Expression of NCAM recapitulates tubulogenic development in kidneys recovering from acute ischemia.

Recovery of the kidney from acute renal failure relies on a sequence of events including epithelial cell dedifferentiation and proliferation followed by differentiation and restoration of the functional integrity of the nephron. The factors responsible for, and the significance of, reversion to a less differentiated cell phenotype and its relationship to the proliferative response after ischemia are poorly understood. In an attempt to identify adhesion molecules that may be influential in the recovery process, the expression of neural cell adhesion molecule (NCAM) and markers of epithelial differentiation and proliferation were analyzed at various times after an ischemic insult. In maturing nephrons, NCAM is detectable by immunohistochemistry in renal vesicles, S-shaped bodies, and early tubules. There is minimal cellular NCAM expression in normal tubules of the adult kidney. In contrast, in postischemic kidneys, NCAM expression is abundant in S3 proximal tubule cells 5 days after reperfusion. As in developing tubules, NCAM is concentrated in basal and lateral aspects of cells that have no apical gp330 or dipeptidyl peptidase IV detectable on their brush border. The expression of NCAM is preceded by disassembly of the brush border and proliferation of surviving S3 cells, which is most prominent at 2 days postischemia. NCAM expression persists in some flattened and dedifferentiated cells for up to 7 wk after ischemia. Thus proximal tubule epithelial cells of the postischemic kidney express NCAM in a pattern that recapitulates the expression of NCAM in the developing kidney. Such reversion of phenotype extends at least back to the early stages of renal vesicle formation, and this reversion may represent a critical step in the reestablishment of a normal tubule. NCAM-matrix interactions may mediate the motogenic and mitogenic responses of the dedifferentiated epithelium that are critical to reestablishment of a functional proximal tubule.

[1]  J. Bonventre,et al.  Polarity, integrin, and extracellular matrix dynamics in the postischemic rat kidney. , 1998, American journal of physiology. Cell physiology.

[2]  F. Walsh,et al.  Neural cell adhesion molecules of the immunoglobulin superfamily: role in axon growth and guidance. , 1997, Annual review of cell and developmental biology.

[3]  J. Bonventre,et al.  Acute renal failure. , 2018, The New England journal of medicine.

[4]  Mart Saarma,et al.  Defects in enteric innervation and kidney development in mice lacking GDNF , 1996, Nature.

[5]  P. Ekblom Genetics of kidney development. , 1996, Current opinion in nephrology and hypertension.

[6]  D. Basile,et al.  Increased transforming growth factor-beta 1 expression in regenerating rat renal tubules following ischemic injury. , 1996, The American journal of physiology.

[7]  D. Drubin,et al.  Origins of Cell Polarity , 1996, Cell.

[8]  R. Scheller,et al.  VAMP/synaptobrevin isoforms 1 and 2 are widely and differentially expressed in nonneuronal tissues , 1996, The Journal of cell biology.

[9]  W. Birchmeier,et al.  Hepatocyte growth factor/scatter factor induces a variety of tissue- specific morphogenic programs in epithelial cells , 1995, The Journal of cell biology.

[10]  A. Bradley,et al.  BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning. , 1995, Genes & development.

[11]  K. Lyons,et al.  A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye. , 1995, Genes & development.

[12]  J. Stevens,et al.  FGF-1 in normal and regenerating kidney: expression in mononuclear, interstitial, and regenerating epithelial cells. , 1995, The American journal of physiology.

[13]  K. Watanabe,et al.  K-glypican: a novel GPI-anchored heparan sulfate proteoglycan that is highly expressed in developing brain and kidney , 1995, The Journal of cell biology.

[14]  S. Miller,et al.  Growth factor gene expression in tubular epithelial injury. , 1995, Current opinion in nephrology and hypertension.

[15]  M. Noble,et al.  Roles of hepatocyte growth factor/scatter factor and the met receptor in the early development of the metanephros , 1995, The Journal of cell biology.

[16]  R. U. Margolis,et al.  Immunocytochemical and in situ hybridization studies of the heparan sulfate proteoglycan, glypican, in nervous tissue. , 1994, Journal of cell science.

[17]  F. Walsh,et al.  Activation of the FGF receptor underlies neurite outgrowth stimulated by L1, N-CAM, and N-cadherin , 1994, Neuron.

[18]  S. Miller,et al.  Therapeutic use of growth factors in renal failure. , 1994, Journal of the American Society of Nephrology : JASN.

