Evidence map›Paper›PMID 33417921›Full record

ArticleExperimental cell research2021

Kindlin-3 mutation in mesenchymal stem cells results in enhanced chondrogenesis.

Bethany A Kerr, Lihong Shi, Alexander H Jinnah, Koran S Harris, Jeffrey S Willey, Donald P Lennon, Arnold I Caplan, Tatiana V Byzova

Open access · greenAbstract read
In one paragraph

Article in Experimental cell research, 2021. 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
2.5field-weighted citation impact, top 11% 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.

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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

8 authors at 3 institutions in 1 country.

Bethany A KerrDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA; Department of Orthopaedic Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. Electronic address: bkerr@wakehealth.edu.
Lihong ShiDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Alexander H JinnahDepartment of Orthopaedic Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Koran S HarrisDepartment of Cancer Biology and Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Jeffrey S WilleyDepartment of Orthopaedic Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA; Department of Radiation Biology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Donald P LennonSkeletal Research Center, Department of Biology, Case Western Reserve University, Cleveland, OH, 44106, USA.
Arnold I CaplanSkeletal Research Center, Department of Biology, Case Western Reserve University, Cleveland, OH, 44106, USA.
Tatiana V ByzovaDepartment of Molecular Cardiology, Joseph J. Jacobs Center for Thrombosis and Vascular Biology, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
Wake Forest University · USCase Western Reserve University · USCleveland Clinic Lerner College of Medicine · US

Funding

Structure Basis for Talin-mediated Integrin ActivationP01HL073311 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2004 to 2019
$27.4M
Regulation of Integrins in Neovasculature DevelopmentR01HL071625 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2003 to 2021
$7.3M
Platelets in CancerR01HL142772 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI BYZOVA, TATIANA V · 2018 to 2021
$2.6M
CD117 Signaling as a Mechanism of Prostate Cancer MetastasisK99CA175291 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI KERR, BETHANY AMBER · 2014 to 2015
$182k
Molecular Mechanisms of Prostate Cancer Induced Bone RemodelingF32CA142133 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI KERR, BETHANY AMBER · 2010 to 2013
$116k
NCI NIH HHS F32 CA142133NCI NIH HHS K99 CA175291NHLBI NIH HHS P01 HL073311NHLBI NIH HHS R01 HL071625NHLBI NIH HHS R01 HL142772
6 · The paper itself

Abstract

Identifying patient mutations driving skeletal development disorders has driven our understanding of bone development. Integrin adhesion deficiency disease is caused by a Kindlin-3 (fermitin family member 3) mutation, and its inactivation results in bleeding disorders and osteopenia. In this study, we uncover a role for Kindlin-3 in the differentiation of bone marrow mesenchymal stem cells (BMSCs) down the chondrogenic lineage. Kindlin-3 expression increased with chondrogenic differentiation, similar to RUNX2. BMSCs isolated from a Kindlin-3 deficient patient expressed chondrocyte markers, including SOX9, under basal conditions, which were further enhanced with chondrogenic differentiation. Rescue of integrin activation by a constitutively activated β

Indexed as

AnimalsCell DifferentiationCells, CulturedChondrogenesisCore Binding Factor Alpha 1 SubunitCytoskeletal ProteinsFemaleHumansMaleMembrane ProteinsMesenchymal Stem CellsMiceMice, TransgenicMutationNeoplasm ProteinsCore Binding Factor Alpha 1 SubunitCytoskeletal ProteinsFERMT3 protein, humankindlin-3 protein, mouseMembrane ProteinsNeoplasm ProteinsBone developmentChondrogenesisKindlin-3/FERMT3Mesenchymal stem cellRUNX2/Cbfa-1

Identifiers

PMID33417921
PMCPMC7874523
OpenAlexW3119376040

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.