Literature DB >> 28185196

Dual Detection of Nucleolytic and Proteolytic Markers of Lysosomal Cell Death: DNase II-Type Breaks and Cathepsin D.

Candace L Minchew1, Vladimir V Didenko2.   

Abstract

Lysosomes contain hydrolytic enzymes that can degrade proteins and DNA. Leakage of these reactive compounds through a compromised lysosomal membrane causes lysosomal cell death, which can have apoptotic, necrotic, or mixed morphology. Lysosomal cathepsin proteases, such as cathepsin D, and the lysosomal endonuclease, DNase II, have both been implicated in lysosome-related cell death. Here, we present a fluorescence dual-labeling technique for simultaneous visualization of these two markers of lysosomal activity linked to cell death. The approach labels the intracellular distribution of cathepsin D and the sites with DNase II-type breaks in fixed tissue sections. It determines the lysosomal or extra-lysosomal localization of the markers and can be useful in studying pathways and signals of lysosomal cell death.

Entities:  

Keywords:  Cathepsin D; Clearance of apoptotic cells; DNA breaks; DNase II; DNase II-type breaks; Florescence dual-labeling technique; Lysosomal cell death; Lysosomes; Phagolysosomes; Vaccinia topoisomerase-based labeling

Mesh:

Substances:

Year:  2017        PMID: 28185196      PMCID: PMC5654642          DOI: 10.1007/978-1-4939-6759-9_16

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


  26 in total

Review 1.  Lysosomal acidification mechanisms.

Authors:  Joseph A Mindell
Journal:  Annu Rev Physiol       Date:  2012       Impact factor: 19.318

Review 2.  Trashing the genome: the role of nucleases during apoptosis.

Authors:  Kumiko Samejima; William C Earnshaw
Journal:  Nat Rev Mol Cell Biol       Date:  2005-09       Impact factor: 94.444

Review 3.  Lysosomal cell death at a glance.

Authors:  Sonja Aits; Marja Jäättelä
Journal:  J Cell Sci       Date:  2013-05-01       Impact factor: 5.285

4.  Assessing phagocytic clearance of cell death in experimental stroke by ligatable fluorescent probes.

Authors:  Candace L Minchew; Vladimir V Didenko
Journal:  J Vis Exp       Date:  2014-05-27       Impact factor: 1.355

Review 5.  In situ ligation: a decade and a half of experience.

Authors:  Peter J Hornsby; Vladimir V Didenko
Journal:  Methods Mol Biol       Date:  2011

6.  In situ ligation simplified: using PCR fragments for detection of double-strand DNA breaks in tissue sections.

Authors:  Vladimir V Didenko
Journal:  Methods Mol Biol       Date:  2011

7.  NUC-1, a caenorhabditis elegans DNase II homolog, functions in an intermediate step of DNA degradation during apoptosis.

Authors:  Y C Wu; G M Stanfield; H R Horvitz
Journal:  Genes Dev       Date:  2000-03-01       Impact factor: 11.361

Review 8.  Pathophysiological functions of cathepsin D: Targeting its catalytic activity versus its protein binding activity?

Authors:  Olivier Masson; Anne-Sophie Bach; Danielle Derocq; Christine Prébois; Valérie Laurent-Matha; Sophie Pattingre; Emmanuelle Liaudet-Coopman
Journal:  Biochimie       Date:  2010-05-21       Impact factor: 4.079

Review 9.  Molecular mechanism of L-DNase II activation and function as a molecular switch in apoptosis.

Authors:  Alicia Torriglia; Chloé Leprêtre; Laura Padrón-Barthe; Sabine Chahory; Elisabeth Martin
Journal:  Biochem Pharmacol       Date:  2008-08-09       Impact factor: 5.858

Review 10.  Cathepsin D--many functions of one aspartic protease.

Authors:  Petr Benes; Vaclav Vetvicka; Martin Fusek
Journal:  Crit Rev Oncol Hematol       Date:  2008-04-08       Impact factor: 6.312

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