Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascade.
Animals
Atherosclerosis
/ metabolism
CD47 Antigen
/ metabolism
Cell Lineage
Cell Proliferation
Cloning, Molecular
Complement Activation
Complement C3
/ genetics
Female
Humans
Inflammation
Macrophages
/ metabolism
Male
Mice, Knockout, ApoE
Myocytes, Smooth Muscle
/ cytology
Phagocytosis
/ physiology
Plaque, Atherosclerotic
/ metabolism
Sequence Analysis, RNA
Up-Regulation
CD47
atherosclerosis
clonality
efferocytosis
smooth muscle cells
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
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
15818-15826Subventions
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.
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