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内毒素抑制人牙龈成纤维细胞附着于I型胶原的机制。

Mechanism of endotoxin inhibition of human gingival fibroblast attachment to type I collagen.

作者信息

Pitaru S, Madgar D, Metzger Z, Hekmati H

机构信息

Department of Oral Biology, Maurice and Gabriela Goldschleger School of Dental Medicine, Tel Aviv University, Israel.

出版信息

J Dent Res. 1990 Sep;69(9):1602-6. doi: 10.1177/00220345900690091301.

Abstract

Bacterial endotoxin inhibits the attachment of human gingival fibroblasts to collagen. The present study attempted to elucidate the possible mechanism of this inhibition. Two mechanisms were considered: direct toxicity to the cells and steric interference. Collagen substrates were prepared by rat type I collagen being air-dried in the wells of 24 multi-well plates. Experimental collagen substrates were treated with 50 micrograms of endotoxin/well, while untreated collagen substrates served as controls. Two mL of cell suspension (10(4) cells/mL) was added to each well, and these were incubated at 37 degrees C for two h. The average cell number/mm2 attached to experimental and control substrates was determined. Cell attachment to endotoxin-treated collagen was inhibited by 78%, compared with that to untreated collagen. The washing of the endotoxin-treated collagen for two h did not affect the inhibition of cell attachment, whereas after 24 h of washing, cell attachment was inhibited by 54%, compared with that to untreated collagen. Pre-incubation of the cells in endotoxin for two h did not affect their attachment to collagen. The addition of fetal calf serum (15%) to the experimental system completely reversed the inhibition of fibroblast attachment to endotoxin-treated collagen. These findings suggest that endotoxin interferes with fibroblast attachment to collagen through a steric phenomenon, possibly by blocking the binding sites on the collagen molecule recognized by the membrane receptor for collagen.

摘要

细菌内毒素可抑制人牙龈成纤维细胞与胶原蛋白的附着。本研究试图阐明这种抑制作用的可能机制。考虑了两种机制:对细胞的直接毒性和空间干扰。通过将大鼠I型胶原蛋白在24孔板的孔中空气干燥来制备胶原蛋白底物。实验性胶原蛋白底物用50微克内毒素/孔处理,未处理的胶原蛋白底物用作对照。向每个孔中加入2毫升细胞悬液(10⁴个细胞/毫升),并在37℃下孵育2小时。测定附着在实验性和对照底物上的平均细胞数/平方毫米。与未处理的胶原蛋白相比,附着在内毒素处理的胶原蛋白上的细胞受到78%的抑制。对内毒素处理的胶原蛋白洗涤2小时不影响细胞附着的抑制作用,而洗涤24小时后,与未处理的胶原蛋白相比,细胞附着受到54%的抑制。将细胞在内毒素中预孵育2小时不影响其与胶原蛋白的附着。向实验系统中加入胎牛血清(15%)可完全逆转成纤维细胞附着在内毒素处理的胶原蛋白上的抑制作用。这些发现表明,内毒素通过空间现象干扰成纤维细胞与胶原蛋白的附着,可能是通过阻断胶原蛋白分子上被胶原蛋白膜受体识别的结合位点。

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