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在体外,磷脂酶在人α-淋巴细胞毒素导致细胞破坏的过程中被激活。

Phospholipases are activated during cell destruction by human alpha-lymphotoxin in vitro.

作者信息

Fitzgerald M T, Longmuir K J, Granger G A

机构信息

Department of Molecular Biology and Biochemistry, College of Medicine, University of California, Irvine 92717.

出版信息

Lymphokine Res. 1987 Fall;6(4):319-24.

PMID:3501507
Abstract

These studies investigate the molecular mechanism of destruction of transformed cells induced by recombinant human alpha-lymphotoxin (LT) in vitro. They focus on steps subsequent to binding of LT to specific plasma membrane receptors. L929 cell membrane phospholipids were prelabelled with 14C arachidonic acid and then the cells were treated with lethal levels of LT. We found 14C labelled fatty acids were released into the media soon after LT treatment and levels continued to climb as cells were destroyed. At various time intervals lipid extracts of these same cell cultures were made and separated by thin layer chromatography. Autoradiography revealed that LT-treated cells contain increased levels of free fatty acids first detectable at 4-6 hrs after LT treatment and the levels continued to rise through 21 hrs. Untreated cultures and cultures killed by alternate methods did not show elevated free fatty acid levels in either the media or intracellularly. These results indicate that cellular phospholipases are activated when LT-induced cell destruction occurs and that this activation does not occur when cells are killed by various other methods.

摘要

这些研究调查了重组人α-淋巴毒素(LT)在体外诱导转化细胞破坏的分子机制。它们聚焦于LT与特定质膜受体结合后的步骤。用14C花生四烯酸对L929细胞膜磷脂进行预标记,然后用致死剂量的LT处理细胞。我们发现LT处理后不久,14C标记的脂肪酸就释放到培养基中,并且随着细胞被破坏,其水平持续上升。在不同时间间隔对这些相同细胞培养物进行脂质提取,并通过薄层色谱法进行分离。放射自显影显示,经LT处理的细胞中游离脂肪酸水平升高,在LT处理后4 - 6小时首次可检测到,并且该水平在21小时内持续上升。未处理的培养物以及通过其他方法杀死的培养物在培养基或细胞内均未显示游离脂肪酸水平升高。这些结果表明,当LT诱导细胞破坏发生时,细胞磷脂酶被激活,而当细胞通过其他各种方法被杀死时,这种激活不会发生。

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