Connections Between Connexins, Calcium, and Cataracts in the Lens
Autor: | Thomas W. White, Junyuan Gao, Xiaohua Gong, Richard T. Mathias, Francisco J. Martinez-Wittinghan, Xiurong Sun |
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Rok vydání: | 2004 |
Předmět: |
connexin knockout
Physiology Analytical chemistry Connexin chemistry.chemical_element coupling conductance connexin knockin Calcium Article Cataract Connexins Calcium in biology law.invention Tissue Culture Techniques Mice 03 medical and health sciences 0302 clinical medicine law Lens Crystalline Animals Homeostasis Calcium Signaling Eye Proteins Electrochemical gradient intracellular calcium 030304 developmental biology Mice Knockout Calcium metabolism 0303 health sciences Chemistry Electric Conductivity Gap junction Gap Junctions Mice Inbred C57BL Coupling (electronics) Lens (optics) Spectrometry Fluorescence 030221 ophthalmology & optometry Biophysics sense organs |
Zdroj: | The Journal of General Physiology |
ISSN: | 1540-7748 0022-1295 |
DOI: | 10.1085/jgp.200409121 |
Popis: | There is a good deal of evidence that the lens generates an internal micro circulatory system, which brings metabolites, like glucose, and antioxidants, like ascorbate, into the lens along the extracellular spaces between cells. Calcium also ought to be carried into the lens by this system. If so, the only path for Ca2+ to get out of the lens is to move down its electrochemical gradient into fiber cells, and then move by electrodiffusion from cell to cell through gap junctions to surface cells, where Ca-ATPase activity and Na/Ca exchange can transport it back into the aqueous or vitreous humors. The purpose of the present study was to test this calcium circulation hypothesis by studying calcium homeostasis in connexin (Cx46) knockout and (Cx46 for Cx50) knockin mouse lenses, which have different degrees of gap junction coupling. To measure intracellular calcium, FURA2 was injected into fiber cells, and the gradient in calcium concentration from center to surface was mapped in each type of lens. In wild-type lenses the coupling conductance of the mature fibers was approximately 0.5 S/cm2 of cell to cell contact, and the best fit to the calcium concentration data varied from 700 nM in the center to 300 nM at the surface. In the knockin lenses, the coupling conductance was approximately 1.0 S/cm2 and calcium varied from approximately 500 nM at the center to 300 nM at the surface. Thus, when the coupling conductance doubled, the concentration gradient halved, as predicted by the model. In knockout lenses, the coupling conductance was zero, hence the efflux path was knocked out and calcium accumulated to approximately 2 microM in central fibers. Knockout lenses also had a dense central cataract that extended from the center to about half the radius. Others have previously shown that this cataract involves activation of a calcium-dependent protease, Lp82. We can now expand on this finding to provide a hypothesis on each step that leads to cataract formation: knockout of Cx46 causes loss of coupling of mature fiber cells; the efflux path for calcium is therefore blocked; calcium accumulates in the central cells; at concentrations above approximately 1 microM (from the center to about half way out of a 3-wk-old lens) Lp82 is activated; Lp82 cleaves cytoplasmic proteins (crystallins) in central cells; and the cleaved proteins aggregate and scatter light. |
Databáze: | OpenAIRE |
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