Swarnabh Bhattacharya
@iamzico.bsky.social
62 followers 97 following 19 posts
Stem cell researcher | Organoids | Computational biology | Postdoc | Ramesh Shivdasani Lab | Dana-Farber Cancer Institute | Harvard Medical School | Ph.D @Shalom-Feuerstein Lab | Technion IIT
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Reposted by Swarnabh Bhattacharya
dev-journal.bsky.social
Our next #DevPres webinar focusses on gut development with talks from Surojit Sural @surojitsural.bsky.social, Swarnabh Bhattacharya @iamzico.bsky.social and Brittany Edens, chaired by Alex Eve @amjeve.bsky.social.

📆 17 September, 15:00 BST (UTC+1)

Register here: us02web.zoom.us/webinar/regi...
iamzico.bsky.social
Thanks to @rkzwick.bsky.social for writing this excellent preview and thoughtful discussion on our recent article @cp-cellstemcell.bsky.social (t.co/TkDxt1b3DH)
iamzico.bsky.social
Honored to receive a Pilot & Feasibility grant (P30 DK034854) from the Harvard Digestive Disease Center to explore cellular plasticity and the epigenetic drivers of inflammatory bowel disease. Excited to uncover new insights into IBD pathogenesis!
Reposted by Swarnabh Bhattacharya
sarawickstrom.bsky.social
Check out this exciting preprint from @aznarbenitahlab.bsky.social discovering a new mode of crosstalk between YAP and the circadian regulator BMAL1. Congrats @juliabonjoch.bsky.social and @guiomarsolanas.bsky.social for fantastic work and thank you for the fun collaboration!
juliabonjoch.bsky.social
Hi Bluesky community:)

Our new manuscript is now available as a preprint!⛅️
biorxiv.org/content/10.1...

1/ Here, we describe a novel BMAL1-YAP complex in epidermal cells, which is hijacked during ageing to control the expression of up-regulated inflammation genes through enhancer binding.🧵
BMAL1 and YAP cooperate to hijack enhancers and promote inflammation in the aged epidermis
Ageing is characterised by persistent low-grade inflammation that is linked to impaired tissue homeostasis and functionality. However, the molecular mechanisms driving age-associated inflammation rema...
biorxiv.org
iamzico.bsky.social
I want to give a big shoutout to my mentor Ramesh Shivdasani, my fellow lab members, and all the fantastic collaborators. It was an excellent team effort.
Here is a link to the full text: authors.elsevier.com/c/1kusf6tu0C...
#PanethCell #GobletCell #Epigenetics #IntestinalBiology
iamzico.bsky.social
A minority of enhancers are uniquely activated in Paneth cells under Wnt-favored conditions, shedding light on how epigenetic priming directs cell function along the crypt–villus axis.
iamzico.bsky.social
Beyond phenotypic plasticity, our study maps cis-regulatory dynamics of intestinal secretory differentiation: Tuft and EE cells display thousands of unique enhancers, while many goblet and Paneth enhancers are shared with intestinal stem cells.
iamzico.bsky.social
These insights redefine how we think about cell fate in the intestinal epithelium. Instead of being fixed identities, goblet and Paneth cells may be viewed as flexible, context-dependent states—a paradigm shift with potential implications for understanding intestinal diseases.
iamzico.bsky.social
A striking aspect of our findings is the reversible nature of this phenotypic switch. Even post-mitotic cells can rapidly convert their secretory identity in response to local niche signals—a process underpinned by dynamic chromatin changes.
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iamzico.bsky.social
Under forced Wnt and especially low BMP conditions, goblet cells gain Paneth features; conversely, BMP exposure potently suppresses Paneth markers and enhances goblet gene expression both in mouse and primary human 2D culture cells.
iamzico.bsky.social
Experimentally, we demonstrated this plasticity by altering Wnt/BMP levels in vivo (e.g., via Apc deletion and RSPO modulation) and in organoid cultures.
iamzico.bsky.social
Niche signals play a pivotal role! High Wnt and low BMP signaling, characteristic of the crypt base, push ATOH1+ cells to adopt a Paneth profile, while increased BMP (and lower Wnt) as cells move up the crypt drive a goblet cell phenotype.
iamzico.bsky.social
Our data show that both cell types originate from a common ATOH1+ secretory progenitor. Rather than being independently specified, goblet and Paneth cells share most mRNAs and many regulatory elements—only a few key antimicrobial genes differentiate them.
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media.tenor.com
iamzico.bsky.social
Using lineage tracing with Atoh1Cre-ER mice, along with single-cell RNA and chromatin accessibility (snATAC-seq) analyses, we found an unexpectedly high overlap in the transcriptomes and epigenetic landscapes of goblet and Paneth cells.
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iamzico.bsky.social
The intestinal epithelium renews rapidly from stem cells, generating absorptive enterocytes and secretory cells. While enteroendocrine and tuft cells follow distinct trajectories, goblet and Paneth cells have long been thought of as separate terminal fates—until now.
Reposted by Swarnabh Bhattacharya
labwaggoner.bsky.social
Different fibroblast subtypes propel spatially defined ileal inflammation through TNFR1 signaling in murine ileitis @naturecomms.bsky.social
www.nature.com/articles/s41...
Reposted by Swarnabh Bhattacharya
labwaggoner.bsky.social
Multiple layers of γδ IEL dysregulation and loss of their immunosuppressive capacity occur before the onset of chronic ileitis
www.science.org/doi/10.1126/...
@nbgolovchenko.bsky.social @sciimmunology.bsky.social @edelblumlab.bsky.social
Reposted by Swarnabh Bhattacharya
labwaggoner.bsky.social
Vagal pathway activation links chronic stress to decline in intestinal stem cell function @cp-cellstemcell.bsky.social
www.cell.com/cell-stem-ce...
Reposted by Swarnabh Bhattacharya
cp-cellchembiol.bsky.social
🔦Spotlight of Peter Dempsey, @brumbaugh-lab.bsky.social et al paper: Epigenetic fluidity meets phenotypic malleability in intestinal epithelial cells by @iamzico.bsky.social and Ramesh Shivdasani at @danafarber.bsky.social http://dlvr.it/TJfVRZ
iamzico.bsky.social
It was fun to write this Spotlight article @cp-cellchembiol.bsky.social on the recent NCB paper (rdcu.be/eayN3) by @brumbaugh-lab.bsky.social & Dempsey labs, revealing how epigenetic fluidity drives phenotypic malleability in the intestinal epithelium. www.sciencedirect.com/science/arti...