Cellular Mechanisms for Diminished Scarring with Aging
- 1 April 2000
- journal article
- research article
- Published by Wolters Kluwer Health in Plastic and Reconstructive Surgery
- Vol. 105 (5) , 1591-1599
- https://doi.org/10.1097/00006534-200004050-00001
Abstract
The study of an age-dependent spectrum of scar formation is driven by the desire to understand and recapitulate scarless healing. Although focus in the past has been directed toward scarring in the fetus, less exuberant scarring is a common clinical observation in the elderly. Cell turnover is a major contributor to the development of scar tissue and is governed by the proliferative and apoptotic cellular fractions within a healing wound. We hypothesize that the balance between cell proliferation and apoptosis during late stages of excisional wound healing is, at least in part, responsible for age-related variations in scarring potential. Full-thickness 7-mm ulcers (four per ear), exposing bare cartilage, were made on the inner surface of the ear on 12 young and 12 aged New Zealand White rabbits. Analyses were performed at days 15, 21, and 28 postwounding. A previously described Scar Elevation Index was derived from histomorphometric analysis, along with the quantification of epithelial ingrowth and total cellularity. Apoptotic cellular fractions were derived from TdTmediated dUTP nick end-labeling assay-stained histologic sections; proliferative fractions were derived from proliferating cell nuclear antigen-labeled serial sections. Young rabbits demonstrated significantly greater scar elevation/area. Apoptosis was strongly associated with progress of epithelialization in both groups. Significantly higher proliferative indices were seen in the young and were sustained through day 28, by which time levels had substantially declined in the aged. No differences in apoptotic indices were demonstrated between groups at any time point. The clinical observation of less exuberant scarring with aging is supported by this animal model. Apoptosis follows the progression of epithelialization but does not appear to independently influence scar morphology. A diminished proliferative response during later stages of healing is an important contributing mechanism for the decrease in scar formation seen in the elderly. (Plast. Reconstr. Surg. 105: 1591, 2000.)Keywords
This publication has 18 references indexed in Scilit:
- Aging Is Associated with Reduced Deposition of Specific Extracellular Matrix Components, an Upregulation of Angiogenesis, and an Altered Inflammatory Response in a Murine Incisional Wound Healing ModelJournal of Investigative Dermatology, 1997
- Scar Formation: The Spectral Nature of Fetal and Adult Wound RepairPlastic and Reconstructive Surgery, 1996
- Effects of Ascorbic Acid on Proliferation and Collagen Synthesis in Relation to the Donor Age of Human Dermal FibroblastsJournal of Investigative Dermatology, 1994
- Detection of DNA fragmentation in apoptosis: application of in situ nick translation to cell culture systems and tissue sections.Journal of Histochemistry & Cytochemistry, 1993
- Differential extracellular matrix gene expression by fibroblasts during their proliferative life span in vitro and at senescenceJournal of Cellular Physiology, 1992
- Longitudinal study of in vivo wound repair and in vitro cellular senescence of dermal fibroblastsExperimental Gerontology, 1991
- Studies in fetal wound healing: III. Early deposition of fibronectin distinguishes fetal from adult wound healingJournal of Pediatric Surgery, 1989
- Effects of serum collected from rats of different ages on in vitro cell proliferationMechanisms of Ageing and Development, 1988
- Tissue replacement in the rabbit's earBritish Journal of Surgery, 1966