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用于细胞体外和体内条码化的荧光聚合物纳米颗粒。

Fluorescent Polymer Nanoparticles for Cell Barcoding In Vitro and In Vivo.

机构信息

Laboratoire de Biophotonique et Pharmacologie, UMR 7213 CNRS, Faculté de Pharmacie, Université de Strasbourg, 74, Route du Rhin, BP 60024, 67401, Illkirch, France.

MN3T, Inserm U1109, LabEx Medalis, Fédération de Médecine Translationnelle de Strasbourg (FMTS), Université de Strasbourg, Strasbourg, 67000, France.

出版信息

Small. 2017 Oct;13(38). doi: 10.1002/smll.201701582. Epub 2017 Aug 9.

DOI:10.1002/smll.201701582
PMID:28791769
Abstract

Fluorescent polymer nanoparticles for long-term labeling and tracking of living cells with any desired color code are developed. They are built from biodegradable poly(lactic-co-glycolic acid) polymer loaded with cyanine dyes (DiO, DiI, and DiD) with the help of bulky fluorinated counterions, which minimize aggregation-caused quenching. At the single particle level, these particles are ≈20-fold brighter than quantum dots of similar color. Due to their identical 40 nm size and surface properties, these nanoparticles are endocytosed equally well by living cells. Mixing nanoparticles of three colors in different proportions generates a homogeneous RGB (red, green, and blue) barcode in cells, which is transmitted through many cell generations. Cell barcoding is validated on 7 cell lines (HeLa, KB, embryonic kidney (293T), Chinese hamster ovary, rat basophilic leucemia, U97, and D2A1), 13 color codes, and it enables simultaneous tracking of co-cultured barcoded cell populations for >2 weeks. It is also applied to studying competition among drug-treated cell populations. This technology enabled six-color imaging in vivo for (1) tracking xenografted cancer cells and (2) monitoring morphogenesis after microinjection in zebrafish embryos. In addition to a robust method of multicolor cell labeling and tracking, this work suggests that multiple functions can be co-localized inside cells by combining structurally close nanoparticles carrying different functions.

摘要

研究开发了用于对活细胞进行长期标记和追踪的具有任意所需颜色编码的荧光聚合物纳米粒子。它们由可生物降解的聚(乳酸-共-乙醇酸)聚合物构建而成,聚合物中负载有菁染料(DiO、DiI 和 DiD),并借助大体积氟化抗衡离子的帮助,这些抗衡离子最小化了聚集引起的淬灭。在单个粒子水平上,这些粒子的亮度比类似颜色的量子点高约 20 倍。由于它们具有相同的 40nm 尺寸和表面性质,这些纳米粒子被活细胞同等程度地内吞。将三种颜色的纳米粒子以不同的比例混合,在细胞中生成均匀的 RGB(红、绿、蓝)条码,该条码可以通过多个细胞世代传递。细胞条码化在 7 种细胞系(HeLa、KB、胚胎肾(293T)、中国仓鼠卵巢、大鼠嗜碱性白血病、U97 和 D2A1)、13 种颜色编码上进行了验证,并能同时追踪共培养的条码化细胞群超过 2 周。它还应用于研究经药物处理的细胞群之间的竞争。该技术实现了体内六色成像,用于(1)追踪异种移植的癌细胞,(2)监测斑马鱼胚胎中微注射后的形态发生。除了用于多色细胞标记和追踪的稳健方法外,这项工作还表明,通过组合携带不同功能的结构上接近的纳米粒子,可以将多个功能共定位在细胞内。

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