REPAIR KINETICS OF AMNION CELLS AFTER MICROSURGICAL INJURY

Citation
Ra. Quintero et al., REPAIR KINETICS OF AMNION CELLS AFTER MICROSURGICAL INJURY, Fetal diagnosis and therapy, 11(5), 1996, pp. 348-356
Citations number
6
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
10153837
Volume
11
Issue
5
Year of publication
1996
Pages
348 - 356
Database
ISI
SICI code
1015-3837(1996)11:5<348:RKOACA>2.0.ZU;2-4
Abstract
Objective: There is a paucity of data regarding healing of fetal membr anes, We assessed the repairing ability of a microsurgically-injured m onolayer of amnion-derived cells compared to an endothelial cell line. Materials and Methods: Amnion-derived cells (FL cells) were grown to confluence in 10% fetal calf serum (FCS), A microsurgical incision was performed under an inverted microscope, The area of each incision was measured at times 0, 6, 12 and 24 h using MCID M4 image analysis soft ware, The experiments were repeated using 1% FCS, The observations wer e also made replacing the media at 6 and 12 h, Umbilical-cord-derived endothelial cells were used for comparison, The rate of repair of the incision was measured using three methods: (a) absolute closure rate ( ACR): (A(0)-A(1))/T, where A(0) is the original incisional area, and A (1) is the new area at interval T; (b) relative percentage rate (RPR): (A(0)-A(1))/A(0)/T x 100, and (c) healing rate (HR): (A(0)-A(1))/A(0) x 100, Results: Amnion cells were capable of repairing the microsurgi cal defect. The ACR decreased over time, and was higher with larger de fects, A lower concentration of FCS nor the addition of fresh media al tered the repair process significantly, Endothelial cells were signifi cantly faster than amnion cells or amnion-supplemented cells with endo thelial media, The RPR remained relatively constant for all groups, su ggesting Gompertzian kinetics, Conclusions: Amnion cells are capable o f repairing a surgical defect at a relatively constant percent rate, b ut are slower than an endothelial cell line. The decreased rate of clo sure over time may be due to relative-contact inhibition, Further stud ies will concentrate on the molecular and cellular mechanisms involved in this process.