Radke Jay R, Routes John M, Cook James L
1Research Section, Boise VA Hospital and Idaho Veterans Research and Education Foundation, Boise, ID 83702 USA.
2Section of Allergy and Clinical Immunology, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Cell Death Discov. 2019 Jul 1;5:110. doi: 10.1038/s41420-019-0189-z. eCollection 2019.
Expression of the adenovirus E1A oncogene sensitizes tumor cells to innate immune rejection by NK cells. This increased NK sensitivity is only partly explained by an E1A-induced increase in target cell surface expression of NKG2D ligands. The post-recognition mechanisms by which E1A sensitizes cells to the apoptotic cell death response to NK injury remains to be defined. E1A sensitizes cells to apoptotic stimuli through two distinct mechanisms-repression of NF-κB-dependent antiapoptotic responses and enhancement of caspase-2 activation and related mitochondrial injury. The current studies examined the roles of each of these post-NKG2D-recognition pathways in the increased sensitivity of E1A-positive target cells to NK killing. Sensitization to NK-induced apoptosis was independent of E1A-mediated repression of cellular NF-κB responses but was dependent on the expression of both caspase-2 and the upstream, caspase-2 activating molecule, PIDD. Target cells lacking caspase-2 or PIDD expression retained E1A-induced increased expression of the NKG2D ligand, RAE-1. NK cell-induced mitochondrial injury of E1A-expressing cells did not require expression of the mitochondrial molecules, Bak or Bax. These results define a PIDD/caspase-2-dependent pathway, through which E1A sensitizes cells to NK-mediated cytolysis independently of and complementarily to E1A-enhanced NKG2D/RAE-1 ligand expression.
腺病毒E1A癌基因的表达使肿瘤细胞对自然杀伤细胞(NK细胞)的先天性免疫排斥敏感。这种NK敏感性增加仅部分由E1A诱导的靶细胞表面NKG2D配体表达增加来解释。E1A使细胞对NK损伤的凋亡细胞死亡反应敏感的识别后机制仍有待确定。E1A通过两种不同机制使细胞对凋亡刺激敏感——抑制NF-κB依赖性抗凋亡反应以及增强半胱天冬酶-2激活和相关的线粒体损伤。目前的研究检查了这些NKG2D识别后途径中的每一个在E1A阳性靶细胞对NK杀伤敏感性增加中的作用。对NK诱导的凋亡的敏感性独立于E1A介导的细胞NF-κB反应的抑制,但依赖于半胱天冬酶-2和上游的半胱天冬酶-2激活分子PIDD的表达。缺乏半胱天冬酶-2或PIDD表达的靶细胞保留了E1A诱导的NKG2D配体RAE-1表达增加。NK细胞诱导的表达E1A的细胞的线粒体损伤不需要线粒体分子Bak或Bax的表达。这些结果定义了一条PIDD/半胱天冬酶-2依赖性途径,通过该途径E1A使细胞对NK介导的细胞溶解敏感,这独立于且互补于E1A增强的NKG2D/RAE-1配体表达。