背景介紹：

在生理學(xué)的廣泛背景下，進(jìn)行體內(nèi)巨噬細(xì)胞特異性去除的能力仍然是一種有效的手段，可以揭示巨噬細(xì)胞的功能。與小鼠模型相比，斑馬魚提供了更方便的成像能力，因?yàn)樗鼈儚膯渭?xì)胞階段到整個(gè)幼蟲發(fā)育過(guò)程中都具有光學(xué)透明性。這些特性對(duì)于進(jìn)行體內(nèi)細(xì)胞特異性去除變得非常重要，以便能夠?qū)崟r(shí)跟蹤和驗(yàn)證目標(biāo)細(xì)胞的消除。斑馬魚中去除巨噬細(xì)胞的方法有多種，包括基因去除（例如irf8敲除）、化學(xué)遺傳學(xué)（例如硝基還原酶/甲硝唑系統(tǒng)）和基于毒素的去除（例如使用荷蘭Liposoma的氯膦酸鹽二鈉脂質(zhì)體Clodronateliposomes）。使用氯膦酸鹽二鈉脂質(zhì)體Clodronateliposomes來(lái)誘導(dǎo)吞噬脂質(zhì)體后巨噬細(xì)胞凋亡在去除巨噬細(xì)胞以及測(cè)試它們的吞噬能力方面都是有效的。在這里，我們描述了一種通過(guò)靜脈注射含熒光右旋糖酐的氯膦酸鹽二鈉脂質(zhì)體Clodronateliposomes系統(tǒng)性去除斑馬魚幼蟲巨噬細(xì)胞的詳細(xì)方案。與熒光右旋糖酐的共同注射允許實(shí)時(shí)跟蹤巨噬細(xì)胞的去除，從驗(yàn)證成功的靜脈注射到巨噬細(xì)胞對(duì)分子攝取及其最終死亡。為了驗(yàn)證巨噬細(xì)胞高程度的去除，可以通過(guò)在早期幼蟲階段進(jìn)行氯膦酸鹽二鈉脂質(zhì)體Clodronateliposomes注射時(shí)快速的中性紅活染料染色來(lái)確定腦部巨噬細(xì)胞（小膠質(zhì)細(xì)胞）的消除程度。

Background：

The ability to conduct in vivo macrophage-specific depletion remains an effective means to uncover functions of macrophages in a wide range of physiological contexts. Compared to the murine model, zebrafish offer superior imaging capabilities due to their optical transparency starting from a single-cell stage to throughout larval development. These qualities become important for in vivo cell specific depletions so that the elimination of the targeted cells can be tracked and validated in real time through microscopy. Multiple methods to deplete macrophages in zebrafish are available, including genetic (such as an irf8 knockout), chemogenetic (such as the nitroreductase/metronidazole system), and toxin-based depletions (such as using clodronate liposomes). The use of clodronate-containing liposomes to induce macrophage apoptosis after phagocytosing the liposomes is effective in depleting macrophages as well as testing their ability to phagocytose. Here we describe a detailed protocol for the systemic depletion of macrophages in zebrafish larvae by intravenous injection of liposomal clodronate supplemented with fluorescent dextran conjugates. Co-injection with the fluorescent dextran allows tracking of macrophage depletion in real time starting with verifying the successful intravenous injection to macrophage uptake of molecules and their eventual death. To verify a high degree of macrophage depletion, the level of brain macrophage (microglia) elimination can be determined by a rapid neutral red vital dye staining when clodronate injection is performed at early larval stages.

氯膦酸二鈉脂質(zhì)體清除斑馬魚巨噬細(xì)Protocol解決方案：