Measurement of glutathione levels in intact roots of Arabidopsis

被引:60
作者
Fricker, MD
May, M
Meyer, AJ
Sheard, N
White, NS
机构
[1] Univ Oxford, Dept Plant Sci, Oxford OX1 3RB, England
[2] Plant Genet Syst NV, B-9000 Ghent, Belgium
关键词
Arabidopsis thaliana; confocal laser scanning microscopy; fluorescence attenuation correction; glutathione; glutathione S-transferase; monochlorobimane; roots;
D O I
10.1046/j.1365-2818.2000.00696.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
Levels of glutathione were measured for different cell types in roots of intact Arabidopsis seedlings after labelling with monochlorobimane to give fluorescent glutathione S-bimane (GSB) and imaging using confocal laser scanning microscopy with excitation at 442 nm. Labelling increased to a plateau in most cell types after about 15-20 min and the GSB accumulated rapidly in the vacuole. Formation of GSB in the cytoplasm was not affected by treatment with sodium azide; however, vacuolar transport of GSB was substantially inhibited under these conditions. We infer that vacuolar sequestration was mediated by a tonoplast glutathione S-conjugate pump. Quantitative estimates of the cytoplasmic glutathione concentration involved correction for the loss in fluorescence signal with depth into the specimen using an empirically determined model derived in situ from a permeabilized root. Correction for the dilution experienced on transport into the vacuole also required an estimate of the amount of cytoplasm present in each cell type. This was achieved in two stages: first, the levels of protein were mapped after fixation, permeabilization and labelling with fluroescein isothiocyanate. Second, the corresponding cytoplasmic volume was determined as 40% for epidermal cells in the elongation zone by manual segmentation of the cytoplasm in serial optical sections. Values of relative cytoplasmic volume for other cells were extrapolated in proportion to their protein content. Using this approach, cytoplasmic glutathione concentrations were found to be 2-3 mm in most cell types. There was a marked difference between the central cells and the neighbouring, rapidly dividing initials, and between the columella cells and the outermost cells of the root cap. In the latter case, the difference was equalized in the presence of azide. This might indicate that additional cell-cell movement and preferential sequestration of GSB can occur during the detoxification process in an intact system.
引用
收藏
页码:162 / 173
页数:12
相关论文
共 36 条
[31]   Cell proliferation and hair tip growth in the Arabidopsis root are under mechanistically different forms of redox control [J].
SanchezFernandez, R ;
Fricker, M ;
Corben, LB ;
White, NS ;
Sheard, N ;
Leaver, CJ ;
VanMontagu, M ;
Inze, D ;
May, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2745-2750
[32]   REGULATION OF GLUTATHIONE SYNTHESIS IN LEAVES OF TRANSGENIC POPLAR (POPULUS-TREMULA X POPULUS-ALBA) OVEREXPRESSING GLUTATHIONE SYNTHETASE [J].
STROHM, M ;
JOUANIN, L ;
KUNERT, KJ ;
PRUVOST, C ;
POLLE, A ;
FOYER, CH ;
RENNENBERG, H .
PLANT JOURNAL, 1995, 7 (01) :141-145
[33]   Barley aleurone cells contain two types of vacuoles: Characterization of lytic organelles by use of fluorescent probes [J].
Swanson, SJ ;
Bethke, PC ;
Jones, RL .
PLANT CELL, 1998, 10 (05) :685-698
[34]   Differential expression of genes coding for ABC transporters after treatment of Arabidopsis thaliana with xenobiotics [J].
Tommasini, R ;
Vogt, E ;
Schmid, J ;
Fromentau, M ;
Amrhein, N ;
Martinoia, E .
FEBS LETTERS, 1997, 411 (2-3) :206-210
[35]   Aberration control in quantitative imaging of botanical specimens by multidimensional fluorescence microscopy [J].
White, NS ;
Errington, RJ ;
Fricker, MD ;
Wood, JL .
JOURNAL OF MICROSCOPY-OXFORD, 1996, 181 :99-116
[36]   Degradation of glutathione S-conjugates by a carboxypeptidase in the plant vacuole [J].
Wolf, AE ;
Dietz, KJ ;
Schroder, P .
FEBS LETTERS, 1996, 384 (01) :31-34