TY - JOUR
T1 - Toward a human brain extracellular vesicle atlas
T2 - Characteristics of extracellular vesicles from different brain regions, including small RNA and protein profiles
AU - Huang, Yiyao
AU - Arab, Tanina
AU - Russell, Ashley E.
AU - Mallick, Emily R.
AU - Nagaraj, Rajini
AU - Gizzie, Evan
AU - Redding-Ochoa, Javier
AU - Troncoso, Juan C.
AU - Pletnikova, Olga
AU - Turchinovich, Andrey
AU - Routenberg, David A.
AU - Witwer, Kenneth W.
N1 - Publisher Copyright:
© 2023 The Authors. Interdisciplinary Medicine published by Wiley-VCH GmbH on behalf of Nanfang Hospital, Southern Medical University.
PY - 2023/10
Y1 - 2023/10
N2 - Extracellular vesicles (EVs) are released from different cell types in the central nervous system (CNS) and play roles in regulating physiological and pathological functions. Although brain-derived EVs (bdEVs) have been successfully collected from brain tissue, there is not yet a “bdEV Atlas” of EVs from different brain regions. To address this gap, we separated EVs from eight anatomical brain regions of a single individual and subsequently characterized them by count, size, morphology, and protein and RNA content. The greatest particle yield was from cerebellum, while the fewest particles were recovered from the orbitofrontal, postcentral gyrus, and thalamus regions. EV surface phenotyping indicated that CD81 and CD9 were more abundant than CD63 in all regions. Cell-enriched surface markers varied between brain regions. For example, putative neuronal markers NCAM, CD271, and NRCAM were more abundant in medulla, cerebellum, and occipital regions, respectively. These findings, while restricted to tissues from a single individual, suggest that additional studies are warranted to provide more insight into the links between EV heterogeneity and function in the CNS.
AB - Extracellular vesicles (EVs) are released from different cell types in the central nervous system (CNS) and play roles in regulating physiological and pathological functions. Although brain-derived EVs (bdEVs) have been successfully collected from brain tissue, there is not yet a “bdEV Atlas” of EVs from different brain regions. To address this gap, we separated EVs from eight anatomical brain regions of a single individual and subsequently characterized them by count, size, morphology, and protein and RNA content. The greatest particle yield was from cerebellum, while the fewest particles were recovered from the orbitofrontal, postcentral gyrus, and thalamus regions. EV surface phenotyping indicated that CD81 and CD9 were more abundant than CD63 in all regions. Cell-enriched surface markers varied between brain regions. For example, putative neuronal markers NCAM, CD271, and NRCAM were more abundant in medulla, cerebellum, and occipital regions, respectively. These findings, while restricted to tissues from a single individual, suggest that additional studies are warranted to provide more insight into the links between EV heterogeneity and function in the CNS.
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U2 - 10.1002/INMD.20230016
DO - 10.1002/INMD.20230016
M3 - Article
AN - SCOPUS:85190143105
SN - 2832-6237
VL - 1
JO - Interdisciplinary Medicine
JF - Interdisciplinary Medicine
IS - 4
M1 - e20230016
ER -