Heron M I, Rakusan K
Department of Physiology, Faculty of Medicine, University of Ottawa, Ontario, Canada.
J Mol Cell Cardiol. 1995 Jul;27(7):1393-403. doi: 10.1006/jmcc.1995.0132.
Immunocytochemical techniques examining the expression of cell proliferation-related markers such as proliferating cell nuclear antigen (PCNA), may be employed to provide visual and quantitative evidence of cell proliferation. The efficacy of this method in frozen samples was tested on sections of 2-day-old rat heart. Mouse monoclonal anti-PCNA and goat anti-mouse IgG2a peroxidase-conjugated antibodies were applied to tissue cross-sections. PCNA positive (PCNA+) cells were evident in these sections as intensely stained, dark brown nuclei. This method was then applied to the hearts of four groups of adult rats (1) 1 month hyperthyroid, (2) 1 month hypothyroid, (3) 6 days hyperthyroid following 1 month hypothyroidism, or (4) euthyroid, in order to assess the ability of identifying and quantifying PCNA+cell types (myocyte, endothelial, or remaining, "other" cells). Serial cross-sections were prepared, half of the sections processed using the PCNA technique, while corresponding sections were stained with hematoxylin and eosin. Identification of PCNA+cell types was made by comparison of PCNA with H&E sections. PCNA labeling indices for a given cell type were expressed as the proportion of PCNA+nuclei per 1000 nuclei. No PCNA+myocyte nuclei were observed in any of the adult hearts. Only hypothyroid/hyperthyroid demonstrated significantly higher PCNA labeling of endothelial and "other" nuclei compared to euthyroid. This finding agrees with previous morphometric data which suggested capillary growth in these hearts. Results demonstrate that quantitation of PCNA expression on frozen heart tissue is possible, and can be used to provide direct, discernible evidence for cell proliferation.
免疫细胞化学技术可用于检测细胞增殖相关标志物的表达,如增殖细胞核抗原(PCNA),从而提供细胞增殖的直观和定量证据。该方法在冷冻样本中的有效性已在2日龄大鼠心脏切片上进行了测试。将小鼠单克隆抗PCNA抗体和山羊抗小鼠IgG2a过氧化物酶偶联抗体应用于组织横断面。在这些切片中,PCNA阳性(PCNA+)细胞表现为深染的深褐色细胞核。然后将该方法应用于四组成年大鼠的心脏:(1)甲状腺功能亢进1个月;(2)甲状腺功能减退1个月;(3)甲状腺功能减退1个月后甲状腺功能亢进6天;或(4)甲状腺功能正常,以评估识别和定量PCNA+细胞类型(心肌细胞、内皮细胞或其余“其他”细胞)的能力。制备连续横断面,一半切片采用PCNA技术处理,而相应切片用苏木精和伊红染色。通过将PCNA与苏木精和伊红切片进行比较来识别PCNA+细胞类型。给定细胞类型的PCNA标记指数表示为每1000个细胞核中PCNA+细胞核的比例。在任何成年心脏中均未观察到PCNA+心肌细胞核。与甲状腺功能正常的大鼠相比,只有甲状腺功能减退/甲状腺功能亢进的大鼠在内皮细胞核和“其他”细胞核上表现出明显更高的PCNA标记。这一发现与之前的形态计量学数据一致,该数据表明这些心脏中存在毛细血管生长。结果表明,对冷冻心脏组织中PCNA表达进行定量是可行的,并且可用于为细胞增殖提供直接、可辨别的证据。