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Fungal dissemination is limited by liver macrophage filtration of the blood

Fungal dissemination into the bloodstream is a critical step leading to invasive fungal infections. Here, using intravital imaging, we show that Kupffer cells (KCs) in the liver have a prominent function in the capture of circulating Cryptococcus neoformans and Candida albicans, thereby reducing fun...

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Detalles Bibliográficos
Autores principales: Sun, Donglei, Sun, Peng, Li, Hongmei, Zhang, Mingshun, Liu, Gongguan, Strickland, Ashley B., Chen, Yanli, Fu, Yong, Xu, Juan, Yosri, Mohammed, Nan, Yuchen, Zhou, Hong, Zhang, Xiquan, Shi, Meiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783440/
https://www.ncbi.nlm.nih.gov/pubmed/31594939
http://dx.doi.org/10.1038/s41467-019-12381-5
Descripción
Sumario:Fungal dissemination into the bloodstream is a critical step leading to invasive fungal infections. Here, using intravital imaging, we show that Kupffer cells (KCs) in the liver have a prominent function in the capture of circulating Cryptococcus neoformans and Candida albicans, thereby reducing fungal dissemination to target organs. Complement C3 but not C5, and complement receptor CRIg but not CR3, are involved in capture of C. neoformans. Internalization of C. neoformans by KCs is subsequently mediated by multiple receptors, including CR3, CRIg, and scavenger receptors, which work synergistically along with C5aR signaling. Following phagocytosis, the growth of C. neoformans is inhibited by KCs in an IFN-γ independent manner. Thus, the liver filters disseminating fungi from circulation via KCs, providing a mechanistic explanation for the enhanced risk of cryptococcosis among individuals with liver diseases, and suggesting a therapeutic strategy to prevent fungal dissemination through enhancing KC functions.