ADAM17介导肿瘤坏死因子- α和l -选择素从白细胞膜脱落,而ADAM10不介导。

T. Condon, S. Flournoy, Glenn J. Sawyer, B. Baker, T. Kishimoto, C. Bennett
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引用次数: 79

摘要

不同的实验室已经证明,肿瘤坏死因子- α (tnf - α)从细胞膜释放是由一种崩解素和金属蛋白酶ADAM10或ADAM17控制的。相比之下,只有ADAM17被证明参与了l -选择素的脱落。为了确定ADAM10和ADAM17在tnf - α和l -选择素脱落过程中的具体作用,我们鉴定了针对ADAM10和ADAM17的反义寡核苷酸(ASO)。我们发现ISIS 16337和ISIS 100750在Jurkat和THP-1细胞中以序列特异性和剂量依赖性的方式减少ADAM17 mRNA和ADAM10 mRNA。ADAM17 ASO (ISIS 16337)抑制THP-1细胞中tnf - α的分泌和Jurkat细胞中l -选择素的分泌,而ADAM10 ASO (ISIS 100750)对这两种蛋白的释放均无显著抑制作用。这些结果表明ADAM17是参与l -选择素脱落和tnf - α加工的主要金属蛋白酶之一。ADAM10在Jurkat和THP-1细胞中的生物学底物仍有待阐明。
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ADAM17 but not ADAM10 mediates tumor necrosis factor-alpha and L-selectin shedding from leukocyte membranes.
The release of tumor necrosis factor-alpha (TNF-alpha) from cellular membranes has been shown by different laboratories to be controlled by a disintegrin and metalloprotease, ADAM10 or ADAM17. In contrast, only ADAM17 has shown to be involved in L-selectin shedding. To determine the specific roles of ADAM10 and ADAM17 in the processing of TNF-alpha and L-selectin shedding, antisense oligonucleotides (ASO) targeting both ADAM10 and ADAM17 were identified. We show that ISIS 16337 reduces ADAM17 mRNA and ISIS 100750 reduces ADAM10 mRNA in a sequence-specific and dose-dependent manner in both Jurkat and THP-1 cells. The ADAM17 ASO (ISIS 16337) inhibited both TNF-alpha secretion in THP-1 cells and L-selectin shedding in Jurkat cells, whereas the ADAM10 ASO (ISIS 100750) did not significantly inhibit release of either protein. These results suggest that ADAM17 is one of the major metalloproteases involved in L-selectin shedding as well as TNF-alpha processing. The biologic substrates for ADAM10 in Jurkat and THP-1 cells remain to be elucidated.
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