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机构地区:[1]哈尔滨医科大学附属第一医院胰胆外科,哈尔滨150001
出 处:《中华肝胆外科杂志》2016年第10期718-720,共3页Chinese Journal of Hepatobiliary Surgery
基 金:国家自然科学基金(81100314,81370565);黑龙江省新世纪优秀人才培养计划(1253-NCET-017);哈尔滨医科大学于维汉院士杰出青年基金
摘 要:胰腺腺泡细胞死亡方式是决定急性胰腺炎(AP)病程及预后的重要因素。AP病情轻重与腺泡坏死呈正相关,与腺泡凋亡呈负相关。细胞的三磷酸腺苷(ATP)含量是调控其死亡方式的关键,在多种病理生理过程中扮演了坏死一凋亡转化开关的角色。低水平ATP可加速细胞坏死,高水平ATP则促进其凋亡。缺氧诱导因子-1(HIF-1)是在缺氧条件下高表达的转录因子,可有效调节细胞能量代谢模式,在细胞死亡及炎症损伤调控中发挥了重要作用。本文对HIF-1在AP中的研究进展做一综述,以期为AP发病机制的深入理解和新的治疗靶点的提出提供参考。Pancreatic acinar cell death modality is a significant factor which determines the course and prognosis of acute pancreatitis (AP). The severity of AP is positively corre- lated with acinar necrosis, while negatively correlated with aci- nat apoptosis. Adenosine triphosphate (ATP) level is the key to control the manner of death, and acts as a switch during the con- version of necrosis and apoptosis in a variety of pathophysiologi- cal settings: low levels of ATP can accelerate cell necrosis and high levels of ATP might promote apoptosis. Hypoxia inducible factor 1 (HIF-1) is a highly expressed transcription factor in anoxic conditions which can effectively regulate cell energy me- tabolism and play an important role in regulating cell death and inflammatory injury. Therefore, this review aimed to provide a reference about better understanding of the pathogenesis and new therapeutic targets of HIF-1 in AP.
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