Spandidos Publications Logo
  • About
    • About Spandidos
    • Aims and Scopes
    • Abstracting and Indexing
    • Editorial Policies
    • Reprints and Permissions
    • Job Opportunities
    • Terms and Conditions
    • Contact
  • Journals
    • All Journals
    • Oncology Letters
      • Oncology Letters
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Oncology
      • International Journal of Oncology
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Molecular and Clinical Oncology
      • Molecular and Clinical Oncology
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Experimental and Therapeutic Medicine
      • Experimental and Therapeutic Medicine
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Molecular Medicine
      • International Journal of Molecular Medicine
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Biomedical Reports
      • Biomedical Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Oncology Reports
      • Oncology Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Molecular Medicine Reports
      • Molecular Medicine Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • World Academy of Sciences Journal
      • World Academy of Sciences Journal
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Functional Nutrition
      • International Journal of Functional Nutrition
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Epigenetics
      • International Journal of Epigenetics
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Medicine International
      • Medicine International
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
  • Articles
  • Information
    • Information for Authors
    • Information for Reviewers
    • Information for Librarians
    • Information for Advertisers
    • Conferences
  • Language Editing
Spandidos Publications Logo
  • About
    • About Spandidos
    • Aims and Scopes
    • Abstracting and Indexing
    • Editorial Policies
    • Reprints and Permissions
    • Job Opportunities
    • Terms and Conditions
    • Contact
  • Journals
    • All Journals
    • Biomedical Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Experimental and Therapeutic Medicine
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Epigenetics
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Functional Nutrition
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Molecular Medicine
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • International Journal of Oncology
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Medicine International
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Molecular and Clinical Oncology
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Molecular Medicine Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Oncology Letters
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • Oncology Reports
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
    • World Academy of Sciences Journal
      • Information for Authors
      • Editorial Policies
      • Editorial Board
      • Aims and Scope
      • Abstracting and Indexing
      • Bibliographic Information
      • Archive
  • Articles
  • Information
    • For Authors
    • For Reviewers
    • For Librarians
    • For Advertisers
    • Conferences
  • Language Editing
Login Register Submit
  • This site uses cookies
  • You can change your cookie settings at any time by following the instructions in our Cookie Policy. To find out more, you may read our Privacy Policy.

    I agree
Search articles by DOI, keyword, author or affiliation
Search
Advanced Search
presentation
Molecular Medicine Reports
Join Editorial Board Propose a Special Issue
Print ISSN: 1791-2997 Online ISSN: 1791-3004
Journal Cover
February-2019 Volume 19 Issue 2

Full Size Image

Sign up for eToc alerts
Recommend to Library

Journals

International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

Biomedical Reports

Biomedical Reports

Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

World Academy of Sciences Journal

World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

International Journal of Functional Nutrition

International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

International Journal of Epigenetics

International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

Medicine International

Medicine International

An International Open Access Journal Devoted to General Medicine.

Journal Cover
February-2019 Volume 19 Issue 2

Full Size Image

Sign up for eToc alerts
Recommend to Library

  • Article
  • Citations
    • Cite This Article
    • Download Citation
    • Create Citation Alert
    • Remove Citation Alert
    • Cited By
  • Similar Articles
    • Related Articles (in Spandidos Publications)
    • Similar Articles (Google Scholar)
    • Similar Articles (PubMed)
  • Download PDF
  • Download XML
  • View XML
Article

Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways

  • Authors:
    • Min Wang
    • Guang‑Hua Luo
    • Hong Liu
    • You‑Pu Zhang
    • Bin Wang
    • Dong‑Mei Di
    • Xiang‑Hong Zhan
    • Yang Yu
    • Shuang Yao
    • Xiao‑Ying Zhang
    • Ning Xu
  • View Affiliations / Copyright

    Affiliations: Department of Cardiothoracic Surgery, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, P.R. China, Department of Comprehensive Laboratory, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu 213003, P.R. China, Section of Clinical Chemistry and Pharmacology, Institute of Laboratory Medicine, Lund University, SE‑22185 Lund, Sweden
  • Pages: 1272-1283
    |
    Published online on: December 12, 2018
       https://doi.org/10.3892/mmr.2018.9747
  • Expand metrics +
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Metrics: Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )
Cited By (CrossRef): 0 citations Loading Articles...

