Marsigliante S, Resta L, Muscella A, Vinson G P, Marzullo A, Storelli C
Dipartimento di Biologia, Laboratorio di Fisiologia Generale, Università di Lecce, Italy.
Cancer Lett. 1996 Dec 20;110(1-2):19-27. doi: 10.1016/s0304-3835(96)04449-7.
The presence of the angiotensin type 1 receptor (AT1 Ang II-R) was investigated in normal and diseased human larynx using a specific monoclonal antibody (6313/G2). When tissue AT1 content was studied by SDS electrophoresis with immunoblotting, the receptor was detected in 10/10 laryngeal tumours, and in 7/10 samples of normal tissue from the same patients. Two immunostaining bands, approximately 75 kDa, were present in all cases. Immunocytochemistry performed on sections of 45 formalin-fixed, paraffin-embedded laryngeal tissue samples showed that the receptor was expressed in normal respiratory epithelium only in a perinuclear pattern, above the nucleus toward the cell apex. In addition, the antigen was invariably present in skeletal muscle cells and in the columnar duct epithelium of minor salivary glands. The secretory cells were negative, but the antibody stained the adjacent myoepithelial cell layer. As expected, smooth muscle cells of the vessel walls also expressed Ang II-R. In metaplastic epithelium deriving from respiratory epithelium, the receptors were distributed diffusely throughout the cytoplasm of basal and parabasal cells. In dysplastic epithelium, cells of all layers were strongly positive. Finally, squamous cell tumours showed varying numbers of immunoreactive cells, which stained in a diffuse cytoplasmic and membranous pattern. Computer-assisted image analysis of the stained sections showed that the positivity for Ang II-R dramatically increased in dysplastic and well-differentiated cancer cells (3- and 5.5-fold higher than in normal epithelium, respectively), but there was less in poorly and very poorly differentiated cancer. Receptor abundance was not correlated with tumour size nor lymph node involvement. These results suggest a possible role of Ang II in the growth or function of normal and neoplastic larynx tissue, which is especially significant in early neoplastic change.
使用特异性单克隆抗体(6313/G2)对正常和病变的人喉组织中血管紧张素1型受体(AT1 Ang II-R)的存在情况进行了研究。当通过SDS电泳和免疫印迹法研究组织中的AT1含量时,在10例喉肿瘤以及来自同一患者的10例正常组织样本中的7例中检测到了该受体。所有病例均出现两条免疫染色带,大小约为75 kDa。对45份福尔马林固定、石蜡包埋的喉组织样本切片进行免疫细胞化学分析显示,该受体仅在正常呼吸道上皮细胞核周呈模式表达,位于细胞核上方朝向细胞顶端。此外,该抗原始终存在于骨骼肌细胞和小涎腺的柱状导管上皮中。分泌细胞呈阴性,但抗体对相邻的肌上皮细胞层进行了染色。正如预期的那样,血管壁的平滑肌细胞也表达Ang II-R。在源自呼吸道上皮的化生上皮中,受体弥漫分布于基底细胞和副基底细胞的细胞质中。在发育异常的上皮中,各层细胞均呈强阳性。最后,鳞状细胞肿瘤显示出数量不等的免疫反应性细胞,呈弥漫性细胞质和膜性染色模式。对染色切片进行计算机辅助图像分析显示,发育异常和高分化癌细胞中Ang II-R的阳性率显著增加(分别比正常上皮高3倍和5.5倍),但低分化和未分化癌细胞中的阳性率较低。受体丰度与肿瘤大小和淋巴结受累情况无关。这些结果表明,Ang II在正常和肿瘤性喉组织的生长或功能中可能发挥作用,这在肿瘤早期变化中尤为显著。