Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death

Active involvement of mitochondria in cell death has been well-documented, but local apoptotic signaling between subsets of mitochondria has been poorly explored to date. Using mitochondrially localized CMXRos as a photosensitizer coupled to laser irradiation by confocal laser scanning microscopy, w...

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Main Authors: May-Ghee Lum, Tetsuhiro Minamikawa, Phillip Nagley
Format: Article
Language:English
Published: Hindawi Limited 2002-01-01
Series:The Scientific World Journal
Online Access:http://dx.doi.org/10.1100/tsw.2002.227
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spelling doaj-1214a1cf383a4678adee295e3abebfbb2020-11-25T02:22:58ZengHindawi LimitedThe Scientific World Journal1537-744X2002-01-0121198120810.1100/tsw.2002.227Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell DeathMay-Ghee Lum0Tetsuhiro Minamikawa1Phillip Nagley2Department of Biochemistry and Molecular Biology, PO Box 13D, Monash University, Victoria 3800, AustraliaOlympus Australia Pty. Ltd., 1/104 Ferntree Gully Rd., Oakleigh VIC 3166, AustraliaDepartment of Biochemistry and Molecular Biology, PO Box 13D, Monash University, Victoria 3800, AustraliaActive involvement of mitochondria in cell death has been well-documented, but local apoptotic signaling between subsets of mitochondria has been poorly explored to date. Using mitochondrially localized CMXRos as a photosensitizer coupled to laser irradiation by confocal laser scanning microscopy, we demonstrate that partial irradiation of about half the mitochondria in human 143B TK– cells induces rapid loss of mitochondrial membrane potential (ΔΨm) in nonirradiated mitochondria. Cells so partially irradiated show apoptotic indications, including mobilization of cytochrome c and binding of annexin V within 2 h following irradiation. The loss of ΔΨm in nonirradiated mitochondria did not occur in cells photoirradiated in the absence of CMXRos. Increasing the proportion of irradiated mitochondria in each cell (up to about 50%) generated a correspondingly greater percentage of cells in which nonirradiated mitochondria lost ΔΨm and which also showed apoptotic indications. Only at the highest level of irradiation (global for all mitochondria in one cell) were signs of necrosis evident (judged by uptake of propidium iodide). Because laser irradiation is specific to the subpopulation of mitochondria targeted, the data imply that a signal emanating from irradiated mitochondria is processed by their nonirradiated counterparts. We conclude that intermitochondrial signaling occurs in the subcellular response to induction of apoptosis.http://dx.doi.org/10.1100/tsw.2002.227
collection DOAJ
language English
format Article
sources DOAJ
author May-Ghee Lum
Tetsuhiro Minamikawa
Phillip Nagley
spellingShingle May-Ghee Lum
Tetsuhiro Minamikawa
Phillip Nagley
Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
The Scientific World Journal
author_facet May-Ghee Lum
Tetsuhiro Minamikawa
Phillip Nagley
author_sort May-Ghee Lum
title Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
title_short Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
title_full Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
title_fullStr Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
title_full_unstemmed Microscopic Photosensitization: A New Tool to Investigate the Role of Mitochondria in Cell Death
title_sort microscopic photosensitization: a new tool to investigate the role of mitochondria in cell death
publisher Hindawi Limited
series The Scientific World Journal
issn 1537-744X
publishDate 2002-01-01
description Active involvement of mitochondria in cell death has been well-documented, but local apoptotic signaling between subsets of mitochondria has been poorly explored to date. Using mitochondrially localized CMXRos as a photosensitizer coupled to laser irradiation by confocal laser scanning microscopy, we demonstrate that partial irradiation of about half the mitochondria in human 143B TK– cells induces rapid loss of mitochondrial membrane potential (ΔΨm) in nonirradiated mitochondria. Cells so partially irradiated show apoptotic indications, including mobilization of cytochrome c and binding of annexin V within 2 h following irradiation. The loss of ΔΨm in nonirradiated mitochondria did not occur in cells photoirradiated in the absence of CMXRos. Increasing the proportion of irradiated mitochondria in each cell (up to about 50%) generated a correspondingly greater percentage of cells in which nonirradiated mitochondria lost ΔΨm and which also showed apoptotic indications. Only at the highest level of irradiation (global for all mitochondria in one cell) were signs of necrosis evident (judged by uptake of propidium iodide). Because laser irradiation is specific to the subpopulation of mitochondria targeted, the data imply that a signal emanating from irradiated mitochondria is processed by their nonirradiated counterparts. We conclude that intermitochondrial signaling occurs in the subcellular response to induction of apoptosis.
url http://dx.doi.org/10.1100/tsw.2002.227
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