Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascade.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
07 07 2020
Historique:
pubmed: 17 6 2020
medline: 9 9 2020
entrez: 17 6 2020
Statut: ppublish

Résumé

Atherosclerosis is the process underlying heart attack and stroke. Despite decades of research, its pathogenesis remains unclear. Dogma suggests that atherosclerotic plaques expand primarily via the accumulation of cholesterol and inflammatory cells. However, recent evidence suggests that a substantial portion of the plaque may arise from a subset of "dedifferentiated" vascular smooth muscle cells (SMCs) which proliferate in a clonal fashion. Herein we use multicolor lineage-tracing models to confirm that the mature SMC can give rise to a hyperproliferative cell which appears to promote inflammation via elaboration of complement-dependent anaphylatoxins. Despite being extensively opsonized with prophagocytic complement fragments, we find that this cell also escapes immune surveillance by neighboring macrophages, thereby exacerbating its relative survival advantage. Mechanistic studies indicate this phenomenon results from a generalized opsonin-sensing defect acquired by macrophages during polarization. This defect coincides with the noncanonical up-regulation of so-called don't eat me molecules on inflamed phagocytes, which reduces their capacity for programmed cell removal (PrCR). Knockdown or knockout of the key antiphagocytic molecule CD47 restores the ability of macrophages to sense and clear opsonized targets in vitro, allowing for potent and targeted suppression of clonal SMC expansion in the plaque in vivo. Because integrated clinical and genomic analyses indicate that similar pathways are active in humans with cardiovascular disease, these studies suggest that the clonally expanding SMC may represent a translational target for treating atherosclerosis.

Identifiants

pubmed: 32541024
pii: 2006348117
doi: 10.1073/pnas.2006348117
pmc: PMC7354942
doi:

Substances chimiques

CD47 Antigen 0
Complement C3 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

15818-15826

Subventions

Organisme : NCI NIH HHS
ID : R35 CA220434
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL125863
Pays : United States
Organisme : NHLBI NIH HHS
ID : R35 HL144475
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL125224
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL148239
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA009109
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL123370
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR027431
Pays : United States

Déclaration de conflit d'intérêts

Competing interest statement: I.L.W. and N.J.L. are cofounders of Forty Seven, Inc., an immunooncology company. This company was recently acquired by Gilead Sciences; the purchase did not include stock in Gilead. I.L.W. and N.J.L. do not currently have any consulting agreement with Gilead Sciences.

