Unknown

Dataset Information

0

Myeloid Growth Factors Promote Resistance to Mycobacterial Infection by Curtailing Granuloma Necrosis through Macrophage Replenishment.


ABSTRACT: The mycobacterial ESX-1 virulence locus accelerates macrophage recruitment to the forming tuberculous granuloma. Newly recruited macrophages phagocytose previously infected apoptotic macrophages to become new bacterial growth niches. Granuloma macrophages can then necrose, releasing mycobacteria into the extracellular milieu, which potentiates their growth even further. Using zebrafish with genetic or pharmacologically induced macrophage deficiencies, we find that global macrophage deficits increase susceptibility to mycobacterial infection by accelerating granuloma necrosis. This is because reduction in the macrophage supply below a critical threshold decreases granuloma macrophage replenishment to the point where apoptotic infected macrophages, failing to get engulfed, necrose. Reducing macrophage demand by removing bacterial ESX-1 offsets the susceptibility of macrophage deficits. Conversely, increasing macrophage supply in wild-type fish by overexpressing myeloid growth factors induces resistance by curtailing necrosis. These findings may explain the susceptibility of humans with mononuclear cytopenias to mycobacterial infections and highlight the therapeutic potential of myeloid growth factors in tuberculosis.

SUBMITTER: Pagan AJ 

PROVIDER: S-EPMC4509513 | biostudies-literature | 2015 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Myeloid Growth Factors Promote Resistance to Mycobacterial Infection by Curtailing Granuloma Necrosis through Macrophage Replenishment.

Pagán Antonio J AJ   Yang Chao-Tsung CT   Cameron James J   Swaim Laura E LE   Ellett Felix F   Lieschke Graham J GJ   Ramakrishnan Lalita L  

Cell host & microbe 20150701 1


The mycobacterial ESX-1 virulence locus accelerates macrophage recruitment to the forming tuberculous granuloma. Newly recruited macrophages phagocytose previously infected apoptotic macrophages to become new bacterial growth niches. Granuloma macrophages can then necrose, releasing mycobacteria into the extracellular milieu, which potentiates their growth even further. Using zebrafish with genetic or pharmacologically induced macrophage deficiencies, we find that global macrophage deficits incr  ...[more]

Similar Datasets

| S-EPMC5268069 | biostudies-literature
2016-10-18 | GSE81913 | GEO
| S-EPMC6512360 | biostudies-literature
| S-EPMC4539912 | biostudies-literature
| S-EPMC3677198 | biostudies-literature
| S-EPMC5827556 | biostudies-literature
| S-EPMC10653359 | biostudies-literature
| S-EPMC4288886 | biostudies-literature
| S-EPMC5419324 | biostudies-literature
| S-EPMC5548176 | biostudies-other