James S, Burnstock G
Department of Anatomy, University College London, UK.
Cell Tissue Res. 1991 Sep;265(3):555-65. doi: 10.1007/BF00340880.
We examined the distribution of binding sites for alpha-atrial natriuretic peptide (125I-ANP1-28) and the recently discovered porcine brain natriuretic peptide (125I-pBNP) on immunocytochemically identified cells in dissociated culture preparations of the rat trachea. Specific binding sites for both 125I-ANP1-28 and 125I-pBNP were evenly distributed over distinct subpopulations of smooth muscle myosin-like immunoreactive muscle cells, fibronectin-like immunoreactive fibroblasts and S-100-like immunoreactive glial cells. Neither keratin-like immunoreactive epithelial cells nor protein gene product 9.5-like immunoreactive paratracheal neurones expressed natriuretic peptide binding sites, although autoradiographically labelled glial cells were seen in close association with both neuronal cell bodies and neurites. The binding of each radiolabelled peptide was abolished by the inclusion of either excess (1 microM) unlabelled rat ANP or excess unlabelled porcine BNP, suggesting that ANP and BNP share binding sites in the trachea. Furthermore, the ring-deleted analogue, Des-[Gln18, Ser19, Gly20, Leu21, Gly22]-ANF4-23-NH2, strongly competed for specific 125I-ANP1-28 and 125I-pBNP binding sites in the tracheal culture; this suggests that virtually all binding sites were of the "clearance" (ANP-C or ANF-R2) receptor subtype.
我们研究了α-心房利钠肽(125I-ANP1-28)和最近发现的猪脑利钠肽(125I-pBNP)在大鼠气管解离培养物中经免疫细胞化学鉴定的细胞上的结合位点分布。125I-ANP1-28和125I-pBNP的特异性结合位点均匀分布在平滑肌肌球蛋白样免疫反应性肌细胞、纤连蛋白样免疫反应性成纤维细胞和S-100样免疫反应性神经胶质细胞的不同亚群上。角蛋白样免疫反应性上皮细胞和蛋白基因产物9.5样免疫反应性气管旁神经元均未表达利钠肽结合位点,尽管在放射自显影片上可见标记的神经胶质细胞与神经元细胞体和神经突紧密相连。每种放射性标记肽的结合都可被加入过量(1μM)未标记的大鼠ANP或过量未标记的猪BNP所消除,这表明ANP和BNP在气管中共享结合位点。此外,环缺失类似物Des-[Gln18, Ser19, Gly20, Leu21, Gly22]-ANF4-23-NH2在气管培养物中强烈竞争特异性125I-ANP1-28和125I-pBNP结合位点;这表明几乎所有结合位点均为“清除”(ANP-C或ANF-R2)受体亚型。