Ventura Raúl, Martínez-Ruiz Inma, Hernández-Alvarez María Isabel
Departament de Bioquímica i Biomedicina Molecular, Facultat de Biologia, Universitat de Barcelona, 08028 Barcelona, Spain.
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Biomedicines. 2022 May 23;10(5):1201. doi: 10.3390/biomedicines10051201.
Phospholipids are the basic structure block of eukaryotic membranes, in both the outer and inner membranes, which delimit cell organelles. Phospholipids can also be damaged by oxidative stress produced by mitochondria, for instance, becoming oxidized phospholipids. These damaged phospholipids have been related to prevalent diseases such as atherosclerosis or non-alcoholic steatohepatitis (NASH) because they alter gene expression and induce cellular stress and apoptosis. One of the main sites of phospholipid synthesis is the endoplasmic reticulum (ER). ER association with other organelles through membrane contact sites (MCS) provides a close apposition for lipid transport. Additionally, an important advance in this small cytosolic gap are lipid transfer proteins (LTPs), which accelerate and modulate the distribution of phospholipids in other organelles. In this regard, LTPs can be established as an essential point within phospholipid circulation, as relevant data show impaired phospholipid transport when LTPs are defected. This review will focus on phospholipid function, metabolism, non-vesicular transport, and associated diseases.
磷脂是真核细胞膜的基本结构单元,存在于界定细胞器的内膜和外膜中。磷脂也会受到线粒体产生的氧化应激的损害,例如,变成氧化磷脂。这些受损的磷脂与动脉粥样硬化或非酒精性脂肪性肝炎(NASH)等常见疾病有关,因为它们会改变基因表达并诱导细胞应激和凋亡。磷脂合成的主要场所之一是内质网(ER)。内质网通过膜接触位点(MCS)与其他细胞器的关联为脂质转运提供了紧密的并列关系。此外,在这个小的胞质间隙方面的一个重要进展是脂质转运蛋白(LTPs),它们加速并调节磷脂在其他细胞器中的分布。在这方面,脂质转运蛋白可被确立为磷脂循环中的一个关键点,因为相关数据表明,当脂质转运蛋白存在缺陷时,磷脂转运受损。本综述将聚焦于磷脂的功能、代谢、非囊泡运输及相关疾病。