Urinary calcium oxalate crystal growth inhibitors.

Calcium stones occur because renal tubular fluid and urine are supersaturated with respect to calcium oxalate and phosphate. The process of stone formation includes crystal nucleation, growth, aggregation, and attachment to renal epithelia. Urine contains macromolecules that modify these processes and may protect against stone formation. Attention has focused especially on inhibitors of crystal growth, and several have been isolated from urine, including nephrocalcin, an acidic phosphorylated glycoprotein that contains several residues of gamma-carboxyglutamic acid per molecule; osteopontin (uropontin), a phosphorylated glycoprotein also found in bone matrix; uronic acid-rich protein, which contains a covalently bound glycosaminoglycan residue; and several others. Abnormalities in structure and/or function have been detected in some of these proteins in stone formers' urine. However, the overall ability of urinary macromolecules to inhibit calcium oxalate crystal growth is often normal in stone formers. Recently, attention has been focused on the ability of these molecules to inhibit other stages in stone formation. Nephrocalcin can inhibit crystal nucleation, for example, and both nephrocalcin and Tamm-Horsfall protein inhibit crystal aggregation. Nephrocalcin and Tamm-Horsfall protein from stone formers are less active in preventing aggregation, and under some conditions, Tamm-Horsfall protein may promote the formation of crystal aggregates, especially in the presence of high concentrations of calcium. The structural abnormalities responsible for impaired inhibitory activity are not completely understood.

[1]  E. Worcester,et al.  Expression of osteopontin, a urinary inhibitor of stone mineral crystal growth, in rat kidney. , 1995, Kidney international.

[2]  P. Jaeger,et al.  Citrate and calcium effects on Tamm-Horsfall glycoprotein as a modifier of calcium oxalate crystal aggregation. , 1993, The American journal of physiology.

[3]  R. Ryall,et al.  Immunohistochemical distribution and quantification of crystal matrix protein. , 1993, Kidney international.

[4]  P. Waterhouse,et al.  Heterogeneity of osteopontin expression among nephrons in mouse kidneys and enhanced expression in sclerotic glomeruli. , 1993, Laboratory investigation; a journal of technical methods and pathology.

[5]  J. Lieske,et al.  Regulation of renal epithelial cell endocytosis of calcium oxalate monohydrate crystals. , 1993, The American journal of physiology.

[6]  M. Daudon,et al.  Molecular characteristics of uronic-acid-rich protein, a strong inhibitor of calcium oxalate crystallization in vitro. , 1993, Biochemical and biophysical research communications.

[7]  J. Davison,et al.  Increases in Urinary Inhibitor Activity and Excretion of an Inhibitor of Crystalluria in Pregnancy: A Defense Against the Hypercalciuria of Normal Gestation , 1993 .

[8]  F. Coe,et al.  The pathogenesis and treatment of kidney stones. , 1992, The New England journal of medicine.

[9]  E. Manseau,et al.  Expression and distribution of osteopontin in human tissues: widespread association with luminal epithelial surfaces. , 1992, Molecular biology of the cell.

[10]  E. Worcester,et al.  The calcium oxalate crystal growth inhibitor protein produced by mouse kidney cortical cells in culture is osteopontin , 1992, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[11]  E. Neilson,et al.  Inhibition of calcium oxalate crystal growth in vitro by uropontin: another member of the aspartic acid-rich protein superfamily. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[12]  F. Coe,et al.  Evidence that nephrocalcin and urine inhibit nucleation of calcium oxalate monohydrate crystals. , 1991, The American journal of physiology.

[13]  P. Chang,et al.  1 alpha,25-dihydroxyvitamin D3 stimulates synthesis and secretion of nonphosphorylated osteopontin (secreted phosphoprotein 1) in mouse JB6 epidermal cells. , 1991, Cancer research.

[14]  F. Coe,et al.  Inhibitors within the nephron. , 1991, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[15]  J. Parks,et al.  Molecular abnormality of Tamm-Horsfall glycoprotein in calcium oxalate nephrolithiasis. , 1991, The American journal of physiology.

[16]  A. Hesse,et al.  Significance of glycosaminoglycans for the formation of calcium oxalate stones. , 1991, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[17]  Y. Nakagawa,et al.  Isolation of nephrocalcin from kidney tissue of nine vertebrate species. , 1991, The American journal of physiology.

