Protein corona and exosomes: new challenges and prospects

被引:53
|
作者
Heidarzadeh, Morteza [1 ]
Zarebkohan, Amir [2 ]
Rahbarghazi, Reza [3 ,4 ]
Sokullu, Emel [1 ,5 ]
机构
[1] Koc Univ, Koc Univ Res Ctr Translat Med KUTTAM, Sch Med, Istanbul, Turkiye
[2] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Nanotechnol, Tabriz, Iran
[3] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Appl Cell Sci, Tabriz, Iran
[4] Tabriz Univ Med Sci, Stem Cell Res Ctr, Tabriz, Iran
[5] Koc Univ, Biophys Dept, Sch Med, TR-34450 Istanbul, Turkiye
关键词
Exosomes; Protein corona; Physicochemical properties; Biodistribution; ANTI-PEG IGM; HUMAN SERUM-ALBUMIN; WALL SHEAR-STRESS; BIOMOLECULAR CORONA; BLOOD CLEARANCE; HUMAN AORTA; IN-VIVO; NANOPARTICLES; LIPOSOMES; BINDING;
D O I
10.1186/s12964-023-01089-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent advances in extracellular vesicle (EVs) detection and isolation methods have led to the development of novel therapeutic modalities. Among different types of EVs, exosomes (Exos) can transfer different signaling biomolecules and exhibit several superior features compared to whole-cell-based therapies. Therapeutic factors are normally loaded into the Exo lumen or attached to their surface for improving the on-target delivery rate and regenerative outcomes. Despite these advantages, there are several limitations in the application of Exos in in vivo conditions. It was suggested that a set of proteins and other biological compounds are adsorbed around Exos in aqueous phases and constitute an external layer named protein corona (PC). Studies have shown that PC can affect the physicochemical properties of synthetic and natural nanoparticles (NPs) after introduction in biofluids. Likewise, PC is generated around EVs, especially Exos in in vivo conditions. This review article is a preliminary attempt to address the interfering effects of PC on Exo bioactivity and therapeutic effects.
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收藏
页数:15
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