Evidence map›Paper›PMID 32588068›Full record

ArticleDiabetologia2020

MYDGF attenuates podocyte injury and proteinuria by activating Akt/BAD signal pathway in mice with diabetic kidney disease.

Mingjuan He, Yixiang Li, Li Wang, Bei Guo, Wen Mei, Biao Zhu, Jiajia Zhang, Yan Ding, Biying Meng, Liming Zhang and 5 more

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Article in Diabetologia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed.

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  14. Targeting Grancalcin Accelerates Wound Healing by Improving Angiogenesis in Diabetes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Mingjuan HeThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Yixiang LiDepartment of Hematology and Medical Oncology, School of Medicine, Emory University, Atlanta, GA, USA.
Li WangThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Bei GuoThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Wen MeiDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Biao ZhuDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Jiajia ZhangDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Yan DingThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Biying MengThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Liming ZhangThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China.
Lin XiangDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Jing DongDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Min LiuDepartment of Endocrinology, General Hospital of Central Theater Command, Wuluo Road 627, Wuhan, 430070, Hubei Province, China.
Lingwei XiangICF, 2635 Century Pkwy NE Unit 1000, Atlanta, GA, 30345, USA. Ynp8@cdc.gov.
Guangda XiangThe First School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong Province, China. Guangda64@hotmail.com.ORCID 0000-0002-6044-2308

Funding

National Key Research and Development Program of China 2016YFC1305601Research Project of Health Commission of Hubei Province WJ2017H0031the National Natural Science Foundation of China NSFC 81870573
6 · The paper itself

Abstract

aims/hypothesisMyeloid-derived growth factor (MYDGF), mainly secreted by bone marrow-derived cells, has been known to promote glucagon-like peptide-1 production and improve glucose/lipid metabolism in mouse models of diabetes, but little is known about the functions of MYDGF in diabetic kidney disease (DKD). Here, we investigated whether MYDGF can prevent the progression of DKD.

methodsIn vivo experiments, both loss- and gain-of-function strategies were used to evaluate the effect of MYDGF on albuminuria and pathological glomerular lesions. We used streptozotocin-treated Mydgf knockout and wild-type mice on high fat diets to induce a model of DKD. Then, albuminuria, glomerular lesions and podocyte injury were evaluated in Mydgf knockout and wild-type DKD mice treated with adeno-associated virus-mediated Mydgf gene transfer. In vitro and ex vivo experiments, the expression of slit diaphragm protein nephrin and podocyte apoptosis were evaluated in conditionally immortalised mouse podocytes and isolated glomeruli from non-diabetic wild-type mice treated with recombinant MYDGF.

resultsMYDGF deficiency caused more severe podocyte injury in DKD mice, including the disruption of slit diaphragm proteins (nephrin and podocin) and an increase in desmin expression and podocyte apoptosis, and subsequently caused more severe glomerular injury and increased albuminuria by 39.6% compared with those of wild-type DKD mice (p < 0.01). Inversely, MYDGF replenishment attenuated podocyte and glomerular injury in both wild-type and Mydgf knockout DKD mice and then decreased albuminuria by 36.7% in wild-type DKD mice (p < 0.01) and 34.9% in Mydgf knockout DKD mice (p < 0.01). Moreover, recombinant MYDGF preserved nephrin expression and inhibited podocyte apoptosis in vitro and ex vivo. Mechanistically, the renoprotection of MYDGF was attributed to the activation of the Akt/Bcl-2-associated death promoter (BAD) pathway. CONCLUSIONS/

interpretationThe study demonstrates that MYDGF protects podocytes from injury and prevents the progression of DKD, providing a novel strategy for the treatment of DKD. Graphical abstract.

Indexed as

AlbuminuriaAnimalsApoptosisbcl-Associated Death ProteinDesminDiabetes Mellitus, ExperimentalDiabetic NephropathiesDiet, High-FatGene Transfer TechniquesInterleukinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, KnockoutPodocytesProto-Oncogene Proteins c-aktbcl-Associated Death ProteinDesminInterleukinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMydgf protein, mousenephrinNPHS2 proteinProto-Oncogene Proteins c-aktDiabetic kidney diseaseMyeloid-derived growth factorPodocyte injury

Identifiers

What Socratic holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.