4.7 Article

Isolation and characterization of mouse and human esophageal epithelial cells in 3D organotypic culture

Journal

NATURE PROTOCOLS
Volume 7, Issue 2, Pages 235-246

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2011.437

Keywords

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Funding

  1. US National Institutes of Health (NIH)/National Cancer Institute (NCI) [P01-CA098101]
  2. NIH/National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) [P30-DK050306]
  3. NIH/NCI [U01-CA143056, T32-CA115299]
  4. NIH/NIDDK Center for Molecular Studies in Digestive and Liver Diseases at the University of Pennsylvania [P30-DK050306, R01DK077005]
  5. American Cancer Society
  6. NIH [T32-CA009140-37]

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T his protocol describes the isolation and characterization of mouse and human esophageal epithelial cells and the application of 3D organotypic culture (OTC), a form of tissue engineering. This model system permits the interrogation of mechanisms underlying epithelial-stromal interactions. We provide guidelines for isolating and cultivating several sources of epithelial cells and fibroblasts, as well as genetic manipulation of these cell types, as a prelude to their integration into OTC. The protocol includes a number of important applications, including histology, immunohistochemistry/immunofluorescence, genetic modification of epithelial cells and fibroblasts with retroviral and lentiviral vectors for overexpression of genes or RNA interference strategies, confocal imaging, laser capture microdissection, RNA microarrays of individual cellular compartments and protein-based assays. The OTC (3D) culture protocol takes 15 d to perform.

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