Mukhin Role of podocin gene mutations in assessment of resistance of proteinuric nephritis to standard immunosupressive therapy
- Autores: Girina S.S1, Pulin A.A1, Kornienko V.Y.1, Pinelis V.G1, Tcygin A.N1, Asanov A.Y.1, Kozlovskaya L.V1, Fomin V.V1, N.A N.A1
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Afiliações:
- Edição: Nº 4 (2014)
- Páginas: 4-10
- Seção: Articles
- URL: https://journals.eco-vector.com/2075-3594/article/view/262542
- ID: 262542
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Sobre autores
S. Girina
Email: girina_ss@mail.ru
A. Pulin
V. Kornienko
V. Pinelis
A. Tcygin
A. Asanov
L. Kozlovskaya
V. Fomin
N. N.A
Bibliografia
- Brahm M., Brammer M., Balsløv J.T. et al. Prognosis in glomerulonephritis. III. A longitudinal analysis of changes in serum creatinine and proteinuria during the course of disease: effect of immunosuppressive treatment. Report from Copenhagen Study Group of Renal Diseases // J Intern Med. - 1992. - Vol. 231(4). - P. 339-347.
- Ponticelli C. Membranous nephropathy // J Nephrol. - 2007. - Vol. 20. - P. 268-287.
- van Husen M., Kemper M.J. New therapies in steroid-sensitive and steroid-resistant idiopathic nephrotic syndrome // Pediatr Nephrol. - 2011. - Vol. 26(6). - P. 881-892.
- Carraro M., Caridi G., Bruschi M. et al. Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome // J Am Soc Nephrol. - 2002. - Vol. 13. - P. 1946-1952.
- Benoit G., Machuca E., Antignac C. Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations // Pediatr Nephrol. - 2010. - Vol. 25. - P. 1621-1632.
- Machuca E., Benoit G., Antignac C. Genetics of nephritic syndrome: connecting molecular genetics to podocyte physiology // Hum Mol Genet. - 2009. - Vol. 18. - P. R185-R194.
- Diez-Sampedro A., Lenz O., Fornoni A. Podocytopathy in diabetes: a metabolic and endocrine disorder // Am J Kidney Dis. - 2011. - Vol. 58(4). - P. 637-646.
- Yuan H., Takeuchi E., Taylor G.A. et al. Nephrin dissociates from actin, and its expression is reduced in early experimental membranous nephropathy // J Am Soc Nephrol. - 2002. - Vol. 13. - P. 946-956.
- Shea-Simonds P., Cairns T.D., Roufosse C. et al. Lupus podocytopathy // Rheumatology (Oxford). - 2009. - Vol. 48(12). - P. 1616-1618.
- Чеботарева Н.В., Бобкова И.Н., Козловская Л.В. Нефринурия как показатель структурно-функциональных нарушений гломерулярного фильтра у больных протеинурическими формами нефрита // Клиническая нефрология. - 2010. - № 4. - С. 51-55.
- Корниенко В.Ю., Алябьева Н.М., Вашурина Т.В. и др. Результаты секвенирования гена NPHS2 у детей со стероидрезистентным синдромом // Вопросы диагностики в педиатрии. - 2011. - № 3(5). - С. 26-30.
- Игнатова М.С. Дизэмбриогенез органов мочевой системы и нефропатии // Клиническая нефрология. - 2011. - № 4. - С. 10-15.
- Lowik M., Levtchenko E., Westra D. et al. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerrosis // Nephrol Dial Transplant. - 2008. - Vol. 23. - P. 3146-3151.
- Laakkonen H., Lönnqvist T., Uusimaa J. et al. Muscular dystonia and athetosis in six patients with congenital nephritic syndrome of the Finnish type (NPHS1) // Pediatr Nephrol. - 2006. - Vol. 21. - P. 182-189.
- Koziell A., Grech V., Hussain S. et al. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephritic syndrome advocate a functional inter-relationship in glomerular filtration // Hum Mol Genet. - 2002. - Vol. 11. - P. 379-388.
- Hinkes B., Vlangos C., Heeringa S. et al. Specific Podocin Mutations Correlate With Age of Onset in Steroid-Resistant Nephrotic Syndrome J Am Soc Nephrol. 2008; 19: 365-371.
- Полтавец Н.В., Приходина Л.С., Галеева Н.М. и др. Генетические аспекты наследственной формы нефротического синдрома // Медицинская генетика. - 2006. - № 5(9). - С. 51.
- Löwik M.M., Groenen P.J., Levtchenko E.N. et al. Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis - a review // Eur J Pediatr. - 2009. - Vol. 168. - P. 1291-1304.
- Huber T.B., Kwoh C., Wu H. et al. Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin // J Clin Invest. - 2006. - Vol. 116. - P. 1337-1345.
- Kim J.M., Wu H., Green G. et al. CD2-associatedprotein haplo-insufficiency is linked to glomerular disease susceptibility // Science. - 2003. - Vol. 300. - P. 1298-1300.
- Чеботарева Н.В., Бобкова И.Н., Козловская Л.В. и др. Значение нарушений механизмов самозащиты почки при хроническом гломерулонефрите // Клиническая нефрология. - 2011. - № 1. - С. 8-14.
- Wada T., Pippin J.W., Nangaku M. et al. Dexamethasone’s prosurvival benefits in podocytes require extracellular signalregulated kinase phosphorylation // Nephron Exp Nephrol. - 2008. - Vol. 109. - P. e8-e19.
- Hsu H.H., Hoffmann S., Endlich N. et al. Mechanism of angiotensin signaling on cytoskeleton of podocytes // J Mol Med. - 2007. - Vol. 86. - P. 1379- 1394.
- Wang L., Flannery P.J., Rosenberg P.B. et al. Gq-dependent signaling upregulates COX2 in glomerular podocytes // J Am Soc Nephrol. - 2008. - Vol. 19. - P. 2108-2118.
- Nakajo A., Khoshnoodi J., Takenaka H. et al. Mizoribine corrects defective nephrin biogenesis by restoring intracellular energy balance // J Am Soc Nephrol. - 2007. - Vol. 18. - P. 2554-2564.
- Faul C., Donelly M., Merscher-Gomez S. et al. The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A // Nature Medicine. - 2008. - Vol. 14. - P. 931-938.
- Mathieson P.W. Proteinuria and immunity an overstated relationship?// N Engl J Med. - 2008. - Vol. 359. - P. 2492-2494.
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