Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Standard

Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M. / Christoffersen, Christina; Obinata, Hideru; Kumaraswamy, Sunil B; Galvani, Sylvain; Ahnström, Josefin; Sevvana, Madhumati; Egerer-Sieber, Claudia; Muller, Yves A; Hla, Timothy; Nielsen, Lars Bo; Dahlbäck, Björn.

I: Proceedings of the National Academy of Sciences USA (PNAS), Bind 108, Nr. 23, 2011, s. 9613-8.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Christoffersen, C, Obinata, H, Kumaraswamy, SB, Galvani, S, Ahnström, J, Sevvana, M, Egerer-Sieber, C, Muller, YA, Hla, T, Nielsen, LB & Dahlbäck, B 2011, 'Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M', Proceedings of the National Academy of Sciences USA (PNAS), bind 108, nr. 23, s. 9613-8. https://doi.org/10.1073/pnas.1103187108

APA

Christoffersen, C., Obinata, H., Kumaraswamy, S. B., Galvani, S., Ahnström, J., Sevvana, M., Egerer-Sieber, C., Muller, Y. A., Hla, T., Nielsen, L. B., & Dahlbäck, B. (2011). Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M. Proceedings of the National Academy of Sciences USA (PNAS), 108(23), 9613-8. https://doi.org/10.1073/pnas.1103187108

Vancouver

Christoffersen C, Obinata H, Kumaraswamy SB, Galvani S, Ahnström J, Sevvana M o.a. Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M. Proceedings of the National Academy of Sciences USA (PNAS). 2011;108(23):9613-8. https://doi.org/10.1073/pnas.1103187108

Author

Christoffersen, Christina ; Obinata, Hideru ; Kumaraswamy, Sunil B ; Galvani, Sylvain ; Ahnström, Josefin ; Sevvana, Madhumati ; Egerer-Sieber, Claudia ; Muller, Yves A ; Hla, Timothy ; Nielsen, Lars Bo ; Dahlbäck, Björn. / Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M. I: Proceedings of the National Academy of Sciences USA (PNAS). 2011 ; Bind 108, Nr. 23. s. 9613-8.

Bibtex

@article{1527e1ed85944fee9014ce1699b1ee49,
title = "Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M",
abstract = "Protection of the endothelium is provided by circulating sphingosine-1-phosphate (S1P), which maintains vascular integrity. We show that HDL-associated S1P is bound specifically to both human and murine apolipoprotein M (apoM). Thus, isolated human ApoM(+) HDL contained S1P, whereas ApoM(-) HDL did not. Moreover, HDL in Apom(-/-) mice contains no S1P, whereas HDL in transgenic mice overexpressing human apoM has an increased S1P content. The 1.7-{\AA} structure of the S1P-human apoM complex reveals that S1P interacts specifically with an amphiphilic pocket in the lipocalin fold of apoM. Human ApoM(+) HDL induced S1P(1) receptor internalization, downstream MAPK and Akt activation, endothelial cell migration, and formation of endothelial adherens junctions, whereas apoM(-) HDL did not. Importantly, lack of S1P in the HDL fraction of Apom(-/-) mice decreased basal endothelial barrier function in lung tissue. Our results demonstrate that apoM, by delivering S1P to the S1P(1) receptor on endothelial cells, is a vasculoprotective constituent of HDL.",
keywords = "Animals, Apolipoproteins, Blotting, Western, Cells, Cultured, Crystallography, X-Ray, Endocytosis, Endothelial Cells, Endothelium, Vascular, Enzyme Activation, HEK293 Cells, Humans, Lipocalins, Lipoproteins, HDL, Lysophospholipids, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Mitogen-Activated Protein Kinases, Models, Molecular, Protein Binding, Protein Conformation, Protein Structure, Tertiary, Proto-Oncogene Proteins c-akt, Receptors, Lysosphingolipid, Sphingosine",
author = "Christina Christoffersen and Hideru Obinata and Kumaraswamy, {Sunil B} and Sylvain Galvani and Josefin Ahnstr{\"o}m and Madhumati Sevvana and Claudia Egerer-Sieber and Muller, {Yves A} and Timothy Hla and Nielsen, {Lars Bo} and Bj{\"o}rn Dahlb{\"a}ck",
year = "2011",
doi = "10.1073/pnas.1103187108",
language = "English",
volume = "108",
pages = "9613--8",
journal = "Proceedings of the National Academy of Sciences of the United States of America",
issn = "0027-8424",
publisher = "The National Academy of Sciences of the United States of America",
number = "23",

