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      The insect nephrocyte is a podocyte-like cell with a filtration slit diaphragm

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          Abstract

          The nephron is the basic structural and functional unit of the vertebrate kidney. It is composed of a glomerulus, the site of ultrafiltration, and a renal tubule, along which the filtrate is modified. Although widely regarded as a vertebrate adaptation 1 ‘nephron-like’ features can be found in the excretory systems of many invertebrates, raising the possibility that components of the vertebrate excretory system were inherited from their invertebrate ancestors 2. Here we show that the insect nephrocyte has remarkable anatomical, molecular and functional similarity with the glomerular podocyte, a cell in the vertebrate kidney that forms the main size-selective barrier as blood is ultrafiltered to make urine. In particular, both cell types possess a specialised filtration diaphragm, known as the slit diaphragm in podocytes or the nephrocyte diaphragm in nephrocytes. We find that fly orthologues of the major constituents of the slit diaphragm, including nephrin, neph1, CD2AP, ZO-1 and podocin are expressed in the nephrocyte and form a complex of interacting proteins that closely mirrors the vertebrate slit diaphragm complex. Furthermore, we find the nephrocyte diaphragm is completely lost in flies mutant for nephrin or neph1 orthologues, a phenotype resembling loss of the slit diaphragm in the absence of either nephrin (as in the human kidney disease NPHS1) or neph1. These changes drastically impair filtration function in the nephrocyte. The similarities we describe between invertebrate nephrocytes and vertebrate podocytes provide evidence suggesting the two cell types are evolutionarily related and establish the nephrocyte as a simple model in which to study podocyte biology and podocyte-associated diseases.

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          Most cited references29

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          NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.

          Familial idiopathic nephrotic syndromes represent a heterogeneous group of kidney disorders, and include autosomal recessive steroid-resistant nephrotic syndrome, which is characterized by early childhood onset of proteinuria, rapid progression to end-stage renal disease and focal segmental glomerulosclerosis. A causative gene for this disease, NPHS2, was mapped to 1q25-31 and we report here its identification by positional cloning. NPHS2 is almost exclusively expressed in the podocytes of fetal and mature kidney glomeruli, and encodes a new integral membrane protein, podocin, belonging to the stomatin protein family. We found ten different NPHS2 mutations, comprising nonsense, frameshift and missense mutations, to segregate with the disease, demonstrating a crucial role for podocin in the function of the glomerular filtration barrier.
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            Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.

            Congenital nephrotic syndrome of the Finnish type (NPHS1) is an autosomal-recessive disorder, characterized by massive proteinuria in utero and nephrosis at birth. In this study, the 150 kb critical region of NPHS1 was sequenced, revealing the presence of at least 11 genes, the structures of 5 of which were determined. Four different mutations segregating with the disease were found in one of the genes in NPHS1 patients. The NPHS1 gene product, termed nephrin, is a 1241-residue putative transmembrane protein of the immunoglobulin family of cell adhesion molecules, which by Northern and in situ hybridization was shown to be specifically expressed in renal glomeruli. The results demonstrate a crucial role for this protein in the development or function of the kidney filtration barrier.
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              Congenital nephrotic syndrome in mice lacking CD2-associated protein.

              CD2-associated protein (CD2AP) is an 80-kilodalton protein that is critical for stabilizing contacts between T cells and antigen-presenting cells. In CD2AP-deficient mice, immune function was compromised, but the mice died at 6 to 7 weeks of age from renal failure. In the kidney, CD2AP was expressed primarily in glomerular epithelial cells. Knockout mice exhibited defects in epithelial cell foot processes, accompanied by mesangial cell hyperplasia and extracellular matrix deposition. Supporting a role for CD2AP in the specialized cell junction known as the slit diaphragm, CD2AP associated with nephrin, the primary component of the slit diaphragm.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                3 April 2009
                29 October 2008
                15 January 2009
                15 July 2009
                : 457
                : 7227
                : 322-326
                Affiliations
                [1 ] Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK
                [2 ] Centro de Biología Molecular Severo Ochoa, CSIC, UAM, Cantoblanco, 28049, Madrid, Spain.
                [3 ] Institut für Genetik, Heinrich-Heine-Universität, Düsseldorf, D-40225, Germany
                [4 ] Department of Genetics, University of Valencia, Burjasot, Valencia 46100, Spain
                [5 ] Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany
                Author notes
                Author for correspondence: hs17@ 123456cam.ac.uk
                [*]

                these authors contributed equally to this work

                Author contribution

                B.D., H.S., M.R-G. designed and directed the project. B.D., H.W., M.R-G. and S.P-S. performed the experiments. F.G. and M.W-B. provided invaluable technical assistance. A.G-L. and R.A. provided materials. B.D. and H.S. wrote the paper. All authors discussed results and commented on the manuscript.

                Article
                UKMS4238
                10.1038/nature07526
                2687078
                18971929
                4e359cab-54c0-4cd4-a08b-ea067c20ac8e
                History
                Funding
                Funded by: Wellcome Trust :
                Award ID: 079221 || WT
                Funded by: Wellcome Trust :
                Award ID: 072441 || WT
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