Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study

<p>Abstract</p> <p>Background</p> <p>Despite the great advances in the understanding of programmed cell death, little attention has been paid to the sequence of the events that characterise it. In particular, the course of apoptotic events induced by microtubule-interfe...

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Main Authors: Lapalombella Rosa, Zoli Wainer, Brigliadori Giovanni, Carloni Silvia, Fabbri Francesco, Marini Marina
Format: Article
Language:English
Published: BMC 2006-01-01
Series:BMC Cell Biology
Online Access:http://www.biomedcentral.com/1471-2121/7/6
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spelling doaj-73fcc71d0f6d4a5f9e17ad3b379c4ffc2020-11-25T01:15:04ZengBMCBMC Cell Biology1471-21212006-01-0171610.1186/1471-2121-7-6Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric studyLapalombella RosaZoli WainerBrigliadori GiovanniCarloni SilviaFabbri FrancescoMarini Marina<p>Abstract</p> <p>Background</p> <p>Despite the great advances in the understanding of programmed cell death, little attention has been paid to the sequence of the events that characterise it. In particular, the course of apoptotic events induced by microtubule-interfering agents such as taxanes is poorly understood. In order to increase such knowledge, we studied a number of independent biochemical and cytological modifications using cytometric methods in a bladder cancer cell line treated with the second generation taxane, docetaxel.</p> <p>Results</p> <p>Within a few hours, drug treatment had induced mitochondrial membrane transition, cell shrinkage and a decrease in granularity. Cell cycle was almost completely blocked in G<sub>2</sub>/M phase within 24 hours. The hypodiploid peak started to become prominent 48 hours after the treatment. At the same time, the appearance of a DNA ladder demonstrated caspase-dependent chromatin fragmentation. Concurrently, specific cell surface modifications took place, involving at first glycoprotein syalilation and later phospholipid asymmetry. DNA fragmentation was subsequently detected by TUNEL assay. Over time, cell membranes became permeable to propidium iodide. A very similar time-course of apoptotic events was found after treatment of a myelomonocytic cell line with the same drug.</p> <p>Conclusion</p> <p>After discussing some characteristics of the methods employed and their limitations, a succession of apoptotic events over time is suggested, in which the collapse of mitochondrial transmembrane potential (Δψm) is the earliest sign of apoptosis.</p> http://www.biomedcentral.com/1471-2121/7/6
collection DOAJ
language English
format Article
sources DOAJ
author Lapalombella Rosa
Zoli Wainer
Brigliadori Giovanni
Carloni Silvia
Fabbri Francesco
Marini Marina
spellingShingle Lapalombella Rosa
Zoli Wainer
Brigliadori Giovanni
Carloni Silvia
Fabbri Francesco
Marini Marina
Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
BMC Cell Biology
author_facet Lapalombella Rosa
Zoli Wainer
Brigliadori Giovanni
Carloni Silvia
Fabbri Francesco
Marini Marina
author_sort Lapalombella Rosa
title Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
title_short Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
title_full Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
title_fullStr Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
title_full_unstemmed Sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: A cytometric study
title_sort sequential events of apoptosis involving docetaxel, a microtubule-interfering agent: a cytometric study
publisher BMC
series BMC Cell Biology
issn 1471-2121
publishDate 2006-01-01
description <p>Abstract</p> <p>Background</p> <p>Despite the great advances in the understanding of programmed cell death, little attention has been paid to the sequence of the events that characterise it. In particular, the course of apoptotic events induced by microtubule-interfering agents such as taxanes is poorly understood. In order to increase such knowledge, we studied a number of independent biochemical and cytological modifications using cytometric methods in a bladder cancer cell line treated with the second generation taxane, docetaxel.</p> <p>Results</p> <p>Within a few hours, drug treatment had induced mitochondrial membrane transition, cell shrinkage and a decrease in granularity. Cell cycle was almost completely blocked in G<sub>2</sub>/M phase within 24 hours. The hypodiploid peak started to become prominent 48 hours after the treatment. At the same time, the appearance of a DNA ladder demonstrated caspase-dependent chromatin fragmentation. Concurrently, specific cell surface modifications took place, involving at first glycoprotein syalilation and later phospholipid asymmetry. DNA fragmentation was subsequently detected by TUNEL assay. Over time, cell membranes became permeable to propidium iodide. A very similar time-course of apoptotic events was found after treatment of a myelomonocytic cell line with the same drug.</p> <p>Conclusion</p> <p>After discussing some characteristics of the methods employed and their limitations, a succession of apoptotic events over time is suggested, in which the collapse of mitochondrial transmembrane potential (Δψm) is the earliest sign of apoptosis.</p>
url http://www.biomedcentral.com/1471-2121/7/6
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