Phosphatidylserine-deficient small extracellular vesicle is a major somatic cell-derived sEV subpopulation in blood

被引:25
作者
Matsumoto, Akihiro [1 ]
Takahashi, Yuki [1 ]
Ogata, Kosuke [2 ]
Kitamura, Shimpei [1 ]
Nakagawa, Naoki [1 ]
Yamamoto, Aki [1 ]
Ishihama, Yasushi [2 ]
Takakura, Yoshinobu [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Biopharmaceut & Drug Metab, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Mol & Cellular BioAnal, Kyoto 6068501, Japan
基金
日本学术振兴会;
关键词
EXOSOMES; DELIVERY; LIPIDOMICS; PHENOTYPE; PLATFORM;
D O I
10.1016/j.isci.2021.102839
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Small extracellular vesicles (sEVs) are important mediators of intercellular communication with respect to diverse pathophysiological processes. Here, we determined novel phosphatidylserine (PS)-deficient sEV subpopulations as a major somatic cell-derived sEV subpopulation in blood because of long blood circulation half-life through escape from macrophage uptake. PS(-)-sEVs were identified in various cultured cells as aminor population. However, as a result of rapid uptake of PS(+)-sEVs by macrophages, circulating somatic cell-derived sEVs in the blood were found to be mainly PS(-)-sEVs. These results suggest that endogenous PS(-)-sEVs could indeed be the key player in sEV-mediated intercellular communication, a good target for sEV-based diagnosis, and a potent candidate for sEV-based drug delivery. Our findings bring a paradigm shift in the understanding of the biology and translational applications of sEVs.
引用
收藏
页数:19
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