3d-culturing-organoids-from-intestinal-villi-epithelium-undergoing

3D Culturing of Organoids from the Intestinal Villi Epithelium Undergoing Dedifferentiation

Clonogenicity of organoids from the intestinal epithelium is attributed to the presence of stem cells therein. The mouse small intestinal epithelium is ...

Stevens Institute of Technology

BMP/SMAD signaling is a crucial regulator of intestinal differentiation. However, the molecular underpinnings of the BMP pathway in this context are unknown. Here, we characterize the mechanism by which BMP/SMAD signaling drives enterocyte differentiation. We establish that the transcription factor HNF4A acts redundantly with an intestine-restricted HNF4 paralog, HNF4G, to activate enhancer chromatin and upregulate the majority of transcripts enriched in the differentiated epithelium; cells fail to differentiate on double knockout of both HNF4 paralogs. Furthermore, we show that SMAD4 and HNF4 function via a reinforcing feed-forward loop, activating each other's expression and co-binding to regulatory elements of differentiation genes. This feed-forward regulatory module promotes and stabilizes enterocyte cell identity; disruption of the HNF4-SMAD4 module results in loss of enterocyte fate in favor of progenitor and secretory cell lineages. This intersection of signaling and transcriptional control provides a framework to understand regenerative tissue homeostasis, particularly in tissues with inherent cellular plasticity.

Ansu Perekatt

Department of Biology and Chemical Biology

Stevens Institute of Technology

3D Culturing of Organoids from the Intestinal Villi Epithelium Undergoing Dedifferentiation

Ansu Perekatt

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Biology and Chemical Biology

Stevens Institute of Technology

3D Culturing of Organoids from the Intestinal Villi Epithelium Undergoing Dedifferentiation

Department of Biology and Chemical Biology