Evidence map›Paper›PMID 31049797›Full record

ArticleJournal of molecular histology2019

Role of mTOR complex in IGF-1 induced neural differentiation of DPSCs.

Dan Huang, Shuling Shen, Ming Cai, Lin Jin, Jun Lu, Ke Xu, Jinlong Zhang, Guijuan Feng, Yingzi Hu, Ke Zheng and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular histology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 19 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 5 institutions in 1 country.

Dan HuangDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Shuling ShenDepartment of Stomatology, Affiliated Hospital of Jiangsu University, Zhenjiang, 212000, China.
Ming CaiGeneral Surgery Department, The Second Affiliated Hospital of Nantong University, Nantong, 226001, China.
Lin JinDepartment of Endodontics, Nantong Stomatological Hospital, Nantong, 226001, China.
Jun LuDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Ke XuDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Jinlong ZhangDepartment of Spine Surgery, The Second Affiliated Hospital of Nantong University, Nantong, 226001, China.
Guijuan FengDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China.
Yingzi HuMedical College of Nantong University, Nantong, 226001, China.
Ke ZhengDepartment of Stomatology, Wuxi No.2 People's Hospital, Wuxi, 214000, China. zhengke1000@126.com.
Xingmei FengDepartment of Stomatology, Affiliated Hospital of Nantong University, Nantong, 226001, China. fengxingmeint@126.com.
Affiliated Hospital of Nantong University · CNNantong University · CNAffiliated Hospital of Jiangsu University · CNNantong Tumor Hospital · CNWuxi No.2 People's Hospital · CN

Funding

Chinese National Natural Science Foundation of China Grant NO. 81500809Chinese National Natural Science Foundation of China Grant NO. 81501076
6 · The paper itself

Abstract

Recent studies have demonstrated that IGF-1 modulates the pluripotent differentiation of dental pulp stem cells (DPSCs). Although mTOR pathway activation has been showed as responsible for IGF-1 induced pluripotent differentiation, the mechanism that the IGF-1-mTOR pathway induces the neural differentiation of DPSCs is still unclear. In our research, we have demonstrated that 0-10 ng/mL IGF-1 had no obvious effect on the proliferation of DPSCs, but IGF-1 nonetheless enhances the neural differentiation of DPSCs in a dose-dependent manner. Simultaneously, we found that phosphorylated mTOR was up-regulated, which indicated the involvement of mTOR in the process. Rapamycin, an inhibitor of mTOR activity, can reverse the effect of DPSCs stimulated by IGF-1. Next, we studied the role of mTORC1 and mTORC2, two known mTOR complexes, in the neural differentiation of DPSCs. We found that inhibition of mTORC1 can severely restricts the neural differentiation of DPSCs. However, inhibition of mTORC2 has the opposite effect. This latter effect disappears when both rictor and mTOR are inhibited, showing that the mTORC2 effect is mTORC1 dependent. This study has expanded the role of mTOR in DPSCs neural differentiation regulated by IGF-1.

Indexed as

AdolescentAdultCell DifferentiationCell ProliferationDental PulpFemaleHumansInsulin-Like Growth Factor IMaleMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2PhosphorylationRecombinant ProteinsSignal TransductionSirolimusStem CellsIGF1 protein, humanInsulin-Like Growth Factor ImecaserminMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MTOR protein, humanRecombinant ProteinsSirolimusTOR Serine-Threonine KinasesDental pulp stem cells (DPSCs)Insulin-like growth factor 1 (IGF-1)mTOR signalingNeural differentiation

Identifiers

PMID31049797
OpenAlexW2942659432

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.