The primary function of the ocular lens is as a light-focusing structure. To this end the lens is avascular, with a highly ordered arrangement of cells that acts to reduce light scattering. However, the avascular nature of the lens presents the problem of supplying cells deep within the lens with nutrients and removing waste products of cellular metabolism, i.e. maintaining cellular homeostasis, To solve this problem the lens possesses intercellular channels, called gap junctions, that facilitate cell-to-cell communication and are regulated by changes in the subcellular distribution and age dependent processing of the gap junction protein subunits, called connexins. The lens expresses three types of connexins (Cx): Cx43 in the anterior surface epithelial cells and connexins 46 and 50 in the fibre cells. Therefore, to fully examine the role of GJs in lens homeostasis, regional differences in GJ structure and function need to be quantified. In this thesis I present the results of experiments designed to map the differentiation dependent changes to subcellular distribution and posttranslational processing of Cx46 and Cx50 in mouse and rat lenses. My results quantitatively show for the first time that Cx50 undergoes two discrete cleavage events in a similar manner to that previously shown for Cx46, and that qualitatively Cx46 does the same in the mouse lens' Such posttranslational processing has important effects on the proposed lens circulation model (Mathias et al., 1997) that accounts for lens homeostasis. In addition, I have examined the functional contribution of gap junctions to localized intercellular communication in different regions of wildtype and Cx46-KO mouse lenses, using highly localised uncaging of fluorescein with Two-Photon Excited Flash Photolysis (TPEFP) in half lenses, The results of these experiments have provided the first supporting evidence for a macromolecule-permeable pathway, previously suggested by Shestoplaov and Bassnett (2000, 2003), that acts in conjunction with gap junctions to facilitate intercellular communication in the lens core. My results show that this pathway acts at a localised level to confer cell-to-cell communication that is as effective as that mediated by gap junctions, and therefore a re-evaluation of current models of lens homeostasis is now required. / Whole document restricted, but available by request, use the feedback form to request access.
| Identifer | oai:union.ndltd.org:ADTP/275570 |
| Date | January 2007 |
| Creators | Sisley, Aran Mathew George |
| Publisher | ResearchSpace@Auckland |
| Source Sets | Australiasian Digital Theses Program |
| Language | English |
| Detected Language | English |
| Rights | Whole document restricted but available by request. Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated., http://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm, Copyright: The author |
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