[18]  H. DeLuca,et al.  Identification of a DNA sequence responsible for binding of the 1,25-dihydroxyvitamin D3 receptor and 1,25-dihydroxyvitamin D3 enhancement of mouse secreted phosphoprotein 1 (SPP-1 or osteopontin) gene expression. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[19]  B. B. Mukherjee,et al.  Physiological properties and differential glycosylation of phosphorylated and nonphosphorylated forms of osteopontin secreted by normal rat kidney cells. , 1990, The Journal of biological chemistry.

[20]  Qi Zhang,et al.  Sulphation of secreted phosphoprotein I (SPPI, osteopontin) is associated with mineralized tissue formation. , 1989, Biochemical and biophysical research communications.

[21]  F. Coe,et al.  Elucidation of multiple forms of nephrocalcin by 31P‐NMR spectrometer , 1989, FEBS letters.

[22]  F. Coe,et al.  Inhibition of calcium oxalate monohydrate crystal aggregation by urine proteins. , 1989, The American journal of physiology.

[23]  A. Craig,et al.  Osteopontin, a transformation-associated cell adhesion phosphoprotein, is induced by 12-O-tetradecanoylphorbol 13-acetate in mouse epidermis. , 1989, The Journal of biological chemistry.

[24]  W. Butler,et al.  The nature and significance of osteopontin. , 1989, Connective tissue research.

[25]  F. Coe,et al.  Crystal adsorption and growth slowing by nephrocalcin, albumin, and Tamm-Horsfall protein. , 1988, The American journal of physiology.

[26]  G. Mandel,et al.  Specificity in calcium oxalate adherence to papillary epithelial cells in cultures. , 1988, The American journal of physiology.

[27]  M. Ploug,et al.  Carbohydrate as covalent crosslink in human inter‐α‐trypsin inhibitor: A novel plasma protein structure , 1988, FEBS letters.

[28]  Y. Nakagawa,et al.  Isolation from human calcium oxalate renal stones of nephrocalcin, a glycoprotein inhibitor of calcium oxalate crystal growth. Evidence that nephrocalcin from patients with calcium oxalate nephrolithiasis is deficient in gamma-carboxyglutamic acid. , 1987, The Journal of clinical investigation.

[29]  S. Ljunghall,et al.  Crystal inhibition: the effects of polyanions on calcium oxalate crystal growth. , 1986, Clinica chimica acta; international journal of clinical chemistry.

[30]  F. Coe,et al.  Urine glycoprotein crystal growth inhibitors. Evidence for a molecular abnormality in calcium oxalate nephrolithiasis. , 1985, The Journal of clinical investigation.

[31]  S. Weiner,et al.  Interactions between acidic proteins and crystals: stereochemical requirements in biomineralization. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[32]  E. Kaiser,et al.  Purification and characterization of the principal inhibitor of calcium oxalate monohydrate crystal growth in human urine. , 1983, The Journal of biological chemistry.

[33]  A. Wheeler,et al.  Control of calcium carbonate nucleation and crystal growth by soluble matrx of oyster shell. , 1981, Science.

[34]  R. Ryall,et al.  The effect of urine, pyrophosphate, citrate, magnesium and glycosaminoglycans on the growth and aggregation of calcium oxalate crystals in vitro. , 1981, Clinica chimica acta; international journal of clinical chemistry.

[35]  E. Kaiser,et al.  Purification and characterization of a calcium oxalate monohydrate crystal growth inhibitor from human kidney tissue culture medium. , 1981, The Journal of biological chemistry.

[36]  H. Fleisch Inhibitors and promoters of stone formation. , 1978, Kidney international.

[37]  B. Finlayson,et al.  The expectation of free and fixed particles in urinary stone disease. , 1978, Investigative urology.

[38]  C. Pak,et al.  Nucleation and growth of brushite and calcium oxalate in urine of stone-formers. , 1976, Metabolism: clinical and experimental.

[39]  M. Peacock,et al.  Calcium oxalate crystalluria and inhibitors of crystallization in recurrent renal stone-formers. , 1972, Clinical science.

[40]  E. G. McQueen,et al.  Factors determining the aggregation of urinary mucoprotein , 1966, Journal of clinical pathology.