Immortalized Epithelial Cells Derived From Human Colon Biopsies Express Stem Cell Markers and Differentiate In Vitro
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
© 2010 AGA Institute. Published by Elsevier Inc. All rights reserved.

