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Transcriptomic and H3K27ac chromatin responses of human microglia to acute PFOS exposure and recovery

GSE342612 Homo sapiens (human) ChIP-seq / ATAC-seq (genome binding and open chromatin) 36 samples Submitted 2026/08/06 Platform GPL21697
At a glance

ChIP-seq / ATAC-seq (genome binding and open chromatin) · human · 36 samples

What it is
ChIP-seq / ATAC-seq (genome binding and open chromatin)Where proteins bind the genome, or which regions are open and active.
Organism
Homo sapiens (human)
Samples
36 samples: 6 conditions, mostly in triplicateGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Perfluoroalkyl substance pollutants disrupt microglia function and trigger transcriptional and epigenomic changesToxicology · 2025
Summary (written by the submitters)
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental contaminants associated with adverse neurological effects, but their impact on microglial gene regulation remains unclear. In this study, human HMC3 microglial cells were exposed to vehicle control or perfluorooctane sulfonate (PFOS) at 25 or 50 µM for 24 hours. RNA sequencing was used to characterize transcriptomic changes, and H3K27ac CUT&Tag was used to profile active chromatin.
Read the full summary ↓
Additional samples were collected after PFOS withdrawal and a 24-hour recovery period to assess persistent molecular alterations. These datasets support integrated analysis of acute and persistent PFOS-induced transcriptomic and epigenetic changes in human microglia.
Published in
Perfluoroalkyl substance pollutants disrupt microglia function and trigger transcriptional and epigenomic changes
Cheng Y, Li JR, Yu H et al. · Toxicology 2025 · PMID 40419075 · doi:10.1016/j.tox.2025.154198
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE342612_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Look for peak files (.bed, .narrowPeak) and signal tracks (.bigWig) among the supplementary files; the raw reads are on ENA.

Also filed as BioProject PRJNA1508658 and SRA study SRP724678. Searching any of these in the dataset finder brings you back here.

Study design
6 conditions, mostly in triplicate
vehicle control, 24 h treatment, ×3 25 µM PFOS, 24 h treatment, ×3 50 µM PFOS, 24 h treatment, ×3 vehicle control, 24 h treatment followed by 2… ×3 25 µM PFOS, 24 h treatment followed by 24 h r… ×3 50 µM PFOS, 24 h treatment followed by 24 h r… ×3 vehicle control, 24 h treatment, biological r… ×1 vehicle control, 24 h treatment, biological r… ×1 +16 more

Supports a between-group comparison across 18 samples.

How we read this: 6 replicated groups read from 36 sample titles; they account for 18 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.