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Age alters ADPase positive dendritic (Langerhans) cell response to P. aeruginosa ocular challenge.

Abstract
The morphology, distribution and quantitation of dendritic (Langerhans) cells (LC) was determined by analysis of ADPase stained epithelial flat mounts from 6-8 week young adult (resistant) and 24 month old (susceptible) aged mice before and after experimental infection with P. aeruginosa topically applied to the scarified cornea. The contralateral eye (controls) was also scarified and phosphate buffered saline applied similarly. This study has examined the changes in ADPase positive cell populations of the conjunctival limbal epithelium and corneal epithelium of naturally resistant mice (Swiss-Webster and CD2F1) following corneal infection with Pseudomonas aeruginosa at two different ages, young adult (8 week old) and aged (24 month old). The young adult mice recover from their infection and restore corneal clarity while the aged mice have extensive ocular destruction and corneal scarring. Conjunctival limbal dendritic cell numbers in young adult mice were found to be significantly increased at day seven post infection and then returned to baseline levels. In contrast, conjunctival limbal dendritic cell numbers in aged mice were found to increase slowly and to peak at fourteen days after infection. Other differences between the two ages (young adult and aged) included an initial increase in dendritic cells five hours post infection in the young adult groups and an initial decrease at five hours in the aged groups of mice.
AuthorsL D Hazlett, M M Moon, S Dawisha, R S Berk
JournalCurrent eye research (Curr Eye Res) Vol. 5 Issue 5 Pg. 343-55 (May 1986) ISSN: 0271-3683 [Print] England
PMID3013504 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Phosphoric Monoester Hydrolases
  • Apyrase
Topics
  • Aging
  • Animals
  • Apyrase (metabolism)
  • Cornea (pathology)
  • Corneal Diseases (enzymology, pathology)
  • Female
  • Langerhans Cells (enzymology)
  • Mice
  • Phosphoric Monoester Hydrolases (metabolism)
  • Pseudomonas Infections (enzymology, pathology)

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