{"title":"急性胰腺炎患者胰腺尖细胞中的离子通道:钙、铁和铜信号的串扰。","authors":"Hanli Wang, Jianhua Gao, Lingling Wen, Kejun Huang, Huixian Liu, Linsheng Zeng, Zhongyi Zeng, Yuxiang Liu, Zhizhun Mo","doi":"10.3389/fimmu.2024.1444272","DOIUrl":null,"url":null,"abstract":"<p><p>The initial stages of acute pancreatitis (AP) are characterized by a significant event - acinar ductal metaplasia (ADM). This process is a crucial feature of both acute and chronic pancreatitis, serving as the first step in the development of pancreatic cancer. Ion channels are integral transmembrane proteins that play a pivotal role in numerous biological processes by modulating ion flux. In many diseases, the expression and activity of ion channels are often dysregulated. Metal ions, including calcium ions (Ca<sup>2+</sup>), ferrous ions (Fe<sup>2+</sup>), and Copper ions (Cu<sup>2+</sup>), assume a distinctive role in cellular metabolism. These ions possess specific biological properties relevant to cellular function. However, the interactions among these ions exacerbate the imbalance within the intracellular environment, resulting in cellular damage and influencing the progression of AP. A more in-depth investigation into the mechanisms by which these ions interact with acinar cells is essential for elucidating AP's pathogenesis and identifying novel therapeutic strategies. Currently, treatment for AP primarily focuses on pain relief, complications prevention, and prognosis improvement. There are limited specific treatments targeting acinous cell dedifferentiation or ion imbalance. 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引用次数: 0
摘要
急性胰腺炎(AP)初期有一个重要特征--尖状腺导管增生(ADM)。这一过程是急性和慢性胰腺炎的重要特征,也是胰腺癌发展的第一步。离子通道是一种完整的跨膜蛋白,通过调节离子通量在许多生物过程中发挥着关键作用。在许多疾病中,离子通道的表达和活性经常失调。金属离子,包括钙离子(Ca2+)、亚铁离子(Fe2+)和铜离子(Cu2+),在细胞代谢中发挥着独特的作用。这些离子具有与细胞功能相关的特定生物特性。然而,这些离子之间的相互作用加剧了细胞内环境的失衡,导致细胞损伤并影响 AP 的进展。深入研究这些离子与acinar细胞相互作用的机制,对于阐明AP的发病机制和确定新的治疗策略至关重要。目前,AP 的治疗主要侧重于缓解疼痛、预防并发症和改善预后。针对尖锐湿疣细胞去分化或离子失衡的特殊治疗方法非常有限。本研究旨在通过研究急性胰腺炎背景下尖腺细胞内的离子串扰,探讨潜在的治疗策略。
Ion channels in acinar cells in acute pancreatitis: crosstalk of calcium, iron, and copper signals.
The initial stages of acute pancreatitis (AP) are characterized by a significant event - acinar ductal metaplasia (ADM). This process is a crucial feature of both acute and chronic pancreatitis, serving as the first step in the development of pancreatic cancer. Ion channels are integral transmembrane proteins that play a pivotal role in numerous biological processes by modulating ion flux. In many diseases, the expression and activity of ion channels are often dysregulated. Metal ions, including calcium ions (Ca2+), ferrous ions (Fe2+), and Copper ions (Cu2+), assume a distinctive role in cellular metabolism. These ions possess specific biological properties relevant to cellular function. However, the interactions among these ions exacerbate the imbalance within the intracellular environment, resulting in cellular damage and influencing the progression of AP. A more in-depth investigation into the mechanisms by which these ions interact with acinar cells is essential for elucidating AP's pathogenesis and identifying novel therapeutic strategies. Currently, treatment for AP primarily focuses on pain relief, complications prevention, and prognosis improvement. There are limited specific treatments targeting acinous cell dedifferentiation or ion imbalance. This study aims to investigate potential therapeutic strategies by examining ion crosstalk within acinar cells in the context of acute pancreatitis.
期刊介绍:
Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.