Doughty Michael J
Department of Vision Sciences, Glasgow-Caledonian University, City Campus, Glasgow, Scotland G4 0BA, UK.
Cell Biol Int. 2004;28(2):131-7. doi: 10.1016/j.cellbi.2003.11.012.
The objective was to examine primary cilia at the apical surface of corneal endothelial cells after using different fixatives. Female albino rabbits (2 kg) were euthanised at 15:00 h and the corneas fixed immediately (usually with an isotonic 2% glutaraldehyde-cacodylate fixative) either after dissection, by application fixative at 4 degrees C, by immersion of the eyeball in fixative at room temperature (RT), or by application of an isotonic or a hypertonic (Karnovsky-type) fixative at RT. Images at 2000x were taken from the central corneal region, and number and length of primary cilia assessed. The length was the same regardless of method (overall average of 1.67+/-0.70 microm), but the incidence of primary cilia was hypertonic fixative (87% of cells) >cold drop fixation (71%), >whole globe immersion (68%) >dissect then fix methods (67%) >RT drop fixation (34%). The first four methods however yielded cells with unacceptable artefacts (especially distortion). More details should be provided of the primary fixation method used.
目的是在使用不同固定剂后检查角膜内皮细胞顶端表面的初级纤毛。体重2 kg的雌性白化兔于15:00处死,角膜在解剖后、4℃应用固定剂、室温(RT)下将眼球浸入固定剂或室温下应用等渗或高渗(Karnovsky型)固定剂后立即固定(通常使用等渗2%戊二醛-二甲胂酸盐固定剂)。从角膜中央区域拍摄2000倍的图像,并评估初级纤毛的数量和长度。无论采用何种方法,纤毛长度相同(总体平均值为1.67±0.70微米),但初级纤毛的发生率为高渗固定剂(87%的细胞)>冷滴固定(71%)>全眼球浸入(68%)>解剖后固定方法(67%)>室温滴固定(34%)。然而,前四种方法产生的细胞有不可接受的伪像(尤其是变形)。应提供所使用的初级固定方法的更多细节。