Evidence map›Paper›PMID 27883077›Full record

ArticleScientific reports2016

TGF beta receptor II interacting protein-1, an intracellular protein has an extracellular role as a modulator of matrix mineralization.

Amsaveni Ramachandran, Sriram Ravindran, Chun-Chieh Huang, Anne George

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. The Role of Autophagy in the Mineralization Process of Bone and Dentin.International journal of molecular sciences · 2025
    Review
  2. Review
  3. DMP1-mediated transformation of DPSCs to CD31Frontiers in cell and developmental biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Extracellular Vesicles in Bone Remodeling and Osteoporosis.Advances in experimental medicine and biology · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. [Review for different sources of exosomes in bone tissue engineering research].Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2020
    Review
  14. Review
  15. Support of bone mineral deposition by regulation of pH.American journal of physiology. Cell physiology · 2018
    Article
  16. Article
  17. Exosomes in Extracellular Matrix Bone Biology.Current osteoporosis reports · 2018
    Review
  18. Article
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 1 institution in 1 country.

Amsaveni RamachandranBrodie Tooth Development Genetics &Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, Il 60612, USA.
Sriram RavindranBrodie Tooth Development Genetics &Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, Il 60612, USA.
Chun-Chieh HuangBrodie Tooth Development Genetics &Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, Il 60612, USA.
Anne GeorgeBrodie Tooth Development Genetics &Regenerative Medicine Research Laboratory, Department of Oral Biology, University of Illinois at Chicago, Chicago, Il 60612, USA.
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
NIDCR NIH HHS R01 DE011657NIDCR NIH HHS R56 DE011657
6 · The paper itself

Abstract

Transforming growth factor beta receptor II interacting protein 1 (TRIP-1), a predominantly intracellular protein is localized in the ECM of bone. TRIP-1 lacks a signal peptide, therefore, in this study, we provide evidence that intracellular TRIP-1 can be packaged and exported to the ECM via exosomes. Overexpression of TRIP-1 in MC3T3-E1 cells resulted in increased matrix mineralization during differentiation and knockdown resulted in reduced effects. In vivo function of TRIP-1 was studied by an implantation assay performed using TRIP-1 overexpressing and knockdown cells cultured in a 3-dimmensional scaffold. After 4 weeks, the subcutaneous tissues from TRIP-1 overexpressing cells showed higher calcium and phosphate deposits, arranged collagen fibrils and increased expression of Runx2 and alkaline phosphatase. Nucleation studies on demineralized and deproteinized dentin wafer is a powerful tool to determine the functional role of noncollagenous proteins in matrix mineralization. Using this system, we provide evidence that TRIP-1 binds to Type-I collagen and can promote mineralization. Surface plasmon resonance analysis demonstrated that TRIP-1 binds to collagen with K

Indexed as

AnimalsCalcification, PhysiologicCalcium PhosphatesCell DifferentiationCell LineCollagen Type IEukaryotic Initiation Factor-3Eukaryotic Initiation FactorsExosomesExtracellular MatrixHumansIntracellular Signaling Peptides and ProteinsMaleMice, NudeOsteoblastsOsteogenesiscalcium phosphateCalcium PhosphatesCollagen Type IEIF3I protein, humanEukaryotic Initiation Factor-3Eukaryotic Initiation FactorsIntracellular Signaling Peptides and ProteinsTRIP-1 protein, mouseTRIP-1 protein, rat

Identifiers

PMID27883077
PMCPMC5121659
OpenAlexW2551683928

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.