Castri Paola, Lee Yang-Ja, Ponzio Todd, Maric Dragan, Spatz Maria, Bembry Joliet, Hallenbeck John
Biochim Biophys Acta. 2014 Mar;1843(3):640-51. doi: 10.1016/j.bbamcr.2013.12.005.
Poly(ADP-ribose) polymerase-1 (PARP-1) and its cleavage products regulate cell viability and NF-kappaB activity when expressed in neurons. PARP-1 cleavage generates a 24 kDa (PARP-1(24)) and an 89 kDa fragment (PARP-1(89)). Compared to WT (PARP-1WT), the expression of an uncleavable PARP-1 (PARP-1(UNCL)) or of PARP-1(24) conferred protection from oxygen/glucose deprivation (OGD) or OGD/restoration of oxygen and glucose (ROG) damage in vitro, whereas expression of PARP-1(89) was cytotoxic. Viability experiments were performed in SH-SY5Y, a human neuroblastoma cell line, as well as in rat primary cortical neurons. Following OGD, the higher viability in the presence of PARP-1UNCL or PARP-1(24) was not accompanied with decreased formation of poly(ADP-riboses) or higher NAD levels. PARP-1 is a known cofactor for NF-kappaB, hence we investigated whether PARP-1 cleavage influences the inflammatory response. All PARP-1 constructs mimicked PARP-1WT in regard to induction of NF-kappaB translocation into the nucleus and its increased activation during ischemic challenge. However, expression of PARP-1(89) construct induced significantly higher NF-kB activity than PARP-1WT; and the same was true for NF-kappaB-dependent iNOS promoter binding activity. At a protein level, PARP-1UNCL and PARP-1(24) decreased iNOS (and lower levels of iNOS transcript) and COX-2, and increased Bcl-xL The increased levels of NF-kB and iNOS transcriptional activities, seen with cytotoxic PARP-189, were accompanied by higher protein expression of COX-2 and iNOS (and higher levels of INOS transcript) and lower protein expression of Bcl-xL Taken together, these findings suggest that PARP-1 cleavage products may regulate cellular viability and inflammatory responses in opposing ways during in vitro models of "ischemia".
聚(ADP - 核糖)聚合酶 -1(PARP -1)及其裂解产物在神经元中表达时可调节细胞活力和核因子κB(NF - κB)活性。PARP -1裂解产生一个24 kDa片段(PARP -1(24))和一个89 kDa片段(PARP -1(89))。与野生型PARP -1(PARP -1WT)相比,不可裂解的PARP -1(PARP -1(UNCL))或PARP -1(24)的表达可在体外保护细胞免受氧/葡萄糖剥夺(OGD)或氧和葡萄糖恢复(ROG)损伤,而PARP -1(89)的表达具有细胞毒性。活力实验在人神经母细胞瘤细胞系SH - SY5Y以及大鼠原代皮质神经元中进行。OGD后,在PARP -1(UNCL)或PARP -1(24)存在的情况下细胞较高的活力并非伴随着聚(ADP - 核糖)形成的减少或较高的烟酰胺腺嘌呤二核苷酸(NAD)水平。PARP -1是已知的NF - κB辅因子,因此我们研究了PARP -1裂解是否影响炎症反应。所有PARP -1构建体在诱导NF - κB易位至细胞核及其在缺血刺激期间增加的激活方面都模拟了PARP -1WT。然而,PARP -1(89)构建体的表达诱导的NF - κB活性明显高于PARP -1WT;NF - κB依赖性诱导型一氧化氮合酶(iNOS)启动子结合活性也是如此。在蛋白质水平上,PARP -1(UNCL)和PARP -1(24)降低了iNOS(以及较低水平的iNOS转录本)和环氧化酶 -2(COX -2),并增加了Bcl - xL。细胞毒性的PARP -1(89)导致的NF - κB和iNOS转录活性增加伴随着COX -2和iNOS更高的蛋白质表达(以及更高水平的iNOS转录本)以及Bcl - xL更低的蛋白质表达。综上所述,这些发现表明在“缺血”体外模型中,PARP -1裂解产物可能以相反的方式调节细胞活力和炎症反应。