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首页> 外文期刊>Acta Histochemica: Zeitschrift fur Histologische Topochemie >Quantitative analysis of ciliary ultrastructure in patients with primary ciliary dyskinesia.
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Quantitative analysis of ciliary ultrastructure in patients with primary ciliary dyskinesia.

机译:原发性睫状运动障碍患者睫状超微结构的定量分析。

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The present study was designed to investigate dynein arm and microtubule defects quantitatively in patients with respiratory disease and to establish the clinical relevance of dynein arm deficiency and microtubule abnormalities. Thirty-four patients with recurrent upper and/or lower respiratory infections were included in the study. Nasal mucosal brushings were fixed in glutaraldehyde and routine electron microscopic procedures were carried out. At least 20 cross-sectioned cilia were examined from each subject. Dynein arm and microtubular abnormalities were quantified and a statistical analysis was performed. Twenty-nine percent of the patients showed dynein arm deficiency and a further 21% had possible deficiency (PD). Microtubule defects in patients with dynein arm deficiency and PD were found to be significantly increased compared to the patients with no dynein arm deficiency. The most prominent defect in the dynein arm deficiency group was a translocation of central and/or peripheral microtubules. The high percentage of translocation defect in this group of patients suggests that these defects are primary, rather than secondary to infection.
机译:本研究旨在定量研究呼吸系统疾病患者中的达因臂和微管缺陷,并建立达因臂缺乏和微管异常的临床相关性。该研究纳入了34例反复出现上呼吸道和/或下呼吸道感染的患者。将鼻粘膜刷固定在戊二醛中,并进行常规电子显微镜检查。每个受试者检查至少20个横截面纤毛。定量测量了达力宁手臂和微管异常,并进行了统计分析。 29%的患者表现出动力蛋白缺乏症,另有21%的患者表现为可能的缺乏症(PD)。与没有动力性手臂缺乏症的患者相比,有动力性手臂缺乏和PD的患者的微管缺损明显增加。达因臂缺损组中最突出的缺陷是中央和/或外周微管移位。这组患者中易位缺陷的百分比很高,表明这些缺陷是原发性的,而不是继发于感染的。

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