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• W4214595685 abstract "My research area in the pharmaceutical industry is innate immunity, especially in phagocytic cells. First, I studied the heat-stable growth factor of peripheral macrophages in tumorous ascitic fluid and found that lipoproteins are an influencing factor. Later, my colleagues and I found that lipid-containing substances, namely, oxidized low-density lipoprotein, dead neutrophils, or purified lipids that could be scavenged by macrophages, induce their growth. From the series of this study, I concluded that phagocytic substances induce macrophage growth by autocrine stimulation of granulocyte-macrophage colony-stimulating factor (GM-CSF). During the study, we found that neutrophils have growth-inhibitory effects against a variety of cells. Then, I elucidated that the primary factor is a zinc-binding protein, calprotectin, an abundant protein complex in the neutrophil cytosol. I found that calprotectin induces apoptosis in many cell types, including tumor cells and normal fibroblasts, and that the zinc-binding capacity is essential for its activity. Microscopic observations revealed that neutrophil extract contains factor-inducing three-dimensional cell aggregation of human mammary carcinoma, MCF-7. I elucidated that cathepsin G is responsible for this activity and that its effect is dependent on the activation of insulin-like growth factor-1. I believe that this modest, albeit novel, observation was crucial to my thirty-nine-year-long career researching phagocytic cells." @default.
• W4214595685 created "2022-03-02" @default.
• W4214595685 creator A5076538361 @default.
• W4214595685 date "2022-03-01" @default.
• W4214595685 modified "2023-09-26" @default.
• W4214595685 title "Unintended Observations Leading to Macrophage Growth and Neutrophil Factor Research" @default.
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• W4214595685 doi "https://doi.org/10.1248/yakushi.21-00191" @default.
• W4214595685 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35228378" @default.
• W4214595685 hasPublicationYear "2022" @default.
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