This article is mentioned in:



Abstract

Apolipoprotein M (ApoM) is a type of apolipoprotein. It is well known that high‑density lipoprotein (HDL) decreases inflammatory responses via the apoM‑sphingosine‑1‑phosphate (S1P) pathway. The present study further investigated the importance of ApoM in the inhibitory effects of HDL on inflammation. Mice with an apoM gene deficiency (apoM‑/‑) were employed to investigate the effects of ApoM on the expression of interleukin‑1β (IL‑1β), monocyte chemotactic protein‑1 (MCP‑1), S1P receptor‑1 (S1PR1) and 3β‑hydroxysterol Δ‑24‑reductase (DHCR24), as compared with in wild‑type mice (apoM+/+). Furthermore, cell culture experiments were performed using a permanent human hybrid endothelial cell line (EA.hy926). Cells were cultured in the presence of recombinant human apoM (rec‑apoM) or were induced to overexpress apoM (apoMTg); subsequently, cells were treated with tumor necrosis factor‑α (TNF‑α), in order to investigate the effects of ApoM on IL‑1β and MCP‑1. The results demonstrated that the mRNA expression levels of IL‑1β and MCP‑1 were significantly higher in the liver following administration of lipopolysaccharide in apoM‑/‑ mice compared with in apoM+/+ mice. In cell culture experiments, when cells were pre‑cultured with rec‑apoM or were engineered to overexpress apoM (apoMTg), they exhibited decreased expression levels of IL‑1β and MCP‑1 following TNF‑α treatment compared with in normal apoM‑expressing cells (apoMTgN). Furthermore, the mRNA expression levels of IL‑1β and MCP‑1 were significantly elevated following addition of the S1PR1 inhibitor W146, but not by the scavenger receptor class B type I inhibitor, block lipid transport‑1 (BLT‑1), in apoMTg cells prior to TNF‑α treatment. Conversely, there were no differences in these inflammatory biomarkers under the same conditions in apoMTgN cells. The mRNA expression levels of DHCR24 were significantly reduced by the addition of BLT‑1 prior to TNF‑α treatment in apoMTg cells; however, there was no difference in the expression of this inflammatory biomarker in apoMTgN cells. In conclusion, ApoM displayed inhibitory effects against the inflammatory response in vivo and in vitro; these effects may be induced via the S1PR1 and DHCR24 pathways.
View Figures

Figure 1

Figure 2

Figure 3

Figure 4

Figure 5

View References

1 

Tall AR: An overview of reverse cholesterol transport. Eur Heart J. 19 Suppl A:A31–A35. 1998.PubMed/NCBI

2 

Feig JE, Shamir R and Fisher EA: Atheroprotective effects of HDL: Beyond reverse cholesterol transport. Curr Drug Targets. 9:196–203. 2008. View Article : Google Scholar : PubMed/NCBI

3 

Xu N and Dahlbäck B: A novel human apolipoprotein (apoM). J Biol Chem. 274:31286–31290. 1999. View Article : Google Scholar : PubMed/NCBI

4 

Huang XS, Zhao SP, Hu M and Luo YP: Apolipoprotein M likely extends its anti-atherogenesis via anti-inflammation. Med Hypotheses. 69:136–140. 2007. View Article : Google Scholar : PubMed/NCBI

5 

Arkensteijn BW, Berbée JF, Rensen PC, Nielsen LB and Christoffersen C: The apolipoprotein m-sphingosine-1-phosphate axis: Biological relevance in lipoprotein metabolism, lipid disorders and atherosclerosis. Int J Mol Sci. 14:4419–4431. 2013. View Article : Google Scholar : PubMed/NCBI

6 

Ishii I, Fukushima N, Ye X and Chun J: Lysophospholipid receptors: Signaling and biology. Annu Rev Biochem. 73:321–354. 2004. View Article : Google Scholar : PubMed/NCBI

7 

Potì F, Simoni M and Nofer JR: Atheroprotective role of high-density lipoprotein (HDL)-associated sphingosine-1-phosphate (S1P). Cardiovasc Res. 103:395–404. 2014. View Article : Google Scholar : PubMed/NCBI

