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Flow cytometric analysis of tracheary element differentiation in Zinnia elegans cells
Author(s) -
Weir Iona E.,
Maddumage Ratnasiri,
Allan Andrew C.,
Ferguson Ian B.
Publication year - 2005
Publication title -
cytometry part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.316
H-Index - 90
eISSN - 1552-4930
pISSN - 1552-4922
DOI - 10.1002/cyto.a.20194
Subject(s) - flow cytometry , biology , microbiology and biotechnology , programmed cell death , population , chromatin , prophase , apoptosis , botany , biochemistry , dna , demography , meiosis , sociology , gene
Background Tracheary element (TE) differentiation in single cells in culture isolated from Zinnia elegans leaves involves programmed cell death (PCD) co‐ordinated with key morphological developments. We have used flow cytometry to analyze physiological and nuclear changes in the differentiating cells. Flow cytometry allows the identification of subpopulations, thereby removing the obscuring effect of population heterogeneity that occurs with the use of other techniques. Methods Cell viability, plasma membrane integrity, oxidative activity, intracellular calcium and pH, cell wall thickening, the possible role of microtubule rearrangement, chromatin condensation, and DNA breakdown were followed by flow cytometry from the first stages of TE induction. Results TE differentiation could be enhanced and made more synchronous by a centrifugation step at 72 h after cell isolation. Size and shape changes were the first changes identified in differentiating cells, and these properties could be used to isolate differentiating populations by back‐gating. Chromatin condensation and nDNA breakdown followed patterns characteristic of programmed cell death. Conclusions We have used flow cytometry to characterize the morphological and physiological changes that occur during TE differentiation, and our findings indicate that this process is a form of autophagic PCD in which microtubule rearrangement appears to play a role. © 2005 Wiley‐Liss, Inc.