Department of Pharmacology and The Penn State Hershey Cancer Institute, The Pennsylvania State University College of Medicine and Milton S. Hershey Medical Center, Hershey, PA, USA.
Autophagy. 2011 Dec;7(12):1557-8. doi: 10.4161/auto.7.12.17910.
Our recent study revealed a new role of nucleus accumbens-1 (NAC1), a transcription factor belonging to the BTB/POZ gene family, in regulating autophagy. Moreover, we found that the high-mobility group box 1 (HMGB1), a chromatin-associated nuclear protein acting as an extracellular damage associated molecular pattern molecule (DAMP), is the downstream executor of NAC1 in modulating autophagy. In response to stress such as therapeutic insults, NAC1 increases the expression, cytosolic translocation and release of HMGB1; elevated level of the cytoplasmic HMGB1 leads to activation of autophagy. The NAC1-HMGB1 partnership may represent a previously unrecognized pathway that regulates autophagy in response to various stresses such as chemotherapy.
我们最近的研究揭示了核小体结合结构域 1(NAC1)的一个新作用,NAC1 是属于 BTB/POZ 基因家族的转录因子,可调节自噬。此外,我们发现高迁移率族盒 1(HMGB1),一种作为细胞外损伤相关分子模式分子(DAMP)的染色质相关核蛋白,是 NAC1 调节自噬的下游执行者。在应激反应(如治疗性损伤)中,NAC1 增加 HMGB1 的表达、胞质易位和释放;细胞质 HMGB1 水平升高会导致自噬的激活。NAC1-HMGB1 伙伴关系可能代表了一种以前未被识别的途径,该途径可调节自噬对各种应激(如化疗)的反应。