In Situ Hybridization and Double Immunohistochemistry for the Detection of VEGF-A mRNA and CD34/Collagen IV Proteins in Renal Transplant Biopsies

Methods Mol Biol. 2018:1788:131-143. doi: 10.1007/7651_2017_86.

Abstract

Quantitative metrics on the tissue distribution of different cell phenotypes, extracellular matrix components, and signaling/cell cycle markers hold the promise for the advent of new-generation tissue-based predictive/prognostic biomarkers in clinical diagnostics. The workflow of this approach is composed of three major phases: (1) detection of multiple molecular targets on a single histologic section, (2) image acquisition, and (3) digital image processing and analysis. Here, we present the most prevalent current alternatives for step (1) and describe a three-plex staining and image acquisition platform that captures the spatial distribution of macromolecules from two different species.

Keywords: Fluorescent immunohistochemistry; In situ hybridization; Quantitative image analysis; Whole slide digital imaging.

MeSH terms

  • Animals
  • Antigens, CD34 / analysis*
  • Biopsy / methods
  • Collagen Type IV / analysis*
  • Humans
  • Image Processing, Computer-Assisted / methods*
  • Immunohistochemistry / methods*
  • In Situ Hybridization / methods*
  • Kidney / pathology*
  • Kidney Transplantation
  • Paraffin Embedding / methods
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics
  • Tissue Fixation / methods
  • Vascular Endothelial Growth Factor A / genetics

Substances

  • Antigens, CD34
  • Collagen Type IV
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A