Vascular cell-adhesion molecule 1 (VCAM-1) regulates JunB-mediated IL-8/CXCL1 expression and pathological neovascularization

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Geetika Kaur
Deepti Sharma
Shivantika Bisen
Chandra Sekhar Mukhopadhyay
Katherine Gurdziel
Nikhlesh K. Singh
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[1] Wayne State University,Integrative Biosciences Center
[2] Wayne State University,Department of Ophthalmology, Visual and Anatomical Sciences, School of Medicine
[3] Guru Angad Dev Veterinary and Animal Sciences University,School of Animal Biotechnology
[4] Wayne State University,Institute of Environmental Health Sciences and Department of Pharmacology, School of Medicine
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Vascular adhesion molecules play an important role in various immunological disorders, particularly in cancers. However, little is known regarding the role of these adhesion molecules in proliferative retinopathies. We observed that IL-33 regulates VCAM-1 expression in human retinal endothelial cells and that genetic deletion of IL-33 reduces hypoxia-induced VCAM-1 expression and retinal neovascularization in C57BL/6 mice. We found that VCAM-1 via JunB regulates IL-8 promoter activity and expression in human retinal endothelial cells. In addition, our study outlines the regulatory role of VCAM-1-JunB-IL-8 signaling on retinal endothelial cell sprouting and angiogenesis. Our RNA sequencing results show an induced expression of CXCL1 (a murine functional homolog of IL-8) in the hypoxic retina, and intravitreal injection of VCAM-1 siRNA not only decreases hypoxia-induced VCAM-1-JunB-CXCL1 signaling but also reduces OIR-induced sprouting and retinal neovascularization. These findings suggest that VCAM-1-JunB-IL-8 signaling plays a crucial role in retinal neovascularization, and its antagonism might provide an advanced treatment option for proliferative retinopathies.
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