Literature DB >> 18574255

Synergistic tissue counterstaining and image segmentation techniques for accurate, quantitative immunohistochemistry.

Simone P Zehntner1, M Mallar Chakravarty, Rozica J Bolovan, Christopher Chan, Barry J Bedell.   

Abstract

Quantitative analysis of digitized IHC-stained tissue sections is increasingly used in research studies and clinical practice. Accurate quantification of IHC staining, however, is often complicated by conventional tissue counterstains caused by the color convolution of the IHC chromogen and the counterstain. To overcome this issue, we implemented a new counterstain, Acid Blue 129, which provides homogeneous tissue background staining. Furthermore, we combined this counterstaining technique with a simple, robust, fully automated image segmentation algorithm, which takes advantage of the high degree of color separation between the 3-amino-9-ethyl-carbazole (AEC) chromogen and the Acid Blue 129 counterstain. Rigorous validation of the automated technique against manual segmentation data, using Ki-67 IHC sections from rat C6 glioma and beta-amyloid IHC sections from transgenic mice with amyloid precursor protein (APP) mutations, has shown the automated method to produce highly accurate results compared with ground truth estimates based on the manually segmented images. The synergistic combination of the novel tissue counterstaining and image segmentation techniques described in this study will allow for accurate, reproducible, and efficient quantitative IHC studies for a wide range of antibodies and tissues.

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Year:  2008        PMID: 18574255      PMCID: PMC2544616          DOI: 10.1369/jhc.2008.950345

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  10 in total

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3.  Protein-embedding technique: a potential approach to standardization of immunohistochemistry for formalin-fixed, paraffin-embedded tissue sections.

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7.  Automated selection of DAB-labeled tissue for immunohistochemical quantification.

Authors:  Eric M Brey; Zahid Lalani; Carol Johnston; Mark Wong; Larry V McIntire; Pauline J Duke; Charles W Patrick
Journal:  J Histochem Cytochem       Date:  2003-05       Impact factor: 2.479

8.  High-level neuronal expression of abeta 1-42 in wild-type human amyloid protein precursor transgenic mice: synaptotoxicity without plaque formation.

Authors:  L Mucke; E Masliah; G Q Yu; M Mallory; E M Rockenstein; G Tatsuno; K Hu; D Kholodenko; K Johnson-Wood; L McConlogue
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  10 in total
  9 in total

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Journal:  J Neuropathol Exp Neurol       Date:  2014-01       Impact factor: 3.685

2.  Correlation of amyloid PET ligand florbetapir F 18 binding with Aβ aggregation and neuritic plaque deposition in postmortem brain tissue.

Authors:  Seok Rye Choi; Julie A Schneider; David A Bennett; Thomas G Beach; Barry J Bedell; Simone P Zehntner; Michael J Krautkramer; Hank F Kung; Daniel M Skovronsky; Franz Hefti; Christopher M Clark
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Review 4.  Translational AI and Deep Learning in Diagnostic Pathology.

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Journal:  Front Med (Lausanne)       Date:  2019-10-01

5.  Initial assessment of the spatial learning, reversal, and sequencing task capabilities of knock-in rats with humanizing mutations in the Aβ-coding region of App.

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6.  Quantitative magnetic resonance imaging of cortical multiple sclerosis pathology.

Authors:  Christine L Tardif; Barry J Bedell; Simon F Eskildsen; D Louis Collins; G Bruce Pike
Journal:  Mult Scler Int       Date:  2012-11-18

7.  Automated Ki-67 Quantification of Immunohistochemical Staining Image of Human Nasopharyngeal Carcinoma Xenografts.

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8.  Knock-in rats with homozygous PSEN1L435F Alzheimer mutation are viable and show selective γ-secretase activity loss causing low Aβ40/42 and high Aβ43.

Authors:  Marc D Tambini; Luciano D'Adamio
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9.  Facilitation of glutamate, but not GABA, release in Familial Alzheimer's APP mutant Knock-in rats with increased β-cleavage of APP.

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  9 in total

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