“…Our studies and studies from other laboratories (Craciun and Barbu-Toduran, 2013; Elshennay, 2011; Hammel and Meilijson, 2012; Japaridze et al, 2012; Matsuno et al, 2008; Okuneva et al, 2012; Paredes-Santos et al, 2012; Savigny et al, 2007; Siksou et al, 2007) established porosomes to be secretory portals that perform the specialized task of fractional discharge of intravesicular contents from cells during cell secretion. The significance of the porosome discovery is reflected by several publications involving its structure (Craciun and Barbu-Toduran, 2013; Elshennay, 2011; Hammel and Meilijson, 2012; Japaridze et al, 2012; Matsuno et al, 2008; Okuneva et al, 2012; Paredes-Santos et al, 2012; Savrgny et al, 2007; Siksou et al, 2007), and the associated transient fusion mechanism (Aravanis et al, 2003; Taraska et al, 2003; Thorn et al, 2004) accompanied by fractional discharge of intravesicular contents from cells. Studies in endocrine cells report secretory granules to be recaptured largely intact following stimulated exocytosis (Taraska et al, 2003); in neurons, single synaptic vesicles fuse transiently and successively without loss of vesicle identity (Aravanis et al, 2003); and in the exocrine pancreas, secretion is characterized by long fusion pore openings and preservation of secretory vesicle lipid identity (Thorn et al, 2004).…”