Extracellular vesicles and ciliary signaling in C. elegans help reveal how an ADPKD-associated mutation disrupts polycystin protein localization...
Read More »Tiny Particles in Urine Could Be the Key to Treating a Deadly Childhood Kidney Disease
Healthy donor extracellular vesicles and exosomes restored missing kidney proteins in ARPKD models, showing potential for prenatal treatment of severe...
Read More »Tracking polycystic kidney disease proteins in extracellular vesicles to uncover disease progression
Researchers at Rutgers University discovered how polycystic kidney disease proteins are packaged into extracellular vesicles, offering new insights into...
Read More »Identification of Biomarkers from Urinary Exosomes
Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of ESRD. Affected individuals inherit a defective copy of either PKD1 or PKD2, which encode polycystin-1 (PC1) or polycystin-2 (PC2), respectively. PC1 and PC2 are secreted on urinary exosome-like vesicles ...
Read More »The exocyst complex is centrally involved in “urocrine signaling”
Cilia, organelles that function as cellular antennae, are central to the pathogenesis of “ciliopathies”, including various forms of polycystic kidney disease (PKD). To date, however, the molecular mechanisms controlling ciliogenesis and ciliary function remain incompletely understood. A recently proposed model ...
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