Unbiased metastatic niche-labeling identifies estrogen receptor-positive macrophages as a barrier of T cell infiltration during bone colonization

• Published in: bioRxiv : the preprint server for biology
• Main Authors: Xu, Zhan, Liu, Fengshuo, Ding, Yunfeng, Pan, Tianhong, Wu, Yi-Hsuan, Liu, Jun, Bado, Igor L, Zhang, Weijie, Wu, Ling, Gao, Yang, Hao, Xiaoxin, Yu, Liqun, Edwards, David G, Chan, Hilda L, Aguirre, Sergio, Dieffenbach, Michael Warren, Chen, Elina, Shen, Yichao, Hoffman, Dane, Dominguez, Luis Becerra, Rivas, Charlotte Helena, Chen, Xiang, Wang, Hai, Gugala, Zbigniew, Satcher, Robert L, Zhang, Xiang H-F
• Format: Journal Article
• Language: English
• Published: United States 10.05.2024
• DOI: 10.1101/2024.05.07.593016

Microenvironment niches determine cellular fates of metastatic cancer cells. However, robust and unbiased approaches to identify niche components and their molecular profiles are lacking. We established Sortase A-Based Microenvironment Niche Tagging (SAMENT), which selectively labels cells encountered by cancer cells during metastatic colonization. SAMENT was applied to multiple cancer models colonizing the same organ and the same cancer to different organs. Common metastatic niche features include macrophage enrichment and T cell depletion. Macrophage niches are phenotypically diverse between different organs. In bone, macrophages express the estrogen receptor alpha (ERα) and exhibit active ERα signaling in male and female hosts. Conditional knockout of in macrophages significantly retarded bone colonization by allowing T cell infiltration. ERα expression was also discovered in human bone metastases of both genders. Collectively, we identified a unique population of ERα+ macrophages in the metastatic niche and functionally tied ERα signaling in macrophages to T cell exclusion during metastatic colonization. SAMENT is a robust metastatic niche-labeling approach amenable to single-cell omics.Metastatic niches are typically enriched with macrophages and depleted of T cells.Direct interaction with cancer cells induces ERα expression in niche macrophages. Knockout of in macrophages allows T cell infiltration and retards bone colonization.