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基于体外研究的巨噬细胞极化布尔模型对肿瘤相关巨噬细胞形成的见解

Insights on TAM Formation from a Boolean Model of Macrophage Polarization Based on In Vitro Studies.

作者信息

Marku Malvina, Verstraete Nina, Raynal Flavien, Madrid-Mencía Miguel, Domagala Marcin, Fournié Jean-Jacques, Ysebaert Loïc, Poupot Mary, Pancaldi Vera

机构信息

INSERM, Centre de Recherches en Cancérologie de Toulouse, 2 Avenue Hubert Curien, 31037 Toulouse, France.

Université III Toulouse Paul Sabatier, Route de Narbonne, 31330 Toulouse, France.

出版信息

Cancers (Basel). 2020 Dec 7;12(12):3664. doi: 10.3390/cancers12123664.

Abstract

The tumour microenvironment is the surrounding of a tumour, including blood vessels, fibroblasts, signaling molecules, the extracellular matrix and immune cells, especially neutrophils and monocyte-derived macrophages. In a tumour setting, macrophages encompass a spectrum between a tumour-suppressive (M1) or tumour-promoting (M2) state. The biology of macrophages found in tumours (Tumour Associated Macrophages) remains unclear, but understanding their impact on tumour progression is highly important. In this paper, we perform a comprehensive analysis of a macrophage polarization network, following two lines of enquiry: (i) we reconstruct the macrophage polarization network based on literature, extending it to include important stimuli in a tumour setting, and (ii) we build a dynamical model able to reproduce macrophage polarization in the presence of different stimuli, including the contact with cancer cells. Our simulations recapitulate the documented macrophage phenotypes and their dependencies on specific receptors and transcription factors, while also unravelling the formation of a special type of tumour associated macrophages in an in vitro model of chronic lymphocytic leukaemia. This model constitutes the first step towards elucidating the cross-talk between immune and cancer cells inside tumours, with the ultimate goal of identifying new therapeutic targets that could control the formation of tumour associated macrophages in patients.

摘要

肿瘤微环境是肿瘤周围的环境,包括血管、成纤维细胞、信号分子、细胞外基质和免疫细胞,尤其是中性粒细胞和单核细胞衍生的巨噬细胞。在肿瘤环境中,巨噬细胞涵盖了肿瘤抑制(M1)或肿瘤促进(M2)状态之间的一系列状态。肿瘤中发现的巨噬细胞(肿瘤相关巨噬细胞)的生物学特性仍不清楚,但了解它们对肿瘤进展的影响非常重要。在本文中,我们沿着两条研究路线对巨噬细胞极化网络进行了全面分析:(i)我们根据文献重建巨噬细胞极化网络,将其扩展以纳入肿瘤环境中的重要刺激因素;(ii)我们构建了一个动力学模型,该模型能够在存在不同刺激因素(包括与癌细胞接触)的情况下再现巨噬细胞极化。我们的模拟重现了已记录的巨噬细胞表型及其对特定受体和转录因子的依赖性,同时还揭示了在慢性淋巴细胞白血病体外模型中一种特殊类型的肿瘤相关巨噬细胞的形成。该模型是阐明肿瘤内免疫细胞与癌细胞之间相互作用的第一步,最终目标是识别出能够控制患者体内肿瘤相关巨噬细胞形成的新治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0e/7762229/b9218a98ae84/cancers-12-03664-g001.jpg

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