Evidence map›Paper›PMID 34643893›Full record

ArticleGenes & genomics2022

Subproteomic profiling from renal cortices in OLETF rats reveals mutations of multiple novel genes in diabetic nephropathy.

Zhiguo Li, Hong Shen, Yeqiang Liu, Xuefeng Zhou, Meihua Yan, Hailan He, Tingting Zhao, Haojun Zhang, Ping Li

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In one paragraph

Article in Genes & genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 49% of its field
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Zhiguo LiDepartment of School of Public Health, International Science and Technology Cooperation Base of Geriatric Medicine, The Hebei Key Lab for Organ Fibrosis, The Hebei Key Lab for chronic disease, North China University of Science and Technology, Tangshan, 063000, China.
Hong ShenDepartment of Modern Technology and Education, North China University of Science and Technology, Tangshan, 063000, China.
Yeqiang LiuDepartment of Endocrinology, Kailuan General Hospital, North China University of Science and Technology, Tangshan, 063000, China.
Xuefeng ZhouBeijing Key Lab for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Science, China-Japan Friendship Hospital, 2 Yinghua East Road, Chaoyang District, Beijing, 100029, People's Republic of China.
Meihua YanBeijing Key Lab for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Science, China-Japan Friendship Hospital, 2 Yinghua East Road, Chaoyang District, Beijing, 100029, People's Republic of China.
Hailan HeSchool of Graduate Studies, North China University of Science and Technology, Tangshan, 063000, China.
Tingting ZhaoBeijing Key Lab for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Science, China-Japan Friendship Hospital, 2 Yinghua East Road, Chaoyang District, Beijing, 100029, People's Republic of China.
Haojun ZhangBeijing Key Lab for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Science, China-Japan Friendship Hospital, 2 Yinghua East Road, Chaoyang District, Beijing, 100029, People's Republic of China. zhhj529@163.com.ORCID 0000-0002-5993-5260
Ping LiBeijing Key Lab for Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Science, China-Japan Friendship Hospital, 2 Yinghua East Road, Chaoyang District, Beijing, 100029, People's Republic of China. lp8675@163.com.
China-Japan Friendship Hospital · CNNorth China University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic nephropathy (DN) is a serious threat to human health, but its pathogenesis is not fully understood. Otsuka Long-Evans Tokushima Fatty (OLETF) rats are very similar to human DN in many aspects such as pathological changes and processes, and are deemed to be an ideal rodent model.

objectiveThis study was aimed to explore the pathogenesis of DN by analyzing the protein expression profile from renal cortices in OLETF rats.

methodsThirty-six-week-old diabetic OLETF rats and normal control Long-Evans Tokushima Otsuka (LETO) rats were nephrectomized, and the renal cortices were isolated. The proteins were separated by soluble and insoluble high-resolution subproteomics methods for the analysis and identification of differential proteins.

resultsThirty-six differentially expressed proteins were found. Among them, 11 proteins had different isoelectric points and molecular weights between OLETF and LETO rats. Further sequencing identified point mutations in genes encoding eight of these proteins, which are involved in many biological processes closely related to DN, including oxidative stress and inflammation. Five of these eight proteins have not been reported in DN.

conclusionThis study reveals mutations of multiple novel genes in diabetic OLETF rats, providing some new potential targets for the pathogenesis of DN and helping to better understand the pathogenesis of DN.

Indexed as

MutationAmino Acid SequenceAnimalsDiabetes Mellitus, Type 2Diabetic NephropathiesDisease Models, AnimalElectrophoresis, Gel, Two-DimensionalHumansKidneyMaleProteomeProteomicsRatsRats, Inbred OLETFSequence Analysis, DNASequence Homology, Amino AcidProteomeDiabetic nephropathyGene mutationOLETF ratProteomicsTwo-dimensional difference gel electrophoresis

Identifiers

PMID34643893
OpenAlexW3206812151

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