Macrophage morphology correlates with single-cell diversity and prognosis in colorectal liver metastasis

形态学(生物学) 转移 结直肠癌 巨噬细胞 多样性(政治) 医学 生物 内科学 癌症 动物 人类学 遗传学 体外 社会学
作者
Matteo Donadon,Guido Torzilli,Nina Cortese,Cristiana Soldani,Luca Di Tommaso,Barbara Franceschini,Roberta Carriero,Marialuisa Barbagallo,Alessandra Rigamonti,Achille Anselmo,Federico Colombo,Giulia Maggi,Ana Lleò,Javier Cibella,Clelia Peano,Paolo Kunderfranco,Massimo Roncalli,Alberto Mantovani,Federica Marchesi
出处
期刊:Journal of Experimental Medicine [Rockefeller University Press]
卷期号:217 (11) 被引量:127
标识
DOI:10.1084/jem.20191847
摘要

It has long been known that in vitro polarized macrophages differ in morphology. Stemming from a conventional immunohistology observation, we set out to test the hypothesis that morphology of tumor-associated macrophages (TAMs) in colorectal liver metastasis (CLM) represents a correlate of functional diversity with prognostic significance. Density and morphological metrics of TAMs were measured and correlated with clinicopathological variables. While density of TAMs did not correlate with survival of CLM patients, the cell area identified small (S-TAM) and large (L-TAM) macrophages that were associated with 5-yr disease-free survival rates of 27.8% and 0.2%, respectively (P < 0.0001). RNA sequencing of morphologically distinct macrophages identified LXR/RXR as the most enriched pathway in large macrophages, with up-regulation of genes involved in cholesterol metabolism, scavenger receptors, MERTK, and complement. In single-cell analysis of mononuclear phagocytes from CLM tissues, S-TAM and L-TAM signatures were differentially enriched in individual clusters. These results suggest that morphometric characterization can serve as a simple readout of TAM diversity with strong prognostic significance.

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