8 

De Palma C, Meacci E, Perrotta C, Bruni P and Clementi E: Endothelial nitric oxide synthase activation by tumor necrosis factor alpha through neutral sphingomyelinase 2, sphingosine kinase 1, and sphingosine 1 phosphate receptors: A novel pathway relevant to the pathophysiology of endothelium. Arterioscler Thromb Vasc Biol. 26:99–105. 2006. View Article : Google Scholar : PubMed/NCBI

9 

Christoffersen C, Obinata H, Kumaraswamy SB, Galvani S, Ahnström J, Sevvana M, Egerer-Sieber C, Muller YA, Hla T, Nielsen LB and Dahlbäck B: Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M. Proc Natl Acad Sci USA. 108:9613–9618. 2011. View Article : Google Scholar : PubMed/NCBI

10 

Zerenturk EJ, Sharpe LJ, Ikonen E and Brown AJ: Desmosterol and DHCR24: Unexpected new directions for a terminal step in cholesterol synthesis. Prog Lipid Res. 52:666–680. 2013. View Article : Google Scholar : PubMed/NCBI

11 

McGrath KC, Li XH, Puranik R, Liong EC, Tan JT, Dy VM, DiBartolo BA, Barter PJ, Rye KA and Heather AK: Role of 3beta-hydroxysteroid-delta 24 reductase in mediating antiinflammatory effects of high-density lipoproteins in endothelial cells. Arterioscler Thromb Vasc Biol. 29:877–882. 2009. View Article : Google Scholar : PubMed/NCBI

12 

Wei J, Shi Y, Zhang X, Feng Y, Luo G, Zhang J, Mu Q, Tang Y, Yu Y, Pan L, et al: Estrogen upregulates hepatic apolipoprotein M expression via the estrogen receptor. Biochim Biophys Acta. 1811:1146–1151. 2011. View Article : Google Scholar : PubMed/NCBI

13 

Benvenuti S, Luciani P, Vannelli GB, Gelmini S, Franceschi E, Serio M and Peri A: Estrogen and selective estrogen receptor modulators exert neuroprotective effects and stimulate the expression of selective Alzheimer's disease indicator-1, a recently discovered antiapoptotic gene, in human neuroblast long-term cell cultures. J Clin Endocrinol Metab. 90:1775–1782. 2005. View Article : Google Scholar : PubMed/NCBI

14 

Nofer JR and van Eck M: HDL scavenger receptor class B type I and platelet function. Curr Opin Lipidol. 22:277–282. 2011. View Article : Google Scholar : PubMed/NCBI

15 

Pei Y, Chen X, Aboutouk D, Fuller MT, Dadoo O, Yu P, White EJ, Igdoura SA and Trigatti BL: SR-BI in bone marrow derived cells protects mice from diet induced coronary artery atherosclerosis and myocardial infarction. PLoS One. 8:e724922013. View Article : Google Scholar : PubMed/NCBI

16 

Tao H, Yancey PG, Babaev VR, Blakemore JL, Zhang Y, Ding L, Fazio S and Linton MF: Macrophage SR-BI mediates efferocytosis via Src/PI3K/Rac1 signaling and reduces atherosclerotic lesion necrosis. J Lipid Res. 56:1449–1460. 2015. View Article : Google Scholar : PubMed/NCBI

17 

Linton MF, Tao H, Linton EF and Yancey PG: SR-BI: A multifunctional receptor in cholesterol homeostasis and atherosclerosis. Trends Endocrinol Metab. 28:461–472. 2017. View Article : Google Scholar : PubMed/NCBI

18 

Pan B, Ma Y, Ren H, He Y, Wang Y, Lv X, Liu D, Ji L, Yu B, Wang Y, et al: Diabetic HDL is dysfunctional in stimulating endothelial cell migration and proliferation due to down regulation of SR-BI expression. PLoS One. 7:e485302012. View Article : Google Scholar : PubMed/NCBI

19 

van Wijk DF, Stroes ES and Dallinga-Thie GM: Novel insights into anti-inflammatory actions of HDL. Atherosclerosis. 212:388–389. 2010. View Article : Google Scholar : PubMed/NCBI

