Literature DB >> 2916437

Tracheobronchial epithelium in the adult rhesus monkey: a quantitative histochemical and ultrastructural study.

C G Plopper1, J G Heidsiek, A J Weir, J A George, D M Hyde.   

Abstract

Previous studies of the intrapulmonary conducting airways of sheep and rabbit have demonstrated marked diversity in the epithelial populations lining them. Because studies of trachea and centriacinar regions of macaque monkeys suggested that primates may be even more diverse, the present study was designed to characterize the epithelial population throughout the airway tree of one primate species, the rhesus monkey. Trachea and intrapulmonary airways of the right cranial and middle lobes of glutaraldehyde/paraformaldehyde-infused lungs of five adult rhesus monkeys were microdissected following the axial pathway. Each branch was assigned a binary number indicating its specific location within the tree. The trachea and six generations of intrapulmonary airway from the right cranial lobe were evaluated for ultrastructure and quantitative histology as were those of the right middle lobe for quantitative carbohydrate histochemistry. Four cell types were identified throughout the tree: ciliated, mucous goblet, small mucous granule, and basal. The tallest epithelium lined the trachea; the shortest, the respiratory bronchiole. The most cells per unit length of basement membrane were in proximal intrapulmonary bronchi; the least, in the respiratory bronchiole. The nonciliated bronchiolar epithelial or Clara cell was restricted to respiratory bronchioles. Sulfomucins were present in the vast majority of surface goblet cells in the trachea and proximal bronchi. In proximal bronchi, neutral glycoconjugates predominated in glands and acidic glycoconjugates in surface epithelium. In terminal and respiratory bronchioles the ratio of acidic glycoconjugate to neutral glycoconjugate equaled that in proximal bronchi, although glands were not present. Sulfomucins were minimal in terminal airways. We conclude that the characteristics of the epithelial lining of the mammalian tracheobronchial airway tree are very species-specific. The lining of the rhesus monkey does not have the diversity in cell types in different airway generations observed in sheep and rabbit. Also, the populations lining these airways in the rhesus are very different from either the sheep or rabbit in number, proportions of different cell types, glycoconjugate content, and distribution of specific cell types.

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Year:  1989        PMID: 2916437     DOI: 10.1002/aja.1001840104

Source DB:  PubMed          Journal:  Am J Anat        ISSN: 0002-9106


  20 in total

1.  Endothelin, vasopressin, and substance P like immunoreactivity in cultured and intact epithelium from rabbit trachea.

Authors:  R E Rennick; A Loesch; G Burnstock
Journal:  Thorax       Date:  1992-12       Impact factor: 9.139

2.  Airway generation-specific differences in the spatial distribution of immune cells and cytokines in allergen-challenged rhesus monkeys.

Authors:  L A Miller; S D Hurst; R L Coffman; N K Tyler; M Y Stovall; D L Chou; L F Putney; L J Gershwin; E S Schelegle; C G Plopper; D M Hyde
Journal:  Clin Exp Allergy       Date:  2005-07       Impact factor: 5.018

3.  Mucus strands from submucosal glands initiate mucociliary transport of large particles.

Authors:  Anthony J Fischer; Maria I Pino-Argumedo; Brieanna M Hilkin; Cullen R Shanrock; Nicholas D Gansemer; Anna L Chaly; Keyan Zarei; Patrick D Allen; Lynda S Ostedgaard; Eric A Hoffman; David A Stoltz; Michael J Welsh; Mahmoud H Abou Alaiwa
Journal:  JCI Insight       Date:  2019-01-10

4.  Ozone-induced airway epithelial cell death, the neurokinin-1 receptor pathway, and the postnatal developing lung.

Authors:  Shannon R Murphy; Karen L Oslund; Dallas M Hyde; Lisa A Miller; Laura S Van Winkle; Edward S Schelegle
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-07-25       Impact factor: 5.464

5.  An official research policy statement of the American Thoracic Society/European Respiratory Society: standards for quantitative assessment of lung structure.

Authors:  Connie C W Hsia; Dallas M Hyde; Matthias Ochs; Ewald R Weibel
Journal:  Am J Respir Crit Care Med       Date:  2010-02-15       Impact factor: 21.405

Review 6.  Airway mucus function and dysfunction.

Authors:  John V Fahy; Burton F Dickey
Journal:  N Engl J Med       Date:  2010-12-02       Impact factor: 91.245

7.  Differentiated bronchiolar epithelium in alveolar ducts of rats exposed to ozone for 20 months.

Authors:  K E Pinkerton; D E Dodge; J Cederdahl-Demmler; V J Wong; J Peake; C J Haselton; P W Mellick; G Singh; C G Plopper
Journal:  Am J Pathol       Date:  1993-03       Impact factor: 4.307

8.  Allergen and ozone exacerbate serotonin-induced increases in airway smooth muscle contraction in a model of childhood asthma.

Authors:  Brian D Moore; Dallas Hyde; Lisa Miller; Emily Wong; Jessica Frelinger; Edward S Schelegle
Journal:  Respiration       Date:  2012-04-13       Impact factor: 3.580

9.  Airway epithelial wounds in rhesus monkey generate ionic currents that guide cell migration to promote healing.

Authors:  Yao-Hui Sun; Brian Reid; Justin H Fontaine; Lisa A Miller; Dallas M Hyde; Alex Mogilner; Min Zhao
Journal:  J Appl Physiol (1985)       Date:  2011-06-30

10.  Persistence of serotonergic enhancement of airway response in a model of childhood asthma.

Authors:  Brian D Moore; Dallas M Hyde; Lisa A Miller; Emily M Wong; Edward S Schelegle
Journal:  Am J Respir Cell Mol Biol       Date:  2014-07       Impact factor: 6.914

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