Transcriptomics

Dataset Information

0

The lung environment controls alveolar macrophage metabolism and responsiveness during type-2 inflammation.


ABSTRACT: Fine control of macrophage activation is required to prevent inflammatory disease, particularly at barrier sites such as the lung. However, the dominant mechanisms that regulate pulmonary MΦs during inflammation are currently poorly understood. Here we show that airway MΦs are substantially less able to respond to the canonical type-2 cytokine IL-4, which underpins allergic disease and parasite worm infections, than lung tissue or peritoneal cavity MΦs. We reveal that MΦ hypo-responsiveness to IL-4 is dictated by the lung environment, though independent of the host microbiota or the prominent lung extracellular matrix components surfactant protein D and mucin 5b. Rather, compared to cavity MΦs,  airway MΦs display severely dysregulated metabolism. Strikingly, upon removal from the lung, alveolar MΦs regain IL-4 responsiveness in a process dependent upon glycolysis. Thus, we propose that impaired glycolysis within the pulmonary niche is a central determinant for regulation of MΦ responsiveness during type-2 inflammation.

ORGANISM(S): Mus musculus

PROVIDER: GSE126309 | GEO | 2019/03/26

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2021-06-18 | ST001835 | MetabolomicsWorkbench
2024-11-07 | GSE267506 | GEO
2019-02-13 | GSE123289 | GEO
2024-09-08 | GSE276428 | GEO
2022-09-12 | GSE167465 | GEO
2022-09-12 | GSE167464 | GEO
2022-09-12 | GSE167461 | GEO
2022-09-12 | GSE167460 | GEO
2022-09-12 | GSE167463 | GEO
2023-08-28 | GSE239696 | GEO