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A neutrophil elastase-generated mature form of IL-33 is a potent regulator of endothelial cell activation and proliferative retinopathy.

Authors :
Bisen S
Verma SK
Mukhopadhyay CS
Singh NK
Source :
Experimental & molecular medicine [Exp Mol Med] 2024 Aug; Vol. 56 (8), pp. 1703-1716. Date of Electronic Publication: 2024 Aug 01.
Publication Year :
2024

Abstract

Human interleukin-33 (IL-33) is a 270 amino acid protein that belongs to the IL-1 cytokine family and plays an important role in various inflammatory disorders. Neutrophil proteases (Cathepsin G and Elastase) and mast cell proteases (tryptase and chymase) regulate the activity of IL-33 by processing full-length IL-33 into its mature form. There is little evidence on the role of these mature forms of IL-33 in retinal endothelial cell signaling and pathological retinal angiogenesis. Here, we cloned, expressed, and purified the various mature forms of human IL-33 and then evaluated the effects of IL-33 <subscript>95-270</subscript> , IL-33 <subscript>99-270</subscript> , IL-33 <subscript>109-270</subscript> , and IL-33 <subscript>112-270</subscript> on angiogenesis in human retinal microvascular endothelial cells (HRMVECs). We observed that IL-33 <subscript>95-270</subscript> , IL-33 <subscript>99-270</subscript> , IL-33 <subscript>109-270</subscript> , and IL-33 <subscript>112-270</subscript> significantly induced HRMVEC migration, tube formation and sprouting angiogenesis. However, only IL-33 <subscript>99-270</subscript> could induce HRMVEC proliferation. We used a murine model of oxygen-induced retinopathy (OIR) to assess the role of these mature forms of IL-33 in pathological retinal neovascularization. Our 3'-mRNA sequencing and signaling studies indicated that IL-33 <subscript>99-270</subscript> and IL-33 <subscript>109-270</subscript> were more potent at inducing endothelial cell activation and angiogenesis than the other mature forms. We found that genetic deletion of IL-33 significantly reduced OIR-induced retinal neovascularization in the mouse retina and that intraperitoneal administration of mature forms of IL-33, mainly IL-33 <subscript>99-270</subscript> and IL-33 <subscript>109-270</subscript> , significantly restored ischemia-induced angiogenic sprouting and tuft formation in the hypoxic retinas of IL-33 <superscript>-/-</superscript> mice. Thus, our study results suggest that blockade or inhibition of IL-33 cleavage by neutrophil proteases could help mitigate pathological angiogenesis in proliferative retinopathies.<br /> (© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)

Details

Language :
English
ISSN :
2092-6413
Volume :
56
Issue :
8
Database :
MEDLINE
Journal :
Experimental & molecular medicine
Publication Type :
Academic Journal
Accession number :
39085349
Full Text :
https://doi.org/10.1038/s12276-024-01279-y