Evidence map›Paper›PMID 21569876›Full record

ArticleBone2011

Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass.

Isabelle Gennero, Sara Laurencin-Dalicieux, Françoise Conte-Auriol, Fabienne Briand-Mésange, Danielle Laurencin, Jackie Rue, Nicolas Beton, Nicole Malet, Marianne Mus, Akira Tokumura and 6 more

Open access · greenAbstract read
In one paragraph

Article in Bone, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 74 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Lysophosphatidic acid signaling via LPAJournal of neurochemistry · 2022
    Article
  8. Autotaxin/Lysophosphatidic Acid Axis: From Bone Biology to Bone Disorders.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Role of Metabolism in Bone Development and Homeostasis.International journal of molecular sciences · 2020
    Review
  11. Conditional Lpar1 gene targeting identifies cell types mediating neuropathic pain.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Gs/Gi Regulation of Bone Cell Differentiation: Review and Insights from Engineered Receptors.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2016
    Review
  20. Observational
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

16 authors at 9 institutions in 4 countries.

Isabelle GenneroINSERM Unité 1043 (Centre de Physiopathologie de Toulouse Purpan), Université Paul-Sabatier, Hôpital Purpan, CHU de Toulouse, 31059 Toulouse Cedex 9, France. gennero.i@chu-toulouse.fr
Sara Laurencin-Dalicieux
Françoise Conte-Auriol
Fabienne Briand-Mésange
Danielle Laurencin
Jackie Rue
Nicolas Beton
Nicole Malet
Marianne Mus
Akira Tokumura
Philippe Bourin
Laurence Vico
Gérard Brunel
Richard O C Oreffo
Jerold Chun
Jean Pierre Salles
Université Toulouse III - Paul Sabatier · FRInserm · FRCentre de Physiopathologie de Toulouse-Purpan · FRHôpital Purpan · FRÉcole Nationale Supérieure de Chimie de Montpellier · FRÉtablissement Français du Sang · FRLa Jolla Institute for Immunology · USTokushima University · JPUniversity of Southampton · GB

Funding

RECEPTOR-MEDIATED LPA SIGNALING IN CORTICAL DEVELOPMENTR01MH051699 · NIMH · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI CHUN, JEROLD · 2001 to 2009
$3.3M
Lysophospholipids roles for Schwann cell &myelinationR01NS048478 · NINDS · SCRIPPS RESEARCH INSTITUTE, THE · PI CHUN, JEROLD · 2004 to 2008
$2.4M
CELL LINES FOR FINDING DEVELOPMENTAL NEOCORTICAL GENESR29MH051699 · NIMH · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI CHUN, JEROLD · 1994 to 1998
–
Biotechnology and Biological Sciences Research Council E18596NIMH NIH HHS MH051699NIMH NIH HHS R01 MH051699NINDS NIH HHS NS048478NINDS NIH HHS R01 NS048478
6 · The paper itself

Abstract

Lysophosphatidic acid (LPA) is a lipid mediator that acts in paracrine systems via interaction with a subset of G protein-coupled receptors (GPCRs). LPA promotes cell growth and differentiation, and has been shown to be implicated in a variety of developmental and pathophysiological processes. At least 6 LPA GPCRs have been identified to date: LPA1-LPA6. Several studies have suggested that local production of LPA by tissues and cells contributes to paracrine regulation, and a complex interplay between LPA and its receptors, LPA1 and LPA4, is believed to be involved in the regulation of bone cell activity. In particular, LPA1 may activate both osteoblasts and osteoclasts. However, its role has not as yet been examined with regard to the overall status of bone in vivo. We attempted to clarify this role by defining the bone phenotype of LPA1((-/-)) mice. These mice demonstrated significant bone defects and low bone mass, indicating that LPA1 plays an important role in osteogenesis. The LPA1((-/-)) mice also presented growth and sternal and costal abnormalities, which highlights the specific roles of LPA1 during bone development. Microcomputed tomography and histological analysis demonstrated osteoporosis in the trabecular and cortical bone of LPA1((-/-)) mice. Finally, bone marrow mesenchymal progenitors from these mice displayed decreased osteoblastic differentiation. These results suggest that LPA1 strongly influences bone development both qualitatively and quantitatively and that, in vivo, its absence results in decreased osteogenesis with no clear modification of osteoclasis. They open perspectives for a better understanding of the role of the LPA/LPA1 paracrine pathway in bone pathophysiology.

Indexed as

AnimalsBiomarkersBone and BonesBone DensityBone Marrow CellsCell DifferentiationLysophospholipidsMesenchymal Stem CellsMiceMice, Inbred C57BLMice, KnockoutNutritional StatusOsteoblastsOsteoclastsOsteogenesisProtein IsoformsBiomarkerslysophosphatidic acidLysophospholipidsProtein IsoformsReceptors, Lysophosphatidic Acid

Identifiers

PMID21569876
PMCPMC3697734
OpenAlexW2155233266

What OpenQuestion holds

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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.