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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
 
 
 
 

Pulmonary endocrine cells in infancy and childhood.

Lung sections from 22 infants and children who died of noncardiopulmonary diseases (control) and from 12 infants with hyaline membrane disease/bronchopulmonary dysplasia (HMD/BPD) were immunostained for bombesin (BOM), calcitonin ( CT), calcitonin gene-related peptide ( CGRP), leu-enkephalin (ENK), and serotonin (5HT). The numbers of immunoreactive cells per millimeter airway epithelial length were counted and determined by morphometry. In lungs from the control group, BOM-immunoreactive (IR) solitary cells (SCs) were numerous at the bronchiolar level, and remained so for 4 to 7 months after birth. The number of CT-IR SCs increased markedly around term. At the bronchial level these cells continued to increase postnatally apparently in inverse proportion to the number of BOM-IR SCs in later childhood. The number of CGRP-IR SCs was high only during the neonatal period. 5HT-IR SCs were relatively few and showed no clear developmental change in number. No unequivocal ENK-IR SCs were observed in any case. BOM-IR neuroepithelial bodies (NEBs) were observed more frequently than any other type of NEBs and remained relatively numerous throughout childhood. In lungs of infants with HMD/BPD, endocrine cells of all types except for ENK-IR cells were markedly increased in number during periods of regeneration, to the chronic stage. It is concluded that each of these types of pulmonary endocrine cell demonstrates a characteristic developmental pattern in distribution and frequency during infancy and childhood, probably reflecting the various functional roles of these cells in early life. In HMD/BPD, there is alteration in the number and/or peptide and serotonin content of pulmonary endocrine cells, possibly a result of acute hypoxia, oxygen administration, and epithelial regenerative activity.[1]

References

  1. Pulmonary endocrine cells in infancy and childhood. Nakatani, Y. Pediatric pathology / affiliated with the International Paediatric Pathology Association. (1991) [Pubmed]
 
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