The Technical Feasibility of Digital Spatial Profiling in Immune/Inflammation Study of Thrombosis

Jianjun Jiang, Yang Liu Department of General Surgery, Vascular Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, People's Republic of ChinaCorrespondence: Yang Liu, Department of General Surgery, Vascular Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, Peo...

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Main Authors: Jiang J (Author), Liu Y (Author)
Format: Book
Published: Dove Medical Press, 2023-06-01T00:00:00Z.
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100 1 0 |a Jiang J  |e author 
700 1 0 |a Liu Y  |e author 
245 0 0 |a The Technical Feasibility of Digital Spatial Profiling in Immune/Inflammation Study of Thrombosis 
260 |b Dove Medical Press,   |c 2023-06-01T00:00:00Z. 
500 |a 1178-7031 
520 |a Jianjun Jiang, Yang Liu Department of General Surgery, Vascular Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, People's Republic of ChinaCorrespondence: Yang Liu, Department of General Surgery, Vascular Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, People's Republic of China, Tel +86 18560088317, Email liuyang_sdu@126.comBackground: A comprehensive study of the distribution and role of immune/inflammatory cells in thrombosis is still lacking because traditional pathology techniques cannot accomplish the analysis of numerous protein and genetic data simultaneously. We aimed to evaluate the feasibility of digital spatial profiling (DSP) to study immune/inflammation reaction in thrombosis progression.Methods and Results: An 82-year-old male patient underwent iliofemoral thrombectomy at our institution. The white, mixed and red thrombi were fixed in formalin, dehydrated in ethanol and embedded in paraffin, which were incubated with morphology-labeled fluorescent antibodies (CD45, SYTO13) and the entire target mixture in GeoMx Whole Transcriptome Atlas panel. DSP system was applied to investigate the regions of interest from fluorescence imaging. Fluorescence imaging showed infiltration of immune/inflammation cells in white, mixed and red thrombosis. Whole genome sequencing revealed 16 genes differentially expressed. Pathway enrichment analysis revealed that these genes were significantly enriched in ligand binding and uptake related signaling pathways of the scavenger receptor. The distribution of immune/inflammation cell subsets was different in white, mixed and red thrombosis. The abundance of endothelial cells, CD8 naive T cells, and macrophages in red thrombosis was significantly higher than in mixed and white thrombosis.Conclusion: The results showed that DSP can facilitate efficient analysis using very few thrombosis samples and provide valuable new leads, suggesting that DSP may be a viable and important new tool to study thrombosis and inflammation.Keywords: digital spatial profiling, immune/inflammation cell, arterial thrombosis, whole genome sequencing, scavenger receptor 
546 |a EN 
690 |a digital spatial profiling 
690 |a immune/inflammation cell 
690 |a arterial thrombosis 
690 |a whole genome sequencing 
690 |a scavenger receptor 
690 |a Pathology 
690 |a RB1-214 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Inflammation Research, Vol Volume 16, Pp 2431-2436 (2023) 
787 0 |n https://www.dovepress.com/the-technical-feasibility-of-digital-spatial-profiling-in-immuneinflam-peer-reviewed-fulltext-article-JIR 
787 0 |n https://doaj.org/toc/1178-7031 
856 4 1 |u https://doaj.org/article/3cde7cc447e74628abf70e76e9f379aa  |z Connect to this object online.