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Apolipoprotein M: Research Progress and Clinical Perspective
1Comprehensive Laboratory, The Third Affiliated Hospital of Soochow University, Changzhou, People's Republic of China.
Abstract:
Apolipoprotein M (apoM) was first identified and characterized to the apolipoprotein family in 1999. Human apoM gene is located in a highly conserved segment in the major histocompatibility complex (MHC) class III locus on chromosome 6 and codes for an about 23 kDa protein that structurally belongs to the lipocalin superfamily. ApoM is selectively expressed in hepatocytes and in the tubular epithelium of kidney. In human plasma, apoM is mainly confined to the high-density lipoprotein (HDL) particles, but it may also occur in other lipoprotein classes, such as in the triglyceride-rich particles after fat intake. It has been demonstrated that apoM is critical for the formation of HDL, notably pre-beta HDL1. The antiatherogenic function of HDL is well established, and its ability to promote cholesterol efflux from foam cells in the atherosclerotic lesions is generally regarded as one of the key mechanisms behind this protective function. However, HDL could also display a variety of properties that may affect the complex atherosclerotic processes by other mechanisms, thus being involved in processes related to antioxidant defense, immune system, and systemic effects in septicemia, which may be partly contributed via its apolipoproteins and/or phospholipids. Moreover, it has been demonstrated that apoM functions as a natural carrier of sphingosin-1-phosphate (S1P) in vivo which may be related to its antiatherosclerotic and protective effects on endothelial cell barrier and anti-inflammatory properties. These may also provide a link between the diverse effects of HDL.
Insights
Apolipoprotein M (apoM) is a protein crucial for forming high-density lipoprotein (HDL), which helps remove cholesterol from arteries. ApoM also carries sphingosine-1-phosphate (S1P), contributing to HDL
Area of Science:
- Lipid metabolism and cardiovascular research
- Biochemistry and molecular biology
- Atherosclerosis and lipoprotein research
Background:
- Apolipoprotein M (apoM) is a 23 kDa protein belonging to the lipocalin superfamily.
- The human apoM gene is located on chromosome 6 within the major histocompatibility complex (MHC) class III locus.
- ApoM is primarily expressed in hepatocytes and kidney tubular epithelium.
Purpose of the Study:
- To investigate the role of apolipoprotein M (apoM) in high-density lipoprotein (HDL) metabolism and function.
- To explore the association of apoM with antiatherogenic properties of HDL.
- To elucidate the function of apoM as a carrier of sphingosine-1-phosphate (S1P).
Main Methods:
- Characterization of apoM structure and gene location.
- Analysis of apoM expression in human tissues.
- Investigation of apoM's presence in different lipoprotein classes in plasma.
- Assessment of apoM's role in HDL formation, particularly pre-beta HDL1.
- Evaluation of apoM's function as an S1P carrier in vivo.
Main Results:
- ApoM is critical for the formation of HDL, especially pre-beta HDL1.
- ApoM is mainly found on HDL particles in human plasma but can associate with triglyceride-rich lipoproteins.
- ApoM acts as a natural carrier of sphingosine-1-phosphate (S1P) in vivo.
- These findings suggest apoM contributes to HDL's antiatherogenic, endothelial protective, and anti-inflammatory effects.
Conclusions:
- Apolipoprotein M plays a vital role in HDL biogenesis and function.
- ApoM's ability to carry S1P links it to HDL's diverse protective mechanisms against atherosclerosis.
- Further research into apoM may reveal new therapeutic targets for cardiovascular diseases.
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