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
Comparative Study
. 2004 Aug;28(4):207-14.
doi: 10.1023/b:ifla.0000049045.41784.59.

Macrophages restrain contraction of an in vitro wound healing model

Affiliations
Comparative Study

Macrophages restrain contraction of an in vitro wound healing model

P M Newton et al. Inflammation. 2004 Aug.

Abstract

Significant numbers of macrophages are present during all stages of dermal wound repair, but the functional significance of these macrophages, especially during the later contraction and remodelling stages of repair, remains unclear. We investigated the effect of macrophages on wound contraction using a novel in vitro model based upon the contracting dermal equivalent (DE). Macrophages were found to reversibly restrain DE contraction, a rapid and sustained effect that was enhanced by lipolysaccharide (LPS) treatment of macrophages and partially inhibited by hydrocortisone. Prolonged inhibition of contraction was strongly correlated with an inhibition of fibroblast proliferation. The rapid contraction-inhibiting effect of the macrophages was mediated through activation of protein kinase C (PKC). These results suggest that inflammatory macrophages restrain the later stages of wound repair, namely matrix contraction and remodeling. The novel in vitro model established here provides a useful system for examining fibroblast-macrophage interactions in the healing wound.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Br J Plast Surg. 1997 Jul;50(5):362-8 - PubMed
    1. Am J Pathol. 1985 Apr;119(1):111-26 - PubMed
    1. Arch Surg. 1990 May;125(5):636-40 - PubMed
    1. Am J Physiol. 1999 Jul;277(1 Pt 1):C1-9 - PubMed
    1. Chem Biol. 2001 Dec;8(12):1123-9 - PubMed

Publication types

Substances

LinkOut - more resources