TY - JOUR
T1 - Single-cell resolution three-dimensional imaging of intact organoids
AU - van Ineveld, Ravian L.
AU - Ariese, Hendrikus C.R.
AU - Wehrens, Ellen J.
AU - Dekkers, Johanna F.
AU - Rios, Anne C.
N1 - Publisher Copyright:
© 2020 Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
PY - 2020
Y1 - 2020
N2 - Organoid technology, in vitro 3D culturing of miniature tissue, has opened a new experimental window for cellular processes that govern organ development and function as well as disease. Fluorescence microscopy has played a major role in characterizing their cellular composition in detail and demonstrating their similarity to the tissue they originate from. In this article, we present a comprehensive protocol for high-resolution 3D imaging of whole organoids upon immunofluorescent labeling. This method is widely applicable for imaging of organoids differing in origin, size and shape. Thus far we have applied the method to airway, colon, kidney, and liver organoids derived from healthy human tissue, as well as human breast tumor organoids and mouse mammary gland organoids. We use an optical clearing agent, FUnGI, which enables the acquisition of whole 3D organoids with the opportunity for single-cell quantification of markers. This three-day protocol from organoid harvesting to image analysis is optimized for 3D imaging using confocal microscopy.
AB - Organoid technology, in vitro 3D culturing of miniature tissue, has opened a new experimental window for cellular processes that govern organ development and function as well as disease. Fluorescence microscopy has played a major role in characterizing their cellular composition in detail and demonstrating their similarity to the tissue they originate from. In this article, we present a comprehensive protocol for high-resolution 3D imaging of whole organoids upon immunofluorescent labeling. This method is widely applicable for imaging of organoids differing in origin, size and shape. Thus far we have applied the method to airway, colon, kidney, and liver organoids derived from healthy human tissue, as well as human breast tumor organoids and mouse mammary gland organoids. We use an optical clearing agent, FUnGI, which enables the acquisition of whole 3D organoids with the opportunity for single-cell quantification of markers. This three-day protocol from organoid harvesting to image analysis is optimized for 3D imaging using confocal microscopy.
KW - 3D imaging
KW - Biology
KW - Confocal microscopy
KW - Immunolabelling
KW - Issue 160
KW - Optical clearing
KW - Organoid
KW - Single-cell resolution
UR - http://www.scopus.com/inward/record.url?scp=85086325903&partnerID=8YFLogxK
U2 - 10.3791/60709
DO - 10.3791/60709
M3 - Article
C2 - 32568249
AN - SCOPUS:85086325903
VL - 2020
SP - 1
EP - 8
JO - Journal of Visualized Experiments
JF - Journal of Visualized Experiments
SN - 1940-087X
IS - 160
M1 - e60709
ER -