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Characterization of TLR signaling in Ticam2-/- macrophages

GSE321707 Mus musculus Expression profiling by high throughput sequencing 30 samples Submitted 2026/08/07 Platform GPL24247
Summary
Early Toll-like receptor (TLR) signaling termination in TRAM (Ticam2) KO macrophages selectively impairs activation of secondary response genes (SRG) and interferon-stimulated genes (ISGs), whereas primary response gene (PRG) induction remains largely intact. We performed bulk RNA-Seq on LTA- or LPS-stimulated primary WT and Ticam2-/- BMDMs after 2 h and 6 h of PAMP-treatment to analyze this phenomenom.
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Direct links to NCBI, no account and no request form: the whole study as GSE321707_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 30 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1429322 and SRA study SRP679818. Searching any of these in the dataset finder brings you back here.

Study design
10 conditions, mostly in triplicate
primary TRAM (Ticam2) KO macrophages, LPS-tre… ×3 primary TRAM (Ticam2) KO macrophages, LTA-tre… ×3 primary TRAM (Ticam2) KO macrophages, ×3 primary TRAM (Ticam2) KO macrophages, LPS-tre… ×3 primary TRAM (Ticam2) KO macrophages, LTA-tre… ×3 primary WT macrophages, LPS-treated, 6 hrs, ×3 primary WT macrophages, LTA-treated, 6 hrs, ×3 primary WT macrophages, ×3 +2 more

Supports a case/control comparison: 12 samples read as cases, 3 as controls.

10 replicated groups read from 30 sample titles; they account for 30 of them. Check it against the sample list below before relying on it.

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