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Fluorescence Visualization of Branchial Collagen Columns Embraced by Pillar Cells
Author(s) -
H Kudo,
Akira Kato,
Shigehisa Hirose
Publication year - 2006
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/jhc.6a7047.2006
Subject(s) - extracellular matrix , lamella (surface anatomy) , green fluorescent protein , concanavalin a , pillar , fluorescence microscope , microbiology and biotechnology , lectin , tissue transglutaminase , fluorescence , biophysics , chemistry , anatomy , biology , biochemistry , optics , physics , structural engineering , enzyme , engineering , in vitro , gene
A collagen column is a structure of the extracellular matrix that helps to maintain the flatness and width of gill lamella. Collagen columns are unique in that they are enfolded by plasma membrane of pillar cells that form two-dimensional vascular networks between parallel sheets of respiratory epithelia. Despite their unique structure and fundamental importance in the physiology of aquatic animals, little is known about their properties and molecular components, owing to the lack of detection methods. In this study we demonstrated that collagen columns can be visualized by staining with fluorescence-labeled concanavalin A (ConA), a lectin that specifically recognizes the trimannoside core of N-glycosylated proteins and histidine-tagged green fluorescent protein (His(6)-Xpress-GFP), a fluorescent substrate for transglutaminase. We constructed a three-dimensional image of a pillar cell and visualized the spatial relationship between collagen columns and contractile apparatuses within the pillar cell body. This manuscript contains online supplemental material at (www.jhc.org). Please visit this article online to view these materials.

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