Changes in symplastic permeability during adventitious shoot regeneration in tobacco thin cell layers.
کلید واژه ها
خلاصه
Thin cell layer (TCL) explants of tobacco (Nicotiana tabacum L.) were cultured in either a regeneration medium that resulted in formation of adventitious vegetative shoots or a non-regeneration (control) medium that maintained the TCLs but did not promote shoot formation. Microinjections were conducted on epidermal cells at 1- or 2-day intervals during the culture period (14 days) and also on meristematic regions as they appeared in regenerating TCLs. A fluorescein isothiocyanate-labelled peptide (F(Glu)3 MW 799) was used to assess the permeability of the symplast during adventitious shoot regeneration. A period of increased symplastic movement of F(Glu)3 was detected during day 2 of culture and was significantly greater in regenerating TCLs than in non-regenerating TCLs. This corresponded to the period of the first cell divisions and represents the re-initiation of a meristematic type of symplastic linkage between epidermal cells. A smaller increase in cell-to-cell movement within non-regenerating TCLs indicated a possible stress response as a factor in these changes. Movement of F(Glu)3 throughout the epidermal symplast of regenerating TCLs returned to pre-culture levels by the time of shoot primordia formation. F(Glu)3 movement was further down-regulated in non-regenerating TCLs, with a high degree of cell isolation observed. Within newly formed shoots, symplastic movement of F(Glu)3 cycled between high and low levels.