Delineation of the healthy rabbit lung by immunohistochemistry - a technical note

Acta Histochem. 2020 Dec;122(8):151648. doi: 10.1016/j.acthis.2020.151648. Epub 2020 Oct 31.

Abstract

Investigation and studies of pulmonary diseases and injuries require pre-clinical animal models. The rabbit lung model is widely used and allows for a diverse set of readouts. Among them, histology and immunohistochemistry are of invaluable merit because qualitative and quantitative information about tissue morphology and composition can be easily obtained. In this technical note, we performed several histological and immunohistochemical stainings in the rabbit healthy naïve lung tissue. Overnight formalin fixation with subsequent paraffin embedding was compared to cryopreservation with a subsequent 10-minute formalin fixation prior to staining. Antigen retrieval (AR) for paraffin embedded sections proved to enhance the corresponding signals compared to analogous staining without AR. Advantages and disadvantages of chromogenic versus immunofluorescence stainings were discussed. In addition, several morphological structures, such as the intrapulmonary bronchus with its mucosal folds, the pulmonary artery, the alveoli and the lymph nodes, were stained with various stainings at the same site in order to give a comprehensive picture of their composition. Besides Haematoxylin&Eosin and Elastica van Gieson staining, collagen I, collagen III, fibronectin, α-SMA, ki-67 and protease-activated receptor-2 (PAR-2) immunohistochemistry was performed. Collagen I, collagen III and fibronectin expression was positive at the outer rim of the pulmonary arteries, while the inner rim was collagen III positive. Moreover, the fibronectin staining in the intrapulmonary bronchus showed an opposite trend when compared to the collagen III staining. The alveoli exhibited PAR-2 expression, while PAR-2 was not expressed in lymph nodes of the healthy rabbit lung.

Keywords: Rabbit lung; alveoli; antigen retrieval; bronchus; cryosection; immunofluorescence; lymph node.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Animals
  • Biomarkers / metabolism
  • Bronchi / blood supply
  • Bronchi / cytology*
  • Bronchi / metabolism
  • Collagen Type I / genetics
  • Collagen Type I / metabolism
  • Collagen Type III / genetics
  • Collagen Type III / metabolism
  • Eosine Yellowish-(YS)
  • Female
  • Fibronectins / genetics
  • Fibronectins / metabolism
  • Fixatives / chemistry
  • Formaldehyde / chemistry
  • Hematoxylin
  • Immunohistochemistry / methods*
  • Ki-67 Antigen / genetics
  • Ki-67 Antigen / metabolism
  • Lymph Nodes / blood supply
  • Lymph Nodes / cytology
  • Lymph Nodes / metabolism
  • Paraffin Embedding / methods*
  • Pulmonary Alveoli / blood supply
  • Pulmonary Alveoli / cytology
  • Pulmonary Alveoli / metabolism
  • Rabbits
  • Receptor, PAR-2 / genetics
  • Receptor, PAR-2 / metabolism
  • Staining and Labeling / methods*
  • Tissue Fixation / methods*

Substances

  • Actins
  • Biomarkers
  • Collagen Type I
  • Collagen Type III
  • Fibronectins
  • Fixatives
  • Ki-67 Antigen
  • Receptor, PAR-2
  • Formaldehyde
  • Eosine Yellowish-(YS)
  • Hematoxylin