Glycopatterns of Urinary Protein as New Potential Diagnosis Indicators for Diabetic Nephropathy

Author:

Zhu Hanyu1,Liu Moyan2,Yu Hanjie3ORCID,Liu Xiawei3ORCID,Zhong Yaogang3,Shu Jian3,Fu Xinle3,Cai Guangyan1,Chen Xiangmei1,Geng Wenjia1,Yang Xiaoli1,Wu Minghui1,Li Zheng3ORCID,Zhang Dong1ORCID

Affiliation:

1. Department of Nephrology, Chinese PLA General Hospital, Chinese PLA Institute of Nephrology, State Key Laboratory of Kidney Diseases, National Clinical Research Center of Kidney Diseases, Beijing Key Laboratory of Kidney Disease, Beijing, China

2. Department of Nephrology, General Hospital of Jinan Military Command, Jinan, China

3. Laboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi’an, China

Abstract

Diabetic nephropathy is a major cause of chronic kidney disease and end-stage kidney disease. However, so little is known about alterations of the glycopatterns in urine with the development of diabetic nephropathy. Presently, we interrogated glycopatterns in urine specimens using a lectin microarray. The results showed that expression levels of Siaα2-6Gal/GalNAc recognized by SNA exhibited significantly increased tendency with the development of diabetic nephropathy; moreover, SNA blotting indicated glycoproteins (90 kDa, 70 kDa, and 40 kDa) in urine may contribute to this alteration. Furthermore, the glycopatterns of(GlcNAc)2–4recognized by STL exhibited difference between diabetic and nondiabetic nephropathy. The results of urinary protein microarray fabricated by another 48 urine specimens also indicated(GlcNAc)2–4is a potential indictor to differentiate the patients with diabetic nephropathy from nondiabetic nephropathy. Furtherly, STL blotting showed that the 50 kDa glycoproteins were correlated with this alteration. In conclusion, our data provide pivotal information to monitor the development of diabetic nephropathy and distinguish between diabetic nephropathy and nondiabetic renal disease based on precise alterations of glycopatterns in urinary proteins, but further studies are needed in this regard.

Funder

National Key Research and Development Program

Publisher

Hindawi Limited

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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