# 3D4 cells exhibit transcriptional features inconsistent with alveolar macrophage identity

**Authors:** Wenjuan Ma, Frieder Hadlich, Nares Trakooljul, Klaus Wimmers, Eduard Murani

PMC · DOI: 10.1186/s13567-025-01638-1 · Veterinary Research · 2025-10-20

## TL;DR

This study shows that 3D4 cells, commonly used as pig alveolar macrophage models, actually have features of respiratory epithelial cells, not macrophages.

## Contribution

The study reveals that 3D4 cells are misclassified and lack key macrophage traits, challenging their use in immunological research.

## Key findings

- 3D4 cells show extensive transcriptomic differences compared to primary porcine alveolar macrophages.
- 3D4 cells lack expression of key macrophage markers and pathogen recognition genes.
- Human Lung Cell Atlas analysis confirms 3D4 cells resemble respiratory epithelial cells.

## Abstract

The 3D4 cell lines are widely used as porcine alveolar macrophage models in immunological research. However, our preliminary experiments revealed that 3D4/21 cells failed to respond to lipopolysaccharide stimulation. We challenged both 3D4/21 and 3D4/2 clones with various Toll-like receptor (TLR)4 (LPS, Ultrapure LPS, Kdo2-Lipid A) and TLR2/TLR1 (Pam3CSK4) ligands. Strikingly, all stimulants failed to activate pro-inflammatory responses (IL1B and TNF expression). To clarify the lack of response of 3D4 cells, we isolated primary porcine alveolar macrophages (PAM) from piglets using lung lavage, and analyzed the transcriptome of unstimulated or Kdo2-Lipid A-stimulated 3D4/21 cells compared with equally treated PAM. We identified extensive transcriptomic differences, with 10,718 differentially expressed genes between untreated 3D4/21 cells and PAM (adjusted p-value < 0.05). Key alveolar macrophage markers and lineage-determining factors (SPI1 and IRF8) were weakly expressed or absent in 3D4/21 cells. Important pathogen recognition genes (TLR1, TLR2, TLR4, TLR6, TLR7, TLR8, TLR9, CGAS, IFI16, and NOD2) showed very low abundance or complete absence compared with PAM. Accordingly, 3D4/21 cells failed to respond to Kdo2-Lipid A stimulation, while PAM showed 2945 regulated genes. Functional annotation revealed that genes preferentially expressed in 3D4/21 cells were enriched for epithelial characteristics. Human Lung Cell Atlas analysis corroborated that 3D4/21 cells originate from respiratory epithelial cells. Similar patterns were observed in 3D4/2 cells, with low macrophage markers (CD163, SPI1, CD14, TLR2, and TLR4) and high epithelial markers (TP63, EGFR, and KRT5). Our data strongly suggest that 3D4 cell lines were misclassified as myeloid cells and actually possess respiratory epithelial characteristics.

The online version contains supplementary material available at 10.1186/s13567-025-01638-1.

## Linked entities

- **Genes:** SPI1 (Spi-1 proto-oncogene) [NCBI Gene 6688], IRF8 (interferon regulatory factor 8) [NCBI Gene 3394], TLR1 (toll like receptor 1) [NCBI Gene 7096], TLR2 (toll like receptor 2) [NCBI Gene 7097], TLR4 (toll like receptor 4) [NCBI Gene 7099], TLR6 (toll like receptor 6) [NCBI Gene 10333], TLR7 (toll like receptor 7) [NCBI Gene 51284], TLR8 (toll like receptor 8) [NCBI Gene 51311], TLR9 (toll like receptor 9) [NCBI Gene 54106], CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004], IFI16 (interferon gamma inducible protein 16) [NCBI Gene 3428], NOD2 (nucleotide binding oligomerization domain containing 2) [NCBI Gene 64127], CD163 (CD163 molecule) [NCBI Gene 9332], CD14 (CD14 molecule) [NCBI Gene 929], TP63 (tumor protein p63) [NCBI Gene 8626], EGFR (epidermal growth factor receptor) [NCBI Gene 1956], KRT5 (keratin 5) [NCBI Gene 3852]
- **Chemicals:** Kdo2-Lipid A (PubChem CID 11355423), Pam3CSK4 (PubChem CID 130704)
- **Species:** Mus musculus (taxon 10090), Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** TLR8 (toll like receptor 8) [NCBI Gene 397384] {aka TLR7}, TNF (tumor necrosis factor) [NCBI Gene 397086] {aka TNFSF2, TNFa}, TP63 (tumor protein p63) [NCBI Gene 100625258], IL1B (interleukin 1 beta) [NCBI Gene 397122] {aka IL1B1}, CD14 [NCBI Gene 100620530], TLR2 (Toll-like receptor 2 level) [NCBI Gene 101055400], CD163 (CD163 molecule) [NCBI Gene 397031], EGFR (epidermal growth factor receptor) [NCBI Gene 397070], LOC100156073 (myeloid cell nuclear differentiation antigen-like protein) [NCBI Gene 100156073] {aka IFI16}, TLR6 (toll like receptor 6) [NCBI Gene 396621] {aka TLR-6}, TLR1 (toll like receptor 1) [NCBI Gene 396607] {aka TLR6}, IRF8 (interferon regulatory factor 8) [NCBI Gene 396645] {aka ICSBP1}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 100516408] {aka MB21D1}, KRT5 (keratin 5) [NCBI Gene 100511564], NOD2 (nucleotide binding oligomerization domain containing 2) [NCBI Gene 100125838], SPI1 (Spi-1 proto-oncogene) [NCBI Gene 414912] {aka PU.1}, TLR4 (toll like receptor 4) [NCBI Gene 399541], TLR7 (toll like receptor 7) [NCBI Gene 100037296], TLR9 (Toll-like receptor 9 level) [NCBI Gene 101055229]
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** LPS (MESH:D008070), Pam3CSK4 (-), Kdo2-Lipid A (MESH:C506188)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 3D4/2 — Sus scrofa (Pig), Transformed cell line (CVCL_0F13), 3D4/21 — Sus scrofa (Pig), Transformed cell line (CVCL_0F14), 3D4 — Mus musculus (Mouse), Hybridoma (CVCL_DD28)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12539023/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12539023/full.md

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Source: https://tomesphere.com/paper/PMC12539023