The presence of delta-crystallin in the plasma membrane of chick lens fiber cells*1

1977 ◽  
Vol 109 (1) ◽  
pp. 63-69 ◽  
Author(s):  
J ALCALA
Author(s):  
Ronald H. Bradley ◽  
Jose Alcala ◽  
Harry Maisel

Filaments (average diameter, 12 nm) are a prominent feature of the water- insoluble fraction of chick lens fiber cells (1) (fig. 1). Isolation of the filaments was achieved in the following manner. The lens fiber mass was homogenized in standard salt solution pH 7.2 to which 10 mM B-mercaptoethanol was added. The homogenate was centrifuged at 37,000 g for 20 min. and the pellet washed in buffer until free of soluble proteins (lens crystallins) when tested with antisera to the crystallins. The pellet was then extracted in 8M urea and centrifuged at 77,000 g for 15 min. The membrane-rich pellet was discarded and the urea-soluble fraction was dialysed against the buffer to remove the urea. Negative stain analysis showed that intact filaments were present in the urea-free solution (UFS).A pellet rich in filaments was obtained by centrifugation of the UFS at 77,000 g for 1 hr. (fig. 2).


1980 ◽  
Vol 159 (4) ◽  
pp. 395-410 ◽  
Author(s):  
J. Kuszak ◽  
J. Alcala ◽  
H. Maisel

2017 ◽  
Vol 8 (5) ◽  
pp. 3523-3528 ◽  
Author(s):  
Peter S. Sherin ◽  
Ismael López-Duarte ◽  
Michael R. Dent ◽  
Markéta Kubánková ◽  
Aurimas Vyšniauskas ◽  
...  

Using fluorescent probes, we demonstrate that the plasma membrane of porcine eye lens fiber cells displays an unprecedentedly high degree of lipid ordering.


2012 ◽  
Vol 23 (16) ◽  
pp. 3266-3274 ◽  
Author(s):  
Miguel Jarrin ◽  
Tanushree Pandit ◽  
Lena Gunhaga

In embryonic and adult lenses, a balance of cell proliferation, cell cycle exit, and differentiation is necessary to maintain physical function. The molecular mechanisms regulating the transition of proliferating lens epithelial cells to differentiated primary lens fiber cells are poorly characterized. To investigate this question, we used gain- and loss-of-function analyses to modulate fibroblast growth factor (FGF) and/or bone morphogenetic protein (BMP) signals in chick lens/retina explants. Here we show that FGF activity plays a key role for proliferation independent of BMP signals. Moreover, a balance of FGF and BMP signals regulates cell cycle exit and the expression of Ccdc80 (also called Equarin), which is expressed at sites where differentiation of lens fiber cells occurs. BMP activity promotes cell cycle exit and induces Equarin expression in an FGF-dependent manner. In contrast, FGF activity is required but not sufficient to induce cell cycle exit or Equarin expression. Furthermore, our results show that in the absence of BMP activity, lens cells have increased cell cycle length or are arrested in the cell cycle, which leads to decreased cell cycle exit. Taken together, these findings suggest that proliferation, cell cycle exit, and early differentiation of primary lens fiber cells are regulated by counterbalancing BMP and FGF signals.


1978 ◽  
Vol 27 (4) ◽  
pp. 495-498 ◽  
Author(s):  
J. Kuszak ◽  
H. Maisel ◽  
C.V. Harding

Author(s):  
Camillo Peracchia ◽  
Stephen J. Girsch

The fiber cells of eye lens communicate directly with each other by exchanging ions, dyes and metabolites. In most tissues this type of communication (cell coupling) is mediated by gap junctions. In the lens, the fiber cells are extensively interconnected by junctions. However, lens junctions, although morphologically similar to gap junctions, differ from them in a number of structural, biochemical and immunological features. Like gap junctions, lens junctions are regions of close cell-to-cell apposition. Unlike gap junctions, however, the extracellular gap is apparently absent in lens junctions, such that their thickness is approximately 2 nm smaller than that of typical gap junctions (Fig. 1,c). In freeze-fracture replicas, the particles of control lens junctions are more loosely packed than those of typical gap junctions (Fig. 1,a) and crystallize, when exposed to uncoupling agents such as Ca++, or H+, into pseudo-hexagonal, rhombic (Fig. 1,b) and orthogonal arrays with a particle-to-particle spacing of 6.5 nm. Because of these differences, questions have been raised about the interpretation of the lens junctions as communicating junctions, in spite of the fact that they are the only junctions interlinking lens fiber cells.


2007 ◽  
Vol 75 (8) ◽  
pp. 737-744 ◽  
Author(s):  
Hasan Mahmud Reza ◽  
Hirofumi Nishi ◽  
Kohsuke Kataoka ◽  
Yoshiko Takahashi ◽  
Kunio Yasuda

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