CD31 in Endothelial Cells: Function, Biomarker, and Target

Endothelial cells form the inner lining of all blood and lymphatic vessels, creating a barrier between circulating blood and body tissues. This single layer of cells plays a role in maintaining vascular health and regulating various physiological processes. A protein found abundantly on their surface is CD31, also known as Platelet Endothelial Cell Adhesion Molecule-1 (PECAM-1).

Understanding Endothelial Cells and CD31

Endothelial cells are flattened cells that create a lining throughout the entire vascular network, including arteries, veins, and capillaries. This lining acts as a semi-permeable barrier, controlling the passage of substances between the bloodstream and surrounding tissues. Their location allows them to respond to changes in blood flow and chemical signals, influencing processes like blood clotting and inflammation.

CD31, or PECAM-1, is a cell surface glycoprotein expressed on endothelial cells, particularly concentrated at their junctions. It is also found on certain immune cells, such as platelets, monocytes, neutrophils, and some T-cell subsets. As a member of the immunoglobulin superfamily, CD31 serves as a definitive marker for identifying and distinguishing endothelial cells from other cell types in various biological contexts.

CD31’s Multifaceted Roles

CD31 plays a part in maintaining the structural integrity of blood vessels through cell adhesion and junctional stability. It forms homophilic interactions, where CD31 molecules on one endothelial cell bind to those on an adjacent cell, effectively “zipping” them together. These interactions create tight junctions that resist mechanical forces and maintain the vessel wall’s barrier function, controlling vascular permeability.

The protein also contributes to angiogenesis, the process by which new blood vessels form from existing ones. CD31 is involved in the migration and assembly of endothelial cells into tube-like structures, a step in new vessel development. This role is important in physiological processes like wound healing and tissue repair, which require new blood supply. CD31’s influence on cell migration highlights its involvement in vascular remodeling.

CD31 facilitates the movement of immune cells from the bloodstream into tissues, a process called diapedesis or leukocyte transmigration. During inflammation, white blood cells exit the vessel to reach sites of infection or injury. CD31 on endothelial cells interacts with CD31 on immune cells, guiding them through the endothelial barrier. This passage prevents tissue damage while enabling an effective immune response.

Beyond its adhesive functions, CD31 also acts as a signaling molecule, transmitting information into the cell. Its intracellular domain contains specific motifs that, upon activation, can recruit other proteins to initiate various cellular responses. This signaling capability influences diverse cellular processes, including cell survival and the regulation of immune responses, demonstrating CD31’s roles in vascular biology.

CD31 as a Biomarker and Therapeutic Target

CD31 is utilized in scientific research and diagnostics as a biomarker for endothelial cells. In laboratory settings, techniques like immunohistochemistry and flow cytometry employ antibodies against CD31 to identify, isolate, and quantify endothelial cells in tissue samples and cell cultures. This enables researchers to visualize blood vessels within tissues and study their density and distribution.

Alterations in CD31 expression or function are associated with various diseases. In cancer, for example, CD31 is used to assess tumor angiogenesis, as tumors often develop their own blood supply to grow and metastasize. High levels of CD31 expression can indicate increased vessel formation within a tumor, correlating with aggressive tumor growth and serving as a relevant indicator for disease progression.

Because of its involvement in angiogenesis and immune cell trafficking, CD31 and its pathways are explored as potential therapeutic targets. In cancer, strategies aim to inhibit new blood vessel formation by targeting CD31-mediated processes, thereby starving tumors of nutrients. In inflammatory diseases, modulating CD31 could help control immune cell migration into affected tissues.

Research also investigates CD31’s role in cardiovascular diseases, such as atherosclerosis, where its disruption might contribute to vascular dysfunction. Maintaining its proper function is important for vascular health. The development of molecules that can influence CD31’s activity, such as specific antibodies or peptides, holds promise for future therapies aimed at conditions involving abnormal blood vessel formation or immune responses.

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