TY - JOUR
T1 - X-ray phase-contrast in vivo microtomography probes new aspects of Xenopus gastrulation
AU - Moosmann, Julian
AU - Ershov, Alexey
AU - Altapova, Venera
AU - Baumbach, Tilo
AU - Prasad, Maneeshi S.
AU - LaBonne, Carole
AU - Xiao, Xianghui
AU - Kashef, Jubin
AU - Hofmann, Ralf
N1 - Funding Information:
Acknowledgements We would like to acknowledge discussions with J. Wittbrodt, H. Steinbeisser, R. Winklbauer and D. Moss. R. Keller and D. Shook helped us with interpreting the data. D. Wedlich and M. Köhl commented on the manuscript. Discussions with M. Köhl on data analysis are gratefully acknowledged. We also would liketothankT.vandeKamp and D.Karpovfor their helpvisualisingtheset-up,aswellas F. de Carlo and K. Fezza for allocating beamtime at 2-BM-B station and at 32-ID, respectively, of Advanced Photon Source, Argonne National Laboratory. Use of the Advanced Photon Source, an Office of Science User Facility operated for the US Department of Energy (DOE) Office of Science by Argonne National Laboratory, was supported by the US DOE under Contract No. DE-AC02-06CH11357. E. Becker, C. Huang, A. Merks and R. Langhe helped analysing blastopore radii. J.K.’s Young Investigator Group received financial support from the ‘Concept for the Future’ programme of Karlsruhe Institute of Technology within the framework of the German Excellence Initiative. Thisresearchpartially was fundedby the German FederalMinistry of Education and Research under grant numbers 05K12CK2 and 05K12VH1.
PY - 2013/5/16
Y1 - 2013/5/16
N2 - An ambitious goal in biology is to understand the behaviour of cells during development by imaging-in vivo and with subcellular resolution-changes of the embryonic structure. Important morphogenetic movements occur throughout embryogenesis, but in particular during gastrulation when a series of dramatic, coordinated cell movements drives the reorganization of a simple ball or sheet of cells into a complex multi-layered organism. In Xenopus laevis, the South African clawed frog and also in zebrafish, cell and tissue movements have been studied in explants, in fixed embryos, in vivo using fluorescence microscopy or microscopic magnetic resonance imaging. None of these methods allows cell behaviours to be observed with micrometre-scale resolution throughout the optically opaque, living embryo over developmental time. Here we use non-invasive in vivo, time-lapse X-ray microtomography, based on single-distance phase contrast and combined with motion analysis, to examine the course of embryonic development. We demonstrate that this powerful four-dimensional imaging technique provides high-resolution views of gastrulation processes in wild-type X. laevis embryos, including vegetal endoderm rotation, archenteron formation, changes in the volumes of cavities within the porous interstitial tissue between archenteron and blastocoel, migration/confrontation of mesendoderm and closure of the blastopore. Differential flow analysis separates collective from relative cell motion to assign propulsion mechanisms. Moreover, digitally determined volume balances confirm that early archenteron inflation occurs through the uptake of external water. A transient ectodermal ridge, formed in association with the confrontation of ventral and head mesendoderm on the blastocoel roof, is identified. When combined with perturbation experiments to investigate molecular and biomechanical underpinnings of morphogenesis, our technique should help to advance our understanding of the fundamentals of development.
AB - An ambitious goal in biology is to understand the behaviour of cells during development by imaging-in vivo and with subcellular resolution-changes of the embryonic structure. Important morphogenetic movements occur throughout embryogenesis, but in particular during gastrulation when a series of dramatic, coordinated cell movements drives the reorganization of a simple ball or sheet of cells into a complex multi-layered organism. In Xenopus laevis, the South African clawed frog and also in zebrafish, cell and tissue movements have been studied in explants, in fixed embryos, in vivo using fluorescence microscopy or microscopic magnetic resonance imaging. None of these methods allows cell behaviours to be observed with micrometre-scale resolution throughout the optically opaque, living embryo over developmental time. Here we use non-invasive in vivo, time-lapse X-ray microtomography, based on single-distance phase contrast and combined with motion analysis, to examine the course of embryonic development. We demonstrate that this powerful four-dimensional imaging technique provides high-resolution views of gastrulation processes in wild-type X. laevis embryos, including vegetal endoderm rotation, archenteron formation, changes in the volumes of cavities within the porous interstitial tissue between archenteron and blastocoel, migration/confrontation of mesendoderm and closure of the blastopore. Differential flow analysis separates collective from relative cell motion to assign propulsion mechanisms. Moreover, digitally determined volume balances confirm that early archenteron inflation occurs through the uptake of external water. A transient ectodermal ridge, formed in association with the confrontation of ventral and head mesendoderm on the blastocoel roof, is identified. When combined with perturbation experiments to investigate molecular and biomechanical underpinnings of morphogenesis, our technique should help to advance our understanding of the fundamentals of development.
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U2 - 10.1038/nature12116
DO - 10.1038/nature12116
M3 - Article
C2 - 23676755
AN - SCOPUS:84878077428
SN - 0028-0836
VL - 497
SP - 374
EP - 377
JO - Nature
JF - Nature
IS - 7449
ER -