Xu Zhou lab @ BCH & HMS
@xuzhoulab.bsky.social
440 followers 640 following 47 posts
AP @BostonChildrens @harvardmed AM @broadinstitute inflammation, tissue biology, quant.&systems immunology #1stGen #ImmigrantScientists #NewPI
Posts Media Videos Starter Packs
Pinned
xuzhoulab.bsky.social
Beyond excited to share our #NewPaper in @cellcellpress.bsky.social! Inflamed environments acidify intracellular #pH. BRD4 senses this via transcriptional condensates, tuning #macrophage responses to match demand and consequences of #inflammation authors.elsevier.com/sd/article/S...
xuzhoulab.bsky.social
Super excited to see our recent @cellcellpress.bsky.social paper featured in a Life Metabolism preview! Huge thanks to Christoopher Glass @ucsdmedschool.bsky.social for the thoughtful highlight. 🔗 academic.oup.com/lifemeta/adv...
#inflammation #macrophage #chromatin #pH #biomolecularcondensates
Reposted by Xu Zhou lab @ BCH & HMS
jkagan1.bsky.social
TLR4 endocytosis continues to be the centerpiece of TRIF-Interferon signaling. Kasper et al report diverse structures of Bacteroides LPS and their impact on TLR4 endocytosis and signaling. Functional consequences on Treg induction in the gut.
www.cell.com/cell/abstrac...
Structure of gut microbial glycolipid modulates host inflammatory response
Structural variations in the number of acyl chains and phosphate groups of gram-negative microbial lipid A differentially modulate DC-derived IFN-β responses, which are mechanistically regulated by TL...
www.cell.com
xuzhoulab.bsky.social
hhmi.org
HHMI @hhmi.org · 19d
🎉 Congratulations to HHMI Investigators Clifford Brangwynne and Akiko Iwasaki, the two winners of the 30th annual Keio Medical Science Prize. This international prize, awarded by Keio University in Tokyo, honors scientists who have made major contributions to the fields of medical or life sciences.
xuzhoulab.bsky.social
Thank you so much Igor! It was a fun journey :)
xuzhoulab.bsky.social
This long journey started ~10yr ago when I was postdoc with @rmedzhitov.bsky.social. twists and turns along the way&many hypotheses proven wrong. This journey is impossible without generous support from my former mentor and labmates, talented people in my own group and collaborators&colleagues.
xuzhoulab.bsky.social
last but not least, BRD4 are broadly expressed in different cell types. We found consistent pH-dependent regulation across immune, stromal, epithelial and tumor cells, including both mouse and human. More examples are accumulating in-house. feel free to dm / email me if anybody is interested.
xuzhoulab.bsky.social
we hypothesize that BRD4 condensates could function as an internal pH meter to gauge cellular state linked to inflammatory activation and metabolism, by controlling the expression of key metabolic genes. 22/n
xuzhoulab.bsky.social
and a similar response happens in vivo! 21/n
xuzhoulab.bsky.social
As immune activation tends to increase intracellular and extracellular acidification, we turned to look at what happens just with LPS stimulation. And it is sufficient to reduce BRD4 condensates in vitro 20/n
xuzhoulab.bsky.social
for anybody who is curious what make a gene dependent or not on BRD4 condensates: we don't have the answer yet, but we found that pH-sensitive genes seem to have the most recruitment of BRD4 to their enhancers. In another words, BRD4 recruitment might be a predictor of pH-sensitive expression.19/n
xuzhoulab.bsky.social
disruption of BRD4 condensates leads to disruption of MED1 condensates, which likely explains the suppressed the inflammatory activation in macrophages (more to come about these mechanisms!) 18/n
xuzhoulab.bsky.social
surprisingly, we found that only histidine residues in selective regions of BRD4-IDR are required for pH sensitivity, and that consecutive histidine can give rise to pH-sensitivity in biomolecular condensates at physiological pH range.
17/n
xuzhoulab.bsky.social
Swapping histidines (ph sensitive around 6-7) to alanine can reverse the pH-dependent regulation on transcriptional condensates. 16/n
xuzhoulab.bsky.social
This response is regulated by enriched and conserved histidines on BRD4-IDR 15/n
xuzhoulab.bsky.social
with suggestions from reviewers, we brought up our game to super-resolution microscopy to characterize the changes of native BRD4 condensates with STED scope & thanks to help from Krishnan Raghunathan and Thiagarajah lab👍
xuzhoulab.bsky.social
@bsabari.bsky.social @richardyonck.com @whiteheadinstitute.bsky.social Arup Chakraborty @mitpress.bsky.social among other pioneers in biomolecular #condensates showed that BRD4 forms transcriptional condensates. We found that these condensates native to macrophages are disrupted by acidic pH. 13/n
xuzhoulab.bsky.social
Based on features of the disordered loop in yeast SNF5. Diana Leung in my lab did an in silico screening and found mammalian BRD4 as putative pH sensor. Happy to chat about the bioinformatic work if anyone is interested. 12/n
xuzhoulab.bsky.social
But how does it happen? We tested differential signaling, protein translation, global epigenetic modification etc. all proven wrong. a few good years of negative data 10/n
xuzhoulab.bsky.social
this analysis suggested that inflammatory genes partition into functions for immediate microbial defense and propagations of inflammatory cascade in a pH-dependent manner 9/n
xuzhoulab.bsky.social
And even more surprise, pH-dependent response is independent of well-known pH sensors in macrophages. To understand better how it happens, we developed a #deconvolution model to quantify how pH and immune signals interact to activate each gene.
Alert 🔥 A computational pipeline will be online soon.