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  1. Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology
  2. Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6
  3. Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6, Issue 1, March 2012
  4. Fluorescence of plant microspores as biosensors
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Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 11
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 10
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 9
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 8
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 7
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6, Issue 4, October 2012
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6, Issue 3, July 2012
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6, Issue 2, April 2012
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 6, Issue 1, March 2012
Presynaptic receptors regulating the time course of neurotransmitter release from vertebrate nerve endings
MTOR kinase and its role in the cell stress response
Receptor and tissue specificity of the effects of peptides corresponding to intracellular regions of the serpentine type receptors
Two mechanisms of calcium oscillations in adipocytes
Convergence of Ca$^{2+}$ signaling pathways in adipocytes. The role of L-arginine and protein kinase G in generation of transient and periodic Ca$^{2+}$ signals
Mitochondrial lipid pore in the mechanism of glutamate-induced calcium deregulation of brain neurons
Activated protein C is the regulator of the NF-κB activity under the conditions of glutamate toxicity
Small G-proteins Ras, Rac and Rho in the regulation of the neutrophil respiratory burst induced by formyl peptide
Rosiglitazone as a regulator of innate immunity in a cell model of hyperglycemia
The synthetic peptide octraphin TPLVTLFK is a selective agonist of nonopioid β-endorphin receptor
Role of mitochondrial thiols of different localization in the generation of reactive oxygen species
The effects of inhibitors and magnesium ions on the activity of the thermostable extracellular cAMP-Specific phosphodiesterase of Physarum polycephalum plasmodium
Fluorescence of plant microspores as biosensors
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 5
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 4
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 3
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 2
Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology : Volume 1

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Fluorescence of plant microspores as biosensors

Content Provider Springer Nature Link
Author Roshchina, V. V. Yashin, V. A. Vikhlyantsev, I. M.
Copyright Year 2012
Abstract Possibilities of fluorescent microscopic single-cell analysis on plant microspores as biosensors for study of chemosignaling involving neurotransmitters and mechanisms of action of fluorescent medicinal compounds—antagonists of neurotransmitters were studied on some examples. By methods of luminescence microscopy, microspectrofluorimetry and laser scanning confocal microscopy using as an example field horsetail Equisetum arvense microspores, the penetration of these compounds into the cell and associate it with individual compartments (estimated as the changes in their autofluorescence) has been analyzed. Fluorescent in blue antagonists of neurotransmitters d-tubocurarine, yohimbine and azulene (blockers of cholinoreceptor, adrenoreceptor, and histamine receptor, respectively) decreased the number of the E. arvense cells with red fluorescence. Tubocurarine and yohimbine bound to the cellular surface and did not penetrate into the cells. Azulene was found both on the cell surface and inside cells, demonstrating blue (excitation 360–380 nm) or green (excitation 420 nm) fluorescence of DNA-containing organelles. The effects of lipophilic (lecithin and amphotericin B) and proteinous (albumin, enzyme cholinesterase, cytoskeleton proteins actin, myosin, and titin) compounds on the manifestation of the effects of the neurotransmitters and antagonist d-tubocurarine have been shown. The intensity of the red light at 680 nm, has evolved in many variants. Most notable was the decline of the emission in the presence of albumin and cholinesterase as compared with the action of dopamine itself. After the addition of the cytoskeleton proteins and cholinesterase to the medium, the decrease of red fluorescence intensity, usually induced by d-tubocurarine, was not observed.
Starting Page 105
Ending Page 112
Page Count 8
File Format PDF
ISSN 19907478
Journal Biochemistry (Moscow) Supplement Series A: Membrane and Cell Biology
Volume Number 6
Issue Number 1
e-ISSN 19907494
Language English
Publisher SP MAIK Nauka/Interperiodica
Publisher Date 2012-02-25
Publisher Place Dordrecht
Access Restriction One Nation One Subscription (ONOS)
Subject Keyword biosensors vegetative microspores Equisetum arvense microspectrofluorimetry d-tubocurarine neurotransmitters lecithin amphotericin B albumin cholinesterase actin myosin titin cytoskeleton Cell Biology
Content Type Text
Resource Type Article
Subject Cell Biology Biochemistry Biophysics
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