Literature DB >> 34859401

Probes for Fluorescent Visualization of Specific Cellular Organelles.

Timothy Paul Foster1.   

Abstract

The defining characteristic of eukaryotic cells is the segregation of critical cellular functions within various membrane bound cellular organelles, including the nucleus, endoplasmic reticulum, Golgi apparatus, lysosomes, and mitochondria. Cell biologists therefore have extensively utilized organelle specific counterstains to help identify the localization of specific proteins or other targets of interest in order to garner an understanding of either their potential functions or their effects on the cell. There currently is a wide array of fluorescent dyes and reagents that can be utilized in live and fixed cells to identify organelles, thereby creating challenges in both choosing between the plethora of options and optimizing their use. Here we present a discussion of commonly utilized commercially available organelle dyes and summarize the factors that influence selection of the various dyes for: a given organelle; live versus fixed cellular conditions; adaptation to a specific protocol; spectral multiplexing; or matching excitation/emission spectra to available imaging equipment. Also presented are recommended protocols for a typical example reagent that can be reliably utilized to visualize its target cellular organelle.
© 2022. Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Actin; Cell biology; Endoplasmic reticulum; Fluorescent dyes; Fluorescent labeling; Golgi; Lysosome; Mitochondria; Nucleus; Organelles; Plasma membrane

Mesh:

Substances:

Year:  2022        PMID: 34859401     DOI: 10.1007/978-1-0716-1948-3_7

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  73 in total

1.  Intracellular accumulation and oligosaccharide processing of alkaline phosphatase under disassembly of the Golgi complex caused by brefeldin A.

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Journal:  Eur J Biochem       Date:  1990-12-27

2.  Overexpression of gK in gK-transformed cells collapses the Golgi apparatus into the endoplasmic reticulum inhibiting virion egress, glycoprotein transport, and virus-induced cell fusion.

Authors:  Timothy P Foster; Galena V Rybachuk; Xavier Alvarez; Olga Borkhsenious; Konstantin G Kousoulas
Journal:  Virology       Date:  2003-12-20       Impact factor: 3.616

3.  Fluorescence spectrophotometry of reduced phosphopyridine nucleotide in intact cells in the near-ultraviolet and visible region.

Authors:  L N DUYSENS; J AMESZ
Journal:  Biochim Biophys Acta       Date:  1957-04

Review 4.  Cell-death assessment by fluorescent and nonfluorescent cytosolic and nuclear staining techniques.

Authors:  N Atale; S Gupta; U C S Yadav; V Rani
Journal:  J Microsc       Date:  2014-05-15       Impact factor: 1.758

5.  Brefeldin A, a drug that blocks secretion, prevents the assembly of non-clathrin-coated buds on Golgi cisternae.

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Journal:  Cell       Date:  1991-03-22       Impact factor: 41.582

6.  Fluorescent conjugates of brefeldin A selectively stain the endoplasmic reticulum and Golgi complex of living cells.

Authors:  Y Deng; J R Bennink; H C Kang; R P Haugland; J W Yewdell
Journal:  J Histochem Cytochem       Date:  1995-09       Impact factor: 2.479

7.  The Brefeldin A-induced retrograde transport from the Golgi apparatus to the endoplasmic reticulum depends on calcium sequestered to intracellular stores.

Authors:  N E Ivessa; C De Lemos-Chiarandini; D Gravotta; D D Sabatini; G Kreibich
Journal:  J Biol Chem       Date:  1995-10-27       Impact factor: 5.157

8.  A Golgi-related structure remains after the brefeldin A-induced formation of an ER-Golgi hybrid compartment.

Authors:  C De Lemos-Chiarandini; N E Ivessa; V H Black; Y S Tsao; I Gumper; G Kreibich
Journal:  Eur J Cell Biol       Date:  1992-08       Impact factor: 4.492

9.  Effects of brefeldin-A on Golgi morphology in human cultured fibroblasts observed in three-dimensional stereo scanning electron microscopy.

Authors:  D Y So; R J Temkin; P J Lea
Journal:  Scanning       Date:  1995 May-Jun       Impact factor: 1.932

10.  A method for measuring mitochondrial mass and activity.

Authors:  Maria Agnello; Giovanni Morici; Anna Maria Rinaldi
Journal:  Cytotechnology       Date:  2008-06-24       Impact factor: 2.058

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  1 in total

1.  2,7-Diaminobenzopyrylium Dyes Are Live-Cell Mitochondrial Stains.

Authors:  Sambashiva Banala; Ariana N Tkachuk; Ronak Patel; Pratik Kumar; Timothy A Brown; Luke D Lavis
Journal:  ACS Bio Med Chem Au       Date:  2022-02-28
  1 in total

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