Evidence map›Paper›PMID 30005867›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

Therapeutic Effects of Adipose Stem Cells from Diabetic Mice for the Treatment of Type 2 Diabetes.

Mengmeng Wang, Lili Song, Charlie Strange, Xiao Dong, Hongjun Wang

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
12.1field-weighted citation impact, top 1% 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

67 citing papers in PubMed, 147 citations in OpenAlex.

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  15. Comprehensive Review on Fruit ofMolecules (Basel, Switzerland) · 2024
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7 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 2 countries.

Mengmeng WangCollege of Life Science, Qingdao Agricultural University, Qingdao, Shandong 266109, China.
Lili SongChina Agricultural University, Beijng 100094, China.
Charlie StrangeDepartment of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Xiao DongCollege of Life Science, Qingdao Agricultural University, Qingdao, Shandong 266109, China. Electronic address: 1163155358@qq.com.
Hongjun WangDepartment of Surgery, Medical University of South Carolina, Charleston, SC 29425, USA. Electronic address: wangho@musc.edu.
Medical University of South Carolina · USQingdao Agricultural University · CNChina Agricultural University · CN

Funding

Alpha1 Anti-trypsin Enhances Islet Autograft SurvivalR01DK105183 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI WANG, HONGJUN · 2016 to 2020
$2.0M
NIDDK NIH HHS R01 DK105183
6 · The paper itself

Abstract

To assess the potential therapeutic effects of adipose tissue-derived mesenchymal stem cells (ASCs) for the treatment of type 2 diabetes (T2D), we compared the phenotype and functionality of ASCs isolated from high-fat diet and streptozotocin (STZ)-induced T2D and the leptin receptor-deficient (db/db) mice with cells from healthy C57BL/6 mice. ASCs from T2D or db/db mice showed similar expression patterns of cellular markers and abilities to differentiate into adipocytes, osteoblasts, and chondrocytes. However, the rate of proliferation was reduced. ASCs from db/db mice secreted less hepatocyte growth factor (HGF). T2D mice receiving a single intravenous injection of T2D or db/db ASCs showed increased insulin sensitivity, reduced inflammation and fat content in adipose tissue and the liver and increased pancreatic β cell mass through 5 weeks post-infusion. Our data show that, although ASCs from T2D or db/db mice had inferior proliferative capacity compared to cells from healthy controls, improved insulin sensitivity and less β cell death was seen in T2D mice receiving mesenchymal stem cell (MSC) therapy. This study offers evidence that ASCs from diabetic donors have the potential to be used for cell therapy in the treatment of insulin resistance and T2D.

Indexed as

Adipose TissueAnimalsCells, CulturedDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diet, High-FatDisease Models, AnimalInsulin ResistanceInsulin-Secreting CellsMaleMesenchymal Stem Cell TransplantationMiceMice, Inbred C57BLReceptors, LeptinStreptozocinleptin receptor, mouseReceptors, LeptinStreptozocinadipose stem cellscell therapydb/db miceinsulin resistancetype 2 diabetestype 2 diabetes mouse modelβ cell mass

Identifiers

PMID30005867
PMCPMC6094391
OpenAlexW2809112830

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.