Electron microscope 3D reconstruction of branched collagen fibrils in vivo

T. Starborg, Y. Lu, A. Huffman, D. F. Holmes, K. E. Kadler

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The ability of tendon to withstand tensile forces is largely attributable to an extracellular matrix containing parallel collagen fibrils organized into fascicles. A major belief is that force is transmitted between collagen fibrils via interactions of molecules at the fibril surface. However, there is existing evidence (reviewed here) for persistent connections between fibrils formed by interfibrillar fusion. Furthermore, in vitro studies have shown the ability of the ends of fibrils to fuse together. In this study, we show using serial section electron microscopy of embryonic mouse-tail tendon further evidence for interfibril fusion in vivo. We showed: (1) fibrils fused via Y-shaped branches without disruption of the 67 nm D-periodicity, (2) the frequency of the branches was ∼1:20 000 D-periods, and (3) the small angle of the Y ranged from 4° to 10°, indicating a structure-based mechanism of branch formation. The regular occurrence of Y-shaped branches between collagen fibrils suggests direct force transmission between fibrils. Furthermore, the formation of the Y-shaped branches by tip-to-shaft fusion would explain the paucity of fibril tips in vivo. © 2009 John Wiley & Sons A/S.
    Original languageEnglish
    Pages (from-to)547-552
    Number of pages5
    JournalScandinavian Journal of Medicine and Science in Sports
    Volume19
    Issue number4
    DOIs
    Publication statusPublished - Aug 2009

    Keywords

    • Branch
    • Branching
    • Bridging
    • Electron microscopy
    • Fibrillogenesis
    • Fusion
    • Split

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