Open AccessSlit Diaphragms Contain Tight Junction Proteins
Author(s) -
Hirotaka Fukasawa,
Scott J. Bornheimer,
Krystyna Kudlicka,
Marilyn G. Farquhar
Publication year - 2009
Publication title -
journal of the american society of nephrology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2008101117
Subject(s) - adherens junction , tight junction , nephrin , podocin , slit diaphragm , microbiology and biotechnology , occludin , cell junction , slit , immunogold labelling , podocalyxin , biology , vinculin , claudin , cytoskeleton , immunoprecipitation , spectrin , intermediate filament , intercalated disc , septate junctions , podocyte , cadherin , anatomy , ultrastructure , biochemistry , intracellular , gap junction , focal adhesion , signal transduction , cell , neuroscience , proteinuria , endocrinology , gene , kidney
Slit diaphragms are essential components of the glomerular filtration apparatus, as changes in these junctions are the hallmark of proteinuric diseases. Slit diaphragms, considered specialized adherens junctions, contain both unique membrane proteins (e.g., nephrin, podocin, and Neph1) and typical adherens junction proteins (e.g., P-cadherin, FAT, and catenins). Whether slit diaphragms also contain tight junction proteins is unknown. Here, immunofluorescence, immunogold labeling, and cell fractionation demonstrated that rat slit diaphragms contain the tight junction proteins JAM-A (junctional adhesion molecule A), occludin, and cingulin. We found these proteins in the same protein complexes as nephrin, podocin, CD2AP, ZO-1, and Neph1 by cosedimentation, coimmunoprecipitation, and pull-down assays. PAN nephrosis increased the protein levels of JAM-A, occludin, cingulin, and ZO-1 several-fold in glomeruli and loosened their attachment to the actin cytoskeleton. These data extend current information about the molecular composition of slit diaphragms by demonstrating the presence of tight junction proteins, although slit diaphragms lack the characteristic morphologic features of tight junctions. The contribution of these proteins to the assembly of slit diaphragms and potential signaling cascades requires further investigation.