About this Research Topic
In the past years, many studies have focused on podocyte proteins as potential therapeutic targets. Recently, an increasing number of evidence indicates that activation of autophagy could be a potent tool to prevent podocyte loss in diabetic nephropathy. On the other hand, there is a close relationship between podocyte structure and function. Recent results of studies in vitro indicate that GTPase and microRNA –mediated regulation of actin dynamics is a target in CKD. Thus, preventing changes and restoring podocyte morphology by stabilization of F-actin cytoskeleton and other structural proteins seems to be a promising approach.
Structure , function and viability of podocytes is directly regulated by various hormones, such as natriuretic peptides, angiotensin II or insulin. Recent studies emphasize a detrimental role of growth hormone in podocytes in diabetic kidney. Podocytes express also a number of nuclear hormone receptors (NR) whose ligands could serve as potential treatments in podocytopathies. While the renoprotective roles of some hormones , such as glucocorticoids or estrogens has been known for years, their direct role on podocyte function is still emerging. Further exploring the NR functions in podocyte development and disorders may shed a new light on the possibilities of a podocyte-specific therapy.
In their excellent articles, the Authors contributing to our previous Research Topic (“Podocyte Pathology and Nephropathy”) have summarized the advances in knowledge and presented new findings on podocytes in health and disease. Now, after some years have passed, this is a good time to update the state of our knowledge. We encourage the contributors to submit mini-reviews, original research articles and review articles.
Keywords: podocytes, diabetes, kidney disease, glomerulopathy, therapy
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