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首页> 外文期刊>Folia histochemica et cytobiologica >Immunohistochemical detection of angiotensin receptors ATI and AT2 in normal rat pituitary gland, estrogen-induced rat pituitary tumor and human pituitary adenomas
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Immunohistochemical detection of angiotensin receptors ATI and AT2 in normal rat pituitary gland, estrogen-induced rat pituitary tumor and human pituitary adenomas

机译:正常大鼠垂体,雌激素诱导的大鼠垂体瘤和人垂体腺瘤中血管紧张素受体ATI和AT2的免疫组织化学检测

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摘要

Male rat pituitary glands, diethylstilbestrol (DES)-induced rat pituitary tumors and 12 human pituitary adenomas were immunostained with antibodies raised against ATI and AT2 angiotensin receptor proteins Positive immunostaining of ATI was observed in a subpopulation of anterior and intermediate pituitary lobe cells as well as in some nerve endings of the neurohypophysis. In the DES-induced rat pituiary tumors, the subpopulation of ATl-immunnopositive cells was smaller than in the non-tumoral anterior pituitary In human pituitary adenomas, weak ATI immunostaining was found in 5 tumors. In the remaining adenomas, the ATI immunostaining was trace (doubtful) or absent. The ATI immunostaining in the peritumoral non-neoplastic pituitary tissue was stronger than that observed in the tumors The normal rat pituitaries and rat tumors did not show immunostaining with anti-AT2 antibody. In human pituitary adenomas, the tumoral cells were AT2- negative but moderate to strong AT2 immunostaining was observed in intratumoral blood vessel walls. The data suggest that the experimental (in rat) and spontaneous (in man) pituitary tumorigenesis is associated with the down-regulation of ATI receptors. The expression of AT2 receptors, in turn, may be connected with the process of tumoral neo-angiogenesis
机译:用针对ATI和AT2血管紧张素受体蛋白的抗体对雄性大鼠垂体腺,己烯雌酚(DES)诱导的大鼠垂体瘤和12个人类垂体腺瘤进行了免疫染色,在垂体前叶和中叶垂体细胞亚群中观察到ATI的阳性免疫染色在神经垂体的一些神经末梢。在DES诱导的大鼠垂体肿瘤中,AT1免疫阳性细胞的亚群小于非肿瘤性垂体前叶。在人类垂体腺瘤中,在5个肿瘤中发现了较弱的ATI免疫染色。在其余的腺瘤中,ATI免疫染色为痕迹(可疑)或不存在。肿瘤周围非肿瘤性垂体组织中的ATI免疫染色比在肿瘤中观察到的要强。正常的大鼠垂体和大鼠肿瘤未显示抗AT2抗体的免疫染色。在人垂体腺瘤中,肿瘤细胞为AT2阴性,但在瘤内血管壁中观察到中等至强AT2免疫染色。数据表明,实验性(大鼠)和自发性(人类)垂体肿瘤发生与ATI受体的下调有关。反过来,AT2受体的表达可能与肿瘤新血管生成的过程有关

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