The programmed elimination of nuclei and other cytoplasmic organelles from cells in the deep cortex of the ocular lens is one of the most striking aspects of terminal differentiation in this tissue. Organelles are light scattering structures and their removal ensures the transparency of the lens substance. The abnormal persistence of organelles is a characteristic feature of cataracts in mice and humans. During the last grant period we completed a morphometric analysis of organelle loss in the developing lens. In the current proposal we will address three related questions that arise directly from these studies: What factors trigger organelle loss? What are the biochemical mechanisms underlying this process and, once the organelles have disappeared, what accounts for the extraordinary longevity of certain mRNAs? In considering possible triggering mechanisms, we will evaluate the role of tissue/matrix interactions and lenticular oxygen gradients. There are some striking similarities between organelle loss in the lens and classical apoptosis. We will determine which elements of the apoptotic pathway are utilized during organelle loss. We will also test the putative involvement of 15-lipoxygenase (an enzyme implicated in erythrocyte organelle loss) in fiber cell denucleation. Finally, our preliminary data indicate that following dissolution of the fiber cell nuclei, specific mRNAs are extraordinarily long lived. We will examine the role of cis- and trans-acting factors in stabilizing one such mRNA, delta crystallin. Together these experiments will provide important new information on lens organelle loss, fiber cell differentiation and cataractogenesis.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY009852-10
Application #
6327115
Study Section
Visual Sciences A Study Section (VISA)
Program Officer
Liberman, Ellen S
Project Start
1992-09-30
Project End
2006-09-29
Budget Start
2001-09-30
Budget End
2002-09-29
Support Year
10
Fiscal Year
2001
Total Cost
$269,500
Indirect Cost
Name
Washington University
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
De Maria, Alicia; Zhao, Haiqing; Bassnett, Steven (2018) Expression of potassium-dependent sodium-calcium exchanger in the murine lens. Exp Eye Res 167:18-24
Bassnett, Steven; Costello, M Joseph (2017) The cause and consequence of fiber cell compaction in the vertebrate lens. Exp Eye Res 156:50-57
Šiki?, Hrvoje; Shi, Yanrong; Lubura, Snježana et al. (2017) A full lifespan model of vertebrate lens growth. R Soc Open Sci 4:160695
Bassnett, Steven; Šiki?, Hrvoje (2017) The lens growth process. Prog Retin Eye Res 60:181-200
Mesa, Rosana; Tyagi, Manoj; Harocopos, George et al. (2016) Somatic Variants in the Human Lens Epithelium: A Preliminary Assessment. Invest Ophthalmol Vis Sci 57:4063-75
De Maria, Alicia; Bassnett, Steven (2015) Birc7: A Late Fiber Gene of the Crystalline Lens. Invest Ophthalmol Vis Sci 56:4823-34
Šiki?, Hrvoje; Shi, Yanrong; Lubura, Snježana et al. (2015) A stochastic model of eye lens growth. J Theor Biol 376:15-31
Shi, Yanrong; De Maria, Alicia; Lubura, Snježana et al. (2015) The penny pusher: a cellular model of lens growth. Invest Ophthalmol Vis Sci 56:799-809
Mesa, Rosana; Bassnett, Steven (2013) UV-B-induced DNA damage and repair in the mouse lens. Invest Ophthalmol Vis Sci 54:6789-97
Shi, Yanrong; Tu, Yidong; De Maria, Alicia et al. (2013) Development, composition, and structural arrangements of the ciliary zonule of the mouse. Invest Ophthalmol Vis Sci 54:2504-15

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