Literature DB >> 10986414

Flow cytometry of apoptotic cell death.

I Vermes1, C Haanen, C Reutelingsperger.   

Abstract

The term apoptosis or programmed cell death defines a genetically encoded cell death program, which is morphologically and biochemically distinct from necrosis or accidental cell death. The characteristic morphological signs of apoptosis (cellular shrinkage, membrane blebbing, nuclear condensation and fragmentation) are the final results of a complex biochemical cascade of events which is an integral part of physiological homeostasis. Techniques designed to identify, quantitate and characterize apoptosis are numerous, but flow cytometry (FCM) remains the methodology of choice to study the apoptotic cascade in relation to cell type, trigger and time. This review outlines the main stages of the apoptotic cascade together with current FCM methods. All FCM apoptosis assays described have a solid experimental basis and have been used successfully in basic research on molecular and biochemical mechanisms of apoptosis. In various clinical settings the ability to follow the apoptotic process in patient samples may offer the rationale for optimal treatment schedules.

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Year:  2000        PMID: 10986414     DOI: 10.1016/s0022-1759(00)00233-7

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  144 in total

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2.  IKCa1 activity is required for cell shrinkage, phosphatidylserine translocation and death in T lymphocyte apoptosis.

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Review 5.  Plant DNA flow cytometry and estimation of nuclear genome size.

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6.  Human AdV-specific T cells: persisting in vitro functionality despite lethal irradiation.

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Journal:  Antimicrob Agents Chemother       Date:  2013-11-11       Impact factor: 5.191

9.  Ruthenium-Clotrimazole complex has significant efficacy in the murine model of cutaneous leishmaniasis.

Authors:  Eva Iniguez; Armando Varela-Ramirez; Alberto Martínez; Caresse L Torres; Roberto A Sánchez-Delgado; Rosa A Maldonado
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Review 10.  Use of fluorescently labeled caspase inhibitors as affinity labels to detect activated caspases.

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Journal:  Hum Cell       Date:  2002-03       Impact factor: 4.174

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