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Morphological investigations into the development of the mammalian corneal endothelium using the mouse model

Includes bibliographical references (leaves 83-89).

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Main Author: Mgwebi, Thandiswa
Other Authors: Kidson, Sue
Format: Thesis
Language:English
Published: Department of Human Biology 2014
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access_status_str Open Access
author Mgwebi, Thandiswa
author2 Kidson, Sue
author_browse Kidson, Sue
Mgwebi, Thandiswa
author_facet Kidson, Sue
Mgwebi, Thandiswa
author_sort Mgwebi, Thandiswa
collection Thesis
description Includes bibliographical references (leaves 83-89).
format Thesis
id oai:open.uct.ac.za:11427/3268
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:11.035Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Human Biology
publisherStr Department of Human Biology
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/3268 Morphological investigations into the development of the mammalian corneal endothelium using the mouse model Mgwebi, Thandiswa Kidson, Sue Medicine Includes bibliographical references (leaves 83-89). The corneal endothelium (CE), a mesenchyme-derived tissue, is a monolayer of squamous cells on the inner corneal surface. In Foxc1-1• mice, the CE fails to form. The understanding of the cause of this defect has implications for the study of human eye disorders that are related to FOXC1 mutations. To understand the basis of CE defects in Foxc1-1- mice, an analysis of normal CE development was performed using scanning electron microscopy. Results showed that in normal mice the transformation from mesenchyme to endothelium was initiated at embryonic day (E) 12.5 and was characterised by a change from stellate to cobblestone shape and the formation of junctions. In FoxcN- mice, the process was initiated but a cobblestone shape not attained. The expression of adherens (N-cadherin) and tight junction (Z0-1) proteins was investigated by immunoflouresence microscopy. In the normal embryo, the expression of N-cadherin was initially in cytoplasmic vesicles and later at the cell membranes. ZO-l was first detected at the cell peripheries at E13.5. In Foxct-I- mice, N-cadherin peripheral bands failed to form. ZO-l was not expressed. These results suggest that the failure to form a monolayered CE in Foxc1 mice is due to incomplete mesenchyme-endothelial conversion. Junction formation was further investigated in vitro. N-cadherin was cytoplasmic in pre-confluent cells and at cell edges in confluent cells. ZO-l was not detected. These results suggest that in vitro, these cells are either unable to form tight junctions or the culture medium does not contain the appropriate signalling molecules. 2014-07-28T18:17:30Z 2014-07-28T18:17:30Z 2004 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/3268 eng application/pdf Department of Human Biology Faculty of Health Sciences University of Cape Town
spellingShingle Medicine
Mgwebi, Thandiswa
Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
thesis_degree_str Doctoral
title Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
title_full Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
title_fullStr Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
title_full_unstemmed Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
title_short Morphological investigations into the development of the mammalian corneal endothelium using the mouse model
title_sort morphological investigations into the development of the mammalian corneal endothelium using the mouse model
topic Medicine
url http://hdl.handle.net/11427/3268
work_keys_str_mv AT mgwebithandiswa morphologicalinvestigationsintothedevelopmentofthemammaliancornealendotheliumusingthemousemodel