Summary: This protocol is intended as a guide for implementing or refining the usage of the air-liquid interface (ALI) model system to generate airway mucociliary tissue in vitro. We present a streamlined protocol for isolating the stem cells from inferior nasal turbinates of donors, allowing for a simple and low-cost supply of primary cells for research. We also provide our detailed protocols for ALI tissue processing and immunofluorescence to aid in the standardization of these techniques between research groups.For complete details on the use and execution of this protocol, please refer to Hussain et al., (2014) Yang et al., (2016) Im et al., (2019)
In recent years, there has been a significant increase in the registration of drugs for nasal applic...
The nasal mucosa provides first line defense against inhaled pathogens while creating a unique micro...
Fresh nasal brushings and air-liquid interface (ALI) cultures of nasal epithelial cells are frequent...
In vitro differentiation of airway epithelium is of interest for respiratory tissue engineering and ...
BACKGROUND: Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop ...
Background: Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop ...
In vitro models using human primary epithelial cells are essential in understanding key functions of...
Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop a well-diffe...
Different in vitro culture systems have been used to study the functional properties of respiratory ...
ABSTRACT − Growing interest in the nasal route as a drug delivery system calls for a reliable in vit...
Introduction: ex vivo airway epithelial cell models provide a biologically representative platform f...
Background and Objectives:The purpose of this study was to subculture normal human nasal epithelial ...
Air-liquid interface (ALI) cell culture of primary airway progenitors enables the differentiation an...
The purpose of this study was to develop a subculturing technique that allows the formation of large...
7 pagesInternational audienceAbstractBackgroundBronchial epithelium plays a key role in orchestratin...
In recent years, there has been a significant increase in the registration of drugs for nasal applic...
The nasal mucosa provides first line defense against inhaled pathogens while creating a unique micro...
Fresh nasal brushings and air-liquid interface (ALI) cultures of nasal epithelial cells are frequent...
In vitro differentiation of airway epithelium is of interest for respiratory tissue engineering and ...
BACKGROUND: Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop ...
Background: Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop ...
In vitro models using human primary epithelial cells are essential in understanding key functions of...
Primary human airway epithelial cells cultured in an air-liquid interface (ALI) develop a well-diffe...
Different in vitro culture systems have been used to study the functional properties of respiratory ...
ABSTRACT − Growing interest in the nasal route as a drug delivery system calls for a reliable in vit...
Introduction: ex vivo airway epithelial cell models provide a biologically representative platform f...
Background and Objectives:The purpose of this study was to subculture normal human nasal epithelial ...
Air-liquid interface (ALI) cell culture of primary airway progenitors enables the differentiation an...
The purpose of this study was to develop a subculturing technique that allows the formation of large...
7 pagesInternational audienceAbstractBackgroundBronchial epithelium plays a key role in orchestratin...
In recent years, there has been a significant increase in the registration of drugs for nasal applic...
The nasal mucosa provides first line defense against inhaled pathogens while creating a unique micro...
Fresh nasal brushings and air-liquid interface (ALI) cultures of nasal epithelial cells are frequent...