Skip to main content
Top
Published in: International Urology and Nephrology 2/2013

01-04-2013 | Nephrology - Original Paper

Mycophenolic acid reverses IgA1 aberrant glycosylation through up-regulating Cosmc expression in IgA nephropathy

Authors: Linshen Xie, Chunyu Tan, Junming Fan, Ping Fu, Yi Tang, Ye Tao, Wei Qin

Published in: International Urology and Nephrology | Issue 2/2013

Login to get access

Abstract

Objective

Impaired core I β3-Gal-T-specific molecular chaperone (Cosmc) expression-caused IgA1 aberrant O-glycosylation is one of the main pathogeneses of IgA nephropathy (IgAN).This study tried to elucidate whether mycophenolic acid (MPA) could up-regulate Cosmc expression of peripheral lymphocytes in IgAN patients and reverse the dys-O-glycosylation.

Method

Peripheral lymphocytes of eighteen IgAN patients and twelve normal controls were isolated and cultured for 3–7 days with or without lipopolysaccharide (LPS) and MPA. Cosmc mRNA and protein expression levels were measured by real-time RT-PCR and western blot. IgA1 and O-glycosylation level were determined by enzyme-linked immunosorbent assay (ELISA) and VV lectin-binding test. Correlation analysis was performed between Cosmc expression levels and IgA1 O-glycosylation level.

Results

Cosmc mRNA expression and IgA1 O-glycosylation level in IgAN patients were significantly lower than normal controls. Treatment of LPS could obviously inhibit the Cosmc expression and increase the IgA1 secretion in peripheral lymphocytes of IgAN patients, which resulted in a significantly increase in IgA1 aberrant glycosylation level. Addition of MPA could significantly increase the Cosmc expression level along with a decrease in IgA1 secretion, leading to a reverse of aberrant glycosylation. A significant positive correlation between the Cosmc expression and IgA1 O-glycosylation level was noticed.

