Evidence map›Paper›PMID 32080264›Full record

ArticleScientific reports2020

NIPA2 regulates osteoblast function by modulating mitophagy in type 2 diabetes osteoporosis.

Wei Zhao, Weilin Zhang, Hongdong Ma, Maowei Yang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% of its field
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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Wei Zhao *Department of Orthopedics, the Fourth Hospital of China Medical University, Shenyang, Liaoning, China.ORCID http://orcid.org/0000-0002-7196-1357
Weilin Zhang *Department of Orthopedics, the Fourth Hospital of China Medical University, Shenyang, Liaoning, China.
Hongdong MaDepartment of Orthopedics, the First Hospital of China Medical University, Shenyang, Liaoning, China.
Maowei YangDepartment of Orthopedics, the First Hospital of China Medical University, Shenyang, Liaoning, China. mwyang@cmu.edu.cn.ORCID http://orcid.org/0000-0003-4304-7661
First Hospital of China Medical University · CNFourth Affiliated Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The highly selective magnesium transporter non-imprinted in Prader-Willi/Angelman syndrome region protein 2 (NIPA2) has recently been associated with the development and progression of type 2 diabetes osteoporosis, but the mechanisms involved are still poorly understood. Because mitophagy is involved in the pathology of type 2 diabetes osteoporosis, the present study aimed to explore the relationship among NIPA2, mitophagy and osteoblast osteogenic capacity. NIPA2 expression was reduced in C57BKS background db/db mice and in vitro models of type 2 diabetes osteoporosis, and the activation of mitophagy in primary culture osteoblast-derived from db/db mice and in high glucose-treated human fetal osteoblastic cells (hFOB1.19) was observed. Knockdown, overexpression of NIPA2 and pharmacological inhibition of peroxisome proliferator-activated receptor γ coactivator 1-α (PGC-1α) showed that NIPA2 increased osteoblast function, which was likely regulated by PTEN induced kinase 1 (PINK1)/E3 ubiquitin ligase PARK2 (Parkin)-mediated mitophagy via the PGC-1α/forkhead box O3a(FoxO3a)/mitochondrial membrane potential (MMP) pathway. Furthermore, the negative effect of mitophagy on osteoblast function was confirmed by pharmacological regulation of mitophagy and knockdown of Parkin. Taken together, these results suggest that NIPA2 positively regulates the osteogenic capacity of osteoblasts via the mitophagy pathway in type 2 diabetes.

Indexed as

MitophagyAlkaline PhosphataseAnimalsBone and BonesCation Transport ProteinsCells, CulturedCollagen Type ICore Binding Factor Alpha 1 SubunitDiabetes Mellitus, Type 2Down-RegulationForkhead Box Protein O3GlucoseHumansMagnesiumMaleMice, Inbred C57BLAlkaline PhosphataseCation Transport ProteinsCollagen Type ICore Binding Factor Alpha 1 SubunitForkhead Box Protein O3FoxO3 protein, mouseGlucoseMagnesiumNIPA2 protein, mouseOsteocalcinOsteoprotegerinPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPpargc1a protein, mouseRNA, Messenger

Identifiers

PMID32080264
PMCPMC7033235
OpenAlexW3008653976

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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 OpenQuestion graph.