The role of collagen arrangement change during tendon healing demonstrated by scanning electron microscopy.

Bibliographic Details
Title: The role of collagen arrangement change during tendon healing demonstrated by scanning electron microscopy.
Authors: Kaoru Sasaki, Naoto Yamamoto, Tomoharu Kiyosawa, Mitsuru Sekido
Source: Journal of Electron Microscopy; Oct2012, Vol. 61 Issue 5, p327-334, 8p
Subject Terms: COLLAGEN, SCANNING electron microscopy, ACHILLES tendon injuries, CELL physiology, TISSUES, SURGERY
Abstract: The dry weight of tendon tissue is accounted for mainly by collagen fibers. Accordingly, the tendon-healing process primarily involves repair of collagen fibers. During the remodeling phase of tendon healing, newly proliferating collagen fibers are transformed into a mature repaired tendon. Despite the importance of this phenomenon, the details of fibrous rebuilding have not been reported previously. The aim of this study was to visualize the ultrastructural changes and to obtain a clear understanding of the reorganization of the collagen fibers in the tendon repair site, using rat Achilles tendons. We used scanning electron microscopy (SEM) with cell maceration as the main method of analysis. Pretreatment with cell maceration removed the cellular components successfully. This allowed precise visualization of each collagen fiber and the three-dimensional network of the fibers. This study was the first to apply the cell-maceration/SEM method to observe tendon tissue. Seven days after surgery, new collagen fibers grew extensively in the repair site in a random arrangement. Fourteen days after surgery, the collagen fibers began to form an axial arrangement. Near the tendon stump, this change progressed from the outer layer to the core region. On the other hand, in the middle of the repair site, it progressed from the core to the outer layer. Change in the axial arrangement of collagen fibers contributes to the connection between the repair site and the tendon stump and to the separation of the repair site from the paratenon. [ABSTRACT FROM AUTHOR]
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Database: Complementary Index
More Details
ISSN:00220744
DOI:10.1093/jmicro/dfs057
Published in:Journal of Electron Microscopy
Language:English