Analyze Diet
Archives of biochemistry and biophysics2006; 456(1); 71-78; doi: 10.1016/j.abb.2006.09.014

Fatty acid transport in articular cartilage.

Abstract: Articular cartilage extracellular matrix imposes a significant transport barrier to albumin, the principal carrier of fatty acids. It has not been previously established whether it also influences the transport of fatty acids important for chondrocyte metabolism. Albumin was labelled with rhodamine-maleimide and bound to NBD-labelled lauric acid. Plugs of fresh equine metacarpal-phalangeal cartilage and subchondral bone were incubated with the complex at 4 degrees C for 2-160 h. The fluorophore distribution was quantified using quantitative microscopy in histological sections. The fluorescence intensity of both fluorophores fell steeply over 300 microm below the articular surface and remained relatively uniform through the mid zone but the ratio of lauric acid to albumin was higher than in the incubation medium. The effective diffusivity of lauric acid in the mid zone was (2.2+/-0.7) x 10(-12) m2 s(-1) (n = 33), higher than that of the carrier albumin, suggesting dissociation in the surface layer. Lauric acid accumulated reversibly at the tidemark.
Publication Date: 2006-10-06 PubMed ID: 17084376DOI: 10.1016/j.abb.2006.09.014Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research presents an investigation into the transport mechanisms of fatty acids, which are essential for chondrocyte metabolism, in articular cartilage. The study found that the effective diffusivity of lauric acid, a fatty acid, was higher than that of its carrier, albumin, suggesting a dissociation in the surface layer.

Background and Methodology

  • The study focused on articular cartilage, a connective tissue found in joints. This tissue’s extracellular matrix is a significant obstacle for albumin transport, the predominant carrier for fatty acids.
  • Researchers were particularly interested in whether this matrix also imposes transport restrictions on fatty acids, which play a crucial role in chondrocyte metabolism. Chondrocytes are the only cells driving cartilage production, so understanding the transport mechanisms within this tissue is vital.
  • To carry out their investigation, the team used a combination of rhodamine-maleimide-labelled albumin and NBD-labelled lauric acid.
  • They placed plugs of fresh equine metacarpal-phalangeal cartilage and subchondral bone in this complex and incubated them at 4 degrees Celsius for time intervals ranging from 2 to 160 hours.
  • Significant quantitative observations were derived by studying sections of the samples under a microscope.

Results and Interpretations

  • The microscopy results revealed that fluorescence intensity, related to the presence of both albumin and lauric acid, showed a sharp decrease 300 microm below the articular surface.
  • The intensity was relatively consistent through the mid-zone, though the proportion of lauric acid to albumin was found to be higher than in the incubation medium. These observations suggest a probable dissociation of lauric acid from its carrier, albumin, at the surface layer of the tissue.
  • The effective diffusivity, an indicator of how fast these substances can move through the tissue, for lauric acid in the mid zone was calculated to be (2.2+/-0.7) x 10(-12) m2 s(-1) (n = 33). Interestingly, this measure was higher than that of albumin, the carrier protein. These results provide additional evidence for the hypothesis that dissociation is taking place.
  • Moreover, the lauric acid was found to accumulate reversibly at the tidemark, an essential transitional zone between the non-calcified and calcified cartilage within a joint, indicating that it tends to move freely in the tissue.

Conclusion and Implications

  • The study provides valuable insights into the internal dynamics of fatty acid transport within articular cartilage.
  • The discovery that lauric acid diffuses faster than its carrier albumin and accumulates at the tidemark deepens our understanding of chondrocyte metabolism and the health of articular cartilage.
  • This research could aid therapeutic strategies targeting improved nutrient delivery to chondrocytes, potentially improving treatment outcomes in osteoarthritis and other joint diseases.

