# HDAC1 and SATB1 positively regulate immune responses in chicken macrophages

**Authors:** Bowen Niu, Junda Hu, Zixuan Fan, Zihao Gao, Yuchen Jie, Xinyu Wu, Xingying Chen, Sirui Chen, Li-Wa Shao

PMC · DOI: 10.1016/j.psj.2026.106607 · 2026-02-10

## TL;DR

This study shows that HDAC1 and SATB1 proteins help chicken immune cells fight infections, offering new ways to improve poultry health and disease resistance.

## Contribution

The study reveals a novel synergistic mechanism of HDAC1 and SATB1 in regulating immune responses in chicken macrophages.

## Key findings

- HDAC1 and SATB1 are up-regulated in chicken macrophages during immune stimulation.
- Disruption of HDAC1 or SATB1 reduces the expression of key immune effectors like IFN-β and TNF-α.
- HDAC1 and SATB1 are evolutionarily conserved and physically interact in chicken cells.

## Abstract

The avian immune system constitutes the primary barrier against pathogen invasion, and its regulatory efficiency directly determines animal health, productive performance, and food safety. Elucidating the molecular and cellular networks that maintain immune homeostasis in poultry has therefore become a pivotal entry point for improving disease prevention and achieving environmentally sustainable production. Histone deacetylase 1 (HDAC1) and special AT-rich sequence-binding protein 1 (SATB1) are reported modulators of immunity in some species such as mammals, yet their roles in avian species remain undefined. Here, we employed chicken macrophages (HD11) stimulated with lipopolysaccharide (LPS) to establish an in vitro immune-response model. Both HDAC1 and SATB1 were markedly activated and up-regulated upon LPS challenge. Using cell transfection and CRISPR/Cas9 genome editing, we generated HD11 cell lines with stable disruption of either HDAC1 or SATB1. In these modified cells, the LPS-induced elevation of key immune effectors—including IFN-β, IRF7, STAT1, TNF-α, and IFIH1 was significantly attenuated. Amino-acid sequence alignment, protein complex prediction, and co-immunoprecipitation further suggest that HDAC1 and SATB1 are evolutionarily conserved and physically interact. Collectively, our study uncovers a novel mechanism by which HDAC1 and SATB1 act synergistically to positively regulate immune responses in chicken macrophages. These findings not only provide new theoretical insights into avian immune regulation but also establishes a molecular foundation for the development of next-generation immune enhancers and breeding strategies that enhance disease resistance.

## Linked entities

- **Genes:** HDAC1 (histone deacetylase 1) [NCBI Gene 3065], SATB1 (SATB homeobox 1) [NCBI Gene 6304], IFNB1 (interferon beta 1) [NCBI Gene 3456], IRF7 (interferon regulatory factor 7) [NCBI Gene 3665], STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 6772], TNF (tumor necrosis factor) [NCBI Gene 7124], IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135]
- **Proteins:** HDAC1 (histone deacetylase 1), SATB1 (SATB homeobox 1)
- **Species:** Gallus gallus (taxon 9031), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 424185] {aka MDA5, chMDA5}, SATB1 (SATB homeobox 1) [NCBI Gene 420647], IFNA3 (interferon) [NCBI Gene 396398] {aka IFN-alpha, IFN-gamma, IFNA, IFNA1, IFNA2, IFNA6}, HDAC1 (histone deacetylase 1) [NCBI Gene 373961] {aka HDAC1A}, MYC (v-myc avian myelocytomatosis viral oncogene homolog) [NCBI Gene 420332] {aka c-myc}, IFNW1 (interferon omega 1) [NCBI Gene 554219] {aka IFN-beta, IFN2, IFNB, IFN_B}, LITAF (lipopolysaccharide induced TNF factor) [NCBI Gene 374125] {aka TNF-alpha}, STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 424044], hda-1 (Histone deacetylase 1) [NCBI Gene 179959], IRF7 (interferon regulatory factor 7) [NCBI Gene 396330] {aka IRF3, cIRF-3}, ACTB (actin, beta) [NCBI Gene 396526] {aka Bact, actin}
- **Diseases:** influenza (MESH:D007251), inflammatory (MESH:D007249), Newcastle disease (MESH:D009521), cytotoxic (MESH:D064420), infection (MESH:D007239)
- **Chemicals:** Triton X-100 (MESH:D017830), acetonitrile (MESH:C032159), streptomycin (MESH:D013307), EDTA (MESH:D004492), formic acid (MESH:C030544), NaCl (MESH:D012965), ethanol (MESH:D000431), thiourea (MESH:D013890), HCl (MESH:D006851), SDS (MESH:D012967), isopropanol (MESH:D019840), TRIzol (MESH:C411644), water (MESH:D014867), urea (MESH:D014508), glycerol (MESH:D005990), puromycin (MESH:D011691), penicillin (MESH:D010406), NaBt (-), PBS (MESH:D007854), hydrogen (MESH:D006859), PVDF (MESH:C024865), chloroform (MESH:D002725), LPS (MESH:D008070), agarose (MESH:D012685), sodium butyrate (MESH:D020148)
- **Species:** Caenorhabditis elegans (species) [taxon 6239], Mus musculus (house mouse, species) [taxon 10090], Salmonella (genus) [taxon 590], Homo sapiens (human, species) [taxon 9606], Gallus gallus (bantam, species) [taxon 9031], unidentified influenza virus (species) [taxon 11309]
- **Cell lines:** HD11 — Gallus gallus (Chicken), Transformed cell line (CVCL_4685)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925555/full.md

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Source: https://tomesphere.com/paper/PMC12925555