Journal article
Glycogen depletion can increase the specificity of mucin detection in airway tissues
BMC research notes, Vol.11(1), pp.763-763
10/25/2018
DOI: 10.1186/s13104-018-3855-y
PMCID: PMC6203197
PMID: 30359291
Abstract
Mucin is an important parameter for detection and assessment in studies of airway disease including asthma and cystic fibrosis. Histochemical techniques are often used to evaluate mucin in tissues sections. Periodic acid Schiff (PAS) is a common technique to detect neutral mucins in tissue, but this technique also detects other tissue components including cellular glycogen. We tested whether depletion of glycogen, a common cellular constituent, could impact the detection of mucin in the surface epithelium of the trachea.
Normal tissues stained by PAS had significantly more staining than serial sections of glycogen-depleted tissue with PAS staining (i.e. dPAS technique) based on both quantitative analysis and semiquantitative scores. Most of the excess stain by the PAS technique was detected in ciliated cells adjacent to goblet cells. We also compared normal tissues using the Alcian blue technique, which does not have reported glycogen staining, with the dPAS technique. These groups had similar amounts of staining consistent with a high degree of mucin specificity. Our results suggest that when using PAS techniques to stain airways, the dPAS approach is preferred as it enhances the specificity for airway mucin.
Details
- Title: Subtitle
- Glycogen depletion can increase the specificity of mucin detection in airway tissues
- Creators
- David K Meyerholz - University of IowaAmanda P Beck - Albert Einstein College of MedicineJ Adam Goeken - University of IowaMariah R Leidinger - University of IowaGeorgina K Ofori-Amanfo - University of IowaHannah C Brown - University of IowaThomas R Businga - University of IowaDavid A Stoltz - University of IowaLeah R Reznikov - University of FloridaHeather A Flaherty - Iowa State University
- Resource Type
- Journal article
- Publication Details
- BMC research notes, Vol.11(1), pp.763-763
- DOI
- 10.1186/s13104-018-3855-y
- PMID
- 30359291
- PMCID
- PMC6203197
- NLM abbreviation
- BMC Res Notes
- ISSN
- 1756-0500
- eISSN
- 1756-0500
- Grant note
- P30 ES005605 / NIEHS NIH HHS HL51670 / National Heart, Lung, and Blood Institute HL136813 / National Heart, Lung, and Blood Institute HL119560 / National Heart, Lung, and Blood Institute R00 HL119560 / NHLBI NIH HHS HL091842 / National Heart, Lung, and Blood Institute DK54759 / National Institute of Diabetes and Digestive and Kidney Diseases P01 HL091842 / NHLBI NIH HHS UIOWA / Cystic Fibrosis Foundation R01 HL136813 / NHLBI NIH HHS P01 HL051670 / NHLBI NIH HHS P30 DK054759 / NIDDK NIH HHS K99 HL119560 / NHLBI NIH HHS OT2 OD023854 / NIH HHS
- Language
- English
- Date published
- 10/25/2018
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Pulmonary, Critical Care, and Occupational Medicine; Pathology; Internal Medicine
- Record Identifier
- 9984186405902771
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