Evidence map›Paper›PMID 20686067›Full record

ArticleAmerican journal of physiology. Cell physiology2010

Characterization of hTERT-immortalized osteoblast cell lines generated from wild-type and connexin43-null mouse calvaria.

Mia M Thi, Marcia Urban-Maldonado, David C Spray, Sylvia O Suadicani

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Cell Immortality:Life (Basel, Switzerland) · 2024
    Review
  4. Connexin 43 hemichannels and prostaglandin EFrontiers in cell and developmental biology · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Role of pannexin 1 channels in load-induced skeletal response.Annals of the New York Academy of Sciences · 2019
    Article
  9. Osteocyte calcium signals encode strain magnitude and loading frequency in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Connexins and Pannexins in Bone and Skeletal Muscle.Current osteoporosis reports · 2017
    Review
  11. Connexin43 and Runx2 Interact to Affect Cortical Bone Geometry, Skeletal Development, and Osteoblast and Osteoclast Function.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Article
  20. Matrix-dependent adhesion mediates network responses to physiological stimulation of the osteocyte cell process.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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.

Mia M ThiDepartment of Orthopaedic Surgery, Albert Einstein College of Medicine of Yeshiva University, Bronx, NY 10461, USA. mia.thi@einstein.yu.edu
Marcia Urban-Maldonado
David C Spray
Sylvia O Suadicani
Yeshiva University · US

Funding

Osteocyte Integrity and Bone RemodelingR01AR041210 · NIAMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHAFFLER, MITCHELL B · 1997 to 2019
$5.8M
The Astrocyte Nexus: CX43-Protein InteractionsR01NS041282 · NINDS · YESHIVA UNIVERSITY · PI SPRAY, DAVID C · 2002 to 2011
$3.3M
Structural, Molecular, and Functional Specialization in Osteocyte MechanosensingR01AR057139 · NIAMS · CITY COLLEGE OF NEW YORK · PI SCHAFFLER, MITCHELL B, SPRAY, DAVID C · 2010 to 2014
$2.5M
Urothelial ATP Signaling and Diabetic Bladder DysfunctionR01DK081435 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SUADICANI, SYLVIA OTTILIE · 2009 to 2013
$1.7M
LUMINESCENCE IMAGING: MOLECULES, CELLS AND TISSUESS10RR020949 · NCRR · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SPRAY, DAVID · 2006 to 2006
$209k
Decoding gap junction communication under shear stressF32HL082130 · NHLBI · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI THI, MIA M · 2005 to 2007
$107k
NCRR NIH HHS S10 RR020949NCRR NIH HHS S10RR-020949NHLBI NIH HHS F32 HL082130NHLBI NIH HHS F32HL-082130NIAMS NIH HHS AR-057139NIAMS NIH HHS R01 AR041210NIAMS NIH HHS R01 AR057139NIDDK NIH HHS DK-081435NIDDK NIH HHS R01 DK081435NINDS NIH HHS NS-041282NINDS NIH HHS R01 NS041282
6 · The paper itself

Abstract

The gap junction protein connexin43 (Cx43) has been proposed to play key roles in bone differentiation and mineralization, but underlying cellular mechanisms are not totally understood. To further explore roles of Cx43 in these processes, we immortalized calvarial osteoblasts from wild-type and Cx43-null mice using human telomerase reverse transcriptase (hTERT). Osteoblastic (MOB) cell lines were generated from three individual wild-type and three individual Cx43-null mouse calvaria. Average population doubling times of the cell lines were higher than of the primary osteoblasts but did not greatly differ with regard to genotype. Modest to high level of Cx45 expression was detected in MOBs of both genotypes. Most of the cell lines expressed osteoblastic markers [Type I collagen, osteopontin, osteocalcin, parathyroid hormone/parathyroid hormone-related peptide receptor (PTH/PTHrP), periostin (OSF-2), osterix (Osx), runt-related transcription factor 2 (Runx2), alkaline phosphatase (ALP)], and mineralization was comparable to that of primary osteoblasts. Two MOB cell lines from each genotype with most robust maintenance of osteoblast lineage markers were analyzed in greater detail, revealing that the Cx43-null cell lines showed a significant delay in early differentiation (up to 9 days in culture). Matrix mineralization was markedly delayed in one of the Cx43-null lines and slightly delayed in the other. These findings comparing new and very stable wild-type and Cx43-null osteoblastic cell lines define a role for Cx43 in early differentiation and mineralization stages of osteoblasts and further support the concept that Cx43 plays important role in the cellular processes associated with skeleton function.

Indexed as

Cell LineAnimalsBiomarkersCalcification, PhysiologicCell DifferentiationConnexin 43Gap JunctionsHumansMiceMice, Inbred C57BLMice, KnockoutOsteoblastsPhenotypeSkullTelomeraseBiomarkersConnexin 43TelomeraseTERT protein, human

Identifiers

PMID20686067
PMCPMC2980299
OpenAlexW2084069949

What OpenQuestion holds

Textmetadata
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.