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.

Cells
|March 11, 2023
PubMed

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.

Related Concept Videos

Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
2.6K
Intracellular Signaling Affects Focal Adhesions01:17

Intracellular Signaling Affects Focal Adhesions

Integrins act both as extracellular input receivers and as intracellular processing activators. As their name suggests, integrins are entirely integrated into the membrane structure. Their hydrophobic membrane-spanning regions interact with the phospholipid bilayer's hydrophobic region. These membrane receptors provide extracellular attachment sites for effectors like hormones and growth factors. They activate intracellular response cascades when their effectors are bound and active.
Some...
2.7K
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
12.2K