TY - JOUR
T1 - Development of a 3D atlas of the embryonic pancreas for topological and quantitative analysis of heterologous cell interactions
AU - Glorieux, Laura
AU - Sapala, Aleksandra
AU - Willnow, David
AU - Moulis, Manon
AU - Salowka, Anna
AU - Darrigrand, Jean Francois
AU - Edri, Shlomit
AU - Schonblum, Anat
AU - Sakhneny, Lina
AU - Schaumann, Laura
AU - Gómez, Harold F.
AU - Lang, Christine
AU - Conrad, Lisa
AU - Guillemot, Fabien
AU - Levenberg, Shulamit
AU - Landsman, Limor
AU - Iber, Dagmar
AU - Pierreux, Christophe E.
AU - Spagnoli, Francesca M.
N1 - Publisher Copyright:
© 2022. Published by The Company of Biologists Ltd.
PY - 2022/2
Y1 - 2022/2
N2 - Generating comprehensive image maps, while preserving spatial three-dimensional (3D) context, is essential in order to locate and assess quantitatively specific cellular features and cell-cell interactions during organ development. Despite recent advances in 3D imaging approaches, our current knowledge of the spatial organization of distinct cell types in the embryonic pancreatic tissue is still largely based on two-dimensional histological sections. Here, we present a light-sheet fluorescence microscopy approach to image the pancreas in three dimensions andmap tissue interactions at key timepoints in the mouse embryo.We demonstrate the utility of the approach by providing volumetric data, 3D distribution of three main cellular components (epithelial, mesenchymal and endothelial cells) within the developing pancreas, and quantification of their relative cellular abundance within the tissue. Interestingly, our 3D images show that endocrine cells are constantly and increasingly in contact with endothelial cells forming small vessels, whereas the interactions with mesenchymal cells decrease over time. These findings suggest distinct cell-cell interaction requirements for early endocrine cell specification and late differentiation. Lastly, we combine our image data in an open-source online repository (referred to as the Pancreas Embryonic Cell Atlas).
AB - Generating comprehensive image maps, while preserving spatial three-dimensional (3D) context, is essential in order to locate and assess quantitatively specific cellular features and cell-cell interactions during organ development. Despite recent advances in 3D imaging approaches, our current knowledge of the spatial organization of distinct cell types in the embryonic pancreatic tissue is still largely based on two-dimensional histological sections. Here, we present a light-sheet fluorescence microscopy approach to image the pancreas in three dimensions andmap tissue interactions at key timepoints in the mouse embryo.We demonstrate the utility of the approach by providing volumetric data, 3D distribution of three main cellular components (epithelial, mesenchymal and endothelial cells) within the developing pancreas, and quantification of their relative cellular abundance within the tissue. Interestingly, our 3D images show that endocrine cells are constantly and increasingly in contact with endothelial cells forming small vessels, whereas the interactions with mesenchymal cells decrease over time. These findings suggest distinct cell-cell interaction requirements for early endocrine cell specification and late differentiation. Lastly, we combine our image data in an open-source online repository (referred to as the Pancreas Embryonic Cell Atlas).
KW - Cell-cell interactions
KW - Endothelial cells
KW - Light-sheet fluorescence microscopy
KW - Mesenchyme
KW - Mouse embryo
KW - Pancreas
UR - http://www.scopus.com/inward/record.url?scp=85124056735&partnerID=8YFLogxK
U2 - 10.1242/dev.199655
DO - 10.1242/dev.199655
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C2 - 35037942
AN - SCOPUS:85124056735
SN - 0950-1991
VL - 149
JO - Development (Cambridge)
JF - Development (Cambridge)
IS - 3
M1 - dev199655
ER -