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固定-包埋方案如何影响促性腺激素亚基免疫细胞化学染色的特异性和效率。

How the fixation-embedding protocol affects the specificity and efficiency of immunocytochemical stains for gonadotropin subunits.

作者信息

Childs G V, Unabia G, Tibolt R

出版信息

Am J Anat. 1985 Dec;174(4):409-17. doi: 10.1002/aja.1001740405.

Abstract

This report describes a study designed to test factors that may affect the efficiency and specificity of stains for gonadotropins. These include chemical or freeze-fixation and dehydration, heat polymerization of the plastic embedding compound, dehydration in organic solvents, and etching. Specifically, postembedding stains for LH or FSH subunits were applied to 1-micron sections of 1) Araldite-embedded pituitaries that were either chemically fixed and dehydrated or freeze-fixed and freeze-dried; 2) Aldehyde-fixed pituitaries that were dehydrated in water-soluble glycol methacrylate (GMA) and embedded in GMA at 4 degrees C; and 3) p-formaldehyde-fixed pituitaries that were embedded in paraffin. A fourth group of pituitaries was dispersed and grown in monolayers for 1-3 days. These were stained following glutaraldehyde fixation. The optimal dilution of the primary antisera varied with the protocol; however, the percentage of cells staining for beta subunits did not change. In contrast, postembedding stains showed that alpha subunit reactivity is masked or destroyed in pituitaries that are fixed in glutaraldehyde and embedded in Araldite. Alpha chain reactivity was detected (in 14% of cells) either after freeze-fixation and freeze-drying followed by Araldite embedding, or after 4% paraformaldehyde fixation and GMA embedding (in 17% of cells). Staining in paraffin-embedded pituitaries was seen in only 10% of the cells. Preembedding stains for alpha chains were strikingly sensitive, however, and immunoreactivity was seen in 18-26% of the population of monolayer cells. Thus, whereas the percentages of cells staining for beta subunits do not change following the use of most of the fixation and embedding protocols, alpha chain reactivity is destroyed by all but the mildest. These findings show that one can control or improve the specificity of the stains for LH and FSH by the fixation-embedding protocol.

摘要

本报告描述了一项旨在测试可能影响促性腺激素染色效率和特异性的因素的研究。这些因素包括化学固定或冷冻固定及脱水、塑料包埋剂的热聚合、在有机溶剂中脱水以及蚀刻。具体而言,将针对促黄体生成素(LH)或促卵泡生成素(FSH)亚基的包埋后染色应用于以下1微米切片:1)用环氧树脂包埋的垂体,这些垂体要么经过化学固定和脱水,要么经过冷冻固定和冷冻干燥;2)用醛固定的垂体,在水溶性甲基丙烯酸乙二醇酯(GMA)中脱水,并在4摄氏度下用GMA包埋;3)用对甲醛固定的垂体,用石蜡包埋。第四组垂体被分散并单层培养1 - 3天。这些在戊二醛固定后进行染色。一抗的最佳稀释度因方案而异;然而,染色的β亚基细胞百分比没有变化。相比之下,包埋后染色显示,在戊二醛固定并用环氧树脂包埋的垂体中,α亚基反应性被掩盖或破坏。在冷冻固定和冷冻干燥后用环氧树脂包埋后,或在4%多聚甲醛固定和GMA包埋后(17%的细胞)检测到α链反应性(14%的细胞)。石蜡包埋的垂体中只有10%的细胞出现染色。然而,α链的包埋前染色非常敏感,在单层细胞群体中有18 - 26%的细胞出现免疫反应性。因此,虽然在使用大多数固定和包埋方案后,染色的β亚基细胞百分比没有变化,但除了最温和的方案外,所有方案都会破坏α链反应性。这些发现表明,可以通过固定 - 包埋方案来控制或提高LH和FSH染色的特异性。

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