridization combined with immunocytochemistry, using 32P-radiolabelled and non-radioactive digoxigenin labelled complementary RNA probes. Human ANP mRNAs are mainly localized in the endothelial cells of the umbilical vein and, to a lesser extent, in the endothelial cells of the umbilical artery. The autoradiographic labelling and the intensity of digoxigenin staining were significantly reduced by treatment with RNase before in situ hybridization. This study provides unequivocal evidence for the expression of the ANP gene in the endothelial cells of human umbilical vessels, confirming that these endothelial cells have the ability to synthesize this peptide. The functional significance of the presence of the ANP mRNA in the endothelial cells of human umbilical vessels is discussed.
在培养的人脐静脉内皮细胞(HUVEC)以及脐静脉和动脉的组织标本中,对编码前心钠素(ANP)的mRNA进行了定位研究。所采用的技术是原位杂交以及原位杂交结合免疫细胞化学,使用了32P放射性标记和非放射性地高辛标记的互补RNA探针。人ANP mRNA主要定位于脐静脉的内皮细胞,在脐动脉内皮细胞中的定位程度较低。原位杂交前用核糖核酸酶处理可使放射自显影标记和地高辛染色强度显著降低。本研究为ANP基因在人脐血管内皮细胞中的表达提供了明确证据,证实这些内皮细胞具有合成该肽的能力。文中还讨论了人脐血管内皮细胞中存在ANP mRNA的功能意义。