Accession Number : ADA181668
Title : Role of Fibronectin in Wound Healing.
Descriptive Note : Annual rept. 1 Oct 85-31 Mar 86, Final rept. 1 Oct 83-31 Mar 86,
Corporate Author : MEDICAL COLL OF GEORGIA AUGUSTA RESEARCH INSTITUTE
Personal Author(s) : Reese,Andy C
PDF Url : ADA181668
Report Date : 12 Sep 1986
Pagination or Media Count : 32
Abstract : The purpose of the project was to determine if local or systemic manipulation of circulating fibronection (Fn, a normal plasma and extracellular matrix glycoprotein) levels affects the rate of wound healing. Initial experiments were designed to determine if Fn is involved in opsonization of effete cells and tissue debris for removal by tissue macrophages. Within two hours after wounding and injection of fluorescene-labeled Fn, tissue debris at the wound site was coated with Fn, and dammaged cells were also coated by 24 hrs. By 48 hrs, macrophages at the site of injury had phagocytized Fn coated tissue debris and/or cells. Thus, effete materials at the wound site are quickly labeled by plasma Fn for removal by tissue macrophages. Subsequent experiments were done to determine if Fn enhanced the healing rate of dermal injuries. Rat Fn was suspended in various inert carriers and used to treat full thickness skin lesions on rats. Fn in several carriers was effective in stimulating significantly faster wound healing than was seen with the carrier mixed with PBS. Further experiments showed that treatment once a day for two days was as effective in enhancing wound healing as more prolonged treatment. A single treatment with Fn on the day of the injury enhanced wound healing but not as much as treatment for two days. One could also delay starting treatment for a few hours after injury and still significantly improve the healing rate.
Descriptors : *WOUNDS AND INJURIES, *GLYCOPROTEINS, *BLOOD COAGULATION, *HEALING, PHAGOCYTES, DELAY, INJECTION, LESIONS, RATES, RATS, SITES, SKIN(ANATOMY), STARTING, THICKNESS, TOLERANCES(PHYSIOLOGY), MICROORGANISMS, BLOOD PLASMA, BLOOD PLATELETS, BLOOD PROTEINS, BIOCHEMISTRY
Subject Categories : Biochemistry
Anatomy and Physiology
Medicine and Medical Research
Distribution Statement : APPROVED FOR PUBLIC RELEASE