基质金属蛋白酶
分子生物学
污渍
基质凝胶
生物
细胞外基质
酶谱
明胶酶A
细胞生物学
细胞
生物化学
基因
作者
Myoung Hee Kim,Richard P. Kitson,Per Albertsson,Ulf Nannmark,Per Basse,Peter J.K. Kuppen,Marianne Hokland,Ronald H. Goldfarb
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2000-06-01
卷期号:164 (11): 5883-5889
被引量:68
标识
DOI:10.4049/jimmunol.164.11.5883
摘要
Abstract We have previously documented that rat IL-2-activated NK (A-NK) cells produce matrix metalloproteinase-2 (MMP-2) and MMP-9. In this study, we describe mouse A-NK cell-derived MMPs, including MT-MMPs, and also TIMPs. RT-PCR analysis from cDNA of mouse A-NK cells revealed mRNA for MMP-2, MMP-9, MMP-11, MMP-13, MT1-MMP, MT2-MMP, TIMP-1, and TIMP-2. MMP-2 and MMP-9 expression was confirmed by gelatin zymography. Moreover, we report for the first time that MT-MMPs are expressed by NK cells, i.e., large granular lymphocytes as determined by both RT-PCR and Western blots. TIMP-1 expression was detected as a 29-kDa protein in Western blots. It is intriguing that TIMP-2 protein from A-NK cells was also detected as a 29-kDa protein, which is clearly different from the previously reported molecular mass of 21 kDa in mouse and human cells. In addition, inhibition of MMPs by BB-94, a selective inhibitor of MMP, significantly inhibited the ability of mouse A-NK cells to migrate through Matrigel, a model basement membrane. Taken together, these findings suggest that A-NK cells may therefore use multiple MMPs in various cellular functions, including degradation of various extracellular matrix molecules as they extravasate from blood vessels and accumulate within cancer metastases following their adoptive transfer.
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