Scholarlink

<p>Rodents are widely used in immunology but do not always recapitulate human immune functions. The tree shrew (<i>Tupaia belangeri</i>) is phylogenetically closer to primates than rodents and may help bridge this gap, yet its immune system has not been comprehensively characterised at single-cell resolution. Here, we present a single-cell transcriptomic atlas of the tree shrew immune system, profiling 39 cell types across 12 tissues. We uncover human-like tonsillar structures and two transcriptionally distinct splenic macrophage subsets: an NR1H3<sup>+</sup> immunoregulatory subset and an IRF8<sup>+</sup> pro-inflammatory subset. During acute Epstein-Barr virus infection, NR1H3<sup>+</sup> macrophages undergo pronounced inflammatory reprogramming and emerge as a major intercellular signalling hub. Cross-species integration of single-cell datasets from seven vertebrate species indicates that NR1H3<sup>+</sup> macrophage gene programmes are evolutionarily conserved. Functional analyses further support a shared anti-inflammatory programme mediated by NR1H3-dependent suppression of the non-canonical NF-κB pathway in both tree shrew and human macrophages. Together, these findings provide a reference resource for tree shrew immunology and support the tree shrew as a complementary model alongside rodent and primate systems.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Tree shrew immune cell atlas identifies NR1H3⁺ tissue macrophages with conserved anti-inflammatory function

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年4月9日

查看全文
  • Wei Xia,
  • Nan Shi,
  • Yongjing Lai,
  • Yiwei Feng,
  • Zhenqiu Luo,
  • Fangfang Chen,
  • Zongjian Huang,
  • Mao Xie,
  • Jingyu Li,
  • Xiang Bin,
  • Xiang Yi,
  • Min He,
  • Chaoqian Li,
  • Guangyao He,
  • Anzhou Tang

摘要

Rodents are widely used in immunology but do not always recapitulate human immune functions. The tree shrew (Tupaia belangeri) is phylogenetically closer to primates than rodents and may help bridge this gap, yet its immune system has not been comprehensively characterised at single-cell resolution. Here, we present a single-cell transcriptomic atlas of the tree shrew immune system, profiling 39 cell types across 12 tissues. We uncover human-like tonsillar structures and two transcriptionally distinct splenic macrophage subsets: an NR1H3+ immunoregulatory subset and an IRF8+ pro-inflammatory subset. During acute Epstein-Barr virus infection, NR1H3+ macrophages undergo pronounced inflammatory reprogramming and emerge as a major intercellular signalling hub. Cross-species integration of single-cell datasets from seven vertebrate species indicates that NR1H3+ macrophage gene programmes are evolutionarily conserved. Functional analyses further support a shared anti-inflammatory programme mediated by NR1H3-dependent suppression of the non-canonical NF-κB pathway in both tree shrew and human macrophages. Together, these findings provide a reference resource for tree shrew immunology and support the tree shrew as a complementary model alongside rodent and primate systems.