Pharmacological validation of targets regulating CD14 during macrophage differentiation
Journal Title
EBioMedicine
Publication Type
Journal Article
Abstract
The signalling receptor for LPS, CD14, is a key marker of, and facilitator for, pro-inflammatory macrophage function. Pro-inflammatory macrophage differentiation remains a process facilitating a broad array of disease pathologies, and has recently emerged as a potential target against cytokine storm in COVID19. Here, we perform a whole-genome CRISPR screen to identify essential nodes regulating CD14 expression in myeloid cells, using the differentiation of THP-1 cells as a starting point. This strategy uncovers many known pathways required for CD14 expression and regulating macrophage differentiation while additionally providing a list of novel targets either promoting or limiting this process. To speed translation of these results, we have then taken the approach of independently validating hits from the screen using well-curated small molecules. In this manner, we identify pharmacologically tractable hits that can either increase CD14 expression on non-differentiated monocytes or prevent CD14 upregulation during macrophage differentiation. An inhibitor for one of these targets, MAP2K3, translates through to studies on primary human monocytes, where it prevents upregulation of CD14 following M-CSF induced differentiation, and pro-inflammatory cytokine production in response to LPS. Therefore, this screening cascade has rapidly identified pharmacologically tractable nodes regulating a critical disease-relevant process.
Publisher
eLife Sciences
Research Division(s)
Inflammation
PubMed ID
33038762
Open Access at Publisher's Site
https://doi.org/10.1016/j.ebiom.2020.103039
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2020-11-02 04:55:16
Last Modified: 2020-11-02 05:01:15
An error has occurred. This application may no longer respond until reloaded. Reload 🗙