Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Modulation of osteoblast function by prostaglandins.

D T Yamaguchi1, J Green, B S Merritt

  • 1Laboratory of Membrane Biology, Cedars-Sinai Medical Center, Los Angeles 90048.

The American Journal of Physiology
|November 1, 1989
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Fuller Albright and our current understanding of calcium and phosphorus regulation and primary hyperparathyroidism.

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia·2011
Same author

Body weight reduction in rats by oral treatment with zinc plus cyclo-(His-Pro).

British journal of pharmacology·2009
Same author

Angiogenic CXC chemokine expression during differentiation of human mesenchymal stem cells towards the osteoblastic lineage.

Journal of cellular biochemistry·2007
Same author

KC chemokine expression by TGF-beta in C3H10T1/2 cells induced towards osteoblasts.

Biochemical and biophysical research communications·2004
Same author

Serial passage of MC3T3-E1 cells down-regulates proliferation during osteogenesis in vitro.

Cell proliferation·2004
Same author

Extracellular matrix alters the relationship between tritiated thymidine incorporation and proliferation of MC3T3-E1 cells during osteogenesis in vitro.

Cell proliferation·2002

Naturally occurring prostaglandins (PGs) activate key signaling pathways in osteoblasts, influencing calcium levels, cAMP production, and cell proliferation. Different PGs exhibit varying potencies in these cellular responses.

Area of Science:

  • Biochemistry
  • Cell Biology
  • Endocrinology

Background:

  • Prostaglandins (PGs) are crucial lipid compounds involved in various physiological processes.
  • Osteoblasts are bone-forming cells critical for skeletal maintenance and repair.
  • Understanding PG signaling in osteoblasts is vital for bone biology research.

Purpose of the Study:

  • To investigate the effects of naturally occurring prostaglandins on intracellular calcium ([Ca2+]i) and cyclic AMP (cAMP) levels.
  • To determine the impact of prostaglandins on osteoblast proliferation.
  • To establish the potency ranking of different PGs for these cellular responses.

Main Methods:

  • Utilized the osteoblastic cell line UMR-106-01 and primary osteoblast cultures.
  • Measured changes in free cytosolic Ca2+ concentrations ([Ca2+]i) and cAMP levels.

Related Experiment Videos

  • Assessed cell proliferation via thymidine uptake assays.
  • Main Results:

    • All tested PGs increased [Ca2+]i, primarily through intracellular calcium release.
    • PG potency for [Ca2+]i increase: PGF2α > PGD2 > PGE2 > TxB2 > PGE1 > PGI2 > PGA2.
    • PGs differentially affected osteoblast proliferation, with some stimulating and others inhibiting it, correlating with cAMP production.

    Conclusions:

    • Naturally occurring prostaglandins activate both Ca2+ and cAMP signal transduction pathways in osteoblasts.
    • The potency and effect of PGs on osteoblast proliferation are linked to their ability to modulate cAMP levels.