20 

Zhang QH, Zu XY, Cao RX, Liu JH, Mo ZC, Zeng Y, Li YB, Xiong SL, Liu X, Liao DF and Yi GH: An involvement of SR-B1 mediated PI3K-Akt-eNOS signaling in HDL-induced cyclooxygenase 2 expression and prostacyclin production in endothelial cells. Biochem Biophys Res Commun. 420:17–23. 2012. View Article : Google Scholar : PubMed/NCBI

21 

Yuhanna IS, Zhu Y, Cox BE, Hahner LD, Osborne-Lawrence S, Lu P, Marcel YL, Anderson RG, Mendelsohn ME, Hobbs HH and Shaul PW: High-density lipoprotein binding to scavenger receptor-BI activates endothelial nitric oxide synthase. Nat Med. 7:853–857. 2001. View Article : Google Scholar : PubMed/NCBI

22 

Lee MH, Appleton KM, El-Shewy HM, Sorci-Thomas MG, Thomas MJ, Lopes-Virella MF, Luttrell LM, Hammad SM and Klein RL: S1P in HDL promotes interaction between SR-BI and S1PR1 and activates S1PR1-mediated biological functions: Calcium flux and S1PR1 internalization. J Lipid Res. 58:325–338. 2017. View Article : Google Scholar : PubMed/NCBI

23 

Wang Z, Luo G, Feng Y, Zheng L, Liu H, Liang Y, Liu Z, Shao P, Berggren-Söderlund M, Zhang X and Xu N: Decreased splenic CD4(+) T-lymphocytes in apolipoprotein M gene deficient mice. Biomed Res Int. 2015:2935122015. View Article : Google Scholar : PubMed/NCBI

24 

Livak KJ and Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 25:402–408. 2001. View Article : Google Scholar : PubMed/NCBI

25 

Christoffersen C, Jauhiainen M, Moser M, Porse B, Ehnholm C, Boesl M, Dahlbäck B and Nielsen LB: Effect of apolipoprotein M on high density lipoprotein metabolism and atherosclerosis in low density lipoprotein receptor knock-out mice. J Biol Chem. 283:1839–1847. 2008. View Article : Google Scholar : PubMed/NCBI

26 

Zheng L, Luo G, Zhang J, Mu Q, Shi Y, Berggren-Söderlund M, Nilsson-Ehle P, Zhang X and Xu N: Decreased activities of apolipoprotein m promoter are associated with the susceptibility to coronary artery diseases. Int J Med Sci. 11:365–372. 2014. View Article : Google Scholar : PubMed/NCBI

27 

Thacker SG, Zarzour A, Chen Y, Alcicek MS, Freeman LA, Sviridov DO, Demosky SJ Jr and Remaley AT: High-density lipoprotein reduces inflammation from cholesterol crystals by inhibiting inflammasome activation. Immunology. 149:306–319. 2016. View Article : Google Scholar : PubMed/NCBI

28 

Wolfrum C, Poy MN and Stoffel M: Apolipoprotein M is required for prebeta-HDL formation and cholesterol efflux to HDL and protects against atherosclerosis. Nat Med. 11:418–422. 2005. View Article : Google Scholar : PubMed/NCBI

29 

Mulya A, Seo J, Brown AL, Gebre AK, Boudyguina E, Shelness GS and Parks JS: Apolipoprotein M expression increases the size of nascent pre beta HDL formed by ATP binding cassette transporter A1. J Lipid Res. 51:514–524. 2010. View Article : Google Scholar : PubMed/NCBI

30 

Ren K, Tang ZL, Jiang Y, Tan YM and Yi GH: Apolipoprotein M. Clin Chim Acta. 446:21–29. 2015. View Article : Google Scholar : PubMed/NCBI

31 

Kumaraswamy SB, Linder A, Åkesson P and Dahlbäck B: Decreased plasma concentrations of apolipoprotein M in sepsis and systemic inflammatory response syndromes. Crit Care. 16:R602012. View Article : Google Scholar : PubMed/NCBI

32 

Christoffersen C and Nielsen LB: Apolipoprotein M-a new biomarker in sepsis. Crit Care. 16:1262012. View Article : Google Scholar : PubMed/NCBI

