Related Experiment Video
Updated: May 31, 2026

A Time Differential Staining Technique Coupled with Full Bilateral Gill Denervation to Study Ionocytes in Fish
Published on: March 19, 2015
Claudins in a primary cultured puffer fish (Tetraodon nigroviridis) gill epithelium
Abstract:
A primary cultured gill epithelium from the model organism Tetraodon nigroviridis (spotted green puffer fish) has been developed for the study of claudin tight junction (TJ) proteins and their potential role in the regulation of paracellular permeability across the gills of fishes. The cultured preparation is composed of polygonal epithelial cells that exhibit TJ protein immunoreactivity around the periphery and develop a surface morphology of concentric apical microridges. There is an absence of cells exhibiting intense Na+-K+-ATPase immunoreactivity and taken together, these characteristics indicate that the epithelium is composed of gill pavement cells only. In Tetraodon, 52 genes encoding for claudin isoforms (Tncldn) have been identified and 32 of these genes are expressed in whole gill tissue. Of these genes, 12 are responsive to alterations in environmental salinity in vivo (Tncldn3a, -3c, -6, -8d, -10d, -10e, -11a, -23b, -27a, -27c, -32a, and -33b). All claudin isoforms found in whole gill tissue can be found in cultured pavement cell gill epithelia with the exception of Tncldn6, -10d, and -10e. The cultured preparation is suitable for studying the "molecular machinery" of TJ proteins in fish gill pavement cells.
Related Concept Videos
Tight Junctions
Patch Clamp
In this method, a glass micropipette containing electrolyte solution is tightly sealed against a small portion of the cell membrane. As a result, a patch of the cell...

