利用糖原诱导的豚鼠多形核白细胞检测人血清中的趋化抑制剂。

Diagnostic immunology Pub Date : 1985-01-01
R C Judd, J A Rudbach
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引用次数: 0

摘要

利用糖原诱导的豚鼠多形核白细胞(PMNs)进行实验,旨在建立酪蛋白刺激的趋化性的最佳条件。随后,研究表明,在无血清培养基中,豚鼠PMNs容易受到正常或患病人血清中发现的三种不同类型的细胞定向趋化抑制剂的迁移抑制。比较豚鼠和人外周血PMNs对迁移的抑制作用表明,豚鼠和人外周血PMNs对创伤患者血清的抑制作用同样敏感;这种抑制剂的分子量约为10,000 d。人类PMNs比豚鼠PMNs更容易受到正常人血清中发现的约110,000 d抑制剂的迁移抑制。另一方面,豚鼠PMNs在某种程度上更容易受到大约400000 d的趋化抑制剂的迁移抑制,这种抑制剂类似于在无能血清中发现的抑制剂。这一信息表明,在无血清培养基中,豚鼠pmn可以在这些人血清因子的定量分析中替代人细胞。
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The use of glycogen-induced guinea pig polymorphonuclear leukocytes to detect inhibitors of chemotaxis found in human serum.

Glycogen-induced guinea pig polymorphonuclear leukocytes (PMNs) were employed in experiments designed to establish the optimal conditions for casein-stimulated chemotaxis. Subsequently, it was shown that guinea pig PMNs, in a serum-free medium, were susceptible to inhibition of migration by three distinct types of cell-directed inhibitors of chemotaxis found in normal or diseased human sera. Comparison of inhibition of migration of both guinea pig and human peripheral PMNs showed that guinea pig and human PMNs were equally susceptible to inhibition by sera from trauma victims; this inhibitor had a molecular weight of about 10,000 d. Human PMNs were slightly more susceptible than were guinea pig PMNs to inhibition of migration by a approximately 110,000-d inhibitor found in normal human sera. On the other hand, guinea pig PMNs were somewhat more susceptible to inhibition of migration by a approximately 400,000-d inhibitor of chemotaxis that was analogous to the inhibitor found in anergic serum. This information shows that guinea pig PMNs, in a serum-free medium, may be substituted for human cells in quantitative assays for these human serum factors.

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