Conclusion

MPA can up-regulate the Cosmc expression and reverse the IgA1 aberrant O-glycosylation level in peripheral lymphocytes of IgAN patients, which might be the underlying mechanism of mycophenolate mofetil (MMF) therapy used in treating IgAN.
Literature
2.
go back to reference Giannakakis K, Feriozzi S, Perez M et al (2007) Aberrantly glycosylated IgA1 in glomerular immune deposits of IgA nephropathy. J Am Soc Nephrol 18(12):3139–3146PubMedCrossRef Giannakakis K, Feriozzi S, Perez M et al (2007) Aberrantly glycosylated IgA1 in glomerular immune deposits of IgA nephropathy. J Am Soc Nephrol 18(12):3139–3146PubMedCrossRef
3.
go back to reference Narita I, Gejyo F (2008) Pathogenetic significance of aberrant glycosylation of IgA1 in IgA nephropathy. Clin Exp Nephrol 12(5):332–338PubMedCrossRef Narita I, Gejyo F (2008) Pathogenetic significance of aberrant glycosylation of IgA1 in IgA nephropathy. Clin Exp Nephrol 12(5):332–338PubMedCrossRef
4.
go back to reference Allen AC, Topham PS, Harper SJ et al (1997) Leucocyte beta 1,3 galactosyltransferase activity in IgA nephropathy. Nephrol Dial Transplant 12(4):701–706PubMedCrossRef Allen AC, Topham PS, Harper SJ et al (1997) Leucocyte beta 1,3 galactosyltransferase activity in IgA nephropathy. Nephrol Dial Transplant 12(4):701–706PubMedCrossRef
5.
go back to reference Qin W, Zhou Q, Yang LC et al (2005) Peripheral B lymphocyte beta1, 3-galactosyltransferase and chaperone expression in immunoglobulin A nephropathy. J Intern Med 258(5):467–477PubMedCrossRef Qin W, Zhou Q, Yang LC et al (2005) Peripheral B lymphocyte beta1, 3-galactosyltransferase and chaperone expression in immunoglobulin A nephropathy. J Intern Med 258(5):467–477PubMedCrossRef
6.
go back to reference Qin W, Zhong X, Fan JM et al (2008) External suppression causes the low expression of the Cosmc gene in IgA nephropathy. Nephrol Dial Transplant 23(5):1608–1614PubMedCrossRef Qin W, Zhong X, Fan JM et al (2008) External suppression causes the low expression of the Cosmc gene in IgA nephropathy. Nephrol Dial Transplant 23(5):1608–1614PubMedCrossRef
7.
go back to reference Xie LS, Qin W, Fan JM et al (2011) The role of C1GALT1C1 in lipopolysaccharide-induced IgA1 aberrant O-glycosylation in IgA nephropathy. Clin Invest Med 33(1):E5–E13 Xie LS, Qin W, Fan JM et al (2011) The role of C1GALT1C1 in lipopolysaccharide-induced IgA1 aberrant O-glycosylation in IgA nephropathy. Clin Invest Med 33(1):E5–E13
8.
go back to reference Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29(9):e45PubMedCrossRef Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29(9):e45PubMedCrossRef
9.
go back to reference Moriyama T, Nakayama K, Iwasaki C et al (2012) Severity of nephrotic IgA nephropathy according to the Oxford classification. Int Urol Nephrol 44(4):1177–1184PubMedCrossRef Moriyama T, Nakayama K, Iwasaki C et al (2012) Severity of nephrotic IgA nephropathy according to the Oxford classification. Int Urol Nephrol 44(4):1177–1184PubMedCrossRef
10.
go back to reference Zhu C, Mertens PR (2012) IgA nephropathy and oxidative stress: news on clinically evaluated biomarkers hits the stage. Int Urol Nephrol 44(4):1277–1280PubMedCrossRef Zhu C, Mertens PR (2012) IgA nephropathy and oxidative stress: news on clinically evaluated biomarkers hits the stage. Int Urol Nephrol 44(4):1277–1280PubMedCrossRef
11.
go back to reference Xu LX, Zhao MH (2005) Aberrantly glycosylated serum IgA1 are closely associated with pathologic phenotypes of IgA nephropathy. Kidney Int 68(1):167–172PubMedCrossRef Xu LX, Zhao MH (2005) Aberrantly glycosylated serum IgA1 are closely associated with pathologic phenotypes of IgA nephropathy. Kidney Int 68(1):167–172PubMedCrossRef
12.
go back to reference Ju T, Cummings RD (2002) A unique molecular chaperone Cosmc required for activity of the mammalian core 1 beta 3-galactosyltransferase. Proc Natl Acad Sci USA 99(26):16613–16618PubMedCrossRef Ju T, Cummings RD (2002) A unique molecular chaperone Cosmc required for activity of the mammalian core 1 beta 3-galactosyltransferase. Proc Natl Acad Sci USA 99(26):16613–16618PubMedCrossRef
13.
go back to reference Felner KM, Dinter A, Cartron JP et al (1998) Repressed beta-1,3-galactosyltransferase in the Tn syndrome. Biochim Biophys Acta 1406(1):115–125PubMedCrossRef Felner KM, Dinter A, Cartron JP et al (1998) Repressed beta-1,3-galactosyltransferase in the Tn syndrome. Biochim Biophys Acta 1406(1):115–125PubMedCrossRef
14.
go back to reference Tang SC, Tang AW, Wong SS et al (2010) Long-term study of mycophenolate mofetil treatment in IgA nephropathy. Kidney Int. 77(6): 543–549 Tang SC, Tang AW, Wong SS et al (2010) Long-term study of mycophenolate mofetil treatment in IgA nephropathy. Kidney Int. 77(6): 543–549
15.
go back to reference Tang S, Leung JC, Chan LY et al (2005) Mycophenolate mofetil alleviates persistent proteinuria in IgA nephropathy. Kidney Int 68(2):802–812PubMedCrossRef Tang S, Leung JC, Chan LY et al (2005) Mycophenolate mofetil alleviates persistent proteinuria in IgA nephropathy. Kidney Int 68(2):802–812PubMedCrossRef
16.
go back to reference Xu G, Tu W, Jiang D et al (2009) Mycophenolate mofetil treatment for IgA nephropathy: a meta-analysis. Am J Nephrol 29(5):362–367PubMedCrossRef Xu G, Tu W, Jiang D et al (2009) Mycophenolate mofetil treatment for IgA nephropathy: a meta-analysis. Am J Nephrol 29(5):362–367PubMedCrossRef
17.
18.
go back to reference Inoue TH, Sugiyama M, Kitagawa et al (2011) Abnormalities of glycogenes in tonsillar lymphocytes in IgA nephropathy. Adv Otorhinolaryngol 72:71–74 Inoue TH, Sugiyama M, Kitagawa et al (2011) Abnormalities of glycogenes in tonsillar lymphocytes in IgA nephropathy. Adv Otorhinolaryngol 72:71–74
Metadata
Title
Mycophenolic acid reverses IgA1 aberrant glycosylation through up-regulating Cosmc expression in IgA nephropathy
Authors
Linshen Xie
Chunyu Tan
Junming Fan
Ping Fu
Yi Tang
Ye Tao
Wei Qin
Publication date
01-04-2013
Publisher
Springer Netherlands
Published in
International Urology and Nephrology / Issue 2/2013
Print ISSN: 0301-1623
Electronic ISSN: 1573-2584
DOI
https://doi.org/10.1007/s11255-012-0313-y

Other articles of this Issue 2/2013

International Urology and Nephrology 2/2013 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine