PUBLICATION

Cell lineage reconstruction of early zebrafish embryos using label-free nonlinear microscopy

Authors
Olivier, N., Luengo-Oroz, M.A., Duloquin, L., Faure, E., Savy, T., Veilleux, I., Solinas, X., Débarre, D., Bourgine, P., Santos, A., Peyriéras, N., and Beaurepaire, E.
ID
ZDB-PUB-100826-4
Date
2010
Source
Science (New York, N.Y.)   329(5994): 967-971 (Journal)
Registered Authors
Duloquin, Louise, Peyriéras, Nadine, Savy, Thierry
Keywords
none
MeSH Terms
  • Animals
  • Blastula/cytology
  • Cell Cycle
  • Cell Lineage*
  • Embryo, Nonmammalian/cytology*
  • Image Processing, Computer-Assisted
  • Microscopy/methods*
  • Zebrafish/embryology*
PubMed
20724640 Full text @ Science
Abstract
Quantifying cell behaviors in animal early embryogenesis remains a challenging issue requiring in toto imaging and automated image analysis. We designed a framework for imaging and reconstructing unstained whole zebrafish embryos for their first 10 cell division cycles and report measurements along the cell lineage with micrometer spatial resolution and minute temporal accuracy. Point-scanning multiphoton excitation optimized to preferentially probe the innermost regions of the embryo provided intrinsic signals highlighting all mitotic spindles and cell boundaries. Automated image analysis revealed the phenomenology of cell proliferation. Blastomeres continuously drift out of synchrony. After the 32-cell stage, the cell cycle lengthens according to cell radial position, leading to apparent division waves. Progressive amplification of this process is the rule, contrasting with classical descriptions of abrupt changes in the system dynamics.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping