Tetraspanin heterogeneity of small extracellular vesicles in human biofluids and brain tissue

被引:15
作者
Okada-Tsuchioka, Mami [1 ]
Kajitani, Naoto [1 ,2 ]
Omori, Wataru [1 ,3 ]
Kurashige, Takashi [4 ]
Boku, Shuken [2 ]
Takebayashi, Minoru [1 ,2 ]
机构
[1] Natl Hosp Org Kure Med Ctr & Chugoku, Inst Clin Res, Canc Ctr, Div Psychiat & Neurosci, 3-1 Aoyama, Kure 7370023, Japan
[2] Kumamoto Univ, Fac Life Sci, Dept Neuropsychiat, 1-1-1 Honjo,Chuo Ku, Kumamoto 8608556, Japan
[3] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Psychiat & Neurosci, 1-2-3 Kasumi,Minami Ku, Hiroshima 7348551, Japan
[4] Natl Hosp Org Kure Med Ctr & Chugoku, Canc Ctr, Dept Neurol, 3-1 Aoyama, Kure 7370023, Japan
基金
日本学术振兴会;
关键词
sEV; Tetraspanin; Brain; Biofluids; Heterogeneity; EXOSOMES; PROTEIN; CELL;
D O I
10.1016/j.bbrc.2022.08.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extracellular vesicles (EVs) are particles released from most cell types delimited by a lipid bilayer. Small EVs (sEVs) are nanosized (<200 nm) and include exosomes. Brain-derived sEVs may provide a source for new biomarkers of brain status. CD9, CD63, and CD81 are major members of the tetraspanin family frequently used as sEV markers. However, according to a recent report, tetraspanins were not equally expressed in all sEVs, but rather show heterogeneity that reflects the expression levels in their secretory cells. We therefore investigated tetraspanin heterogeneity of sEVs in biofluids commonly used for clinical laboratory tests, and those in the brain. Expression levels and distributions of CD9, CD63 and CD81 on sEVs were determined in serum, plasma, and cerebrospinal fluid (CSF) samples collected from each healthy donor, and in post-mortem brain tissue samples. We found heterogeneous mixes of sEVs with various tetraspanin combinations among sEVs, and the predominant types and heterogeneous patterns of tetraspanins were specific to sample type. Hierarchical clustering revealed that brain sEVs were similar to those in the CSF, but different from those in peripheral blood. Our findings both provide basic information and contribute to the development of biomarkers for neurological and psychiatric disorders.(c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:146 / 151
页数:6
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