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Published on: December 9, 2021
IL-33 via PKCμ/PRKD1 Mediated α-Catenin Phosphorylation Regulates Endothelial Cell-Barrier Integrity and
Deepti Sharma1,2, Geetika Kaur1,2, Shivantika Bisen1,2
1Integrative Biosciences Center, Wayne State University, Detroit, MI 48202, USA.
Insights
Interleukin-33 (IL-33) disrupts the inner blood-retinal barrier (iBRB) by phosphorylating alpha-catenin, a key adhesion protein. Blocking this IL-33 signaling pathway reduces vascular leakage in retinopathy models.
Area of Science:
- Ophthalmology
- Vascular Biology
- Cell Adhesion
Background:
- Endothelial cell-cell adhesion is crucial for blood-retinal barrier (BRB) integrity and function.
- The cadherin-catenin complex mediates cell adhesion and regulates BRB homeostasis.
- The precise role of cadherins and catenins in BRB structure and function requires further elucidation.
Purpose of the Study:
- To investigate the role of Interleukin-33 (IL-33) in retinal endothelial barrier disruption and abnormal angiogenesis.
- To identify the molecular mechanisms underlying IL-33-mediated endothelial dysfunction.
- To assess the therapeutic potential of targeting IL-33 signaling in oxygen-induced retinopathy (OIR).
Main Methods:
- Utilized a murine model of oxygen-induced retinopathy (OIR) and human retinal microvascular endothelial cells (HRMVECs).
- Employed electric cell-substrate impedance sensing (ECIS) and FITC-dextran permeability assays to measure endothelial barrier function.
- Investigated protein phosphorylation using mass spectrometry (MS) and Western blotting, and analyzed signaling pathways (PKCμ/PRKD1-p38 MAPK).
Main Results:
- IL-33 (20 ng/mL) induced endothelial barrier disruption in HRMVECs.
- IL-33 triggered alpha-catenin phosphorylation at Ser/Thr residues, specifically at Thr654.
- PKCμ/PRKD1-p38 MAPK signaling pathway was identified as a regulator of IL-33-induced alpha-catenin phosphorylation and barrier integrity.
- Genetic deletion of IL-33 reduced vascular leakage and suppressed the PKCμ/PRKD1-p38 MAPK-alpha-catenin signaling cascade in OIR models.
Conclusions:
- IL-33 significantly contributes to endothelial permeability and inner blood-retinal barrier (iBRB) dysfunction.
- The IL-33-induced PKCμ/PRKD1-p38 MAPK-alpha-catenin signaling pathway is a critical mediator of iBRB integrity.
- Targeting IL-33 signaling presents a potential therapeutic strategy for managing retinal vascular diseases characterized by increased permeability.
Abstract:
Angiogenesis, neovascularization, and vascular remodeling are highly dynamic processes, where endothelial cell-cell adhesion within the vessel wall controls a range of physiological processes, such as growth, integrity, and barrier function. The cadherin-catenin adhesion complex is a key contributor to inner blood-retinal barrier (iBRB) integrity and dynamic cell movements. However, the pre-eminent role of cadherins and their associated catenins in iBRB structure and function is not fully understood. Using a murine model of oxygen-induced retinopathy (OIR) and human retinal microvascular endothelial cells (HRMVECs), we try to understand the significance of IL-33 on retinal endothelial barrier disruption, leading to abnormal angiogenesis and enhanced vascular permeability. Using electric cell-substrate impedance sensing (ECIS) analysis and FITC-dextran permeability assay, we observed that IL-33 at a 20 ng/mL concentration induced endothelial-barrier disruption in HRMVECs. The adherens junction (AJs) proteins play a prominent role in the selective diffusion of molecules from the blood to the retina and in maintaining retinal homeostasis. Therefore, we looked for the involvement of adherens junction proteins in IL-33-mediated endothelial dysfunction. We observed that IL-33 induces α-catenin phosphorylation at serine/threonine (Ser/Thr) residues in HRMVECs. Furthermore, mass-spectroscopy (MS) analysis revealed that IL-33 induces the phosphorylation of α-catenin at Thr654 residue in HRMVECs. We also observed that PKCμ/PRKD1-p38 MAPK signaling regulates IL-33-induced α-catenin phosphorylation and retinal endothelial cell-barrier integrity. Our OIR studies revealed that genetic deletion of IL-33 resulted in reduced vascular leakage in the hypoxic retina. We also observed that the genetic deletion of IL-33 reduced OIR-induced PKCμ/PRKD1-p38 MAPK-α-catenin signaling in the hypoxic retina. Therefore, we conclude that IL-33-induced PKCμ/PRKD1-p38 MAPK-α-catenin signaling plays a significant role in endothelial permeability and iBRB integrity.
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