Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1991 Jan;16(1):24-30.
doi: 10.1016/s0363-5023(10)80006-1.

Intrinsic healing of the laceration site in human superficialis flexor tendons in vitro

Affiliations

Intrinsic healing of the laceration site in human superficialis flexor tendons in vitro

D P Mass et al. J Hand Surg Am. 1991 Jan.

Abstract

The intrinsic capability of the human superficialis flexor tendon to heal a reapproximated laceration site in vitro was examined. Segments of lacerated and sutured human superficialis flexor tendons from zone II were cultured for two, four, or eight weeks in vitro and analyzed by use of light and electron microscopy. We noted a specific pattern of intrinsic healing at the repair site during the incubation period. After two weeks, the cells of the epitenon from both tendon stumps proliferated and appeared to migrate into the repair site. Elongated cells of the thickened epitenon bridged the laceration and synthesized new collagen fibers. By eight weeks, a smooth contiguous tendon surface was restored and the internal collagen bundles were brought into intimate contact. The fibroblasts bridging the laceration, both in the epitenon and centrally in the repair site, were oriented perpendicular to the cut surfaces. The cells in the repair site were active in protein synthesis, and new collagen fibers were present. No cellular necrosis was observed in the internal repair site. Our results indicate that human superficialis tendons possess an intrinsic capacity to heal with diffusion and without dependence on extratendinous cells or on adhesions.

PubMed Disclaimer

Publication types

LinkOut - more resources