Localization of wheat-germ agglutinin in developing wheat embryos and those cultured in abscisic acid

Planta ◽  
1986 ◽  
Vol 168 (4) ◽  
pp. 433-440 ◽  
Author(s):  
N. V. Raikhel ◽  
R. S. Quatrano
Keyword(s):  
Abscisic Acid ◽  
Wheat Germ Agglutinin ◽  
Wheat Germ ◽  
Wheat Embryos

Drought-induced increase in wheat germ agglutinin (WGA) accumulation in developing wheat embryos appears to be independent of ABA

1999 ◽  
Vol 26 (8) ◽  
pp. 787 ◽  
Author(s):  
Priya Bhaglal ◽  
Prabhjeet Singh ◽  
S. S. Bhullar
Keyword(s):  
Triticum Aestivum ◽  
Abscisic Acid ◽  
Water Stress ◽  
Wheat Germ Agglutinin ◽  
Wheat Germ ◽  
Triticum Aestivum L ◽  
Stress Conditions ◽  
Grain Development ◽  
Natural Conditions ◽  
Wheat Embryos

Accumulation of wheat germ agglutinin (WGA) in the developing embryos of three different wheat (Triticum aestivum L.) cultivars, PBW-138, PBW-299 and C-306, was studied in relation to abscisic acid (ABA) accumulation under water stress conditions at 18, 24 and 30 days post anthesis (DPA) under natural conditions. Imposition of water stress in all three cultivars resulted in enhanced ABA levels in the embryos at all stages of grain development. On the contrary, the increase in WGA accumulation in the embryos in response to drought was stage- and cultivar-dependent. Our results suggest that apart from ABA, other factors that are temporally expressed may be involved in drought-induced regulation of the WGA gene.

scholarly journals Stress-Induced Accumulation of Wheat Germ Agglutinin and Abscisic Acid in Roots of Wheat Seedlings

1989 ◽  
Vol 91 (4) ◽  
pp. 1432-1435 ◽  
Author(s):  
Bruno P. A. Cammue ◽  
Willem F. Broekaert ◽  
Jan T. C. Kellens ◽  
Natasha V. Raikhel ◽  
Willy J. Peumans
Keyword(s):  
Abscisic Acid ◽  
Wheat Germ Agglutinin ◽  
Wheat Germ ◽  
Wheat Seedlings

scholarly journals Immunocytochemical localization of wheat germ agglutinin in wheat.

1982 ◽  
Vol 92 (3) ◽  
pp. 753-764 ◽  
Author(s):  
M Mishkind ◽  
N V Raikhel ◽  
B A Palevitz ◽  
K Keegstra
Keyword(s):  
Wheat Germ Agglutinin ◽  
Direct Contact ◽  
Fungal Pathogens ◽  
Adventitious Roots ◽  
Wheat Germ ◽  
Wheat Embryos ◽  
Secondary Antibodies ◽  
Germination And Growth ◽  
Subcellular Level ◽  
Adult Plants

Immunocytological techniques were developed to localize the plant lectin, wheat germ agglutinin (WGA), in the tissues and cells of wheat plants. In a previous study we demonstrated with a radioimmunoassay that the lectin is present in wheat embryos and adult plants both in the roots and at the base of the stem. We have now found, using rhodamine, peroxidase, and ferritin-labeled secondary antibodies, that WGA is located in cells and tissues that establish direct contact with the soil during germination and growth of the plant In the embryo, WGA is found in the surface layer of the radicle, the first adventitious roots, the coleoptile, and the scutellum. Although found throughout the coleorhiza and epiblast, it is at its highest levels within the cells at the surface of these organs. In adult plants, WGA is located only in the caps and tips of adventitious roots. Reaction product for WGA was not visualized in embryonic or adult leaves or in other tissues of adult plants. At the subcellular level, WGA is located at the periphery of protein bodies, within electron-translucent regions of the cytoplasm, and at the cell wall-protoplast interface. Since WGA is found at potential infection sites and is known to have fungicidal properties, it may function in the defense against fungal pathogens.

