斑马鱼肾髓质离体巨噬细胞的提取。

IF 1.2
Zebrafish Pub Date : 2025-10-01 Epub Date: 2025-09-24 DOI:10.1177/15458547251366984
Leonel Witcoski Junior, André Guilherme Portela de Paula, Jordana Dinorá de Lima, Mariana Abrantes do Amaral, Barbara Nunes Padovani, Mariana Rodrigues Davanso, Niels Olsen Saraiva Camara, Karin Braun Prado, Tarcio Teodoro Braga
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引用次数: 0

摘要

斑马鱼(Danio rerio)被认为是造血研究的通用模型,因为它的透明度,与人类的遗传相似性和易于操作。本研究描述了一种利用转基因细胞系和L929细胞条件培养基(LCCM)作为重组M-CSF的替代品,从斑马鱼肾髓质中体外提取和分化巨噬细胞的方案。成年TgMpegmCherry斑马鱼保持在受控条件下。安乐死后,分离肾髓细胞,用抗生素处理,并在LCCM或重组人M-CSF中培养。使用共聚焦显微镜(mCherry)、流式细胞术和功能性吞噬试验评估巨噬细胞分化。该方案能够有效地将祖细胞分化为巨噬细胞,在LCCM中7天后平均有49.1%的mCherry+细胞,优于重组M-CSF。分化的细胞表现出较强的吞噬活性,证实了巨噬细胞的功能。该方法为获得斑马鱼来源的离体巨噬细胞提供了一种可行的方法,使免疫和造血研究成为可能,并允许与传统的小鼠巨噬细胞方案进行功能比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Extraction of Ex Vivo Macrophages from the Renal Medulla of Zebrafish (Danio rerio).

Zebrafish (Danio rerio) is recognized as a versatile model for hematopoietic studies due to its transparency, genetic similarity to humans, and ease of manipulation. This study describes a protocol for the ex vivo extraction and differentiation of macrophages from the renal medulla of zebrafish using transgenic lines and L929 cell-conditioned medium (LCCM) as an alternative to recombinant M-CSF. Adult TgMpegmCherry zebrafish were maintained under controlled conditions. Following euthanasia, renal medullary cells were isolated, treated with antibiotics, and cultured in either LCCM or recombinant human M-CSF. Macrophage differentiation was assessed using confocal microscopy (mCherry), flow cytometry, and functional phagocytosis assays. The protocol enabled efficient differentiation of progenitor cells into macrophages, with an average of 49.1% mCherry+ cells after 7 days in LCCM, outperforming recombinant M-CSF. Differentiated cells demonstrated strong phagocytic activity, confirming macrophage functionality. This method provides an accessible approach to obtaining ex vivo zebrafish-derived macrophages, enabling immunological and hematopoietic studies and allowing for functional comparisons with traditional murine macrophage protocols.

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