}

RIS

TY - JOUR

T1 - Endothelium-protective sphingosine-1-phosphate provided by HDL-associated apolipoprotein M

AU - Christoffersen, Christina

AU - Obinata, Hideru

AU - Kumaraswamy, Sunil B

AU - Galvani, Sylvain

AU - Ahnström, Josefin

AU - Sevvana, Madhumati

AU - Egerer-Sieber, Claudia

AU - Muller, Yves A

AU - Hla, Timothy

AU - Nielsen, Lars Bo

AU - Dahlbäck, Björn

PY - 2011

Y1 - 2011

N2 - Protection of the endothelium is provided by circulating sphingosine-1-phosphate (S1P), which maintains vascular integrity. We show that HDL-associated S1P is bound specifically to both human and murine apolipoprotein M (apoM). Thus, isolated human ApoM(+) HDL contained S1P, whereas ApoM(-) HDL did not. Moreover, HDL in Apom(-/-) mice contains no S1P, whereas HDL in transgenic mice overexpressing human apoM has an increased S1P content. The 1.7-Å structure of the S1P-human apoM complex reveals that S1P interacts specifically with an amphiphilic pocket in the lipocalin fold of apoM. Human ApoM(+) HDL induced S1P(1) receptor internalization, downstream MAPK and Akt activation, endothelial cell migration, and formation of endothelial adherens junctions, whereas apoM(-) HDL did not. Importantly, lack of S1P in the HDL fraction of Apom(-/-) mice decreased basal endothelial barrier function in lung tissue. Our results demonstrate that apoM, by delivering S1P to the S1P(1) receptor on endothelial cells, is a vasculoprotective constituent of HDL.

AB - Protection of the endothelium is provided by circulating sphingosine-1-phosphate (S1P), which maintains vascular integrity. We show that HDL-associated S1P is bound specifically to both human and murine apolipoprotein M (apoM). Thus, isolated human ApoM(+) HDL contained S1P, whereas ApoM(-) HDL did not. Moreover, HDL in Apom(-/-) mice contains no S1P, whereas HDL in transgenic mice overexpressing human apoM has an increased S1P content. The 1.7-Å structure of the S1P-human apoM complex reveals that S1P interacts specifically with an amphiphilic pocket in the lipocalin fold of apoM. Human ApoM(+) HDL induced S1P(1) receptor internalization, downstream MAPK and Akt activation, endothelial cell migration, and formation of endothelial adherens junctions, whereas apoM(-) HDL did not. Importantly, lack of S1P in the HDL fraction of Apom(-/-) mice decreased basal endothelial barrier function in lung tissue. Our results demonstrate that apoM, by delivering S1P to the S1P(1) receptor on endothelial cells, is a vasculoprotective constituent of HDL.

KW - Animals

KW - Apolipoproteins

KW - Blotting, Western

KW - Cells, Cultured

KW - Crystallography, X-Ray

KW - Endocytosis

KW - Endothelial Cells

KW - Endothelium, Vascular

KW - Enzyme Activation

KW - HEK293 Cells

KW - Humans

KW - Lipocalins

KW - Lipoproteins, HDL

KW - Lysophospholipids

KW - Mice

KW - Mice, Inbred C57BL

KW - Mice, Knockout

KW - Mice, Transgenic

KW - Mitogen-Activated Protein Kinases

KW - Models, Molecular

KW - Protein Binding

KW - Protein Conformation

KW - Protein Structure, Tertiary

KW - Proto-Oncogene Proteins c-akt

KW - Receptors, Lysosphingolipid

KW - Sphingosine

U2 - 10.1073/pnas.1103187108

DO - 10.1073/pnas.1103187108

M3 - Journal article

C2 - 21606363

VL - 108

SP - 9613

EP - 9618

JO - Proceedings of the National Academy of Sciences of the United States of America

JF - Proceedings of the National Academy of Sciences of the United States of America

SN - 0027-8424

IS - 23

ER -

ID: 38431877