Literature DB >> 20622939

Time-Saving Benefits of Intravital Staining.

Catherine Macgillivray1, Jeremy Sylvan, Richard T Lee, Hayden Huang.   

Abstract

One of the challenges in labeling tissues for fluorescence microscopy is minimizing sample processing while maintaining or improving the information generated by the fluorescent label. Generally, tissues are extracted, fixed, and embedded in mounting media (such as paraffin), sectioned, and then postprocessed by removing the paraffin, blocking, labeling, and washing. Despite all of these steps, the consistency of labeling quality can vary as a result of several factors, including heterogeneity in labeling efficiency from slide to slide, the necessity of postprocessing to obtain information on sequential sections of tissue, interference from the mounting media, and loss of native three-dimensional structural information, especially in thicker sections. A method for embedding and processing tissues that have been labeled by intravital staining is described in this study. Intravital staining is the process in which live-cell dyes and other labels are injected into the bloodstream before fixation of the tissues. Tissues processed this way can be imaged upon sectioning without further staining and retain their native, three-dimensional information, thereby improving the information retained by the labels and speeding up sample processing.

Entities:  

Year:  2008        PMID: 20622939      PMCID: PMC2901106          DOI: 10.1179/his.2008.31.3.129

Source DB:  PubMed          Journal:  J Histotechnol        ISSN: 0147-8885            Impact factor:   0.714


  4 in total

1.  High-resolution whole organ imaging using two-photon tissue cytometry.

Authors:  Timothy Ragan; Jeremy D Sylvan; Ki Hean Kim; Hayden Huang; Karsten Bahlmann; Richard T Lee; Peter T C So
Journal:  J Biomed Opt       Date:  2007 Jan-Feb       Impact factor: 3.170

2.  Cardiomyocyte hypertrophy and degradation of connexin43 through spatially restricted autocrine/paracrine heparin-binding EGF.

Authors:  Jun Yoshioka; Robin N Prince; Hayden Huang; Scott B Perkins; Francisco U Cruz; Catherine MacGillivray; Douglas A Lauffenburger; Richard T Lee
Journal:  Proc Natl Acad Sci U S A       Date:  2005-07-14       Impact factor: 11.205

3.  Peroxisome proliferator activated-receptor agonism and left ventricular remodeling in mice with chronic myocardial infarction.

Authors:  Stefan Frantz; Kai Hu; Julian Widder; Barbara Bayer; Catharina Clara Witzel; Isabel Schmidt; Paolo Galuppo; Jörg Strotmann; Georg Ertl; Johann Bauersachs
Journal:  Br J Pharmacol       Date:  2003-12-08       Impact factor: 8.739

4.  Targeted deletion of thioredoxin-interacting protein regulates cardiac dysfunction in response to pressure overload.

Authors:  Jun Yoshioka; Kenichi Imahashi; Scott A Gabel; William A Chutkow; Aurora A Burds; Joseph Gannon; P Christian Schulze; Catherine MacGillivray; Robert E London; Elizabeth Murphy; Richard T Lee
Journal:  Circ Res       Date:  2007-10-04       Impact factor: 17.367

  4 in total
  1 in total

1.  Three-dimensional cardiac architecture determined by two-photon microtomy.

Authors:  Hayden Huang; Catherine Macgillivray; Hyuk-Sang Kwon; Jan Lammerding; Jeffrey Robbins; Richard T Lee; Peter So
Journal:  J Biomed Opt       Date:  2009 Jul-Aug       Impact factor: 3.170

  1 in total

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