[19]  E. Neilson,et al.  Epithelial differentiation of metanephric mesenchymal cells after stimulation with hepatocyte growth factor or embryonic spinal cord. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[20]  M. Abbate,et al.  Expression of gp330 and gp330/alpha 2-macroglobulin receptor-associated protein in renal tubular differentiation. , 1994, Journal of the American Society of Nephrology : JASN.

[21]  J. Bonventre,et al.  Localization of proliferating cell nuclear antigen, vimentin, c-Fos, and clusterin in the postischemic kidney. Evidence for a heterogenous genetic response among nephron segments, and a large pool of mitotically active and dedifferentiated cells. , 1994, The Journal of clinical investigation.

[22]  S. Frisch,et al.  Disruption of epithelial cell-matrix interactions induces apoptosis , 1994, The Journal of cell biology.

[23]  E. Bock,et al.  Transmembrane neural cell-adhesion molecule (NCAM), but not glycosyl-phosphatidylinositol-anchored NCAM, down-regulates secretion of matrix metalloproteinases. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[24]  D. Rueger,et al.  Osteogenic protein-1 regulates L1 and neural cell adhesion molecule gene expression in neural cells. , 1993, The Journal of biological chemistry.

[25]  S. Dauwe,et al.  Stage- and segment-specific expression of cell-adhesion molecules N-CAM, A-CAM, and L-CAM in the kidney. , 1993, Kidney international.

[26]  R. Bloch Clusters of neural cell adhesion molecule at sites of cell-cell contact , 1992, The Journal of cell biology.

[27]  F. Toback,et al.  Regeneration after acute tubular necrosis. , 1992, Kidney international.

[28]  J. Sunshine,et al.  NCAM polysialic acid can regulate both cell-cell and cell-substrate interactions , 1991, The Journal of cell biology.

[29]  B. Molitoris Ischemia-induced loss of epithelial polarity: potential role of the actin cytoskeleton. , 1991, The American journal of physiology.

[30]  P. Lackie,et al.  Polysialic acid and N-CAM localisation in embryonic rat kidney: mesenchymal and epithelial elements show different patterns of expression. , 1990, Development.

[31]  C. Goridis,et al.  Modulation of NCAM expression by transforming growth factor-beta, serum, and autocrine factors , 1990, The Journal of cell biology.

[32]  L. Fine,et al.  Molecular events in the organization of renal tubular epithelium: from nephrogenesis to regeneration. , 1989, The American journal of physiology.

[33]  P. Ekblom Developmentally regulated conversion of mesenchyme to epithelium , 1989, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[34]  E. J. Gutmann,et al.  Colchicine-induced redistribution of an apical membrane glycoprotein (gp330) in proximal tubules. , 1989, The American journal of physiology.

[35]  R. Akeson,et al.  Identification of a heparin binding domain of the neural cell adhesion molecule N-CAM using synthetic peptides , 1989, Neuron.

[36]  D. Bitter‐Suermann,et al.  Presence of the long chain form of polysialic acid of the neural cell adhesion molecule in Wilms' tumor. Identification of a cell adhesion molecule as an oncodevelopmental antigen and implications for tumor histogenesis. , 1988, The American journal of pathology.

[37]  T. Jessell,et al.  Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons , 1988, Neuron.

[38]  C. Goridis,et al.  Neural cell adhesion molecules during embryonic induction and development of the kidney. , 1988, Development.

[39]  G. Edelman,et al.  Neural cell adhesion molecule: structure, immunoglobulin-like domains, cell surface modulation, and alternative RNA splicing. , 1987, Science.

[40]  L. Saxén Organogenesis of the kidney , 1987 .

[41]  L. Braiterman,et al.  Identification of rat hepatocyte plasma membrane proteins using monoclonal antibodies , 1985, The Journal of cell biology.

[42]  G. Edelman,et al.  Ontogenetic expression of cell adhesion molecules: L-CAM is found in epithelia derived from the three primary germ layers. , 1984, Developmental biology.

[43]  I. W. Mclean,et al.  PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY , 1974, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[44]  R. Jennings,et al.  Alterations in renal cortex following ischemic injury. I. PAH uptake by slices of cortex after ischemia or autolysis. , 1971, Laboratory investigation; a journal of technical methods and pathology.

[45]  W. Clapp Development and gross anatomy of the kidney , 1944 .