Hyperplasia of Alveolar Neuroendocrine Cells in Rat Lung Carcinogenesis by Silica with Selective Expression of Proadrenomedullin-Derived Peptides and Amidating Enzymes

• Published in: Laboratory investigation 2001-12, Vol.81 (12), p.1627-1638
• Main Authors: Elizegi, Eider, Pino, Irene, Vicent, Silvestre, Blanco, David, Saffiotti, Umberto, Montuenga, Luis M
• Format: Article
• Language: English
• Subjects: Adrenomedullin; Amides - metabolism; Animals; Biological and medical sciences; Cell Division; Cricetinae; Enzymes - metabolism; Female; Fetus - metabolism; Hyperplasia; Laboratory Medicine; Lung Neoplasms - chemically induced; Lung Neoplasms - metabolism; Lung Neoplasms - pathology; Medical sciences; Medicine; Medicine & Public Health; Mesocricetus; Mice; Mice, Inbred Strains; Neurosecretory Systems - embryology; Neurosecretory Systems - metabolism; Neurosecretory Systems - pathology; Pathology; Peptide Fragments - metabolism; Peptides - metabolism; Pneumology; Protein Precursors - metabolism; Proteins - metabolism; Pulmonary Alveoli - embryology; Pulmonary Alveoli - pathology; Rats; Rats, Inbred F344; Reference Values; Silicon Dioxide; Tumors of the respiratory system and mediastinum
• ISSN: 0023-6837; 1530-0307
• DOI: 10.1038/labinvest.3780376

Pulmonary neuroendocrine (NE) cells are found as clusters called neuroepithelial bodies (NEBs) or as single cells scattered in the respiratory epithelium. They express a variety of bioactive peptides, and they are thought to be the origin of NE lung tumors. Proadrenomedullin N-terminal 20 peptide (PAMP) is a peptide derived from the same precursor as adrenomedullin (AM). AM and PAMP are C-terminally amidated during their processing by a well-characterized amidating enzyme, peptidylglycine alpha-amidating monooxygenase (PAM). We explored AM, PAMP, and PAM expression as markers for NE hyperplasia in three rodent species (Fischer 344 rats, Syrian golden hamsters, and A/J mice) after a single intratracheal instillation of crystalline silica (quartz), which was previously found to induce different reactions in the three species. Rats developed a marked silicosis, with alveolar and bronchiolar hyperplasia and formation of peripheral lung epithelial tumors. Mice developed a moderate degree of silicosis, but not epithelial hyperplasia or tumors. Hamsters showed dust-storage lesions, but not silicosis or tumors. NE cells were immunolabeled for calcitonin gene-related peptide (CGRP), AM, PAMP, and PAM in serial sections of each lung. The numbers of positive NEBs per lung area and positive cells per NEB were quantified. A marked hyperplastic reaction in the NEBs of silica treated rats occurred only in alveolar NEBs, but not in bronchiolar NEBs. From Month 11 onwards, there were marked differences in the number of alveolar NEBs per section and in the number of cells per alveolar NEB immunoreactive for CGRP. No hyperplastic NE cell reaction was observed in silica-treated mice and hamsters. Significant PAMP and PAM expression was seen only in rat hyperplastic alveolar and in bronchiolar NEBs from Month 11 onwards. In E18, rat fetal lung NEBs were found to be strongly positive for PAMP and PAM.