RRC ID 54103
著者 Emam SE, Ando H, Lila ASA, Shimizu T, Okuhira K, Ishima Y, Mahdy MA, Ghazy FS, Sagawa I, Ishida T.
タイトル Liposome co-incubation with cancer cells secreted exosomes (extracellular vesicles) with different proteins expressions and different uptake pathways.
ジャーナル Sci Rep
Abstract We recently showed that in vitro incubation of cells with liposomes of varying compositions can increase exosome secretion and increase the yield of harvested exosomes (extracellular vesicles, EVs). This might foster their potential therapeutic implementations. In the current study, we investigated the surface proteins and the uptake of the harvested exosomes (EVs) to see if the incubation of cells with liposomes would change the biological properties of these exosomes (EVs). Interestingly, exosomes (EVs) induced by solid cationic liposomes lacked some major exosome marker proteins such as CD9, flotillin-1, annexin-A2 and EGF, and subsequently had lower levels of cellular uptake upon re-incubation with donor cancer cells. However, exosomes (EVs) induced under normal condition and by fluid cationic liposomes, displayed the entire spectrum of proteins, and exhibited higher uptake by the donor cancer cells. Although endocytosis was the major uptake pathway of exosomes (EVs) by tumor cells, endocytosis could occur via more than one mechanism. Higher exosome uptake was observed in donor B16BL6 cells than in allogeneic C26 cells, indicating that donor cells might interact specifically with their exosomes (EVs) and avidly internalize them. Taken together, these results suggest a technique for controlling the characteristics of secreted exosomes (EVs) by incubating donor cancer cells with liposomes of varying physiochemical properties.
巻・号 8(1)
ページ 14493
公開日 2018-9-27
DOI 10.1038/s41598-018-32861-w
PII 10.1038/s41598-018-32861-w
PMID 30262875
PMC PMC6160473
MeSH Animals Cell Line, Tumor Endocytosis* Exosomes / metabolism* Gene Expression Regulation, Neoplastic* Liposomes Melanoma, Experimental / metabolism* Melanoma, Experimental / pathology Mice Neoplasm Proteins / metabolism*
IF 3.998
引用数 6
リソース情報
ヒト・動物細胞 B16/BL6(RCB2638)