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载脂蛋白M:研究进展、调控及代谢功能(综述)

Apolipoprotein M: Research progress, regulation and metabolic functions (Review).

作者信息

Huang Li-Zhu, Gao Jia-Lin, Pu Chun, Zhang Pu-Hong, Wang Li-Zhuo, Feng Gang, Zhang Yao

机构信息

Department of Biochemistry and Molecular Biology, Wannan Medical College, Wuhu, Anhui 241001, P.R. China.

Department of Endocrinology and Genetic Metabolism, Yijishan Hospital of Wannan Medical College, Wuhu, Anhui 241002, P.R. China.

出版信息

Mol Med Rep. 2015 Aug;12(2):1617-24. doi: 10.3892/mmr.2015.3658. Epub 2015 Apr 22.

Abstract

Apolipoprotein M (ApoM) is a novel lipoprotein-associated plasma protein of the apolipoprotein family. It is predominantly enriched in high-density lipoprotein (HDL), and is also present in small quantities in low-density lipoprotein (LDL) and in very low-density lipoprotein. Transgenic animal experiments have suggested that ApoM can be transformed into various lipoproteins and may be involved in lipoprotein metabolism. ApoM has five subtypes, however, their biological functions remain to be elucidated. The α-helix, formed by ApoM through hydrophobic signal peptides, is anchored to the phospholipid monomolecular layers of HDL. Hydrophobic domains can associate with small lipophilic ligands and perform biological functions. ApoM may affect HDL metabolism and exhibit anti-atherosclerotic functions. Human HDL, containing ApoM subfractions, can protect LDL from oxidation and regulate cholesterol efflux more effectively than HDL without ApoM. Therefore, it is highly correlated with plasma cholesterol levels in the human body. Although previous studies have reported no difference in ApoM between groups of patients with coronary heart disease (CHD) and a normal control groups, the anti-atherosclerotic effect of ApoM is evident. ApoM is highly expressed in renal proximal tubule cells and is secreted into the urine in tubule cells. However, it is usually reabsorbed by giantin-associated proteins in a process, which is also affected in kidney disease. In addition to liver and kidney cells, low expression levels of ApoM occur in the intestinal tract and are associated with lymph node metastasis of colorectal cancer. ApoM gene polymorphism is associated with CHD, diabetes and other immune-associated diseases. Investigations into the gene regulation of ApoM may assist in further clarifying the role of ApoM in blood glucose and lipid metabolism. Genetic modification of the mouse ApoM gene is an essential technique to investigate the gene expression and regulation of ApoM, and to clarify the potential roles of ApoM in lipoprotein metabolism, atherosclerosis, diabetes and renal diseases.

摘要

载脂蛋白M(ApoM)是载脂蛋白家族中一种新型的脂蛋白相关血浆蛋白。它主要富集于高密度脂蛋白(HDL)中,在低密度脂蛋白(LDL)和极低密度脂蛋白中也有少量存在。转基因动物实验表明,ApoM可转化为多种脂蛋白,并可能参与脂蛋白代谢。ApoM有五个亚型,但其生物学功能仍有待阐明。ApoM通过疏水信号肽形成的α螺旋锚定在HDL的磷脂单分子层上。疏水结构域可与小的亲脂性配体结合并发挥生物学功能。ApoM可能影响HDL代谢并具有抗动脉粥样硬化功能。含有ApoM亚组分的人HDL比不含ApoM的HDL能更有效地保护LDL免受氧化并调节胆固醇流出。因此,它与人体血浆胆固醇水平高度相关。尽管先前的研究报道冠心病(CHD)患者组和正常对照组之间的ApoM没有差异,但ApoM的抗动脉粥样硬化作用是明显的。ApoM在肾近端小管细胞中高表达,并在小管细胞中分泌到尿液中。然而,它通常在一个过程中被巨蛋白相关蛋白重新吸收,这个过程在肾脏疾病中也会受到影响。除了肝脏和肾脏细胞外,ApoM在肠道中的表达水平较低,并且与结直肠癌的淋巴结转移有关。ApoM基因多态性与CHD、糖尿病和其他免疫相关疾病有关。对ApoM基因调控的研究可能有助于进一步阐明ApoM在血糖和脂质代谢中的作用。对小鼠ApoM基因进行基因改造是研究ApoM基因表达和调控、阐明ApoM在脂蛋白代谢、动脉粥样硬化、糖尿病和肾脏疾病中潜在作用的一项重要技术。

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