NutriGenetic Research Institute, Ephrata, PA 17522, USA.
Integrative Medicine Fellow, University of Arizona College of Medicine, Tucson, AZ 85724, USA.
Cells. 2024 Sep 15;13(18):1554. doi: 10.3390/cells13181554.
Intercellular adhesion molecule 1 (ICAM-1/CD54), a transmembrane glycoprotein, has been considered as one of the most important adhesion molecules during leukocyte recruitment. It is encoded by the gene and plays a central role in inflammation. Its crucial role in many inflammatory diseases such as ulcerative colitis and rheumatoid arthritis are well established. Given that neuroinflammation, underscored by microglial activation, is a key element in neurodegenerative diseases such as Parkinson's disease (PD), we investigated whether ICAM-1 has a role in this progressive neurological condition and, if so, to elucidate the underpinning mechanisms. Specifically, we were interested in the potential interaction between ICAM-1, glial cells, and ferroptosis, an iron-dependent form of cell death that has recently been implicated in PD. We conclude that there exist direct and indirect (via glial cells and T cells) influences of ICAM-1 on ferroptosis and that further elucidation of these interactions can suggest novel intervention for this devastating disease.
细胞间黏附分子 1(ICAM-1/CD54)是一种跨膜糖蛋白,被认为是白细胞募集过程中最重要的黏附分子之一。它由 基因编码,在炎症中发挥核心作用。其在溃疡性结肠炎和类风湿关节炎等许多炎症性疾病中的关键作用已得到充分证实。鉴于神经炎症(以小胶质细胞激活为特征)是帕金森病(PD)等神经退行性疾病的关键因素,我们研究了 ICAM-1 是否在这种进行性神经疾病中发挥作用,如果有,阐明其潜在机制。具体来说,我们对 ICAM-1 与神经胶质细胞和铁死亡之间的潜在相互作用感兴趣,铁死亡是一种最近被认为与 PD 相关的铁依赖性细胞死亡形式。我们得出结论,ICAM-1 对铁死亡存在直接和间接(通过神经胶质细胞和 T 细胞)的影响,进一步阐明这些相互作用可以为这种毁灭性疾病提供新的干预措施。