Evidence map›Paper›PMID 18703865›Full record

ArticleCells, tissues, organs2009

Autophagy: a new phase in the maturation of growth plate chondrocytes is regulated by HIF, mTOR and AMP kinase.

Vickram Srinivas, Jolene Bohensky, Irving M Shapiro

Open access · bronzeAbstract read
In one paragraph

Article in Cells, tissues, organs, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

49 citing papers in PubMed, 91 citations in OpenAlex.

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  12. Autophagy coordinates chondrocyte development and early joint formation in zebrafish.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  13. Review
  14. AMPK Signaling in Energy Control, Cartilage Biology, and Osteoarthritis.Frontiers in cell and developmental biology · 2021
    Review
  15. Review
  16. Review
  17. Review
  18. The physiological roles of autophagy in the mammalian life cycle.Biological reviews of the Cambridge Philosophical Society · 2019
    Review
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Vickram SrinivasDepartment of Orthopaedic Surgery, Thomas Jefferson University, Philadelphia, Pa. 19107, USA.
Jolene Bohensky
Irving M Shapiro
Thomas Jefferson University · US

Funding

BONE GROWTH IN DENTAL, CRANIAL AND SKELETAL TISSUESR01DE010875 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI SHAPIRO, IRVING M · 1994 to 2006
$2.4M
Oxygen Sensing and Growth Plate Chrondrocyte MaturationR01DE016383 · NIDCR · THOMAS JEFFERSON UNIVERSITY · PI SRINIVAS, VICKRAM · 2005 to 2009
$1.4M
CRANIOFACIAL DEVELOPMENT: METABOLIC CONTROL OF APOPTOSISR01DE013319 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI SHAPIRO, IRVING M · 1999 to 2003
$1.1M
HIF Prolyl Hydroxylases and Chondrocyte MaturationR03DE015694 · NIDCR · THOMAS JEFFERSON UNIVERSITY · PI SRINIVAS, VICKRAM · 2004 to 2005
$157k
NIDCR NIH HHS DE 010875NIDCR NIH HHS DE 013319NIDCR NIH HHS DE 015694NIDCR NIH HHS DE 016383NIDCR NIH HHS R01 DE010875NIDCR NIH HHS R01 DE013319NIDCR NIH HHS R01 DE016383NIDCR NIH HHS R03 DE015694
6 · The paper itself

Abstract

The overall goal of the investigation was to examine autophagy in the growth plate and to ascertain how this process was regulated. Herein, we show that in the postmitotic maturing zone of the growth plate, chondrocytes express an autophagic phenotype. This robust and particulate immunohistochemical response provides direct evidence that autophagy is a new and transient stage in the chondrocyte maturation pathway. We found that induction of autophagy was regulated by mTOR, a sensor of cellular metabolism. When mTOR was inhibited, changes in LC3 fluorescence indicated that this kinase regulated development of the autophagic state. To determine if AMP kinase was required for chondrocyte autophagy, we suppressed its expression in N1511 cells using siRNA technology. When these cells were serum starved, a condition that triggers autophagy, there was no change in LC3 distribution. This result confirmed that AMP kinase was required for the induction of the autophagic response. Based on the 2 studies described above, and our previous observation that HIF-1 is required for the induction of autophagy, we put forward the hypothesis that autophagy is regulated by the activities of AMP kinase and mTOR in a HIF-1-dependent manner. Once autophagy is activated, the postmitotic chondrocytes would be expected to remain viable in their unique microenvironment and complete their life cycle.

Indexed as

AutophagyAdenylate KinaseAnimalsCell DifferentiationCell LineChondrocytesGrowth PlateHypoxia-Inducible Factor 1, alpha SubunitMiceMicrotubule-Associated ProteinsProtein KinasesTOR Serine-Threonine KinasesAdenylate KinaseHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitMap1lc3b protein, mouseMicrotubule-Associated ProteinsmTOR protein, mouseProtein KinasesTOR Serine-Threonine Kinases

Identifiers

PMID18703865
PMCPMC2677069
OpenAlexW2088437980

What OpenQuestion holds

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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.