CD24 can be used to isolate Lgr5+ putative colonic epithelial stem cells in mice

Am J Physiol Gastrointest Liver Physiol. 2012 Aug 15;303(4):G443-52. doi: 10.1152/ajpgi.00087.2012. Epub 2012 Jun 21.

Abstract

A growing body of evidence has implicated CD24, a cell-surface protein, as a marker of colorectal cancer stem cells and target for antitumor therapy, although its presence in normal colonic epithelium has not been fully characterized. Previously, our group showed that CD24-based cell sorting can be used to isolate a fraction of murine small intestinal epithelial cells enriched in actively cycling stem cells. Similarly, we hypothesized that CD24-based isolation of colonic epithelial cells would generate a fraction enriched in actively cycling colonic epithelial stem cells (CESCs). Immunohistochemistry performed on mouse colonic tissue showed CD24 expression in the bottom half of proximal colon crypts and the crypt base in the distal colon. This pattern of distribution was similar to enhanced green fluorescent protein (EGFP) expression in Lgr5-EGFP mice. Areas expressing CD24 contained actively proliferating cells as determined by ethynyl deoxyuridine (EdU) incorporation, with a distinct difference between the proximal colon, where EdU-labeled cells were most frequent in the midcrypt, and the distal colon, where they were primarily at the crypt base. Flow cytometric analyses of single epithelial cells, identified by epithelial cell adhesion molecule (EpCAM) positivity, from mouse colon revealed an actively cycling CD24(+) fraction that contained the majority of Lgr5-EGFP(+) putative CESCs. Transcript analysis by quantitative RT-PCR confirmed enrichment of active CESC markers [leucine-rich-repeat-containing G protein-coupled receptor 5 (Lgr5), ephrin type B receptor 2 (EphB2), and CD166] in the CD24(+)EpCAM(+) fraction but also showed enrichment of quiescent CESC markers [leucine-rich repeats and immunoglobin domains (Lrig), doublecortin and calmodulin kinase-like 1 (DCAMKL-1), and murine telomerase reverse transcriptase (mTert)]. We conclude that CD24-based sorting in wild-type mice isolates a colonic epithelial fraction highly enriched in actively cycling and quiescent putative CESCs. Furthermore, the presence of CD24 expression in normal colonic epithelium may have important implications for the use of anti-CD24-based colorectal cancer therapies.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, Neoplasm / metabolism
  • Biomarkers / metabolism
  • CD24 Antigen / metabolism*
  • Cell Adhesion Molecules / metabolism
  • Cell Proliferation
  • Cell Separation / methods*
  • Colon / cytology
  • Colon / immunology*
  • Epithelial Cell Adhesion Molecule
  • Epithelial Cells / immunology*
  • Flow Cytometry*
  • Gene Expression Regulation
  • Green Fluorescent Proteins / biosynthesis
  • Green Fluorescent Proteins / genetics
  • Immunohistochemistry
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Confocal
  • RNA, Messenger / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / immunology*
  • Transcription, Genetic

Substances

  • Antigens, Neoplasm
  • Biomarkers
  • CD24 Antigen
  • Cd24a protein, mouse
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule
  • Lgr5 protein, mouse
  • RNA, Messenger
  • Receptors, G-Protein-Coupled
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins