Dual Roles of Extracellular Histone H3 in Host Defense: Its Differential Regions Responsible for Antimicrobial and Cytotoxic Properties and Their Modes of Action

被引:5
作者
Tanaka, Yuri [1 ]
Yamanaka, Nanako [1 ]
Koyano, Izumi [1 ]
Hasunuma, Itaru [1 ]
Kobayashi, Tetsuya [2 ]
Kikuyama, Sakae [3 ]
Iwamuro, Shawichi [1 ]
机构
[1] Toho Univ, Fac Sci, Dept Biol, Chiba 2748510, Japan
[2] Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Saitama 3388570, Japan
[3] Waseda Univ, Fac Educ & Integrated Arts & Sci, Ctr Adv Biomed Sci, Dept Biol, Tokyo 1628480, Japan
来源
ANTIBIOTICS-BASEL | 2022年 / 11卷 / 09期
关键词
histone H3; antimicrobial activity; cytotoxicity; cell membrane destruction; ELEBA; LYSINE-RICH HISTONES; PROTEINS; MEDIATORS; PEPTIDES; DNA; DEATH; H2A; H1;
D O I
10.3390/antibiotics11091240
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Extracellular histones play a dual role-antimicrobial and cytotoxic-in host defense. In this study, we evaluated the antimicrobial and cytotoxic activities of histone H3 and identified the responsible molecular regions for these properties. Broth microdilution assays indicated that histone H3 exhibits growth inhibitory activity against not only Gram-negative and -positive bacteria but also fungi. Observations under scanning electron microscopy (SEM) revealed that histone H3 induced morphological abnormalities on the cell surface of a wide range of reference pathogens. MTT assays and SEM observations indicated that histone H3 has strong cytotoxic and cell lytic effects on mammalian normal, immortal, and tumor cell lines. Assays using synthetic peptides corresponding to fragments 1-34 (H3DP1), 35-68 (H3DP2), 69-102 (H3DP3), and 103-135 (H3DP4) of histone H3 molecule demonstrated that its antimicrobial activity and cytotoxicity are elicited by the H3DP2 and H3DP3 protein regions, respectively. Enzyme-linked endotoxin binding assays indicated that histones H3 and H3DP1, H3DP2, and H3DP4, but not H3DP3, exhibited high affinities toward lipopolysaccharide and lipoteichoic acid. Our findings are expected to contribute to the development of new histone H3-based peptide antibiotics that are not cytotoxic.
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页数:14
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