Literature DB >> 10602293

Visualization of interstitial cells of Cajal in living, intact tissues.

M Hanani1, V Belzer, A Rich, S M Faussone-Pellegrini.   

Abstract

Interstitial cells of Cajal (ICC) appear to be a major element in pacing and signal transmission in the gastrointestinal tract. A prominent problem in the study of ICC has been the difficulty in observing them in intact tissues. We used several methods to visualize living ICC in freshly-dissected tissues: (1) Placing small crystals of the lipophilic dye DiI in the submucosal-circular muscle border in the mouse colon resulted in the labeling of living ICC-like cells. Two main morphological cell types, bipolar and multipolar, were noted. The DiI stain could be converted into a stable, electron-opaque product. Electron-microscopic observations showed that the labeled cells had the typical appearance of ICC reported in previous studies. (2) Living ICC in the region of the myenteric plexus (ICC-MP) in the small intestines of mice and guinea-pigs were observed with Nomarski optics. This enabled the visualization of ICC in living tissues, and the impalement of the cells with Lucifer yellow-filled microelectrodes. The dye-labeled cells had the morphological features of ICC-MP, and about 30% of them were found to be dye coupled to 1-21 other ICC. The identity of the cells as ICC was verified by electron-microscopy following photoconversion, and by c-kit immunohistochemistry. (3) Living ICC were labeled with a c-kit antibody that does not require tissue fixation. This resulted in the fluorescent staining of the entire ICC network. Single cells were labeled by dye injection, which provided a detailed picture of ICC morphology. This method was found to be suitable for a wide range of tissues. We expect that these three methods for identifying ICC in intact, living tissues will be useful for physiological and pharmacological investigations of ICC in a variety of gastrointestinal tissues. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10602293     DOI: 10.1002/(SICI)1097-0029(19991201)47:5<336::AID-JEMT5>3.0.CO;2-5

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  5 in total

1.  Ano1, a Ca2+-activated Cl- channel, coordinates contractility in mouse intestine by Ca2+ transient coordination between interstitial cells of Cajal.

Authors:  Raman Deep Singh; Simon J Gibbons; Siva Arumugam Saravanaperumal; Peng Du; Grant W Hennig; Seth T Eisenman; Amelia Mazzone; Yujiro Hayashi; Chike Cao; Gary J Stoltz; Tamas Ordog; Jason R Rock; Brian D Harfe; Joseph H Szurszewski; Gianrico Farrugia
Journal:  J Physiol       Date:  2014-07-25       Impact factor: 5.182

2.  Role of interstitial cells and gap junctions in the transmission of spontaneous Ca2+ signals in detrusor smooth muscles of the guinea-pig urinary bladder.

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Journal:  J Physiol       Date:  2004-07-02       Impact factor: 5.182

Review 3.  Lucifer yellow - an angel rather than the devil.

Authors:  Menachem Hanani
Journal:  J Cell Mol Med       Date:  2012-01       Impact factor: 5.310

Review 4.  Transmission Electron Microscopy as a Powerful Tool to Investigate the Interaction of Nanoparticles with Subcellular Structures.

Authors:  Manuela Malatesta
Journal:  Int J Mol Sci       Date:  2021-11-26       Impact factor: 5.923

5.  Simultaneous ultrastructural analysis of fluorochrome-photoconverted diaminobenzidine and gold immunolabelling in cultured cells.

Authors:  M Malatesta; C Zancanaro; M Costanzo; B Cisterna; C Pellicciari
Journal:  Eur J Histochem       Date:  2013-09-16       Impact factor: 3.188

  5 in total

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