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Identification of scavenger receptor B1 as the airway microfold cell receptor for Mycobacterium tuberculosis

Mycobacterium tuberculosis (Mtb) can enter the body through multiple routes, including via specialized transcytotic cells called microfold cells (M cell). However, the mechanistic basis for M cell entry remains undefined. Here, we show that M cell transcytosis depends on the Mtb Type VII secretion m...

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Detalles Bibliográficos
Autores principales: Khan, Haaris S, Nair, Vidhya R, Ruhl, Cody R, Alvarez-Arguedas, Samuel, Galvan Rendiz, Jorge L, Franco, Luis H, Huang, Linzhang, Shaul, Philip W, Kim, Jiwoong, Xie, Yang, Mitchell, Ron B, Shiloh, Michael U
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065847/
https://www.ncbi.nlm.nih.gov/pubmed/32134383
http://dx.doi.org/10.7554/eLife.52551
Descripción
Sumario:Mycobacterium tuberculosis (Mtb) can enter the body through multiple routes, including via specialized transcytotic cells called microfold cells (M cell). However, the mechanistic basis for M cell entry remains undefined. Here, we show that M cell transcytosis depends on the Mtb Type VII secretion machine and its major virulence factor EsxA. We identify scavenger receptor B1 (SR-B1) as an EsxA receptor on airway M cells. SR-B1 is required for Mtb binding to and translocation across M cells in mouse and human tissue. Together, our data demonstrate a previously undescribed role for Mtb EsxA in mucosal invasion and identify SR-B1 as the airway M cell receptor for Mtb.