Evidence map›Paper›PMID 18281278›Full record

ArticleThe Journal of biological chemistry2008

Collagen/annexin V interactions regulate chondrocyte mineralization.

Hyon Jong Kim, Thorsten Kirsch

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Augmentation ofJournal of the Endocrine Society · 2020
    Article
  7. Article
  8. Article
  9. Time-dependent proteomic and genomic alterations in Toll-like receptor-4-activated human chondrocytes: increased expression of lamin A/C and annexins.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  10. Article
  11. Article
  12. On the Collagen Mineralization. A Review.Clujul medical (1957) · 2015
    Review
  13. Annexin-phospholipid interactions. Functional implications.International journal of molecular sciences · 2013
    Article
  14. Long-term administration of AMD3100, an antagonist of SDF-1/CXCR4 signaling, alters fracture repair.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2012
    Article
  15. Article
  16. Article
  17. Proteoliposomes as matrix vesicles' biomimetics to study the initiation of skeletal mineralization.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2010
    Review
  18. Beta-catenin, cartilage, and osteoarthritis.Annals of the New York Academy of Sciences · 2010
    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

2 authors at 1 institution in 1 country.

Hyon Jong KimMusculoskeletal Research Laboratories, Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Thorsten Kirsch
University of Maryland, Baltimore · US

Funding

REGULATION OF MINERALIZATION IN SKELETAL TISSUESR01AR046245 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI KIRSCH, THORSTEN · 1999 to 2009
$2.0M
Collagen-Annexin Interactions in Tissue MineralizationR01AR049074 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI KIRSCH, THORSTEN · 2003 to 2007
$1.4M
NIAMS NIH HHS R01AR046245NIAMS NIH HHS R01AR049074
6 · The paper itself

Abstract

Physiological mineralization in growth plate cartilage is highly regulated and restricted to terminally differentiated chondrocytes. Because mineralization occurs in the extracellular matrix, we asked whether major extracellular matrix components (collagens) of growth plate cartilage are directly involved in regulating the mineralization process. Our findings show that types II and X collagen interacted with cell surface-expressed annexin V. These interactions led to a stimulation of annexin V-mediated Ca(2+) influx resulting in an increased intracellular Ca(2+) concentration, [Ca(2+)](i), and ultimately increased alkaline phosphatase activity and mineralization of growth plate chondrocytes. Consequently, stimulation of these interactions (ascorbate to stimulate collagen synthesis, culturing cells on type II collagen-coated dishes, or overexpression of full-length annexin V) resulted in increase of [Ca(2+)](i), alkaline phosphatase activity, and mineralization of growth plate chondrocytes, whereas inhibition of these interactions (3,4-dehydro-l-proline to inhibit collagen secretion, K-201, a specific annexin channel blocker, overexpression of N terminus-deleted mutant annexin V that does not bind to type II collagen and shows reduced Ca(2+) channel activities) decreased [Ca(2+)](i), alkaline phosphatase activity, and mineralization. In conclusion, the interactions between collagen and annexin V regulate mineralization of growth plate cartilage. Because annexin V is up-regulated during pathological mineralization events of articular cartilage, it is possible that these interactions also regulate pathological mineralization.

Indexed as

Alkaline PhosphataseAnimalsAnnexin A5CalciumCartilage, ArticularCell SurvivalChick EmbryoChondrocytesCollagenCollagen Type IICollagen Type XCytosolLiposomesModels, BiologicalProtein Structure, TertiaryAlkaline PhosphataseAnnexin A5CalciumCollagenCollagen Type IICollagen Type XLiposomes

Identifiers

PMID18281278
PMCPMC2447629
OpenAlexW1998525570

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.