33 

Feingold KR, Shigenaga JK, Chui LG, Moser A, Khovidhunkit W and Grunfeld C: Infection and inflammation decrease apolipoprotein M expression. Atherosclerosis. 199:19–26. 2008. View Article : Google Scholar : PubMed/NCBI

34 

Gao JJ, Hu YW, Wang YC, Sha YH, Ma X, Li SF, Zhao JY, Lu JB, Huang C, Zhao JJ, et al: ApoM Suppresses TNF-α-Induced Expression of ICAM-1 and VCAM-1 Through Inhibiting the Activity of NF-κB. DNA Cell Biol. 34:550–556. 2015. View Article : Google Scholar : PubMed/NCBI

35 

Leyva-López N, Gutierrez-Grijalva EP, Ambriz-Perez DL and Heredia JB: Flavonoids as cytokine modulators: A possible therapy for inflammation-related diseases. Int J Mol Sci. 17(pii): E9212016. View Article : Google Scholar : PubMed/NCBI

36 

Khan R, Spagnoli V, Tardif JC and L'Allier PL: Novel anti-inflammatory therapies for the treatment of atherosclerosis. Atherosclerosis. 240:497–509. 2015. View Article : Google Scholar : PubMed/NCBI

37 

Galea J, Armstrong J, Gadsdon P, Holden H, Francis SE and Holt CM: Interleukin-1 beta in coronary arteries of patients with ischemic heart disease. Arterioscler Thromb Vasc Biol. 16:1000–1006. 1996. View Article : Google Scholar : PubMed/NCBI

38 

Freitas Lima LC, Braga VA, do Socorro de França Silva M, Cruz JC, Sousa Santos SH, de Oliveira Monteiro MM and Balarini CM: Adipokines, diabetes and atherosclerosis: An inflammatory association. Front Physiol. 6:3042015. View Article : Google Scholar : PubMed/NCBI

39 

Stephen SL, Freestone K, Dunn S, Twigg MW, Homer-Vanniasinkam S, Walker JH, Wheatcroft SB and Ponnambalam S: Scavenger receptors and their potential as therapeutic targets in the treatment of cardiovascular disease. Int J Hypertens. 2010:6469292010. View Article : Google Scholar : PubMed/NCBI

40 

Nádró B, Juhász L, Szentpéteri A, Páll D, Paragh G and Harangi M: The role of apolipoprotein M and sphingosine 1-phosphate axis in the prevention of atherosclerosis. Orv Hetil. 159:168–175. 2018.(In Hungarian). View Article : Google Scholar : PubMed/NCBI

41 

Guo S, Yu Y, Zhang N, Cui Y, Zhai L, Li H, Zhang Y, Li F, Kan Y and Qin S: Higher level of plasma bioactive molecule sphingosine 1-phosphate in women is associated with estrogen. Biochim Biophys Acta. 1841:836–846. 2014. View Article : Google Scholar : PubMed/NCBI

42 

Sutter I, Park R, Othman A, Rohrer L, Hornemann T, Stoffel M, Devuyst O and von Eckardstein A: Apolipoprotein M modulates erythrocyte efflux and tubular reabsorption of sphingosine-1-phosphate. J Lipid Res. 55:1730–1737. 2014. View Article : Google Scholar : PubMed/NCBI

43 

Igarashi J, Erwin PA, Dantas AP, Chen H and Michel T: VEGF induces S1P1 receptors in endothelial cells: Implications for cross-talk between sphingolipid and growth factor receptors. Proc Natl Acad Sci USA. 100:10664–10669. 2003. View Article : Google Scholar : PubMed/NCBI

44 

Nofer JR, van der Giet M, Tölle M, Wolinska I, von Wnuck Lipinski K, Baba HA, Tietge UJ, Gödecke A, Ishii I, Kleuser B, et al: HDL induces NO-dependent vasorelaxation via the lysophospholipid receptor S1P3. J Clin Invest. 113:569–581. 2004. View Article : Google Scholar : PubMed/NCBI

45 

Wang X and Wang F: Vascular protection by high-density lipoprotein-associated sphingosine-1-phosphate. J Geriatr Cardiol. 14:696–702. 2017.PubMed/NCBI

