Recently, we performed an immunohistochemical analysis using renal biopsy samples of immunoglobulin

A nephropathy (IgAN) and minor glomerular abnormalities (MGA) that were found in the early stage of disease by a school urinary screening system in Japan [30]. Glomerular AGT is weakly expressed by GEC in MGA patients, but strongly induced at endocapillary sites including GEC and MC in IgAN patients, although they have normal glomerular filtration rate and BP (Fig. 3). The level of glomerular AGT parallels the levels of glomerular Ang II and TGF-β expression in diseased glomeruli. The level of glomerular injury, such as cell proliferation, ECM PF-2341066 accumulation and proteinuria, is also closely correlated with the levels of AGT and Ang II. Additionally, the AGT level seems selleck compound to determine the Ang II level in nephritic glomeruli. Furthermore, several cell culture studies, including ours, have shown that Ang II can stimulate AGT mRNA and AGT protein biosynthesis by renal cells, suggesting that its action might constitute an auto-amplifying loop of the activity of the intrarenal RAS [7, 30]. Therefore, we postulate that

even in the early stage of IgAN, glomerular RAS activation seems to occur as a result of increased GEC- and MC-AGT expression and promotes to the enhanced local generation of Ang II, which leads to clinical and pathological abnormalities. A glomerular Ang II–AGT-positive feedback loop might drive RAS activation for further glomerular injury. The substantial association between glomerular RAS activity (Ang II generation) Selisistat purchase and glomerular TGF-β, ROS generation and pathological alterations was then investigated using

a rat model of crescentic glomerulonephritis (GN) in combination with treatment with ARB (candesartan) [39]. For the ROS-generating system, we focused on the expression of Nox2, a major component of NAD(P)H oxidase, which is well known to be a major source of ROS in the diseased kidney and is activated Tau-protein kinase by Ang II stimulation [37]. Vehicle-treated nephritic rats showed significant proteinuria and severe crescentic nephritis while treatment with ARB significantly attenuated proteinuria, glomerular Ang II accumulation, superoxide production and associated pathological alterations (Fig. 4). Consistent with these histological findings, a biochemical analysis using isolated glomeruli revealed that glomerular production of AGT, Ang II, and TGF-β and Nox2 was enhanced in nephritic rats while treatment with ARB significantly reduced the production of each of these in glomeruli to close to the control level (Fig. 5). These results suggest that a glomerular Ang II-generating system works in vivo and the produced Ang II induces TGF-β expression and superoxide, and finally contributes to the development of crescentic GN in rats. Similarly, Nakamura et al.