巨噬细胞亚型可抑制乳腺癌的培养增殖。

IF 3.1 3区 生物学 Q3 CELL BIOLOGY
Molecular Biology of the Cell Pub Date : 2025-01-01 Epub Date: 2024-11-27 DOI:10.1091/mbc.E24-06-0241
Sophia R S Varady, Daniel Greiner, Minna Roh-Johnson
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引用次数: 0

摘要

巨噬细胞是一种可塑性很强的细胞类型,可根据环境线索采用不同的亚型和功能状态。这些功能状态可以变化很大,不同的巨噬细胞能够显示出截然相反的功能。我们试图了解存在于光谱两端的巨噬细胞亚型如何影响其他细胞的功能。我们利用与原代人类巨噬细胞的共培养系统来探究巨噬细胞亚型对乳腺癌细胞增殖的影响。我们的研究发现了一种令人惊讶的表型,与单独的癌细胞相比,两种巨噬细胞亚型都能抑制癌细胞的增殖。特别有趣的是,我们使用两种不同的乳腺癌细胞系进行了两种不同的增殖试验,结果表明,将巨噬细胞分化成 "亲肿瘤 "亚型会抑制乳腺癌细胞的增殖。这些发现与 "亲肿瘤 "巨噬细胞会促进癌细胞增殖的普遍解释不一致,并建议重新评估这些解释是如何得出的。[媒体:见正文]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophage subtypes inhibit breast cancer proliferation in culture.

Macrophages are a highly plastic cell type that adopt distinct subtypes and functional states depending on environmental cues. These functional states can vary widely, with distinct macrophages capable of displaying opposing functions. We sought to understand how macrophage subtypes that exist on two ends of a spectrum influence the function of other cells. We used a coculture system with primary human macrophages to probe the effects of macrophage subtypes on breast cancer cell proliferation. Our studies revealed a surprising phenotype in which both macrophage subtypes inhibited cancer cell proliferation compared with cancer cells alone. Of particular interest, using two different proliferation assays with two different breast cancer cell lines, we showed that differentiating macrophages into a "protumor" subtype inhibited breast cancer cell proliferation. These findings are inconsistent with the prevailing interpretation that "protumor" macrophages promote cancer cell proliferation and suggest a re-evaluation of how these interpretations are made.

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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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