Evidence map›Paper›PMID 31648392›Full record

ArticleStem cells (Dayton, Ohio)2020

Knockdown of formin mDia2 alters lamin B1 levels and increases osteogenesis in stem cells.

Jeyantt S Sankaran, Buer Sen, Amel Dudakovic, Christopher R Paradise, Tony Perdue, Zhihui Xie, Cody McGrath, Maya Styner, Joshua Newberg, Gunes Uzer and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2020. 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
1.5field-weighted citation impact, top 20% 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, 21 citations in OpenAlex.

  1. Recent advances in nuclear actin research.Nucleus (Austin, Tex.) · 2025
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. The skeleton in a physical world.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  7. Article
  8. Article
  9. Modeling stem cell nucleus mechanics using confocal microscopy.Biomechanics and modeling in mechanobiology · 2021
    Article
  10. Review
  11. Review
  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

12 authors at 3 institutions in 1 country.

Jeyantt S SankaranDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.ORCID 0000-0002-8613-9219
Buer SenDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Amel DudakovicDepartment of Orthopedic Surgery and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.
Christopher R ParadiseGraduate School of Biomedical Sciences and Center for Regenerative Medicine, Mayo Clinic, Rochester, Minnesota.
Tony PerdueDepartment of Biology, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Zhihui XieDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Cody McGrathDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Maya StynerDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.
Joshua NewbergDepartment of Mechanical and Biomedical Engineering, Boise State University, Boise, Idaho.
Gunes UzerDepartment of Mechanical and Biomedical Engineering, Boise State University, Boise, Idaho.
Andre J van WijnenDepartment of Orthopedic Surgery and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-4458-0946
Janet RubinDepartment of Medicine, University of North Carolina Chapel Hill, Chapel Hill, North Carolina.ORCID 0000-0003-3534-8667
University of North Carolina at Chapel Hill · USMayo Clinic · USBoise State University · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
VPS35 D620N inhibits autophagy through disrupted hyaluronic acid-CD44 signalingP20GM109095 · NIGMS · BOISE STATE UNIVERSITY · PI OXFORD, JULIA THOM · 2014 to 2023
$22.7M
Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
Role of force regulated nuclear structure in expression of osteogenesisR01AR075803 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUBIN, JANET E · 2020 to 2024
$2.4M
Marrow Adipose Compartment Physiology in Caloric Restriction and AgingR01AR073264 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI STYNER, MAYA SHALEV · 2019 to 2023
$1.7M
Mechanical regulation of cytoskeleton guides beta-catenin effect on MSC fateR01AR066616 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUBIN, JANET E · 2015 to 2019
$1.7M
NCI NIH HHS P30 CA016086NIAMS NIH HHS R01 AR049069NIAMS NIH HHS R01 AR066616NIAMS NIH HHS R01 AR073264NIAMS NIH HHS R01 AR075803NIGMS NIH HHS P20 GM109095
6 · The paper itself

Abstract

Nuclear actin plays a critical role in mediating mesenchymal stem cell (MSC) fate commitment. In marrow-derived MSCs, the principal diaphanous-related formin Diaph3 (mDia2) is present in the nucleus and regulates intranuclear actin polymerization, whereas Diaph1 (mDia1) is localized to the cytoplasm and controls cytoplasmic actin polymerization. We here show that mDia2 can be used as a tool to query actin-lamin nucleoskeletal structure. Silencing mDia2 affected the nucleoskeletal lamin scaffold, altering nuclear morphology without affecting cytoplasmic actin cytoskeleton, and promoted MSC differentiation. Attempting to target intranuclear actin polymerization by silencing mDia2 led to a profound loss in lamin B1 nuclear envelope structure and integrity, increased nuclear height, and reduced nuclear stiffness without compensatory changes in other actin nucleation factors. Loss of mDia2 with the associated loss in lamin B1 promoted Runx2 transcription and robust osteogenic differentiation and suppressed adipogenic differentiation. Hence, mDia2 is a potent tool to query intranuclear actin-lamin nucleoskeletal structure, and its presence serves to retain multipotent stromal cells in an undifferentiated state.

Indexed as

ActinsAnimalsCell DifferentiationCore Binding Factor Alpha 1 SubunitGene Knockdown TechniquesLamin Type BMesenchymal Stem CellsMiceMicrotubule-Associated ProteinsNADPH DehydrogenaseNuclear EnvelopeOsteoblastsOsteogenesisActinsCore Binding Factor Alpha 1 SubunitDia2 protein, mouseLamin Type BMicrotubule-Associated ProteinsNADPH DehydrogenaseRunx2 protein, mouseintranuclear actinmDia2nucleoskeletonstem cell fate

Identifiers

PMID31648392
PMCPMC6993926
OpenAlexW2981434737

What OpenQuestion holds

Textmetadata
LicenceTDM
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.