46 

Brinck JW, Thomas A, Brulhart-Meynet MC, Lauer E, Frej C, Dahlbäck B, Stenvinkel P, James RW and Frias MA: High-density lipoprotein from end-stage renal disease patients exhibits superior cardioprotection and increase in sphingosine-1-phosphate. Eur J Clin Invest. 48:e128662018. View Article : Google Scholar

47 

Ruiz M, Okada H and Dahlbäck B: HDL-associated ApoM is anti-apoptotic by delivering sphingosine 1-phosphate to S1P1 & S1P3 receptors on vascular endothelium. Lipids Health Dis. 16:362017. View Article : Google Scholar : PubMed/NCBI

48 

Feuerborn R, Becker S, Potì F, Nagel P, Brodde M, Schmidt H, Christoffersen C, Ceglarek U, Burkhardt R and Nofer JR: High density lipoprotein (HDL)-associated sphingosine 1-phosphate (S1P) inhibits macrophage apoptosis by stimulating STAT3 activity and survivin expression. Atherosclerosis. 257:29–37. 2017. View Article : Google Scholar : PubMed/NCBI

49 

Bosteen MH, Madsen Svarrer EM, Bisgaard LS, Martinussen T, Madsen M, Nielsen LB, Christoffersen C and Pedersen TX: Effects of apolipoprotein M in uremic atherosclerosis. Atherosclerosis. 265:93–101. 2017. View Article : Google Scholar : PubMed/NCBI

50 

Frej C, Mendez AJ, Ruiz M, Castillo M, Hughes TA, Dahlbäck B and Goldberg RB: A shift in ApoM/S1P between HDL-particles in women with type 1 diabetes mellitus is associated with impaired anti-inflammatory effects of the ApoM/S1P complex. Arterioscler Thromb Vasc Biol. 37:1194–1205. 2017. View Article : Google Scholar : PubMed/NCBI

51 

Memon AA, Sundquist J, Zöller B, Wang X, Dahlbäck B, Svensson PJ and Sundquist K: Apolipoprotein M and the risk of unprovoked recurrent venous thromboembolism. Thromb Res. 133:322–326. 2014. View Article : Google Scholar : PubMed/NCBI

52 

Ahmad A, Sundquist K, Zöller B, Dahlbäck B, Elf J, Svensson PJ, Strandberg K, Sundquist J and Memon AA: Evaluation of expression level of apolipoprotein M as a diagnostic marker for primary venous thromboembolism. Clin Appl Thromb Hemost. 24:416–422. 2018. View Article : Google Scholar : PubMed/NCBI

53 

Hajny S and Christoffersen C: A novel perspective on the ApoM-S1P axis, highlighting the metabolism of ApoM and its role in liver fibrosis and neuroinflammation. Int J Mol Sci. 18(pii): E16362017. View Article : Google Scholar : PubMed/NCBI

54 

Christensen PM, Liu CH, Swendeman SL, Obinata H, Qvortrup K, Nielsen LB, Hla T, Di Lorenzo A and Christoffersen C: Impaired endothelial barrier function in apolipoprotein M-deficient mice is dependent on sphingosine-1-phosphate receptor 1. FASEB J. 30:2351–2359. 2016. View Article : Google Scholar : PubMed/NCBI

55 

Ruiz M, Frej C, Holmér A, Guo LJ, Tran S and Dahlbäck B: High-density lipoprotein-associated apolipoprotein M limits endothelial inflammation by delivering sphingosine-1-phosphate to the sphingosine-1-phosphate receptor 1. Arterioscler Thromb Vasc Biol. 37:118–129. 2017. View Article : Google Scholar : PubMed/NCBI

56 

Zhu B, Luo GH, Feng YH, Yu MM, Zhang J, Wei J, Yang C, Xu N and Zhang XY: Apolipoprotein M protects against lipopolysaccharide-induced acute lung injury via sphingosine-1-phosphate signaling. Inflammation. 41:643–653. 2018. View Article : Google Scholar : PubMed/NCBI

57 

Patel S, Di Bartolo BA, Nakhla S, Heather AK, Mitchell TW, Jessup W, Celermajer DS, Barter PJ and Rye KA: Anti-inflammatory effects of apolipoprotein A-I in the rabbit. Atherosclerosis. 212:392–397. 2010. View Article : Google Scholar : PubMed/NCBI

