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SRX21637388: GSM7758574: human_DLBCL_region_198; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 3000) run: 3.6M spots, 1.1G bases, 412.5Mb downloads

External Id: GSM7758574_r1
Submitted by: National University of Singapore
Study: Spatially-resolved transcriptomics reveal macrophage heterogeneity and prognostic significance in diffuse large B-cell lymphoma
show Abstracthide Abstract
Macrophages are abundant immune cells in the microenvironment of diffuse large B-cell lymphoma (DLBCL). Macrophage phenotyping by immunohistochemistry has varying prognostic significance across studies in DLBCL and does not provide a comprehensive analysis of macrophage subtypes. We hypothesized that whole-transcriptomic analysis (WTA) of macrophage in-situ would identify new macrophage subsets of biological and clinical significances. Overall design: Using digital spatial profiling with whole transcriptome analysis of CD68+ cells, we characterized macrophages in distinct spatial niches of reactive lymphoid tissues (RLTs) and DLBCL. We reveal previously unrecognized transcriptomic differences between macrophages populating in RLTs (light zone (LZ)/ dark zone (DZ), germinal center (GC)/ interfollicular (IF) regions), and in between disease states (RLTs and DLBCL). And we also captured the CD20+ cells in the same way, which was used for validation.
Sample: human_DLBCL_region_198
SAMN37284598 • SRS18807477 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: GSM7758574
Instrument: Illumina HiSeq 3000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The slides were incubated with blocking Buffer W (200 μL/slide, NanoString) for 30 min in the humidity chamber at room temperature after hybridization.Each slide was stained with corresponding morophology markers. After immunofluorescent staining, the slides were visualized using the GeoMx® DSP instrument to select regions of interest (ROIs). To acquire representative regions, ROI selection was performed by an expert pathologist. The pathologist was blinded to the group assignment during the ROIs selection. Based on fluorescent staining, each ROI was segmented into corresponding areas of interest (AOIs) - CD68+ regions, CD3+ regions, and CD20+ regions. Subsequently, each AOI was exposed to UV light and photocleaved oligos were aspirated from the solution into the wells of a collection plate. Collected photocleaved oligos were PCR amplified with the corresponding GeoMx® Seq Code Primer Plate and Master Mix (NanoString). PCR products were pooled and cleaned with AMPure XP beads (Agilent, Santa Clara, California, USA) twice to obtain the libraries. The quality and concentration of libraries were assessed using a high sensitivity DNA Kit (Agilent) and Bioanalyzer. Subsequently, libraries were sequenced on an illumina sequencing platform (Hiseq or NovaSeq) with standard workflow specifications (dual-indexing and paired-end reads (2 × 27 bp)).
Runs: 1 run, 3.6M spots, 1.1G bases, 412.5Mb
Run# of Spots# of BasesSizePublished
SRR259175653,571,3241.1G412.5Mb2023-11-05

ID:
29272561

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