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Signaling mechanisms in red blood cells: A view through the protein phosphorylation and deformability

Journal

JOURNAL OF CELLULAR PHYSIOLOGY
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/jcp.30958

Keywords

deformability; mechanism; protein phosphorylation; red blood cell; shear stress; signaling

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Intracellular signaling mechanisms in red blood cells (RBCs) involve protein kinases and phosphatases, which regulate the physiological properties of the cell in response to various stimuli. Protein phosphorylation plays a crucial role in intracellular signal transduction, volume regulation, and cytoskeletal organization in RBCs. The structural organization of the membrane and cytoskeleton determines RBC deformability and allows them to pass through narrow capillaries under shear stress.
Intracellular signaling mechanisms in red blood cells (RBCs) involve various protein kinases and phosphatases and enable rapid adaptive responses to hypoxia, metabolic requirements, oxidative stress, or shear stress by regulating the physiological properties of the cell. Protein phosphorylation is a ubiquitous mechanism for intracellular signal transduction, volume regulation, and cytoskeletal organization in RBCs. Spectrin-based cytoskeleton connects integral membrane proteins, band 3 and glycophorin C to junctional proteins, ankyrin and Protein 4.1. Phosphorylation leads to a conformational change in the protein structure, weakening the interactions between proteins in the cytoskeletal network that confers a more flexible nature for the RBC membrane. The structural organization of the membrane and the cytoskeleton determines RBC deformability that allows cells to change their ability to deform under shear stress to pass through narrow capillaries. The shear stress sensing mechanisms and oxygenation-deoxygenation transitions regulate cell volume and mechanical properties of the membrane through the activation of ion transporters and specific phosphorylation events mediated by signal transduction. In this review, we summarize the roles of Protein kinase C, cAMP-Protein kinase A, cGMP-nitric oxide, RhoGTPase, and MAP/ERK pathways in the modulation of RBC deformability in both healthy and disease states. We emphasize that targeting signaling elements may be a therapeutic strategy for the treatment of hemoglobinopathies or channelopathies. We expect the present review will provide additional insights into RBC responses to shear stress and hypoxia via signaling mechanisms and shed light on the current and novel treatment options for pathophysiological conditions.

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