The roles of regional specialization, mechanical forces and epigenetic memory after perturbation and injury of the intestinal stem cell microenvironment

NIH RePORTER · NIH · U01 · $279,654 · view on reporter.nih.gov ↗

Abstract

Project Summary The increased complexity of methods to analyze high-throughput genomic data, particularly single cell datasets, mandates the tight interaction between experimental and computational scientists. Analysis of how different compartments of the intestine interact with each other and react to insults is greatly advanced by studies at the single cell level. This project will accelerate progress of genomic analysis of the intestinal stem cell niche by ISCC members through the following two aims, (1) collaborations on projects from individual centers, and (2) collaboration on a consortium-wide project to determine the minimum set of genetic factors that support the intestinal stem cell niche using a comparative approach. In the previous year of this project, we have established collaborations with four ISCC teams to help with their project; we will now continue these collaborations and initiate two additional collaborations. For the consortium-wide project, we will generate new single-cell gene expression datasets to annotate a set of gene modules and communication modules in the intestinal stem cell niche in mouse and human. This project will deliver a set of conserved and derived factors that participate in the maintenance of the intestinal stem cell niche and a consortium-endorsed nomenclature of all mesenchymal, epithelial, and other cell subtypes in human and mouse intestine.

Key facts

NIH application ID
10439349
Project number
3U01DK103147-08S2
Recipient
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
Principal Investigator
Ophir D Klein
Activity code
U01
Funding institute
NIH
Fiscal year
2021
Award amount
$279,654
Award type
3
Project period
2014-09-05 → 2022-08-31