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线粒体光损伤与光动力疗法诱导的细胞凋亡

Mitochondrial photodamage and PDT-induced apoptosis.

作者信息

Kessel D, Luo Y

机构信息

Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

J Photochem Photobiol B. 1998 Feb;42(2):89-95. doi: 10.1016/s1011-1344(97)00127-9.

Abstract

Four photosensitizers with specific targets (mitochondria, lysosomes and plasma membrane) were used to delineate the mechanism of PDT-induced apoptosis in murine leukemia cells. Additional studies were carried out with two sensitizers which caused photodamage to both mitochondria and lysosomes, but varied with regard to membrane photodamage. PDT induced an apoptotic response after mitochondrial photodamage, but not after selective damage to lysosomes or to the cell membrane. Moreover, the latter could delay or inhibit the appearance of apoptosis after mitochondrial photodamage. We had previously reported that exposure of cells to high porphycene concentrations caused an apoptotic response in the dark; this was also associated with mitochondrial damage. These results are consistent with recent proposals that release of mitochondrial components can trigger an apoptotic response. ATP depletion after mitochondrial photodamage does not appear to play a role in initiation of the apoptotic program.

摘要

使用四种具有特定靶点(线粒体、溶酶体和质膜)的光敏剂来阐明光动力疗法诱导小鼠白血病细胞凋亡的机制。对另外两种对线粒体和溶酶体均造成光损伤但在膜光损伤方面有所不同的光敏剂进行了额外研究。光动力疗法在线粒体光损伤后诱导凋亡反应,但在溶酶体或细胞膜选择性损伤后则不会。此外,后者可延迟或抑制线粒体光损伤后凋亡的出现。我们之前曾报道,细胞暴露于高卟吩浓度会在黑暗中引发凋亡反应;这也与线粒体损伤有关。这些结果与最近提出的线粒体成分释放可触发凋亡反应的观点一致。线粒体光损伤后ATP耗竭似乎在凋亡程序启动中不起作用。

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