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原发性纤毛运动障碍患者中性粒细胞运动功能缺陷。

Defective neutrophil motility in patients with primary ciliary dyskinesia.

作者信息

Valerius N H, Knudsen B B, Pedersen M

出版信息

Eur J Clin Invest. 1983 Dec;13(6):489-94. doi: 10.1111/j.1365-2362.1983.tb00134.x.

Abstract

Microtubules are important in the regulation of the motile functions of a variety of cells, including leukocytes, ciliated cells and spermatozoa. Polymorphonuclear leukocyte function was studied in ten patients with primary ciliary dyskinesia, an inherited disorder of microtubules in sperm tails and cilia. Neutrophil chemotaxis in Boyden chambers was slightly reduced, but only one patient showed a migration below normal values. In vivo mobilization of polymorphonuclear leukocytes into skin windows was also slightly decreased. In contrast, neutrophil polarization and orientation was normal. The bactericidal activity of neutrophils from patients with primary ciliary dyskinesia was normal, while the ingestion of bacteria was decreased. The abnormalities of neutrophil function in patients with primary ciliary dyskinesia are related to motility. It is suggested that the microtubule defect responsible for the abnormal pattern of ciliary beating is a general abnormality also responsible for the depression of polymorphonuclear leukocyte motility.

摘要

微管在调节包括白细胞、纤毛细胞和精子在内的多种细胞的运动功能中起着重要作用。对10例原发性纤毛运动障碍患者的多形核白细胞功能进行了研究,原发性纤毛运动障碍是一种精子尾部和纤毛微管的遗传性疾病。在Boyden小室中,中性粒细胞趋化性略有降低,但只有1例患者的迁移低于正常值。多形核白细胞向皮肤窗口的体内动员也略有减少。相比之下,中性粒细胞的极化和定向是正常的。原发性纤毛运动障碍患者中性粒细胞的杀菌活性正常,而细菌摄取减少。原发性纤毛运动障碍患者中性粒细胞功能异常与运动性有关。有人提出,导致纤毛跳动异常模式的微管缺陷是一种普遍异常,也导致多形核白细胞运动性降低。

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