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

Chondrocyte-matrix attachment complexes mediate survival and differentiation

K K Svoboda1

  • 1Department of Biomedical Sciences, Baylor College of Dentistry, Dallas, Texas 75246, USA. ksvoboda@tambcd.edu

Microscopy Research and Technique
|November 21, 1998
PubMed
Summary

Integrin signals are crucial for chondrocyte survival and differentiation. This review details how cell-matrix interactions, particularly the cell-matrix attachment complex (CMAX), prevent chondrocyte apoptosis.

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

Erk and PI-3 kinase are necessary for collagen binding and actin reorganization in corneal epithelia.

Investigative ophthalmology & visual science·2000
Same author

Hyperbaric oxygen downregulates ICAM-1 expression induced by hypoxia and hypoglycemia: the role of NOS.

American journal of physiology. Cell physiology·2000
Same author

Zyxin and vinculin distribution at the cell-extracellular matrix attachment complex (CMAX) in corneal epithelial tissue are actin dependent.

The Anatomical record·1999
Same author

ECM-stimulated actin bundle formation in embryonic corneal epithelia is tyrosine phosphorylation dependent.

The Anatomical record·1999
Same author

Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.

Current eye research·1998
Same author

Chondrocyte survival and differentiation in situ are integrin mediated.

Developmental dynamics : an official publication of the American Association of Anatomists·1997

Area of Science:

  • Cell Biology
  • Biochemistry
  • Developmental Biology

Background:

  • Integrin-mediated cell-extracellular matrix (ECM) interactions are vital for cell survival and differentiation.
  • Chondrocytes rely on these interactions for maintaining their phenotype and function.
  • Understanding these mechanisms is key to addressing chondrocyte-related pathologies.

Purpose of the Study:

  • To review the role of integrin-mediated signal transduction in chondrocyte differentiation and survival.
  • To discuss signaling pathways activated by ECM components in chondrocytes.
  • To explore the interplay between integrin signaling and factors like parathyroid hormone (PTH) and transforming growth factor-beta (TGF-β).

Main Methods:

  • Literature review of existing studies on chondrocyte biology and integrin signaling.

Related Experiment Videos

  • Analysis of data concerning chondrocyte behavior in vitro and in vivo.
  • Examination of gene expression changes preceding apoptosis.
  • Main Results:

    • Integrin-mediated signaling is essential for chondrocyte survival and differentiation.
    • Specific ECM components activate distinct signal transduction pathways in chondrocytes.
    • Parathyroid hormone and TGF-β may modulate chondrocyte survival in conjunction with integrin signaling.
    • Changes in gene expression patterns precede apoptosis, and integrin signals appear to prevent this.

    Conclusions:

    • Integrin-mediated signals are critical for preventing chondrocyte apoptosis.
    • Anchorage-dependent survival is fundamental for chondrocyte development and differentiation.
    • Further research into integrin signaling pathways can inform therapeutic strategies for cartilage diseases.