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跨组织和疾病的SPP1巨噬细胞全景:综述

The Landscape of SPP1 Macrophages Across Tissues and Diseases: A Comprehensive Review.

作者信息

Palma Alessandro

机构信息

Department of Biology and Biotechnologies "Charles Darwin", Sapienza University of Rome, Rome, Italy.

出版信息

Immunology. 2025 Oct;176(2):179-196. doi: 10.1111/imm.13952. Epub 2025 May 21.

DOI:10.1111/imm.13952
PMID:40395129
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12401812/
Abstract

Macrophages play a critical role in shaping the immune landscape of various diseases, with secreted phosphoprotein 1 (SPP1)-expressing macrophages emerging as a distinct subset implicated in both cancerous and non-cancerous conditions. Leveraging recent advances in single-cell RNA sequencing, numerous studies have identified SPP1 macrophages across diverse pathological contexts, shedding light on their functional heterogeneity. In cancer, SPP1 tumour-associated macrophages contribute to tumour growth, angiogenesis, and immune evasion, often interacting with T cells and stromal components to sustain an immunosuppressive microenvironment. Conversely, in non-cancerous diseases, these macrophages exhibit both profibrotic and disease-promoting properties, depending on the tissue context. This review provides a comprehensive synthesis of the latest findings on SPP1 macrophages, highlighting their roles in tumour progression, immune suppression, tissue remodelling, and fibrosis. By comparing their shared traits and tissue-specific differences, we explore how SPP1 macrophages adapt to distinct microenvironments and influence disease progression. Understanding their conserved and context-dependent functions may open new avenues for therapeutic targeting.

摘要

巨噬细胞在塑造各种疾病的免疫格局中发挥着关键作用,表达分泌型磷蛋白1(SPP1)的巨噬细胞作为一个独特的亚群出现,与癌症和非癌症疾病均有关联。利用单细胞RNA测序的最新进展,众多研究已在不同病理背景下鉴定出SPP1巨噬细胞,揭示了它们的功能异质性。在癌症中,SPP1肿瘤相关巨噬细胞促进肿瘤生长、血管生成和免疫逃逸,常与T细胞和基质成分相互作用以维持免疫抑制微环境。相反,在非癌症疾病中,这些巨噬细胞根据组织背景表现出促纤维化和促进疾病的特性。本综述全面综合了关于SPP1巨噬细胞的最新发现,突出了它们在肿瘤进展、免疫抑制、组织重塑和纤维化中的作用。通过比较它们的共同特征和组织特异性差异,我们探讨了SPP1巨噬细胞如何适应不同的微环境并影响疾病进展。了解它们的保守功能和依赖于背景的功能可能为治疗靶点开辟新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/3e686ca81063/IMM-176-179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/7133c7fd1429/IMM-176-179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/26d5b569461d/IMM-176-179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/3e686ca81063/IMM-176-179-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/7133c7fd1429/IMM-176-179-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/26d5b569461d/IMM-176-179-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/551d/12401812/3e686ca81063/IMM-176-179-g002.jpg

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2
Tissue macrophages: origin, heterogenity, biological functions, diseases and therapeutic targets.组织巨噬细胞:起源、异质性、生物学功能、疾病及治疗靶点。
Signal Transduct Target Ther. 2025 Mar 7;10(1):93. doi: 10.1038/s41392-025-02124-y.
3
Multi-omics analyses reveal biological and clinical insights in recurrent stage I non-small cell lung cancer.
多组学分析揭示了复发性I期非小细胞肺癌的生物学和临床见解。
Nat Commun. 2025 Feb 10;16(1):1477. doi: 10.1038/s41467-024-55068-2.
4
Spatial transcriptomics identifies molecular niche dysregulation associated with distal lung remodeling in pulmonary fibrosis.空间转录组学鉴定出与肺纤维化中远端肺重塑相关的分子微环境失调。
Nat Genet. 2025 Mar;57(3):647-658. doi: 10.1038/s41588-025-02080-x. Epub 2025 Feb 3.
5
SPP1+ macrophages promote head and neck squamous cell carcinoma progression by secreting TNF-α and IL-1β.SPP1 +巨噬细胞通过分泌肿瘤坏死因子-α和白细胞介素-1β促进头颈部鳞状细胞癌进展。
J Exp Clin Cancer Res. 2024 Dec 26;43(1):332. doi: 10.1186/s13046-024-03255-w.
6
Single-cell dissection of multifocal bladder cancer reveals malignant and immune cells variation between primary and recurrent tumor lesions.多灶性膀胱癌的单细胞剖析揭示了原发性和复发性肿瘤病灶之间恶性细胞和免疫细胞的差异。
Commun Biol. 2024 Dec 19;7(1):1659. doi: 10.1038/s42003-024-07343-7.
7
Multi-omic profiling highlights factors associated with resistance to immuno-chemotherapy in non-small-cell lung cancer.多组学分析揭示了与非小细胞肺癌免疫化疗耐药相关的因素。
Nat Genet. 2025 Jan;57(1):126-139. doi: 10.1038/s41588-024-01998-y. Epub 2024 Dec 10.
8
Spatially resolved gene expression profiling of tumor microenvironment reveals key steps of lung adenocarcinoma development.肿瘤微环境的空间分辨基因表达谱揭示了肺腺癌发展的关键步骤。
Nat Commun. 2024 Dec 6;15(1):10637. doi: 10.1038/s41467-024-54671-7.
9
The immune landscape of murine skeletal muscle regeneration and aging.鼠类骨骼肌再生和衰老的免疫图谱。
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