نتایج جستجو برای: lens fiber cells

تعداد نتایج: 1545354  

2011
Junyuan Gao Xiurong Sun Leon C. Moore Thomas W. White Peter R. Brink Richard T. Mathias

We recently modeled fluid flow through gap junction channels coupling the pigmented and nonpigmented layers of the ciliary body. The model suggested the channels could transport the secretion of aqueous humor, but flow would be driven by hydrostatic pressure rather than osmosis. The pressure required to drive fluid through a single layer of gap junctions might be just a few mmHg and difficult t...

2016
Ying Zhang Jieqing Fan Joshua W. K. Ho Tommy Hu Stephen C. Kneeland Xueping Fan Qiongchao Xi Michael A. Sellarole Wilhelmine N. de Vries Weining Lu Salil A. Lachke Richard A. Lang Simon W. M. John Richard L. Maas

The developing lens is a powerful system for investigating the molecular basis of inductive tissue interactions and for studying cataract, the leading cause of blindness. The formation of tightly controlled cell-cell adhesions and cell-matrix junctions between lens epithelial (LE) cells, between lens fiber (LF) cells, and between these two cell populations enables the vertebrate lens to adopt a...

Journal: :The Journal of General Physiology 2004
Junyuan Gao Xiurong Sun Francisco J. Martinez-Wittinghan Xiaohua Gong Thomas W. White Richard T. Mathias

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 fi...

2016
Ying Zhang Jieqing Fan Joshua W. K. Ho Tommy Hu Stephen C. Kneeland Xueping Fan Qiongchao Xi Michael A. Sellarole Wilhelmine N. de Vries Weining Lu Salil A. Lachke Richard A. Lang Simon W. M. John Richard L. Maas

The developing lens is a powerful system for investigating the molecular basis of inductive tissue interactions and for studying cataract, the leading cause of blindness. The formation of tightly controlled cell-cell adhesions and cell-matrix junctions between lens epithelial (LE) cells, between lens fiber (LF) cells, and between these two cell populations enables the vertebrate lens to adopt a...

Journal: :Optics express 2001
C Liang M Descour K B Sung R Richards-Kortum

In-vivo imaging can be achieved with a coherent-fiber-bundle based confocal reflectance microscope. Such a microscope could provide the means to detect pre-cancerous lesions in the cervix by characterizing cells' nuclear-to-cytoplasmic ratio. In this paper we present the design of such a fiber confocal reflectance microscope, with an emphasis on its optical sub-systems. The optical sub-systems ...

Journal: :Investigative ophthalmology & visual science 1993
T Arita Y Murata L R Lin T Tsuji V N Reddy

PURPOSE This study examined the extent to which human lens epithelial (HLE) cells in tissue culture retain the potential for differentiation, expression of lens-specific marker proteins, and the synthesis of lens capsule, the major characteristics of lens epithelium in vivo. METHODS Primary cultures of HLE cells were maintained for up to 450 days. Transmission and immunoelectron microscopy we...

Journal: :The Journal of Cell Biology 1997
Steven Bassnett Danijela Mataic

During development, the lens of the eye becomes transparent, in part because of the elimination of nuclei and other organelles from the central lens fiber cells by an apoptotic-like mechanism. Using confocal microscopy we showed that, at the border of the organelle-free zone (OFZ), fiber cell nuclei became suddenly irregular in shape, with marginalized chromatin. Subsequently, holes appeared in...

Journal: :The Journal of Cell Biology 1983
P G Fitzgerald D Bok J Horwitz

The in situ distribution of the 26-kdalton Main Intrinsic Polypeptide (MIP or MP 26), a putative gap junction protein in ocular lens fibers, was defined at the electron microscope level using indirect immunoferritin labeling of ultrathin frozen sections of rat lens. MIP was found distributed throughout the plasma membrane of the lens fiber cell, with no apparent distinction between junctional a...

Journal: :Investigative Opthalmology & Visual Science 2011

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