We performed an immunohistochemistry study of the normal human bladder so as to understand the interactions of extracellular matrix (ECM) components and the integrins of cell adhesion that accommodate the volume changes and maintain an impermeable barrier to reabsorption of urine in the bladder. The normal human urothelial cell and/or its plasma membrane contained integrins 0~3, c~V, [31, and [34 but did not contain integrin [33. The urothelial basement membrane (UBM) contained collagen type IV and laminin. Fibronectin and integrins (x3 and [~4 were found in or near the U B M area, with types I and III collagen and tenascin abutting the area. The patterns of collagen, laminin, tenascin, vitronectin, fobronectin, and the 0~3, c~V, [31, and [33 integrins in the lamina propria, vessels, nerves, and smooth-muscle layers are described. These findings detail the normal anatomical ECM/integrin relationship that provides the cellular basis for bladder-wall relationships responsible for its impermeable state and other functions.The relationship of the cellular adhesion mechanisms that help secure the urothelial cells to one another as well as to the underlying urothelial basement membrane (UBM) and extracellular matrix (ECM) components would be expected to contribute to the integrity of the impermeable bladder surface. This adhesion involves a family of celladhesion receptors called integrins, heterodimeric molecules expressed on cell surfaces [3]. The family is composed of at least 13 c~ chains and 8 [3 chains which, depending upon pairing, form heterodimers that recognize one or more ligands present on E C M or on opposing cell surfaces. Only limited information is known about the nature of the integrins or their E C M ligands that perform as the adhesion molecules in the bladder wall.The bladder wall of patients with interstitial cystitis, as characterized by varying degrees of chronic inflammaCorrespondence to: