-
Something wrong with this record ?
Differential Polarization Imaging of Plant Cells. Mapping the Anisotropy of Cell Walls and Chloroplasts
JS. Radosavljević, AL. Mitrović, K. Radotić, L. Zimányi, G. Garab, G. Steinbach
Language English Country Switzerland
Document type Journal Article, Review
Grant support
GINOP-2.3.3-15-2016-00003
Nemzetgazdasági Minisztérium
GINOP-2.3.3-15-2016-00030
Nemzetgazdasági Minisztérium
GINOP-2.1.7-15-2016-00713
Nemzetgazdasági Minisztérium
GINOP-2.3.2-15-2016-00001
Nemzetgazdasági Minisztérium
OTKA K 128679
Hungarian Scientific Research Fund
No 451-03-9/2021-14/200053
Science Fund of the Republic of Serbia
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
34299279
DOI
10.3390/ijms22147661
Knihovny.cz E-resources
- MeSH
- Anisotropy MeSH
- Cell Wall ultrastructure MeSH
- Chloroplasts ultrastructure MeSH
- Microscopy, Confocal methods MeSH
- Microscopy, Polarization methods MeSH
- Plant Cells ultrastructure MeSH
- Thylakoids ultrastructure MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Modern light microscopy imaging techniques have substantially advanced our knowledge about the ultrastructure of plant cells and their organelles. Laser-scanning microscopy and digital light microscopy imaging techniques, in general-in addition to their high sensitivity, fast data acquisition, and great versatility of 2D-4D image analyses-also opened the technical possibilities to combine microscopy imaging with spectroscopic measurements. In this review, we focus our attention on differential polarization (DP) imaging techniques and on their applications on plant cell walls and chloroplasts, and show how these techniques provided unique and quantitative information on the anisotropic molecular organization of plant cell constituents: (i) We briefly describe how laser-scanning microscopes (LSMs) and the enhanced-resolution Re-scan Confocal Microscope (RCM of Confocal.nl Ltd. Amsterdam, Netherlands) can be equipped with DP attachments-making them capable of measuring different polarization spectroscopy parameters, parallel with the 'conventional' intensity imaging. (ii) We show examples of different faces of the strong anisotropic molecular organization of chloroplast thylakoid membranes. (iii) We illustrate the use of DP imaging of cell walls from a variety of wood samples and demonstrate the use of quantitative analysis. (iv) Finally, we outline the perspectives of further technical developments of micro-spectropolarimetry imaging and its use in plant cell studies.
Biofotonika Research and Development Ltd 6720 Szeged Hungary
Department of Physics Faculty of Science Ostrava University 709 00 Ostrava Czech Republic
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21025338
- 003
- CZ-PrNML
- 005
- 20211026133914.0
- 007
- ta
- 008
- 211013s2021 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms22147661 $2 doi
- 035 __
- $a (PubMed)34299279
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Radosavljević, Jasna Simonović $u Department of Life Sciences, Institute for Multidisciplinary Research, University of Belgrade, Kneza Višeslava 1, 11000 Belgrade, Serbia
- 245 10
- $a Differential Polarization Imaging of Plant Cells. Mapping the Anisotropy of Cell Walls and Chloroplasts / $c JS. Radosavljević, AL. Mitrović, K. Radotić, L. Zimányi, G. Garab, G. Steinbach
- 520 9_
- $a Modern light microscopy imaging techniques have substantially advanced our knowledge about the ultrastructure of plant cells and their organelles. Laser-scanning microscopy and digital light microscopy imaging techniques, in general-in addition to their high sensitivity, fast data acquisition, and great versatility of 2D-4D image analyses-also opened the technical possibilities to combine microscopy imaging with spectroscopic measurements. In this review, we focus our attention on differential polarization (DP) imaging techniques and on their applications on plant cell walls and chloroplasts, and show how these techniques provided unique and quantitative information on the anisotropic molecular organization of plant cell constituents: (i) We briefly describe how laser-scanning microscopes (LSMs) and the enhanced-resolution Re-scan Confocal Microscope (RCM of Confocal.nl Ltd. Amsterdam, Netherlands) can be equipped with DP attachments-making them capable of measuring different polarization spectroscopy parameters, parallel with the 'conventional' intensity imaging. (ii) We show examples of different faces of the strong anisotropic molecular organization of chloroplast thylakoid membranes. (iii) We illustrate the use of DP imaging of cell walls from a variety of wood samples and demonstrate the use of quantitative analysis. (iv) Finally, we outline the perspectives of further technical developments of micro-spectropolarimetry imaging and its use in plant cell studies.
- 650 _2
- $a anizotropie $7 D016880
- 650 _2
- $a buněčná stěna $x ultrastruktura $7 D002473
- 650 _2
- $a chloroplasty $x ultrastruktura $7 D002736
- 650 _2
- $a konfokální mikroskopie $x metody $7 D018613
- 650 _2
- $a polarizační mikroskopie $x metody $7 D008859
- 650 _2
- $a rostlinné buňky $x ultrastruktura $7 D059828
- 650 _2
- $a tylakoidy $x ultrastruktura $7 D020524
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Mitrović, Aleksandra Lj $u Department of Life Sciences, Institute for Multidisciplinary Research, University of Belgrade, Kneza Višeslava 1, 11000 Belgrade, Serbia
- 700 1_
- $a Radotić, Ksenija $u Department of Life Sciences, Institute for Multidisciplinary Research, University of Belgrade, Kneza Višeslava 1, 11000 Belgrade, Serbia
- 700 1_
- $a Zimányi, László $u Institute of Biophysics, Biological Research Centre, Eötvös Loránd Research Network, 6726 Szeged, Hungary
- 700 1_
- $a Garab, Győző $u Institute of Plant Biology, Biological Research Centre, Eötvös Loránd Research Network, 6726 Szeged, Hungary $u Department of Physics, Faculty of Science, Ostrava University, 709 00 Ostrava, Czech Republic $u Biofotonika Research and Development Ltd., 6720 Szeged, Hungary
- 700 1_
- $a Steinbach, Gábor $u Biofotonika Research and Development Ltd., 6720 Szeged, Hungary $u Cellular Imaging Laboratory, Biological Research Centre, Eötvös Loránd Research Network, 6726 Szeged, Hungary
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 22, č. 14 (2021)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34299279 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20211026133920 $b ABA008
- 999 __
- $a ok $b bmc $g 1714403 $s 1145845
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 22 $c 14 $e 20210717 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a GINOP-2.3.3-15-2016-00003 $p Nemzetgazdasági Minisztérium
- GRA __
- $a GINOP-2.3.3-15-2016-00030 $p Nemzetgazdasági Minisztérium
- GRA __
- $a GINOP-2.1.7-15-2016-00713 $p Nemzetgazdasági Minisztérium
- GRA __
- $a GINOP-2.3.2-15-2016-00001 $p Nemzetgazdasági Minisztérium
- GRA __
- $a OTKA K 128679 $p Hungarian Scientific Research Fund
- GRA __
- $a No 451-03-9/2021-14/200053 $p Science Fund of the Republic of Serbia
- LZP __
- $a Pubmed-20211013