TY - JOUR
T1 - Gut Isolation from Zebrafish Larvae for Single-cell RNA Sequencing
AU - Kakiailatu, Naomi J.M.
AU - Kuil, Laura E.
AU - Bindels, Eric
AU - Zink, Joke T.M.
AU - Vermeulen, Michael
AU - Melotte, Veerle
AU - Alves, Maria M.
N1 - Funding Information:
This work was funded by the friends of Sophia Foundation (SSWO WAR-63).
Funding Information:
This work was funded by the friends of Sophia Foundation
Publisher Copyright:
© 2023 JoVE Journal of Visualized Experiments.
PY - 2023/11/1
Y1 - 2023/11/1
N2 - The gastrointestinal (GI) tract performs a range of functions essential for life. Congenital defects affecting its development can lead to enteric neuromuscular disorders, highlighting the importance to understand the molecular mechanisms underlying GI development and dysfunction. In this study, we present a method for gut isolation from zebrafish larvae at 5 days post fertilization to obtain live, viable cells which can be used for single-cell RNA sequencing (scRNA-seq) analysis. This protocol is based on the manual dissection of the zebrafish intestine, followed by enzymatic dissociation with papain. Subsequently, cells are submitted to fluorescence-activated cell sorting, and viable cells are collected for scRNA-seq. With this method, we were able to successfully identify different intestinal cell types, including epithelial, stromal, blood, muscle, and immune cells, as well as enteric neurons and glia. Therefore, we consider it to be a valuable resource for studying the composition of the GI tract in health and disease, using the zebrafish.
AB - The gastrointestinal (GI) tract performs a range of functions essential for life. Congenital defects affecting its development can lead to enteric neuromuscular disorders, highlighting the importance to understand the molecular mechanisms underlying GI development and dysfunction. In this study, we present a method for gut isolation from zebrafish larvae at 5 days post fertilization to obtain live, viable cells which can be used for single-cell RNA sequencing (scRNA-seq) analysis. This protocol is based on the manual dissection of the zebrafish intestine, followed by enzymatic dissociation with papain. Subsequently, cells are submitted to fluorescence-activated cell sorting, and viable cells are collected for scRNA-seq. With this method, we were able to successfully identify different intestinal cell types, including epithelial, stromal, blood, muscle, and immune cells, as well as enteric neurons and glia. Therefore, we consider it to be a valuable resource for studying the composition of the GI tract in health and disease, using the zebrafish.
U2 - 10.3791/65876
DO - 10.3791/65876
M3 - Article
SN - 1940-087X
VL - 2023
JO - Journal of visualized experiment
JF - Journal of visualized experiment
IS - 201
M1 - e65876
ER -