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- W3043462158 abstract "Abstract Macrophages are a major immune cell type infiltrating tumors and promoting tumor growth and metastasis. To elucidate the mechanism of macrophage recruitment, we utilize an overgrowth tumor model (“undead” model) in larval Drosophila imaginal discs that are attached by numerous macrophages. Here we report that changes to the microenvironment of the overgrown tissue are important for recruiting macrophages. First, we describe a correlation between generation of reactive oxygen species (ROS) and damage of the basement membrane (BM) in all neoplastic, but not hyperplastic, models examined. ROS and the stress kinase JNK mediate the accumulation of matrix metalloproteinase 2 (Mmp2), damaging the BM, which recruits macrophages to the tissue. We propose a model where macrophage recruitment to and activation at overgrowing tissue is a multi-step process requiring ROS- and JNK-mediated Mmp2 upregulation and BM damage. These findings have implications for understanding the role of the tumor microenvironment for macrophage activation." @default.
- W3043462158 created "2020-07-23" @default.
- W3043462158 creator A5027733318 @default.
- W3043462158 creator A5052696262 @default.
- W3043462158 date "2020-07-20" @default.
- W3043462158 modified "2023-10-14" @default.
- W3043462158 title "Basement membrane damage by ROS- and JNK-mediated Mmp2 activation drives macrophage recruitment to overgrown tissue" @default.
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- W3043462158 doi "https://doi.org/10.1038/s41467-020-17399-8" @default.
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