Solberg Lene B, Melhus Gunhild, Brorson Sverre-Henning, Wendel Mikael, Reinholt Finn P
Institute and Department of Pathology, University of Oslo, Rikshospitalet-Radiumhospitalet Trust, Oslo, Norway.
Micron. 2006;37(4):347-54. doi: 10.1016/j.micron.2005.11.010. Epub 2005 Dec 9.
The main purpose of this study was to examine whether antigens can be retrieved by heating Lowicryl sections of paraformaldehyde-fixed (PFF) tissues. Thus the intensity of the immunogold signal for two bone proteins (Nucleobindin (Nuc) and osteoadherin (OSAD)) was compared in retrieved and non-retrieved sections of PFF rat bone. As an additional experiment, the effect of antigen retrieval (for Nuc) in sections of tissue primary stabilized by high pressure freezing with subsequent freeze substitution (HPF-FS) was studied. Finally, the tissue distribution patterns of Nuc labeling were compared in non-retrieved HPF-FS sections to that of retrieved and non-retrieved PFF sections. Antigen retrieval in Lowicryl sections of PFF tissues showed significantly enhanced labeling intensity for both proteins in all compartments where they are known to occur. Retrieved PFF Lowicryl sections showed only minor ultrastructural differences compared to non-retrieved ones. Retrieval of HPF-FS sections exhibited no enhancement of labeling but rather a slight reduction, which was significant in the cytoplasm and in cartilage. Furthermore, striking ultrastructural differences were observed in retrieved HPF-FS sections compared to non-retrieved ones with loss of coherence and structure in sections subjected to heating. Comparison of the distribution patterns of Nuc in the sections of PFF and HPF-FS tissues showed discrepancy in most compartments. Antigen retrieval by heating Lowicryl sections of PFF tissues significantly enhances immunogold labeling in all cell compartments where the bone proteins are known to occur. However, the procedure may distort the tissue distribution pattern of bone proteins.
本研究的主要目的是检测加热经多聚甲醛固定(PFF)组织的Lowicryl切片是否能使抗原得以恢复。因此,在PFF大鼠骨骼的经恢复和未经恢复的切片中,比较了两种骨蛋白(核结合蛋白(Nuc)和骨黏附素(OSAD))的免疫金信号强度。作为一项额外实验,研究了在经高压冷冻随后冷冻置换(HPF-FS)初步固定的组织切片中抗原恢复(针对Nuc)的效果。最后,比较了在未经恢复的HPF-FS切片中Nuc标记的组织分布模式与经恢复和未经恢复的PFF切片中的模式。PFF组织的Lowicryl切片中的抗原恢复显示,在已知这两种蛋白存在的所有区域,其标记强度均显著增强。与未经恢复的切片相比,经恢复的PFF Lowicryl切片仅显示出微小的超微结构差异。HPF-FS切片的恢复并未增强标记,反而略有降低,在细胞质和软骨中这种降低具有显著性。此外,与未经恢复的切片相比,在经恢复的HPF-FS切片中观察到明显的超微结构差异,加热处理的切片出现了连贯性和结构丧失。比较PFF和HPF-FS组织切片中Nuc的分布模式,发现在大多数区域存在差异。加热PFF组织的Lowicryl切片进行抗原恢复,在已知骨蛋白存在的所有细胞区域显著增强了免疫金标记。然而,该操作可能会扭曲骨蛋白的组织分布模式。