This review will focus on biophysical properties and biogenesis of exosomes, their pathophysiological roles and their potential

as biomarkers and therapeutics in kidney diseases. Intercellular communication is vital for the regulation and coordination of many different processes within multicellular organisms. Extracellular membrane-bound vesicles are emerging as a novel and significant mechanism of cell signalling and communication. Exosomes are a specific subset of membrane-bound vesicles of endosomal origin, which are released into the extracellular environment by many cells from different tissues and organs. Exosomes exist in Silmitasertib cost a wide range of biological fluids, including blood and urine. The ubiquitous nature of exosomes has highlighted them as significant vehicles of cellular communication, with many important biological and pathophysiological implications. Exosomes are defined as small vesicles between 30 and 100 nm in diameter, consisting of a limiting lipid bilayer, transmembrane proteins and a hydrophilic core containing proteins, mRNAs and microRNAs (miRNA). They are distinguished from other microparticles by

their size and the fact that they are formed intracellularly within multivesicular endosomes (multivesicular bodies; MVB), while microvesicles (100 to 1000 nm in diameter) MLN8237 supplier are shed from the plasma membrane surface[1] (see Table 1). Cellular breakdown Release from cellular blebs during apoptosis Exosomes contain a defined set of proteins, which varies according to the cell of origin.[6] Common components of exosomes are proteins involved with endosomal trafficking, membrane trafficking and fusion proteins, tetraspanins (CD63, CD81, CD9, CD82), heat shock proteins (HSP70, HSP90), metabolic enzymes, adhesion molecules, signal transduction proteins, lipid rafts and cytoskeletal proteins, in addition to cell type-specific

proteins, such as major histocompatibility complex (MHC) class I and II, α-synuclein, and the A33 antigen.[6] Exosomes have a specific lipid composition distinct from their Calpain parental MVB, although they do reflect their cell of origin, and can also contain bioactive lipids such as prostaglandins, which may contribute to their function.[7] Exosomes contain mRNAs and miRNAs, and RNA profiling of exosomal fractions has identified significant differences to parental cellular RNA.[8, 9] Both mRNAs and miRNAs present in the exosomal fraction maintain their function when transferred to other cells,[8, 10] demonstrating that exosomal RNA transfer may be an important route for epigenetic signalling between cells. However, recent studies suggested that many extracellular miRNAs may not be contained within exosomes, but can be complexed with circulating Argonaute-2 or other ribonucleoprotein complexes.[11-13] Exosomes are formed by the intraluminal budding of late endosomal compartments to create MVB, containing intraluminal vesicles.