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DOI 10.1095/biolreprod47.2.227

Медицинская библиотека · Biology of reproduction · 1992

Histological assessment of the mouse uterus from birth to puberty for the appearance of LGL-1+ natural killer cells.

Kiso Y, McBey B A, Mason L, Croy B A

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The appearance of natural killer (NK) cells during growth and maturation of the murine uterus was studied by immunohistochemistry, using the monoclonal antibody LGL-1. To determine the contributions of microorganisms in the environment and of T-cell and B-cell regulation to the establishment of a uterine NK cell population, uteri from barrier-raised, flora-defined, random-bred CD-1 mice and from genetically T-cell- and B-cell-deficient SCID mice (genotype C.B-17 scid/scid) were compared to uteri from conventionally raised CD-1 mice. Uteri were studied from birth to the ages at which these mice are normally paired for mating (7-10 wk). Absolute uterine weight and the ratio of uterine weight to body weight increased remarkably between 3 and 5 wk of age in each group of animals. Growth continued beyond Week 5 of age, and in all groups the ratio of uterine weight to body weight was similar at puberty, although both the flora-defined CD-1 and SCID mice were significantly smaller than conventionally reared mice. LGL-1+ cells could not be detected in any of the neonatal uteri examined. LGL-1+ cells were first detected at 2 wk of age in uteri from the conventional and flora-defined CD-1 mice. A significant increase in the number of LGL-1+ NK cells occurred in the CD-1 uterus between Weeks 2 and 3 of age and again between Weeks 5 and 7 of age. Environmental conditions did not alter the frequency of LGL-1+ cells between the two groups of CD-1 mice at any age studied.(ABSTRACT TRUNCATED AT 250 WORDS)

Для цитирования: Kiso Y, McBey B A, Mason L, Croy B A. Histological assessment of the mouse uterus from birth to puberty for the appearance of LGL-1+ natural killer cells.. Biology of reproduction. 1992. DOI: 10.1095/biolreprod47.2.227.

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