Gastroenterology
Volume 138, Issue 3 , Pages 1012-1021.e5, March 2010

Immortalized Epithelial Cells Derived From Human Colon Biopsies Express Stem Cell Markers and Differentiate In Vitro

  • Andres I. Roig

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
    • Department of Medicine, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Ugur Eskiocak

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Suzie K. Hight

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Sang Bum Kim

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Oliver Delgado

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Rhonda F. Souza

      Affiliations

    • Department of Medicine, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
    • Veterans Affairs North Texas Health Care System, Dallas, Texas
  • ,
  • Stuart J. Spechler

      Affiliations

    • Department of Medicine, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
    • Veterans Affairs North Texas Health Care System, Dallas, Texas
  • ,
  • Woodring E. Wright

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Jerry W. Shay

      Affiliations

    • Department of Cell Biology, Division of Digestive and Liver Diseases, University of Texas Southwestern Medical Center, Dallas, Texas
    • Corresponding Author InformationReprint requests Address requests for reprints to: Jerry W. Shay, PhD, Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75390. fax: (214) 648-8694

Received 19 August 2009; accepted 20 November 2009. published online 07 December 2009.

Background & Aims

Long-term propagation of human colonic epithelial cells (HCEC) of adult origin has been a challenge; currently used HCEC lines are of malignant origin and/or contain multiple cytogenetic changes. We sought to immortalize human colon biopsy-derived cells expressing stem cell markers and retaining multilineage epithelial differentiation capability.

Methods

We isolated and cultured cells from biopsy samples of 2 patients undergoing routine screening colonoscopy. Cells were immortalized by expression of the nononcogenic proteins cyclin-dependent kinase 4 (Cdk4) and the catalytic component of human telomerase (hTERT) and maintained for more than 1 year in culture.

Results

The actively proliferating HCECs expressed the mesenchymal markers vimentin and α-smooth muscle actin. Upon growth arrest, cells assumed a cuboidal shape, decreased their mesenchymal features, and expressed markers of colonic epithelial cells such as cytokeratin 18, zonula occludens-1, mucins-1 and -2, antigen A33, and dipeptidyl peptidase 4. Immortalized cells expressed stem cell markers that included LGR5, BMI1, CD29, and CD44. When placed in Matrigel in the absence of a mesenchymal feeder layer, individual cells divided and formed self-organizing, cyst-like structures; a subset of cells exhibited mucin-2 or polarized villin staining.

Conclusions

We established immortalized HCECs that are capable of self-renewal and multilineage differentiation. These cells should serve as valuable reagents for studying colon stem cell biology, differentiation, and pathogenesis.

Keywords: Stem/Progenitor Cells, Epithelial Mesenchymal Transition, Self-Renewal, Multilineage Differentiation

Abbreviations used in this paper: BIO, bromoindirubin-3-oxime, 2D, two-dimensional, 3D, three-dimensional, Cdk4, cyclin-dependent kinase-4, EGF, epithelial growth factor, GSK-3β, glycogen synthase kinase-3β, HCEC CT, human colonic epithelial cell immortalized with Cdk4 and hTERT, hTERT, catalytic component of human telomerase, MUC, mucin, PD, population doublings, ZO-1, zonula occludens-1

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 Conflicts of interest The authors disclose no conflicts.

 Funding This work was supported by NASA grant no. NNXO8BA54G and NNX09AU95G to J.W.S., and T32 CA124334 and American Gastroenterology Association Fellow to Faculty Transition Award to A.I.R.

PII: S0016-5085(09)02104-0

doi:10.1053/j.gastro.2009.11.052

Gastroenterology
Volume 138, Issue 3 , Pages 1012-1021.e5, March 2010