DSPE-PEG-Biotin對(duì)循環(huán)中小細(xì)胞外囊泡的直接標(biāo)記

鏈接：https://xueshu.baidu.com/usercenter/paper/show?paperid=111h0820k42y0re09m0a06a0rh159218&site=xueshu_se

作者：Yu, Zi-Li |  Zhao, Yi |  Miao, Fan |  Wu, Min |  Xia, Hou-Fu |  Chen, Zhuo-Kun |  Liu, Hai-Ming |  Zhao, Yi-Fang |  Chen, Gang

Circulating small extracellular vesicles (sEVs) are naturally occurring nanosized membrane vesicles that convey bioactive molecules between cells. Conventionally, to evaluate their behaviors in vivo, circulating sEVs have to be isolated from the bloodstream, then labeled with imaging materials in vitro, and finally injected back into the circulation of animals for subsequent detection. The tedious isolation-labeling-reinfusion procedures might have an undesirable influence on the natural properties of circulating sEVs, thereby changing their behaviors and the detected kinetics in vivo. Herein, we proposed an in situ biotinylation strategy to directly label circulating sEVs with intravenously injected DSPE-PEG-Biotin, aiming to evaluate the in vivo kinetics of circulating sEVs more biofriendly and accurately. Such an analysis strategy is free of isolation-labeling- reinfusion procedures and has no unfavorable influence on the natural behaviors of sEVs. The results showed that the lifetime of generic circulating sEVs in mice was around 3 days. Furthermore, w; for the first time, revealed the distinct in vivo kinetics of circulating sEV subpopulations with different cell sources, among which erythrocyte-derived sEVs showed the longest lifespan. Moreover, compared with circulating sEVs in situ or used as autograft, circulating sEVs used as allograft had the shortest lifetime. In addition, the in situ biotinylation strategy also provides a way for the enrichment of biotinylated circulating sEVs. In summary, this study provides a novel strategy for in situ labeling of circulating sEVs, which would facilitate the accurate characterization of their kinetics in vivo, thereby accelerating their future application as biomarkers and theranositic vectors.   

譯文：

循環(huán)小細(xì)胞外囊泡（sEVs）是天然存在的納米級(jí)膜囊泡，在細(xì)胞之間傳遞生物活性分子。傳統(tǒng)上，為了評(píng)估它們?cè)隗w內(nèi)的行為，循環(huán)的sEV必須從血液中分離出來(lái)，然后在體外用成像材料標(biāo)記，最后注射回動(dòng)物的循環(huán)中進(jìn)行后續(xù)檢測(cè)。繁瑣的分離標(biāo)記再融合程序可能會(huì)對(duì)循環(huán)sEV的自然性質(zhì)產(chǎn)生不利影響，從而改變它們的行為和體內(nèi)檢測(cè)到的動(dòng)力學(xué)。在此，我們提出了一種原位生物素化策略，用靜脈注射的DSPE-PEG生物素直接標(biāo)記循環(huán)sEV，旨在更生物友好和準(zhǔn)確地評(píng)估循環(huán)sEV的體內(nèi)動(dòng)力學(xué)。這種分析策略沒(méi)有隔離標(biāo)記-再融合程序，對(duì)sEV的自然行為沒(méi)有不利影響。結(jié)果顯示，小鼠中通用循環(huán)sEV的壽命約為3天。此外，w；首次揭示了不同細(xì)胞來(lái)源的循環(huán)sEV亞群的不同體內(nèi)動(dòng)力學(xué)，其中紅細(xì)胞來(lái)源的sEV壽命最長(zhǎng)。此外，與原位循環(huán)sEVs或用作自體移植相比，用作同種異體移植的循環(huán)sEVs的壽命最短。此外，原位生物素化策略還為生物素化循環(huán)sEVs的富集提供了一種方法�？傊�，本研究為循環(huán)sEV的原位標(biāo)記提供了一種新策略，這將有助于準(zhǔn)確表征其體內(nèi)動(dòng)力學(xué)，從而加速其作為生物標(biāo)志物和*載體的未來(lái)應(yīng)用。   

DOI：10.1021/acs.analchem.1c01176

西安pg電子官方生物提供相關(guān)產(chǎn)品：

m-PEG-DSPE

m-PEG8-DSPE

m-PEG8-DSPE

m-PEG12-DSPE

m-PEG24-DSPE

mPEG-CLS

mPEG-DEPE

mPEG-DLPE

mPEG-DMPE

mPEG-DOPE

mPEG-DPPE

mPEG-DSPE

mPEG-DSPE CAS No.: 147867-65-0

mPEG-DSPE(ammonium salt)

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