Background: Diabetic kidney disease (DKD) remains a
major cause of end-stage renal disease worldwide, yet
current clinical biomarkers such as albuminuria and estimated glomerular filtration rate lack sufficient sensitivity
to detect early renal injury or predict individual disease
trajectories. Growth differentiation factor 15 (GDF15), a
stress-inducible cytokine belonging to the transforming
growth factor-b superfamily, has emerged as a promising
molecular link between metabolic stress, inflammation,
mitochondrial dysfunction, and renal injury in diabetes.
This review systematically synthesizes current experimental and clinical evidence on the role of GDF15 in
DKD, with emphasis on its mechanistic involvement in
renal pathophysiology and its translational potential as
a biomarker and therapeutic target. Evidence from preclinical models and human studies indicates that GDF15
is upregulated in diabetic kidneys, particularly in tubular
epithelial cells, in response to hyperglycemia-induced
oxidative stress and mitochondrial dysfunction. Mechanistically, GDF15 modulates key pathogenic pathways in
DKD, including NF-kB–mediated inflammation, NLRP3
inflammasome activation, macrophage polarization,
TGF-b/Smad-driven fibrogenesis, and autophagy regulation through PI3K/Akt and AMPK signaling. Clinically, circulating and urinary GDF15 levels correlate with disease
severity and independently predict renal function decline,
suggesting utility in both early diagnosis and prognostic stratification. In addition, emerging evidence supports its
potential role as a pharmacodynamic marker responsive
to interventions such as metformin and SGLT2 inhibitors.
However, its context-dependent biological effects, lack
of assay standardization, and confounding elevation in
systemic diseases remain key challenges. Overall, GDF15
represents a central stress-integrating mediator in DKD
pathogenesis and a promising candidate for precision
nephrology, warranting further validation in longitudinal
multi-omics and interventional studies.
Yu Chen, Min Li, Min Yang et al.· Journal of Medical Biochemis...· 0 citations
Kidney organoids are important tools for modeling human development and disease, especially in chronic kidney disease (CKD), which is a global health challenge. Current treatment strategies focus on delaying disease progression by managing underlying causes, and in this regard, kidney organoids offer a platform for mechanism-based therapeutics. Advances in the understanding of human induced pluripotent stem cells (hiPSCs) and sophisticated 3D organ culture methods have enabled researchers to replicate human kidney development and disease mechanisms in vitro, thereby opening new avenues for drug testing. Although the methods for generating renal cell lineages are well established, new protocols for inducing lineages, such as the ureteric bud and collecting ducts, have emerged over the past 5 years. Patient-derived or genetically edited kidney organoids have been used to successfully model various genetic kidney diseases, notably polycystic kidney disease, and to generate kidney tissues that closely mimic the morphology of real organs. However, achieving more complex disease modeling and generating transplantable synthetic kidneys still has notable challenges. The present review discusses the application of hiPSC-derived 3D organoids in CKD research and addresses the limitations of current organ culture methods. The present review also examines the impact of CRISPR/Cas9 technology, and investigates potential future directions.
Shengxin Cui, Ti-Chou Chen, Yun Zou et al.· Experimental and Therapeutic...· 0 citations