Kessel David, Evans Conor L
Department of Pharmacology, Wayne State University, Detroit, MI.
Wellman Center for Photomedicine, Harvard Medical School Massachusetts General Hospital, Boston, MA.
Photochem Photobiol. 2016 Jul;92(4):620-3. doi: 10.1111/php.12592. Epub 2016 May 18.
Prior studies demonstrated that a low level (LD10-15 ) of lysosomal photodamage can sensitize cells to the apoptotic death that results from subsequent mitochondrial photodamage. We have proposed that this process occurs via a calpain-catalyzed cleavage of the autophagy-associated protein ATG5 to form a proapoptotic fragment. In this report, we provide evidence for the postulated ATG5 cleavage and show that the sequential photodynamic therapy (PDT) protocol can also partly overcome the adverse effect of hypoxia on the initiation of apoptosis. While autophagy can offer cytoprotection after mitochondrial photodamage, this does not appear to apply when lysosomes are the target. This may account for the ability of very low PDT doses directed at lysosomes to evoke ATG5 cleavage. The resulting proapoptotic effect overcomes intrinsic cytoprotection from mitochondrial photodamage along with a further stimulation of phototoxicity.
先前的研究表明,低水平(LD10 - 15)的溶酶体光损伤可使细胞对随后线粒体光损伤导致的凋亡性死亡敏感。我们提出,这一过程是通过钙蛋白酶催化自噬相关蛋白ATG5的裂解形成促凋亡片段来发生的。在本报告中,我们为假定的ATG5裂解提供了证据,并表明序贯光动力疗法(PDT)方案也可部分克服缺氧对凋亡起始的不利影响。虽然自噬可在细胞线粒体光损伤后提供细胞保护作用,但当溶酶体成为靶点时,情况似乎并非如此。这可能解释了针对溶酶体的极低PDT剂量引发ATG5裂解的能力。由此产生的促凋亡效应克服了线粒体光损伤带来的内在细胞保护作用,并进一步增强了光毒性。