Confocal Microscopic Analysis of Scarless Repair in the Fetal Rat: Defining the Transition

&NA; Fetal wounds pass from scarless repair to healing with scar formation during gestation. This transition depends on both the size of the wound and the gestational age of the fetus. This study defines the transition period in the fetal rat model and provides new insight into scarless collagen wound architecture by using confocal microscopy. A total of 16 pregnant Sprague‐Dawley rats were operated on. Open full‐thickness wounds, 2 mm in diameter, were created on fetal rats at gestational ages 14.5 days (E14; n = 10), 16.5 days (E16; n = 42), and 18.5 days (E18; n = 42) (term = 21.5 days). Wounds were harvested at 24 (n = 18 per gestational age) and 72 hours (n = 24 per gestational age). Skin at identical gestational ages to wound harvest was used for controls. The wounds were fixed and stained with hematoxylin and eosin, antibody to type I collagen, and Sirius red for confocal microscopic evaluation. No E14 rat fetuses survived to wound harvest. Wounds created on E16 fetal rats healed completely and without scarring. E16 fetal rat hair follicle formation and collagen architecture was similar to that of normal, nonwounded skin. Wounds created on E18 fetal rats demonstrated slower healing; only 50 percent were completely healed at 72 hours compared with 100 percent of the E16 fetal rat wounds at 72 hours. Furthermore, the E18 wounds healed with collagen scar formation and without hair follicle formation. Confocal microscopy demonstrated that the collagen fibers were thin and arranged in a wispy pattern in E16 fetal rat wounds and in nonwounded dermis. E18 fetal rat wounds had thickened collagen fibers with large interfiber distances. Two‐millimeter excisional E16 fetal rat wounds heal without scar formation and with regeneration of normal dermal and epidermal appendage architecture. E18 fetal rat wounds heal in a pattern similar to that of adult cutaneous wounds, with scar formation and absence of epidermal appendages. Confocal microscopy more clearly defined the dermal architecture in normal skin, scarless wounds, and scars. These data further define the transition period in the fetal rat wound model, which promises to be an effective system for the study of in vivo scarless wound healing.

[1]  D. Cochran,et al.  Development of an in vitro wound healing model for periodontal cells. , 2000, Journal of periodontology.

[2]  S. Ihara,et al.  Ontogenetic transition of wound healing pattern in rat skin occurring at the fetal stage. , 1990, Development.

[3]  M. Longaker,et al.  The Fetal Fibroblast: The Effector Cell of Scarless Fetal Skin Repair , 1995, Plastic and reconstructive surgery.

[4]  M. Longaker,et al.  Scarless wound repair: a human fetal skin model. , 1992, Development.

[5]  M. Longaker,et al.  Rapid epithelialisation of fetal wounds is associated with the early deposition of tenascin. , 1991, Journal of cell science.

[6]  M. Longaker,et al.  Foetal wound healing in a large animal model: the deposition of collagen is confirmed. , 1990, British journal of plastic surgery.

[7]  N. Perelman,et al.  Relative distribution and crosslinking of collagen distinguish fetal from adult sheep wound repair. , 1999, Journal of pediatric surgery.

[8]  M. Longaker,et al.  The in vivo effect of hyaluronan associated protein-collagen complex on wound repair. , 1995, Biochemistry and molecular biology international.

[9]  G. Hallock,et al.  The Ontogenetic Transition of Collagen Deposition in Rat Skin , 1993, Annals of plastic surgery.

[10]  I. K. Cohen,et al.  Biology of fetal wound healing: collagen biosynthesis during dermal repair. , 1992, Journal of pediatric surgery.

[11]  M. Longaker,et al.  Animal models for the study of fetal tissue repair. , 1991, The Journal of surgical research.

[12]  I. K. Cohen,et al.  In Vivo Degradation of Fetal Wound Hyaluronic Acid Results in Increased Fibroplasia, Collagen Deposition, and Neovascularization , 1992, Plastic and reconstructive surgery.

[13]  P. Bartold,et al.  Growth factor modulation of fibroblasts in simulated wound healing. , 1996, Journal of periodontal research.

[14]  M. Longaker,et al.  Wound size and gestational age modulate scar formation in fetal wound repair. , 1997, Journal of pediatric surgery.

[15]  I. K. Cohen,et al.  Collagen induces cytokine release by fetal platelets: implications in scarless healing. , 1997, Journal of pediatric surgery.

[16]  G. Hallock,et al.  Analysis of Collagen Content in the Fetal Wound , 1988, Annals of plastic surgery.

[17]  M. Longaker,et al.  Fetal Wound Healing The Ontogeny of Scar Formation in the Non‐Human Primate , 1993, Annals of surgery.

[18]  M. Longaker,et al.  Studies in fetal wound healing, VI. Second and early third trimester fetal wounds demonstrate rapid collagen deposition without scar formation. , 1990, Journal of pediatric surgery.

[19]  M S Spach,et al.  Conventional and confocal fluorescence microscopy of collagen fibers in the heart. , 1993, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[20]  D. Belford The mechanism of excisional fetal wound repair in vitro is responsive to growth factors. , 1997, Endocrinology.