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脆弱拟杆菌脂多糖在体内产生的兔多形核白细胞趋化因子。II. 抗原性和生物学特性。

Rabbit polymorphonuclear leukocyte chemotactic factor generated in vivo by Bacteroides fragilis lipopolysaccharide. II. Antigenic and biologic properties.

作者信息

Sveen K

出版信息

Acta Pathol Microbiol Scand B. 1978 Aug;86(4):237-45. doi: 10.1111/j.1699-0463.1978.tb00037.x.

Abstract

Preparations of the polymorphonuclear leukocyte (PMN) chemotactic factor isolated from lipopolysaccharide (LPS)-induced inflammatory exudate in rabbits were immunogenic in guinea pigs. Complete fusion of the precipitation lines produced against anti-CF by LPS-CF (molecular weigth 16,000) and material eluted on Sephadex G-200 columns with molecular weights (MW) of 68,000, 16,000 and 7,000 was found. Also, the chemotactically active material with MW of 68,000 and 7,000 eluted on G-75 columns after fractionation of the fraction of MW 16,000 from the G-200 eluate was antigenically identical to LPS-CF in double diffusion in agar. Normal rabbit serum (NRS) incubated with LPS, LPS-induced wound chamber exudate and NRS alone gave lines of precipitation against the anti-LPS-CF sera identical to that of LPS-CF. The capacity of LPS-CF to attract PMNs was significantly higher than that of LPS, and a peak in the number of PMNs in the exudate of wound chambers implanted in rabbits was found 4 h after the local injection of LPS-CF. When injected intraperitoneally in C5 deficient mice, LPS-CF stimulated a PMN migration which was only slightly below that in C5 normal mice. Antisera to LPS-CF inhibited the chemotactic activity of LPS-CF as well as that of LPS-NRS when the supernatants were tested using the Boyden's technique. Also, preincubation of PMNs with LPS-CF suppressed the migration towards a chemotactic gradient of LPS-CF molecules of these PMNs.

摘要

从兔脂多糖(LPS)诱导的炎性渗出物中分离出的多形核白细胞(PMN)趋化因子制剂在豚鼠中具有免疫原性。发现由LPS - CF(分子量16,000)产生的抗CF沉淀线与在Sephadex G - 200柱上洗脱的分子量为68,000、16,000和7,000的物质完全融合。此外,在从G - 200洗脱液中分离出分子量为16,000的级分后,在G - 75柱上洗脱的分子量为68,000和7,000的趋化活性物质在琼脂双向扩散中与LPS - CF抗原性相同。用LPS、LPS诱导的伤口腔渗出液和单独的正常兔血清(NRS)孵育后,针对抗LPS - CF血清产生的沉淀线与LPS - CF的沉淀线相同。LPS - CF吸引PMN的能力明显高于LPS,并且在兔局部注射LPS - CF后4小时,在植入的伤口腔渗出物中发现PMN数量达到峰值。当在C5缺陷小鼠中腹腔注射时,LPS - CF刺激PMN迁移,其迁移率仅略低于C5正常小鼠。当使用博伊登技术检测上清液时,抗LPS - CF血清抑制LPS - CF以及LPS - NRS的趋化活性。此外,用LPS - CF预孵育PMN可抑制这些PMN向LPS - CF分子趋化梯度的迁移。

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