Références

J Clin Med. 2019 Feb 16;8(2):
pubmed: 30781475
Cardiovasc Res. 2007 Nov 1;76(2):340-50
pubmed: 17673191
Immunol Rev. 2016 Nov;274(1):218-232
pubmed: 27782329
Science. 2003 Sep 19;301(5640):1720-5
pubmed: 14500982
Circ Res. 2016 Jan 22;118(2):230-40
pubmed: 26596284
J Cell Sci. 2020 Mar 6;133(5):
pubmed: 31964705
Science. 2016 Aug 19;353(6301):827-30
pubmed: 27540175
Cell. 2011 Apr 29;145(3):341-55
pubmed: 21529710
N Engl J Med. 2017 Jul 13;377(2):111-121
pubmed: 28636844
Immunol Rev. 2016 Nov;274(1):127-140
pubmed: 27782338
Nat Rev Immunol. 2009 Oct;9(10):729-40
pubmed: 19730437
N Engl J Med. 2018 Nov 01;379(18):1711-1721
pubmed: 30380386
Nat Med. 2019 Aug;25(8):1280-1289
pubmed: 31359001
Nat Commun. 2018 Nov 1;9(1):4567
pubmed: 30385745
Nat Commun. 2018 May 25;9(1):2073
pubmed: 29802249
Nat Nanotechnol. 2020 Feb;15(2):154-161
pubmed: 31988506
Circ Res. 2017 Jan 20;120(2):296-311
pubmed: 27834190
N Engl J Med. 1999 Jan 14;340(2):115-26
pubmed: 9887164
Nature. 2016 Aug 4;536(7614):86-90
pubmed: 27437576
Arterioscler Thromb Vasc Biol. 2005 Nov;25(11):2368-75
pubmed: 16141402
Nat Med. 2013 Sep;19(9):1166-72
pubmed: 23933982
N Engl J Med. 2017 Sep 21;377(12):1119-1131
pubmed: 28845751
Circ Res. 2017 Feb 17;120(4):624-626
pubmed: 28209794
Circ Res. 2016 Dec 9;119(12):1313-1323
pubmed: 27682618
J Clin Oncol. 2019 Apr 20;37(12):946-953
pubmed: 30811285
Circulation. 2017 Jan 31;135(5):476-489
pubmed: 28137963
F1000Res. 2018 Dec 21;7:
pubmed: 30613386
PLoS Genet. 2018 Nov 16;14(11):e1007755
pubmed: 30444878
Nature. 2001 Nov 1;414(6859):105-11
pubmed: 11689955
Nature. 2011 May 19;473(7347):317-25
pubmed: 21593864
Cell. 2005 Oct 21;123(2):321-34
pubmed: 16239148
Nat Methods. 2013 Feb;10(2):171-7
pubmed: 23314172
Circ Res. 2014 Sep 12;115(7):662-7
pubmed: 25070003
Nat Commun. 2017 Apr 05;8:14802
pubmed: 28378740
Proc Natl Acad Sci U S A. 1973 Jun;70(6):1753-6
pubmed: 4515934
Cardiovasc Res. 2012 Jul 15;95(2):156-64
pubmed: 22406749
JCI Insight. 2017 Oct 5;2(19):
pubmed: 28978793
J Clin Invest. 2014 Mar;124(3):1083-97
pubmed: 24531546
Nat Med. 2015 Jun;21(6):628-37
pubmed: 25985364
Thromb Haemost. 2014 Jun;111(6):1102-11
pubmed: 24500020

Auteurs

Ying Wang (Y)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.
Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305.

Vivek Nanda (V)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.
Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305.
Department of Molecular and Cellular Pathology, University of Alabama at Birmingham, Birmingham, AL 35294.

Daniel Direnzo (D)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Jianqin Ye (J)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Sophia Xiao (S)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Yoko Kojima (Y)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Kathryn L Howe (KL)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Kai-Uwe Jarr (KU)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Alyssa M Flores (AM)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Pavlos Tsantilas (P)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Noah Tsao (N)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

Abhiram Rao (A)

Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305.
Department of Bioengineering, Stanford University, Stanford, CA 94305.

Alexandra A C Newman (AAC)

Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22904.

Anne V Eberhard (AV)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305.

James R Priest (JR)

Division of Pediatric Cardiology, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305.

Arno Ruusalepp (A)

Department of Cardiac Surgery, Tartu University Hospital, Tartu, Estonia 50406.

Gerard Pasterkamp (G)

Department of Cardiology, University Medical Center Utrecht, 3584CX Utrecht, the Netherlands.
Laboratory of Clinical Chemistry, University Medical Center Utrecht, 3584CX Utrecht, the Netherlands.

Lars Maegdefessel (L)

Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Technical University Munich, 80333 Munich, Germany.
German Center for Cardiovascular Research (DZHK partner site), 10785 Munich, Germany.

Clint L Miller (CL)

Center for Public Health Genomics, Department of Public Health Sciences, University of Virginia, Charlottesville, VA 22904.
Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA 22904.
Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22904.

Lars Lind (L)

Department of Medical Sciences, Uppsala University, SE-751 05 Uppsala, Sweden.

Simon Koplev (S)

Department of Genetics and Genomic Sciences, Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574.

Johan L M Björkegren (JLM)

Department of Genetics and Genomic Sciences, Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029-6574.

Gary K Owens (GK)

Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22904.

Erik Ingelsson (E)

Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305.
Department of Medical Sciences, Uppsala University, SE-751 05 Uppsala, Sweden.
Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305.

Irving L Weissman (IL)

Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305 irv@stanford.edu nleeper@stanford.edu.

Nicholas J Leeper (NJ)

Division of Vascular Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, CA 94305; irv@stanford.edu nleeper@stanford.edu.
Stanford Cardiovascular Institute, Stanford University, Stanford, CA 94305.

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