Purpose. The authors developed an assay to observe the contraction of a single human ciliary muscle cell. Methods. Cultured human ciliary muscle cells were partially detached from the culture dish by incubation with a nonenzymatic dissociation buffer and treated with carbachol or pilocarpine. Contraction was quantified by measuring the cross-sectional surface areas of the cells. Results. Carbachol decreased the cell surface area in a time- dependent manner. Contraction was observed within 1 min after the addition of carbachol and completed in less than 15 min. The effect of carbachol was dose dependent. For example, at 10 min after treatment with 10 μmol/l carbachol, the relative surface areas of cells decreased to 47% ± 4% (mean ± standard error of the mean, n = 7, with surface area at 0 min defined as 100%). The relative surface areas were 74% ± 4% (n = 7) after 1 μmol/l and 100% ± 9% (n = 7) after 0.1 μmol/l carbachol treatment. This contractile effect was antagonized by pretreatment with atropine, a specific muscarinic antagonist. Conclusions. A simple method was established to study the functional changes of human ciliary muscle cells.
|Number of pages||4|
|Journal||Investigative Ophthalmology and Visual Science|
|State||Published - 1 Jan 1993|
- ciliary muscle cell
- single-cell contraction assay