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Detailed survey of an in vitro intestinal epithelium model by single-cell transcriptomics.
Ran, Ran; Muñoz Briones, Javier; Jena, Smrutiti; Anderson, Nicole L; Olson, Matthew R; Green, Leopold N; Brubaker, Douglas K.
Afiliación
  • Ran R; Center for Global Health and Diseases, Department of Pathology, Case Western Reserve University, Cleveland, OH, USA.
  • Muñoz Briones J; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
  • Jena S; Purdue Interdisciplinary Life Science Program, West Lafayette, IN, USA.
  • Anderson NL; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
  • Olson MR; Department of Biological Sciences, Purdue University, West Lafayette, IN, USA.
  • Green LN; Department of Biological Sciences, Purdue University, West Lafayette, IN, USA.
  • Brubaker DK; Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, USA.
iScience ; 27(4): 109383, 2024 Apr 19.
Article en En | MEDLINE | ID: mdl-38523788
ABSTRACT
The co-culture of two adult human colorectal cancer cell lines, Caco-2 and HT29, on Transwell is commonly used as an in vitro gut mimic, yet the translatability of insights from such a system to adult human physiological contexts is not fully characterized. Here, we used single-cell RNA sequencing on the co-culture to obtain a detailed survey of cell type heterogeneity in the system and conducted a holistic comparison with human physiology. We identified the intestinal stem cell-, transit amplifying-, enterocyte-, goblet cell-, and enteroendocrine-like cells in the system. In general, the co-culture was fetal intestine-like, with less variety of gene expression compared to the adult human gut. Transporters for major types of nutrients were found in the majority of the enterocytes-like cells in the system. TLR 4 was not expressed in the sample, indicating that the co-culture model is incapable of mimicking the innate immune aspect of the human epithelium.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: IScience Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: IScience Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos