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Preferential Perinatal Development of Skin-Homing NK1.1(+) Innate Lymphoid Cells for Regulation of Cutaneous Microbiota Colonization

Proper immune cell development at early ontogenic stages is critical for life-long health. How resident immune cells are established in barrier tissues at neonatal stages to provide early protection is an important but still poorly understood question. We herein report that a developmentally program...

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Detalles Bibliográficos
Autores principales: Yang, Jie, Restori, Katherine H., Xu, Ming, Song, Eun Hyeon, Zhao, Luming, Hu, Shaomin, Lyu, Pingyun, Wang, Wei-Bei, Xiong, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155142/
https://www.ncbi.nlm.nih.gov/pubmed/32283522
http://dx.doi.org/10.1016/j.isci.2020.101014
Descripción
Sumario:Proper immune cell development at early ontogenic stages is critical for life-long health. How resident immune cells are established in barrier tissues at neonatal stages to provide early protection is an important but still poorly understood question. We herein report that a developmentally programmed preferential generation of skin-homing group 1 innate lymphoid cells (ILC1s) at perinatal stages helps regulate early skin microbiota colonization. We found that a population of skin-homing NK1.1(+) ILC1s was preferentially generated in the perinatal thymi of mice. Unique thymic environments and progenitor cells are responsible for the preferential generation of skin-homing NK1.1(+) ILC1s at perinatal stages. In the skin, NK1.1(+) ILC1s regulate proper microbiota colonization and control the opportunistic pathogen Pseudomonas aeruginosa in neonatal mice. These findings provide insight into the development and function of tissue-specific immune cells at neonatal stages, a critical temporal window for establishment of local tissue immune homeostasis.