Evidence map›Paper›PMID 25160731›Full record

ArticleJournal of cellular physiology2015

Initial Characterization of Osteoblast Differentiation and Loss of RUNX2 Stability in the Newly Established SK11 Human Embryonic Stem Cell-Derived Cell Line.

Jia-Li Yu, Helty Adisetiyo, Gillian H Little, C Thomas Vangsness, Jianjie Jiang, Hal Sternberg, Michael D West, Baruch Frenkel

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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 2 institutions in 1 country.

Jia-Li YuDepartment of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California.
Helty AdisetiyoDepartment of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California.
Gillian H LittleDepartment of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California.
C Thomas VangsnessDepartment of Orthopaedic Surgery, University of Southern California, Los Angeles, California.
Jianjie JiangBioTime, Inc., 1301 Harbor Bay Parkway, Alameda, California.
Hal SternbergBioTime, Inc., 1301 Harbor Bay Parkway, Alameda, California.
Michael D WestBioTime, Inc., 1301 Harbor Bay Parkway, Alameda, California.
Baruch FrenkelDepartment of Biochemistry and Molecular Biology, University of Southern California, Los Angeles, California.
University of Southern California · USLineage Cell Therapeutics (United States) · US

Funding

Sex Steroids and Runx Signaling in BoneR01DK071122 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI FRENKEL, BARUCH · 2005 to 2013
$2.5M
NIDDK NIH HHS R01 DK071122NIDDK NIH HHS R01DK71122
6 · The paper itself

Abstract

We describe a novel model for investigation of genetically normal human osteoblasts in culture. SK11 is a clonal progenitor cell line derived from human embryonic stem cells. Initially selected based on the expression of chondrogenic markers when differentiated in micromass culture, SK11 cells display typical mRNA expression patterns of bone phenotypic genes under osteogenic conditions. These include osterix, α1(I) collagen, alkaline phosphatase, osteonectin, osteopontin, and osteocalcin. Similar to well-characterized murine osteoblast cultures, the osteoblast master regulator RUNX2 was present during the first few days after plating, but the protein disappeared during the first week of culture. Loss of RUNX2 expression is considered an important regulatory feature for osteoblast maturation. Indeed, following ∼2 weeks of differentiation, SK11 cultures exhibited robust calcium deposition, evidenced by alizarin red staining. We also introduced a lentiviral vector encoding doxycycline (dox)-inducible FLAG-tagged RUNX2 into SK11 cells. Dox-mediated enhancement of RUNX2 expression resulted in accelerated mineralization, which was further increased by co-treatment with BMP-2. Like the endogenous RUNX2, expression of the virally coded FLAG-RUNX2 was lost during the first week of culture despite persistent dox treatment. By following RUNX2 decay after dox withdrawal from day-5 versus day-3 cultures, we demonstrated a developmentally regulated decrease in RUNX2 stability. Availability of culture models for molecular investigation of genetically normal human osteoblasts is important because differences between murine and human osteoblasts, demonstrated here by the regulation of matrix Gla Protein, may have significant biomedical implications.

Indexed as

AnimalsCalcification, PhysiologicCell DifferentiationCell DivisionCell LineCells, CulturedCore Binding Factor Alpha 1 SubunitEmbryonic Stem CellsHumansMiceOsteoblastsOsteogenesisCore Binding Factor Alpha 1 SubunitRUNX2 protein, humanRunx2 protein, mouse

Identifiers

PMID25160731
PMCPMC5770229
OpenAlexW2134698959

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.