Rac Monika
Department of Biochemistry, Pomeranian Medical University, Powstancow Wielkopolskich 72, 70-111 Szczecin, Poland.
Genes (Basel). 2025 Jun 13;16(6):705. doi: 10.3390/genes16060705.
Human CD36 plays an important role in ligand binding, signalling, cell adhesion, and the regulation of angiogenesis. As a scavenging receptor, it is responsible for clearing long-chain fatty acids (LCFAs) and removing approximately 50% of oxidised low-density lipoprotein (ox-LDL) from plasma. The gene is alternatively spliced. It has several alternative promoters and first exons. The alternative transcripts are expressed in multiple tissues, and their expression patterns are highly variable. The molecular mechanisms that regulate gene expression are complex and reflect its multifunctional role in different tissues. CD36 activity has been linked to several metabolic processes, such as inflammation, angiogenesis, phagocytosis, and energy homeostasis. CD36 plays a key role in regulating vascular and cardiovascular health and in the pathogenesis of atherosclerosis. gene mutations in the Caucasian population are rare. Hence, it is extremely difficult to recruit a statistically significant group of CAD patients with these mutations. Nevertheless, this population is largely at risk of cardiovascular disease. Atherosclerosis is a multifactorial disease, but the role of the CD36 receptor in the development of ox-LDL is extremely important. This review aims to introduce readers to issues related to the relationship between CD36 and CAD. The activity of this receptor should be considered when exploring treatment options for atherosclerosis-related complications.
人类CD36在配体结合、信号传导、细胞黏附以及血管生成调节中发挥着重要作用。作为一种清道夫受体,它负责清除长链脂肪酸(LCFA)并从血浆中清除约50%的氧化型低密度脂蛋白(ox-LDL)。该基因存在可变剪接。它有多个可变启动子和首个外显子。可变转录本在多种组织中表达,且其表达模式高度可变。调节该基因表达的分子机制复杂,反映了其在不同组织中的多功能作用。CD36活性与多种代谢过程相关,如炎症、血管生成、吞噬作用和能量稳态。CD36在调节血管和心血管健康以及动脉粥样硬化发病机制中起关键作用。白种人群中的该基因突变罕见。因此,招募一组具有这些突变的冠心病患者并使其具有统计学意义极为困难。然而,这一人群患心血管疾病的风险很大。动脉粥样硬化是一种多因素疾病,但CD36受体在ox-LDL形成过程中的作用极为重要。本综述旨在向读者介绍与CD36和冠心病之间关系相关的问题。在探索动脉粥样硬化相关并发症的治疗方案时,应考虑该受体的活性。
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