Evidence map›Paper›PMID 27632702›Full record

ArticleAging2016

SATB2-Nanog axis links age-related intrinsic changes of mesenchymal stem cells from craniofacial bone.

Peipei Zhou, Geng Wu, Ping Zhang, Rongyao Xu, Jie Ge, Yu Fu, Yuchao Zhang, Yifei Du, Jinhai Ye, Jie Cheng and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 27 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

11 authors at 1 institution in 1 country.

Peipei ZhouJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Geng WuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Ping ZhangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Rongyao XuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Jie GeJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Yu FuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Yuchao ZhangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Yifei DuJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Jinhai YeJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Jie ChengJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Hongbing JiangJiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, 210029 Nanjing, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone mesenchymal stem cells (BMSCs) senescence contributes to age-related bone loss. The alveolar bone in jaws originates from neural crest cells and possesses significant site- and age-related properties. However, such intrinsic characteristics of BMSCs from alveolar bone (AB-BMSCs) and the underlying regulatory mechanisms still remain unknown. Here, we found that the expression of special AT-rich binding protein 2 (SATB2) in human AB-BMSCs significantly decreased with aging. SATB2 knockdown on AB-BMSCs from young donors displayed these aging-related phenotypes in vitro. Meanwhile, enforced SATB2 overexpression could rejuvenate AB-BMSCs from older donors. Importantly, satb2 gene- modified BMSCs therapy could prevent the alveolar bone loss during the aging of rats. Mechanistically, the stemness regulator Nanog was identified as the direct transcriptional target of SATB2 in BMSCs and functioned as a downstream mediator of SATB2. Collectively, our data reveal that SATB2 in AB-BMSCs associates with their age-related properties, and prevents AB-BMSCs senescence via maintaining Nanog expression. These findings highlight the translational potential of transcriptional factor-based cellular reprogramming for anti-aging therapy.

Indexed as

Age FactorsAgingAnimalsBone and BonesGene ExpressionHumansMatrix Attachment Region Binding ProteinsMesenchymal Stem CellsNanog Homeobox ProteinOsteogenesisRatsTranscription FactorsMatrix Attachment Region Binding ProteinsNanog Homeobox ProteinSATB2 protein, humanTranscription Factorsagingbone lossbone mesenchymal stem cellscytotherapypluripotency

Identifiers

PMID27632702
PMCPMC5076449
OpenAlexW2520340320

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.