RIP1 kinase mediates angiogenesis by modulating macrophages in experimental neovascularization.
Animals
Biomarkers
Caspases
/ metabolism
Cells, Cultured
Collagen
Corneal Injuries
/ chemically induced
Corneal Neovascularization
/ enzymology
Drug Combinations
Enzyme Activation
Fibroblast Growth Factor 2
/ pharmacology
GTPase-Activating Proteins
/ antagonists & inhibitors
Human Umbilical Vein Endothelial Cells
Humans
Imidazoles
/ pharmacology
In Situ Nick-End Labeling
Indoles
/ pharmacology
Laminin
Lasers
/ adverse effects
Macrophages
/ classification
Mice
Mice, Inbred C57BL
Models, Animal
Neovascularization, Pathologic
/ enzymology
Oligopeptides
/ pharmacology
Proteoglycans
RNA, Messenger
/ biosynthesis
Receptor-Interacting Protein Serine-Threonine Kinases
/ deficiency
Receptors, Vascular Endothelial Growth Factor
/ therapeutic use
Recombinant Fusion Proteins
/ pharmacology
AMD
RIPK
immune
necrosis
neovascular
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:
19 11 2019
19 11 2019
Historique:
pubmed:
7
11
2019
medline:
21
4
2020
entrez:
6
11
2019
Statut:
ppublish
Résumé
Inflammation plays an important role in pathological angiogenesis. Receptor-interacting protein 1 (RIP1) is highly expressed in inflammatory cells and is known to play an important role in the regulation of apoptosis, necroptosis, and inflammation; however, a comprehensive description of its role in angiogenesis remains elusive. Here, we show that RIP1 is abundantly expressed in infiltrating macrophages during angiogenesis, and genetic or pharmacological inhibition of RIP1 kinase activity using kinase-inactive RIP1
Identifiants
pubmed: 31685620
pii: 1908355116
doi: 10.1073/pnas.1908355116
pmc: PMC6876205
doi:
Substances chimiques
Biomarkers
0
Drug Combinations
0
GTPase-Activating Proteins
0
Imidazoles
0
Indoles
0
Laminin
0
Oligopeptides
0
Proteoglycans
0
RNA, Messenger
0
Ralbp1 protein, mouse
0
Recombinant Fusion Proteins
0
benzyloxycarbonyl-valyl-alanyl-aspartic acid
0
necrostatin-1
0
Fibroblast Growth Factor 2
103107-01-3
matrigel
119978-18-6
aflibercept
15C2VL427D
Collagen
9007-34-5
Receptors, Vascular Endothelial Growth Factor
EC 2.7.10.1
Receptor-Interacting Protein Serine-Threonine Kinases
EC 2.7.11.1
Ripk3 protein, mouse
EC 2.7.11.1
Caspases
EC 3.4.22.-
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
23705-23713Subventions
Organisme : NEI NIH HHS
ID : R01 EY025362
Pays : United States
Organisme : NEI NIH HHS
ID : R21 EY023079
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY003790
Pays : United States
Informations de copyright
Copyright © 2019 the Author(s). Published by PNAS.
Déclaration de conflit d'intérêts
The authors declare no competing interest.
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