Evidence map›Paper›PMID 31572220›Full record

ArticleFrontiers in physiology2019

Endocytic Trafficking of DMP1 and GRP78 Complex Facilitates Osteogenic Differentiation of Human Periodontal Ligament Stem Cells.

Annette Merkel, Yinghua Chen, Anne George

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Role of the GRP78-c-Src signaling pathway on osteoblast differentiation of periodontal ligament fibroblasts induced by cyclic mechanical stretch.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2024
    Article
  4. COVID-19, Obesity, and GRP78: Unraveling the Pathological Link.Journal of obesity & metabolic syndrome · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Dentistry journal · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Review
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

3 authors at 1 institution in 1 country.

Annette MerkelDepartment of Oral Biology, The University of Illinois at Chicago, Chicago, IL, United States.
Yinghua ChenDepartment of Oral Biology, The University of Illinois at Chicago, Chicago, IL, United States.
Anne GeorgeDepartment of Oral Biology, The University of Illinois at Chicago, Chicago, IL, United States.
University of Illinois Chicago · US

Funding

CHARACTERIZATION OF DMP1--DENTIN PHOSPHOPROTEINR01DE011657 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GEORGE, ANNE · 1996 to 2018
$5.2M
Characterization of DMP1 a dentin phosphoproteinR56DE011657 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GEORGE, ANNE · 2008 to 2008
$341k
Endoplasmic Chaperone GRP78 Interacts with DMP1 to Function in BiomineralizationF30DE027601 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MERKEL, ANNETTE C · 2018 to 2021
$204k
NIDCR NIH HHS F30 DE027601NIDCR NIH HHS R01 DE011657NIDCR NIH HHS R56 DE011657
6 · The paper itself

Abstract

Periodontal ligament contains periodontal ligament stem cells that maintain tissue homeostasis. Targeting hPDLSCs (human periodontal ligament cells) is a promising strategy for repair and regeneration of bone tissue destroyed by periodontal diseases. However, the mechanisms by which PDLSCs differentiate into osteoblasts to form a mineralized matrix is unclear. In this study, we demonstrate for the first time the molecular events that contribute to osteogenic differentiation of PDLSCs. Dentin matrix protein 1 (DMP1) and its receptor, Glucose regulated protein-78 (GRP78), are localized in the progenitor cells of the PDL. Our overall goal is to demonstrate the formation of DMP1-GRP78 complex at the plasma membrane and subsequent protein trafficking and nuclear localization to promote osteogenic differentiation. To study the internalization and routing of the complex, we mimic an

Indexed as

cell biologymatrix biologymineralized tissue/developmentmolecular biologyprotein expressionstem cells

Identifiers

PMID31572220
PMCPMC6751249
OpenAlexW2970289756

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.