Rewilding of laboratory mice enhances granulopoiesis and immunity through intestinal fungal colonization

粒细胞生成 生物 殖民地化 免疫 免疫学 白色念珠菌 免疫系统 骨髓 微生物学 先天免疫系统 粒细胞 祖细胞 干细胞 细胞生物学
作者
Ying-Han Chen,Frank Yeung,Keenan A. Lacey,Kimberly Zaldaña,Jian-Da Lin,Gavyn Chern Wei Bee,Caroline McCauley,Ramya S. Barre,Shen-Huan Liang,Christina Hansen,Alexander E. Downie,Kyle Tio,Jeffrey N. Weiser,Victor J. Torres,Richard J. Bennett,P’ng Loke,Andrea L. Graham,Ken Cadwell
出处
期刊:Science immunology [American Association for the Advancement of Science (AAAS)]
卷期号:8 (84) 被引量:25
标识
DOI:10.1126/sciimmunol.add6910
摘要

The paucity of blood granulocyte populations such as neutrophils in laboratory mice is a notable difference between this model organism and humans, but the cause of this species-specific difference is unclear. We previously demonstrated that laboratory mice released into a seminatural environment, referred to as rewilding, display an increase in blood granulocytes that is associated with expansion of fungi in the gut microbiota. Here, we find that tonic signals from fungal colonization induce sustained granulopoiesis through a mechanism distinct from emergency granulopoiesis, leading to a prolonged expansion of circulating neutrophils that promotes immunity. Fungal colonization after either rewilding or oral inoculation of laboratory mice with Candida albicans induced persistent expansion of myeloid progenitors in the bone marrow. This increase in granulopoiesis conferred greater long-term protection from bloodstream infection by gram-positive bacteria than by the trained immune response evoked by transient exposure to the fungal cell wall component β-glucan. Consequently, introducing fungi into laboratory mice may restore aspects of leukocyte development and provide a better model for humans and free-living mammals that are constantly exposed to environmental fungi.
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