Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.814340
Title: In vitro characterisation of human cleft fibroblasts isolated from patients with differing cleft manifestations
Author: Saeed, Naveed
ISNI:       0000 0004 9353 5396
Awarding Body: University of Birmingham
Current Institution: University of Birmingham
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Following surgical correction of cleft lip and palate a number of patients develop post-operative complications including oronasal-fistulae (ONF) and hypertrophic scarring (HTS). As these conditions can form due to pathological wound healing, this study aimed to characterise fibroblast behaviour, derived from patients with differing cleft phenotypes, to identify potential contributing factors. Fibroblasts were isolated from oral mucosal tissues derived from 29 cleft patients and were subsequently characterised and compared in terms proliferation, migration, ECM deposition and gene expression. Cleft fibroblasts were clustered into two statistically distinct migratory groups: fast and slow, with fast migrating fibroblasts secreting greater amounts of collagen. Although these groups did not correlate with cleft phenotype, CL fibroblasts all presented increased motility coupled with increased collagen deposition and upregulation of COL1A1. As both elevated motility and collagen secretion are hallmarks of HTS, it is possible that patients with faster migrating fibroblasts, including those derived from CL, may be at greater risk of pathological wound healing. Further, as fast migrating fibroblasts contained greater quantities of F-actin and upregulated ARP2, a major component of the ARP2/3 complex which acts as an actin filament nucleator, the observed increase in motility may be a result of altered cytoskeletal dynamics.
Supervisor: Not available Sponsor: EPSRC
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.814340  DOI: Not available
Keywords: RK Dentistry
Share: