Development of the conducting airway epithelium in fetal Syrian golden hamsters during normal and diabetic pregnancies
- PMID: 2368922
- DOI: 10.1002/ar.1092270113
Development of the conducting airway epithelium in fetal Syrian golden hamsters during normal and diabetic pregnancies
Abstract
The conducting airway epithelium of fetal Syrian golden hamsters was studied from gestational day 12 to day 15, during normal and uncontrolled diabetic pregnancies. Diabetes was induced in the pregnant hamsters by injecting streptozotocin at 60 mg/kg body weight, subcutaneously, early on gestational day 10. Cells in S-phase were labelled immunochemically with bromodeoxyuridine (BrdU), and the day on which endocrine cells and ciliated cells first appeared was determined. In control fetuses, the BrdU-labelling indices (LI's) of different anatomical airway levels were significantly different from one gestational day to the next. For example, the LI of the lobar bronchus was significantly different on each gestational day (P less than .0001), and the same was true of the bronchioles. Moreover, the difference between LI's of the lobar bronchus and bronchioles-terminal buds was highly significant on day 12 (P less than .0001), and on day 13 the differences between lobar bronchus and bronchioles, lobar bronchus and terminal buds, and bronchioles and terminal buds were also highly significant (P less than .0001). However, on gestational days 14 and 15, the LI's were reduced and were comparable at different airway levels. The BrdU-labelling indices were very consistent among fetuses of the same age, and the differences between the average LI's for pups of different litters was numerically very small. Hyperglycemia (mild, moderate, severe) did not alter LI's in the fetal airway epithelial cells. Furthermore, although glycogen was not depleted from the airway epithelium of the hyperglycemic fetuses as it was in the controls, the endocrine cells first appeared on gestational days 12, 13, and 14, respectively, in the trachea, lobar bronchus and bronchioles, followed 1 day later by the ciliated cells, in the fetuses of control and diabetic mothers. In our experimental model, induction of diabetes in the pregnant hamsters on gestational day 10 did not appear to alter development or differentiation of the fetal conducting airway epithelium.
Similar articles
-
Correlations between blood glucose levels and bromodeoxyuridine labelling indices of pancreatic islet cells following streptozotocin administration to pregnant Syrian golden hamsters.Virchows Arch B Cell Pathol Incl Mol Pathol. 1989;57(4):223-30. doi: 10.1007/BF02899085. Virchows Arch B Cell Pathol Incl Mol Pathol. 1989. PMID: 2569782
-
Immunochemical localization of Clara cell protein by light and electron microscopy in conducting airways of fetal and neonatal hamster lung.Anat Rec. 1990 May;227(1):77-86. doi: 10.1002/ar.1092270109. Anat Rec. 1990. PMID: 2368927
-
Neuroepithelial bodies and growth of the airway epithelium in developing hamster lung.Anat Rec. 1993 May;236(1):15-22; discussion 22-4. doi: 10.1002/ar.1092360106. Anat Rec. 1993. PMID: 8507001
-
[Airway epithelial cells].Arerugi. 1991 Nov;40(11):1357-61. Arerugi. 1991. PMID: 1763957 Review. Japanese. No abstract available.
-
Human airway secretory cells during development and in mature airway epithelium.Eur Respir J. 1992 Jan;5(1):93-104. Eur Respir J. 1992. PMID: 1577157 Review.
Cited by
-
Ontogeny of endocrine cells in the respiratory system of Syrian golden hamsters. I. Larynx and trachea.Cell Tissue Res. 1994 Jan;275(1):143-56. doi: 10.1007/BF00305382. Cell Tissue Res. 1994. PMID: 8118840
-
CGRP-immunoreactive endocrine cell proliferation in normal and hypoxic rat lung studied by immunocytochemical detection of incorporation of 5'-bromodeoxyuridine.Cell Tissue Res. 1992 Apr;268(1):9-15. doi: 10.1007/BF00338049. Cell Tissue Res. 1992. PMID: 1386790
-
Cytodynamics of in vitro developing airways and interaction with extracellular matrix proteins.Lung. 1996;174(6):359-71. doi: 10.1007/BF00164633. Lung. 1996. PMID: 8887931
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical