Saeedi-Boroujeni Ali, Purrahman Daryush, Shojaeian Ali, Poniatowski Łukasz A, Rafiee Fatemeh, Mahmoudian-Sani Mohammad-Reza
Department of Microbiology, School of Medicine, Abadan University of Medical Sciences, Abadan, Iran.
Thalassemia and Hemoglobinopathy Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
J Inflamm (Lond). 2023 Jan 19;20(1):1. doi: 10.1186/s12950-023-00327-0.
Immune dysregulation has been identified as a critical cause of the most common types of cardiovascular diseases (CVDs). Notably, the innate and adaptive immune responses under physiological conditions are typically regulated with high sensitivity to avoid the exacerbation of inflammation, but any dysregulation can probably be associated with CVDs. In this respect, progranulin (PGRN) serves as one of the main components of the regulation of inflammatory processes, which significantly contributes to the immunopathogenesis of such disorders. PGRN has been introduced among the secreted growth factors as one related to wound healing, inflammation, and human embryonic development, as well as a wide variety of autoimmune diseases. The relationship between the serum PGRN and TNF-α ratio with the spontaneous bacterial peritonitis constitute one of the independent predictors of these conditions. The full-length PGRN can thus effectively reduce the calcification of valve interstitial cells, and the granulin precursor (GRN), among the degradation products of PGRN, can be beneficial. Moreover, it was observed that, PGRN protects the heart against ischemia-reperfusion injury. Above all, PGRN also provides protection in the initial phase following myocardial ischemia-reperfusion injury. The protective impact of PGRN on this may be associated with the early activation of the PI3K/Akt signaling pathway. PGRN also acts as a protective factor in hyperhomocysteinemia, probably by down-regulating the wingless-related integration site Wnt/β-catenin signaling pathway. Many studies have further demonstrated that SARS-CoV-2 (COVID-19) has dramatically increased the risks of CVDs due to inflammation, so PGRN has drawn much more attention among scholars. Lysosomes play a pivotal role in the inflammation process, and PGRN is one of the key regulators in their functioning, which contributes to the immunomodulatory mechanism in the pathogenesis of CVDs. Therefore, investigation of PGRN actions can help find new prospects in the treatment of CVDs. This review aims to summarize the role of PGRN in the immunopathogenesis of CVD, with an emphasis on its treatment.
免疫失调已被确认为最常见类型心血管疾病(CVD)的关键病因。值得注意的是,生理条件下的先天性和适应性免疫反应通常受到高度敏感的调节,以避免炎症加剧,但任何失调都可能与CVD相关。在这方面,前颗粒蛋白(PGRN)是炎症过程调节的主要成分之一,对这类疾病的免疫发病机制有显著贡献。PGRN已被列为与伤口愈合、炎症、人类胚胎发育以及多种自身免疫性疾病相关的分泌性生长因子之一。血清PGRN与TNF-α比值与自发性细菌性腹膜炎之间的关系是这些病症的独立预测指标之一。因此,全长PGRN可有效减少瓣膜间质细胞的钙化,而PGRN降解产物中的颗粒蛋白前体(GRN)可能有益。此外,观察到PGRN可保护心脏免受缺血再灌注损伤。最重要的是,PGRN还在心肌缺血再灌注损伤后的初始阶段提供保护。PGRN对此的保护作用可能与PI3K/Akt信号通路的早期激活有关。PGRN在高同型半胱氨酸血症中也作为一种保护因子发挥作用,可能是通过下调无翅相关整合位点Wnt/β-连环蛋白信号通路。许多研究进一步表明,严重急性呼吸综合征冠状病毒2(SARS-CoV-2,即新冠病毒病)由于炎症显著增加了CVD的风险,因此PGRN在学者中受到了更多关注。溶酶体在炎症过程中起关键作用,而PGRN是其功能的关键调节因子之一,这有助于CVD发病机制中的免疫调节机制。因此,研究PGRN的作用有助于找到治疗CVD的新前景。本综述旨在总结PGRN在CVD免疫发病机制中的作用,重点是其治疗作用。