Association of hepatocyte-derived growth factor receptor/caudal type homeobox 2 co-expression with mucosal regeneration in active ulcerative colitis

World J Gastroenterol. 2015 Jul 28;21(28):8569-79. doi: 10.3748/wjg.v21.i28.8569.

Abstract

Aim: To characterize the regeneration-associated stem cell-related phenotype of hepatocyte-derived growth factor receptor (HGFR)-expressing cells in active ulcerative colitis (UC).

Methods: On the whole 38 peripheral blood samples and 38 colonic biopsy samples from 18 patients with histologically proven active UC and 20 healthy control subjects were collected. After preparing tissue microarrays and blood smears HGFR, caudal type homeobox 2 (CDX2), prominin-1 (CD133) and Musashi-1 conventional and double fluorescent immunolabelings were performed. Immunostained samples were digitalized using high-resolution Mirax Desk instrument, and analyzed with the Mirax TMA Module software. For semiquantitative counting of immunopositive lamina propria (LP) cells 5 fields of view were counted at magnification × 200 in each sample core, then mean ± SD were determined. In case of peripheral blood smears, 30 fields of view with 100 μm diameter were evaluated in every sample and the number of immunopositive cells (mean ± SD) was determined. Using 337 nm UVA Laser MicroDissection system at least 5000 subepithelial cells from the lamina propria were collected. Gene expression analysis of HGFR, CDX2, CD133, leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5), Musashi-1 and cytokeratin 20 (CK20) were performed in both laser-microdisscted samples and blood samples by using real time reverse transcription polymerase chain reaction (RT-PCR).

Results: By performing conventional and double fluorescent immunolabelings confirmed by RT-PCR, higher number of HGFR (blood: 6.7 ± 1.22 vs 38.5 ± 3.18; LP: 2.25 ± 0.85 vs 9.22 ± 0.65; P < 0.05), CDX2 (blood: 0 vs 0.94 ± 0.64; LP: 0.75 ± 0.55 vs 2.11 ± 0.75; P < 0.05), CD133 (blood: 1.1 ± 0.72 vs 8.3 ± 1.08; LP: 11.1 ± 0.85 vs 26.28 ± 1.71; P < 0.05) and Musashi-1 (blood and LP: 0 vs scattered) positive cells were detected in blood and lamina propria of UC samples as compared to controls. HGFR/CDX2 (blood: 0 vs 1 ± 0.59; LP: 0.8 ± 0.69 vs 2.06 ± 0.72, P < 0.05) and Musashi-1/CDX2 (blood and LP: 0 vs scattered) co-expressions were found in blood and lamina propria of UC samples. HGFR/CD133 and CD133/CDX2 co-expressions appeared only in UC lamina propria samples. CDX2, Lgr5 and Musashi-1 expressions in UC blood samples were not accompanied by CK20 mRNA expression.

Conclusion: In active UC, a portion of circulating HGFR-expressing cells are committed to the epithelial lineage, and may participate in mucosal regeneration by undergoing mesenchymal-to-epithelial transition.

Keywords: CD133; Caudal type homeobox 2; Hepatocyte-derived growth factor receptor; Leucine-rich repeat-containing G-protein coupled receptor 5; Musashi-1; Regeneration; Ulcerative colitis.

MeSH terms

  • AC133 Antigen
  • Antigens, CD / analysis
  • CDX2 Transcription Factor
  • Case-Control Studies
  • Cell Differentiation
  • Cell Lineage
  • Colitis, Ulcerative / diagnosis
  • Colitis, Ulcerative / genetics
  • Colitis, Ulcerative / metabolism*
  • Colitis, Ulcerative / physiopathology
  • Colon / chemistry*
  • Colon / pathology
  • Colon / physiopathology
  • Fluorescent Antibody Technique
  • Glycoproteins / analysis
  • Homeodomain Proteins / analysis*
  • Homeodomain Proteins / blood
  • Homeodomain Proteins / genetics
  • Humans
  • Intestinal Mucosa / chemistry*
  • Intestinal Mucosa / pathology
  • Intestinal Mucosa / physiopathology
  • Laser Capture Microdissection
  • Nerve Tissue Proteins / analysis
  • Peptides / analysis
  • Phenotype
  • Proto-Oncogene Proteins c-met / analysis*
  • Proto-Oncogene Proteins c-met / blood
  • Proto-Oncogene Proteins c-met / genetics
  • RNA-Binding Proteins / analysis
  • Real-Time Polymerase Chain Reaction
  • Regeneration*
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Stem Cells / chemistry*
  • Stem Cells / pathology

Substances

  • AC133 Antigen
  • Antigens, CD
  • CDX2 Transcription Factor
  • CDX2 protein, human
  • Glycoproteins
  • Homeodomain Proteins
  • MSI1 protein, human
  • Nerve Tissue Proteins
  • PROM1 protein, human
  • Peptides
  • RNA-Binding Proteins
  • MET protein, human
  • Proto-Oncogene Proteins c-met