58 

Wu BJ, Chen K, Shrestha S, Ong KL, Barter PJ and Rye KA: High-density lipoproteins inhibit vascular endothelial inflammation by increasing 3β-hydroxysteroid-Δ24 reductase expression and inducing heme oxygenase-1. Circ Res. 112:278–288. 2013. View Article : Google Scholar : PubMed/NCBI

59 

Connelly MA, de la Llera-Moya M, Monzo P, Yancey PG, Drazul D, Stoudt G, Fournier N, Klein SM, Rothblat GH and Williams DL: Analysis of chimeric receptors shows that multiple distinct functional activities of scavenger receptor, class B, type I (SR-BI), are localized to the extracellular receptor domain. Biochemistry. 40:5249–5259. 2001. View Article : Google Scholar : PubMed/NCBI

60 

Banerjee S, de Freitas A, Friggeri A, Zmijewski JW, Liu G and Abraham E: Intracellular HMGB1 negatively regulates efferocytosis. J Immunol. 187:4686–4694. 2011. View Article : Google Scholar : PubMed/NCBI

61 

Al-Jarallah A, Chen X, González L and Trigatti BL: High density lipoprotein stimulated migration of macrophages depends on the scavenger receptor class B type I, PDZK1 and Akt1 and is blocked by sphingosine 1 phosphate receptor antagonists. PLoS One. 9:e1064872014. View Article : Google Scholar : PubMed/NCBI

62 

Sahoo D, Peng Y, Smith JR, Darlington YF and Connelly MA: Scavenger receptor class B, type I (SR-BI) homo-dimerizes via its C-terminal region: Fluorescence resonance energy transfer analysis. Biochim Biophys Acta. 1771:818–829. 2007. View Article : Google Scholar : PubMed/NCBI

Related Articles

  • Abstract
  • View
  • Download
  • Twitter
Copy and paste a formatted citation
Spandidos Publications style
Wang M, Luo GH, Liu H, Zhang YP, Wang B, Di DM, Zhan XH, Yu Y, Yao S, Zhang XY, Zhang XY, et al: Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways. Mol Med Rep 19: 1272-1283, 2019.
APA
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D. ... Xu, N. (2019). Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways. Molecular Medicine Reports, 19, 1272-1283. https://doi.org/10.3892/mmr.2018.9747
MLA
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D., Zhan, X., Yu, Y., Yao, S., Zhang, X., Xu, N."Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways". Molecular Medicine Reports 19.2 (2019): 1272-1283.
Chicago
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D., Zhan, X., Yu, Y., Yao, S., Zhang, X., Xu, N."Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways". Molecular Medicine Reports 19, no. 2 (2019): 1272-1283. https://doi.org/10.3892/mmr.2018.9747
Copy and paste a formatted citation
x
Spandidos Publications style
Wang M, Luo GH, Liu H, Zhang YP, Wang B, Di DM, Zhan XH, Yu Y, Yao S, Zhang XY, Zhang XY, et al: Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways. Mol Med Rep 19: 1272-1283, 2019.
APA
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D. ... Xu, N. (2019). Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways. Molecular Medicine Reports, 19, 1272-1283. https://doi.org/10.3892/mmr.2018.9747
MLA
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D., Zhan, X., Yu, Y., Yao, S., Zhang, X., Xu, N."Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways". Molecular Medicine Reports 19.2 (2019): 1272-1283.
Chicago
Wang, M., Luo, G., Liu, H., Zhang, Y., Wang, B., Di, D., Zhan, X., Yu, Y., Yao, S., Zhang, X., Xu, N."Apolipoprotein M induces inhibition of inflammatory responses via the S1PR1 and DHCR24 pathways". Molecular Medicine Reports 19, no. 2 (2019): 1272-1283. https://doi.org/10.3892/mmr.2018.9747
Follow us
  • Twitter
  • LinkedIn
  • Facebook
About
  • Spandidos Publications
  • Careers
  • Cookie Policy
  • Privacy Policy
How can we help?
  • Help
  • Live Chat
  • Contact
  • Email to our Support Team