Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice

The immune response to immunogenic stimuli depends on various factors like cytokine context, way of entry, and immune status of the organism. In mice, female chemosignal entry into the male organism via the respiratory system causes activation of the mucosal immune response, which leads to the devel...

Full description

Saved in:
Bibliographic Details
Main Authors: G. V. Kontsevaya, E. A. Litvinova, M. P. Moshkin
Format: Article
Language:English
Published: Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders 2016-12-01
Series:Вавиловский журнал генетики и селекции
Subjects:
Online Access:https://vavilov.elpub.ru/jour/article/view/818
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832575212465422336
author G. V. Kontsevaya
E. A. Litvinova
M. P. Moshkin
author_facet G. V. Kontsevaya
E. A. Litvinova
M. P. Moshkin
author_sort G. V. Kontsevaya
collection DOAJ
description The immune response to immunogenic stimuli depends on various factors like cytokine context, way of entry, and immune status of the organism. In mice, female chemosignal entry into the male organism via the respiratory system causes activation of the mucosal immune response, which leads to the development of enhanced resistance to infections and is of adaptive value. However, the activation of mucosal immunity depends on the genetic predispositions of the immune response. BALB/c and C57BL/6 are prototypically Th2- and Th1-type mouse strains, respectively, therefore, they can serve as perfect model organisms for studying mechanism of lung mucosal immune activation in response to female chemosignals. Respiratory tract mucosal immune response to intranasal application of LPS, urea solution, saline and female urine used as a chemosignal was investigated in BALB/c and C57BL/6 male mice. Application of both female urine and LPS increased total white blood cell count and protein concentration in bronchoalveolar lavage fluid in BALB/c, but not in C57BL/6 male mice, suggesting an important role of Th2 pathway in lung mucosal immune response. At the same time, urine application provoked a significantly lower plasma corticosterone elevation than LPS. Thus, sexual signals associated with infection risks provide genotype-dependent mobilization of innate immunity without significant activation of physiological stress mechanisms.
format Article
id doaj-art-1f9d769be4c541daba8cbccf12daecbb
institution Kabale University
issn 2500-3259
language English
publishDate 2016-12-01
publisher Siberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and Breeders
record_format Article
series Вавиловский журнал генетики и селекции
spelling doaj-art-1f9d769be4c541daba8cbccf12daecbb2025-02-01T09:58:03ZengSiberian Branch of the Russian Academy of Sciences, Federal Research Center Institute of Cytology and Genetics, The Vavilov Society of Geneticists and BreedersВавиловский журнал генетики и селекции2500-32592016-12-0120570470710.18699/VJ15.123533Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male miceG. V. Kontsevaya0E. A. Litvinova1M. P. Moshkin2Institute of Cytology and Genetics SB RASInstitute of Cytology and Genetics SB RASInstitute of Cytology and Genetics SB RASThe immune response to immunogenic stimuli depends on various factors like cytokine context, way of entry, and immune status of the organism. In mice, female chemosignal entry into the male organism via the respiratory system causes activation of the mucosal immune response, which leads to the development of enhanced resistance to infections and is of adaptive value. However, the activation of mucosal immunity depends on the genetic predispositions of the immune response. BALB/c and C57BL/6 are prototypically Th2- and Th1-type mouse strains, respectively, therefore, they can serve as perfect model organisms for studying mechanism of lung mucosal immune activation in response to female chemosignals. Respiratory tract mucosal immune response to intranasal application of LPS, urea solution, saline and female urine used as a chemosignal was investigated in BALB/c and C57BL/6 male mice. Application of both female urine and LPS increased total white blood cell count and protein concentration in bronchoalveolar lavage fluid in BALB/c, but not in C57BL/6 male mice, suggesting an important role of Th2 pathway in lung mucosal immune response. At the same time, urine application provoked a significantly lower plasma corticosterone elevation than LPS. Thus, sexual signals associated with infection risks provide genotype-dependent mobilization of innate immunity without significant activation of physiological stress mechanisms.https://vavilov.elpub.ru/jour/article/view/818female sexual chemosignalslung mucosal immunityth1/th2 immune balancebalb/cc57bl/6
spellingShingle G. V. Kontsevaya
E. A. Litvinova
M. P. Moshkin
Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
Вавиловский журнал генетики и селекции
female sexual chemosignals
lung mucosal immunity
th1/th2 immune balance
balb/c
c57bl/6
title Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
title_full Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
title_fullStr Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
title_full_unstemmed Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
title_short Effects of female sexual chemosignals on mucosal immunity in BALB/c and C57BL/6 male mice
title_sort effects of female sexual chemosignals on mucosal immunity in balb c and c57bl 6 male mice
topic female sexual chemosignals
lung mucosal immunity
th1/th2 immune balance
balb/c
c57bl/6
url https://vavilov.elpub.ru/jour/article/view/818
work_keys_str_mv AT gvkontsevaya effectsoffemalesexualchemosignalsonmucosalimmunityinbalbcandc57bl6malemice
AT ealitvinova effectsoffemalesexualchemosignalsonmucosalimmunityinbalbcandc57bl6malemice
AT mpmoshkin effectsoffemalesexualchemosignalsonmucosalimmunityinbalbcandc57bl6malemice