Failure of 6D1 or Exposure of Platelets to ADP to Affect Agglutination Induced by Wheat Germ Agglutinin

1989 ◽  
Vol 62 (02) ◽  
pp. 815 ◽  
Author(s):  
Marjorie B Zucker ◽  
Robert A Grant ◽  
Evelyn A Mauss
Keyword(s):  
Wheat Germ Agglutinin ◽  
Wheat Germ

Transport Characteristics of Wheat Germ Agglutinin-Modified Insulin-Liposomes and Solid Lipid Nanoparticles in a Perfused Rat Intestinal Model

2006 ◽  
Vol 6 (9) ◽  
pp. 2959-2966 ◽  
Author(s):  
Na Zhang ◽  
Qineng Ping ◽  
Guihua Huang ◽  
Xiuzhen Han ◽  
Yanna Cheng ◽  
...  
Keyword(s):  
Solid Lipid Nanoparticles ◽  
Wheat Germ Agglutinin ◽  
Wheat Germ ◽  
Serum Insulin ◽  
Lipid Nanoparticles ◽  
Solid Lipid ◽  
Mucosal Absorption ◽  
Perfusion Experiment ◽  
Absorption Sites

Wheat germ agglutinin (WGA) modified liposomes and solid lipid nanoparticles (SLNs) were evaluated for improving intestinal absorption of insulin. In an in situ local intestinal perfusion experiment, formulations containing 100 IU/kg insulin were administered to the duodenum, jejunum, and ileum of fasted rats. As hypothesized, ileum was the best intestinal location for the absorption of insulin-containing liposomes. Serum insulin concentrations decreased for the various formulations in different absorption sites according to the following trends: Duodenum > ileum > jejunum for WGA-modified insulin-containing liposomes; duodenum > jejunum > ileum for WGA-modified insulin-containing SLNs; ileum > jejunum > duodenum for insulin-containing liposomes; ileum > duodenum > jejunum for insulin-containing SLNs; and duodenum ≥ ileum > jejunum for aqueous solution of insulin. These results imply that the nanoparticle type and delivery site were important factors with respect to increasing the bioavailability of insulin following oral administration. The proteolytic degradation as well as the epithelial permeability were primary determinants influcing insulin mucosal absorption.

Identification of distinct haemocyte populations from the freshwater bivalves swan mussel (Anodonta cygnea) and duck mussel (Anodonta anatina) using wheat-germ agglutinin

2017 ◽  
Vol 95 (12) ◽  
pp. 937-947 ◽  
Author(s):  
M. Hinzmann ◽  
M. Lopes-Lima ◽  
F. Cerca ◽  
A. Correia ◽  
J. Machado ◽  
...  
Keyword(s):  
Flow Cytometry ◽  
Wheat Germ Agglutinin ◽  
Wheat Germ ◽  
Transmission Microscopy ◽  
Anodonta Cygnea ◽  
Functional Studies ◽  
Lectin Staining ◽  
Surface Staining ◽  
Cytological Features ◽  
Freshwater Bivalves

Haemocytes play a major role in molluscs immunity. Functional studies are, however, impaired by limited available experimental tools to identify and sort distinct haemocyte populations. Therefore, using nonlethal methods, we aimed at evaluating whether lectin staining combined with flow cytometry could be used to distinguish circulating haemocyte populations from two freshwater bivalves of the family Unionidae, the duck mussel (Anodonta anatina (L., 1758)) and the swan mussel (Anodonta cygnea (L., 1758)). Based on classical classification, haemocytes were distinguished as granulocytes and hyalinocytes and cytological features were visualized using transmission microscopy and staining techniques. Size, granularity, viability, and surface staining using lectins as specific probes were analysed by flow cytometry and fluorescence microscopy. The microscopic proportions of granulocytes and hyalinocytes significantly differed, being of 70% and 30% for A. cygnea and of 85% and 15% for A. anatina, respectively. Two haemocyte populations were sorted by flow cytometry based on size and granularity and confirmed as granulocytes and hyalinocytes. Interestingly, two different granulocyte populations could be further discriminated in A. cygnea according to their binding affinity to wheat-germ agglutinin (WGA), whereas granulocytes of A. anatina all stained similarly. Our results show that WGA labelling combined with flow cytometry can be used to better discriminate Anodonta haemocyte populations and obtain purified populations for functional studies.

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