𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Volume regulation in lens epithelial cells and differentiating lens fiber cells

✍ Scribed by David C. Beebe; Judith T. Parmelee; Karla S. Belcher


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
532 KB
Volume
143
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


Previous studies from our laboratory have led us to conclude that lens cell elongation is caused by an increase in cell volume. This volume increase results from an increase in the potassium content of the cells due to decreased potassium efflux. In contrast, an increase in the volume of most cells triggers a regulatory volume decrease (RVD) that is usually mediated by increased potassium efflux.

For this reason, chicken embryo lens epithelial cells were tested to see whether they were capable of typical cell volume regulation. Changes in cell volume during lens fiber differentiation were first estimated by 3H,0 water uptake. Cell water increased in proportion to cell length in elongating lens cells. Treatment of epithelial cells cultured in basal medium with dilute or concentrated medium, or with medium containing 50 m M sucrose, resulted in typical volume regulatory responses. Cells lost or gained volume in response to osmotic stress, then returned to their previous volume. In addition, the elongation and increase in cell volume that accompanies lens fiber cell differentiation occurred normally in either hypoor hypertonic media. This observation showed that the activation of mechanisms to compensate for osmotic stress did not interfere with the increase in volume that accompanies elongation. The ability of elongating cells to volume regulate was also tested. Lens epithelial cells were stimulated to elongate by exposure to embryonic vitreous humor, then challenged with hypotonic medium. These elongating cells regulated their volume as effectively as unstimulated cells. Therefore, cells that were increasing their volume due to reduced potassium efflux could adjust their volume in response to osmotic stress, presumably by increasing potassium efflux. This suggests that the changes in potassium efflux that occur during differentiation and RVD are regulated by distinct mechanisms.


πŸ“œ SIMILAR VOLUMES


pH Regulation in tissue-cultured bovine
✍ M. R. Williams; G. Duncan; P. C. Croghan; R. Riach; S. F. Webb πŸ“‚ Article πŸ“… 1992 πŸ› Springer 🌐 English βš– 812 KB

The intracellular pH (pHi) of tissue-cultured bovine lens epithelial cells was measured in small groups of 6 to 10 cells using the trapped fluorescent dye 2',7'-bis-(2-,carboxyethyl)-5 (and 6)carboxyfluorescein (BCECF). When perifused at 35 degrees C with artificial aqueous humour solution (AAH) con

Lamins of ocular lens epithelial cells
✍ M. Bagchi; T. Petrov; H. Maisel πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 163 KB

## Abstract Experiments were performed to characterize a prominent nuclear matrix (NM) protein isolated from tissue cultured mouse lens epithelial cells. This NM protein was separated by SDS‐PAGE and the stained gel band was analyzed by mass spectroscopy. Blast analysis of the amino acid sequence d

Dedifferentiation of lens epithelial cel
✍ A. J. M. Vermorken; A. A. Groeneveld; J. M. H. C. Hilderink; R. Waal; H. Bloemen πŸ“‚ Article πŸ“… 1977 πŸ› Springer 🌐 English βš– 802 KB

Lens epithelial cells can be kept in their original differentiated state or brought to dedifferentiation depending on the culture conditions. The different stages of differentiation can be identified using specific markers, namely the activity of steroid metabolizing enzymes, and the synthesis of sp

Nonchromatin nuclear proteins of mammali
✍ M. Bagchi; S.A. Ansari; M. Katar; H. Maisel πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 306 KB

The nuclear matrix (NM) proteins of six tissue cultured lens epithelial cell lines and one embryonic rabbit epidermal cell line were analyzed to determine possible tissue and species specificity of these proteins. The NM proteins were isolated by the modified Penman technique. The tissue cultured ce