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Primary cultures of mouse small intestinal epithelial cells using the dissociating enzyme type I collagenase and hyaluronidase
Ren, HJ; Zhang, CL; Liu, RD; Li, N; Li, XG; Xue, HK; Guo, Y; Wang, ZQ; Cui, J; Ming, L.
Affiliation
  • Ren, HJ; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Zhang, CL; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Liu, RD; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Li, N; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Li, XG; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Xue, HK; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Guo, Y; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Wang, ZQ; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Cui, J; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
  • Ming, L; Zhengzhou University. Department of Clinical Laboratory. Zhengzhou. CN
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;50(5): e5831, 2017. tab, graf
Article de En | LILACS | ID: biblio-839293
Bibliothèque responsable: BR1.1
ABSTRACT
The epithelium is a highly dynamic system, which plays a crucial role in the homeostasis of the intestinal tract. However, studies on the physiological and pathophysiological functions of intestinal epithelial cells (IECs) have been hampered due to lack of normal epithelial cell models. In the present study, we established a reproducible method for primary culture of mouse IECs, which were isolated from the viable small intestinal crypts of murine fetuses (on embryonic day 19), using type I collagenase and hyaluronidase in a short span of time (≤20 min). With this method, continuously growing mouse IECs, which can be subcultured over a number of passages, were obtained. The obtained cell lines formed a tight cobblestone-like arrangement, displayed long and slender microvilli, expressed characteristic markers (cytokeratin 18 and Notch-1), and generated increasing transepithelial electrical resistance and low paracellular permeability during in vitro culture. The cells also had enzymatic activities of alkaline phosphatase and sucrase-isomaltase, and secreted various cytokines (IL-1β, IL-6, IL-8, and monocyte chemoattractant protein-1), responding to the stimulation of Escherichia coli. These results show that the primary-cultured mouse IECs obtained by the method established here had the morphological and immunological characteristics of IECs. This culture system can be a beneficial in vitro model for studies on mucosal immunology and toxicology.
Sujet(s)
Mots clés

Texte intégral: 1 Indice: LILACS Sujet Principal: Techniques de culture cellulaire / Cellules épithéliales / Matrix Metalloproteinase 13 / Hyaluronoglucosaminidase / Intestin grêle Type d'étude: Evaluation_studies / Prognostic_studies Limites du sujet: Animals langue: En Texte intégral: Braz. j. med. biol. res / Rev. bras. pesqui. méd. biol Thème du journal: BIOLOGIA / MEDICINA Année: 2017 Type: Article / Project document

Texte intégral: 1 Indice: LILACS Sujet Principal: Techniques de culture cellulaire / Cellules épithéliales / Matrix Metalloproteinase 13 / Hyaluronoglucosaminidase / Intestin grêle Type d'étude: Evaluation_studies / Prognostic_studies Limites du sujet: Animals langue: En Texte intégral: Braz. j. med. biol. res / Rev. bras. pesqui. méd. biol Thème du journal: BIOLOGIA / MEDICINA Année: 2017 Type: Article / Project document