OBJECTIVE: To prepare an in vitro reconstruction of the porcine laryngeal mucosa, for use in cell biological investigations and as a model for the study of laryngeal disease. DESIGN: Using separately obtained epithelial cells and fibroblasts from porcine laryngeal mucosa, we reconstructed the laryngeal mucosa in a three-dimensional collagen gel matrix culture with air-liquid interface. SUBJECTS: Porcine larynges were from 6-month-old pigs obtained from a local abattoir. RESULTS: We successfully reconstructed the laryngeal mucosa in vitro, including epithelium and lamina propria. The epithelial cells showed five to eight cells in thickness and were well differentiated on the reconstructed lamina propria. The differentiation-specific cytokeratin was positive. CONCLUSIONS: To our knowledge, this is the first report of a reconstruction of the laryngeal mucosa in a three-dimensional collagen gel matrix culture. Fibroblasts and air-liquid interface treatment exert a great influence on the proliferation and differentiation of the cultured epithelial cells. This culture system will help to provide an appropriate physiologic environment to study the differentiation and disease of the larynx.
OBJECTIVE: To prepare an in vitro reconstruction of the porcine laryngeal mucosa, for use in cell biological investigations and as a model for the study of laryngeal disease. DESIGN: Using separately obtained epithelial cells and fibroblasts from porcine laryngeal mucosa, we reconstructed the laryngeal mucosa in a three-dimensional collagen gel matrix culture with air-liquid interface. SUBJECTS: Porcine larynges were from 6-month-old pigs obtained from a local abattoir. RESULTS: We successfully reconstructed the laryngeal mucosa in vitro, including epithelium and lamina propria. The epithelial cells showed five to eight cells in thickness and were well differentiated on the reconstructed lamina propria. The differentiation-specific cytokeratin was positive. CONCLUSIONS: To our knowledge, this is the first report of a reconstruction of the laryngeal mucosa in a three-dimensional collagen gel matrix culture. Fibroblasts and air-liquid interface treatment exert a great influence on the proliferation and differentiation of the cultured epithelial cells. This culture system will help to provide an appropriate physiologic environment to study the differentiation and disease of the larynx.
Authors: Mahalakshmi Sivasankar; Elizabeth Erickson; Mark Rosenblatt; Ryan C Branski Journal: Otolaryngol Head Neck Surg Date: 2009-11-22 Impact factor: 3.497
Authors: Changying Ling; Qiyao Li; Matthew E Brown; Yo Kishimoto; Yutaka Toya; Erin E Devine; Kyeong-Ok Choi; Kohei Nishimoto; Ian G Norman; Tenzin Tsegyal; Jack J Jiang; William J Burlingham; Sundaram Gunasekaran; Lloyd M Smith; Brian L Frey; Nathan V Welham Journal: Sci Transl Med Date: 2015-11-18 Impact factor: 17.956