Cite This Article

APA
Arkill KP, Winlove CP. (2006). Fatty acid transport in articular cartilage. Arch Biochem Biophys, 456(1), 71-78. https://doi.org/10.1016/j.abb.2006.09.014

Publication

ISSN: 0003-9861
NlmUniqueID: 0372430
Country: United States
Language: English
Volume: 456
Issue: 1
Pages: 71-78

Researcher Affiliations

Arkill, Kenton Paul
  • Biomedical Physics Group, School of Physics, University of Exeter, Exeter, EX4 4QL, UK. k.p.arkill@ex.ac.uk
Winlove, C Peter

    MeSH Terms

    • Animals
    • Biological Transport, Active / physiology
    • Cartilage, Articular / metabolism
    • Fatty Acids / metabolism
    • Horses
    • In Vitro Techniques
    • Serum Albumin / metabolism

    Grant Funding

    • Wellcome Trust

    Citations

    This article has been cited 9 times.
    1. Cao C, Shi Y, Zhang X, Li Q, Zhang J, Zhao F, Meng Q, Dai W, Liu Z, Yan W, Duan X, Zhang J, Fu X, Cheng J, Hu X, Ao Y. Cholesterol-induced LRP3 downregulation promotes cartilage degeneration in osteoarthritis by targeting Syndecan-4. Nat Commun 2022 Nov 21;13(1):7139.
      doi: 10.1038/s41467-022-34830-4pubmed: 36414669google scholar: lookup
    2. Su Z, Zong Z, Deng J, Huang J, Liu G, Wei B, Cui L, Li G, Zhong H, Lin S. Lipid Metabolism in Cartilage Development, Degeneration, and Regeneration. Nutrients 2022 Sep 25;14(19).
      doi: 10.3390/nᐙ3984pubmed: 36235637google scholar: lookup
    3. Mao X, Fu P, Wang L, Xiang C. Mitochondria: Potential Targets for Osteoarthritis. Front Med (Lausanne) 2020;7:581402.
      doi: 10.3389/fmed.2020.581402pubmed: 33324661google scholar: lookup
    4. Mansfield JC, Winlove CP. Lipid distribution, composition and uptake in bovine articular cartilage studied using Raman micro-spectrometry and confocal microscopy. J Anat 2017 Jul;231(1):156-166.
      doi: 10.1111/joa.12624pubmed: 28508410google scholar: lookup
    5. Villalvilla A, Gómez R, Largo R, Herrero-Beaumont G. Lipid transport and metabolism in healthy and osteoarthritic cartilage. Int J Mol Sci 2013 Oct 16;14(10):20793-808.
      doi: 10.3390/ijms141020793pubmed: 24135873google scholar: lookup
    6. Lee JI, Sato M, Ushida K, Mochida J. Measurement of diffusion in articular cartilage using fluorescence correlation spectroscopy. BMC Biotechnol 2011 Mar 2;11:19.
      doi: 10.1186/1472-6750-11-19pubmed: 21366913google scholar: lookup
    7. Hurst S, Rees SG, Randerson PF, Caterson B, Harwood JL. Contrasting effects of n-3 and n-6 fatty acids on cyclooxygenase-2 in model systems for arthritis. Lipids 2009 Oct;44(10):889-96.
      doi: 10.1007/s11745-009-3347-xpubmed: 19784684google scholar: lookup
    8. Ma Y, Liu Y, Luo D, Guo Z, Xiang H, Chen B, Wu X. Identification of biomarkers and immune infiltration characterization of lipid metabolism-associated genes in osteoarthritis based on machine learning algorithms. Aging (Albany NY) 2024 Apr 17;16(8):7043-7059.
      doi: 10.18632/aging.205740pubmed: 38637111google scholar: lookup
    9. Gögele C, Hahn J, Schulze-Tanzil G. Anatomical Tissue Engineering of the Anterior Cruciate Ligament Entheses. Int J Mol Sci 2023 Jun 5;24(11).
      doi: 10.3390/ijms24119745pubmed: 37298698google scholar: lookup