4.6 Article

Sox9 expression marks a subset of CD24-expressing small intestine epithelial stem cells that form organoids in vitro

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpgi.00470.2009

关键词

SOX factors; intestinal epithelial culture

资金

  1. University of North Carolina (UNC) Center for Gastrointestinal Biology and Disease Imaging and Histology COREs [5P30DK034987]
  2. UNC Neuroscience Confocal Imaging Facility [P30 NS045892-04]
  3. UNC Chapel Hill Mutant Mouse Regional Resource Center
  4. UNC Flow Cytometry CORE
  5. National Institutes of Health [1-K01-DK080181-01]
  6. American Gastroenterological Association
  7. North Carolina Biotechnology Center
  8. UNC-Chapel Hill the Center for Gastrointestinal Biology and Disease [5P30DK034987]

向作者/读者索取更多资源

Gracz AD, Ramalingam S, Magness ST. Sox9 expression marks a subset of CD24-expressing small intestine epithelial stem cells that form organoids in vitro. Am J Physiol Gastrointest Liver Physiol 298: G590-G600, 2010. First published February 25, 2010; doi: 10.1152/ajpgi.00470.2009.-The inability to identify, isolate, and culture intestinal epithelial stem cells (IESCs) has been prohibitive to the study and therapeutic utilization of these cells. Using a Sox9(EGFP) mouse model, we demonstrate that Sox9(EGFP) fluorescence signatures can be used to differentiate between and enrich for progenitors (Sox9(EGFPsubLo)) and multipotent IESCs (Sox9(EGFPlo)). Sox9(EGFPlo) cells generate organoids in a recently defined culture system that mimics the native IESC niche. These organoids possess all four differentiated cell types of the small intestine epithelium, demonstrating the multipotent capacity of Sox9(EGFPlo) cells. Our results are consistent with the previously reported observation that single IESCs generate cryptlike units without a detectable mesenchymal cell component. A prospective search revealed that CD24 is expressed in the Sox9(EGFPlo) population and marks IESCs that form organoids in culture. CD24 represents the first cell surface marker that facilitates fluorescence-activated cell sorting enrichment of IESCs with widely available antibodies without requiring a specialized fluorescent reporter gene mouse model.

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