Toward a ToxAtlas of Carbon-Based Nanomaterials: Single-Cell RNA Sequencing Reveals Initiating Cell Circuits in Pulmonary Inflammation.

Voss, Carola; Han, Lianyong; Ansari, Meshal; Strunz, Maximilian; Haefner, Verena; Angelidis, Ilias; Mayr, Christoph H; Berthing, Trine et al. · ACS Nano · 2025

basic_science · Level V

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Abstract

Understanding how nanomaterial properties drive acute lung inflammation is critical for the development of safer materials, but for low solubility carbon-based nanomaterials (CBNs) the initiation of the inflammatory response is still poorly understood. Leveraging single-cell RNA sequencing of mouse lungs, 12 h after intratracheally instillation with different CBN spherical carbon nanoparticles (CNP), tangled double-walled (DWCNT), and rigid multiwalled carbon nanotubes (MWCNT) and lipopolysaccharide (LPS) as positive control, we identified 41 cell states and delineated material-specific molecular initiation events at single-cell resolution. CBN doses were chosen to cause equal levels of moderate inflammation, assessed by airspace neutrophilia, and exposure-triggered cellular activation was tested for <i>in vitro</i> reproducibility. To advance future development of cell-based assays, we developed a webtool, ToxAtlas, mapping CBN-specific gene responses of interest. Despite chemical similarity, CBN elicited distinct inflammatory cytokine and cell responses via different modes of action. CNP triggered neutrophilia through alveolar epithelial activation and <i>Cxcl1</i> and <i>Csf2</i> expression but without apparent cell damage or macrophage activation. In contrast, CNT induced epithelial and macrophage damage, with alarmin release (IL-1α, IL-33) dominating the MWCNT response. DWCNT caused alveolar epithelial injury, and pro-inflammatory macrophage and fibroblast-derived monocyte attractant (<i>Ccl2</i>, <i>Ccl7</i>) activation. Our initiating cell circuits identify epithelial as well as early fibroblast activation, especially from alveolar type 2 cell-adjacent lipofibroblasts, as central to orchestrating the initiation of CBN-induced inflammation. These findings support the role of mesenchymal cells in early pulmonary defense, eventually priming chronic inflammation, a known cause of MWCNT exposure.

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