Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model.
Menstruation-associated disorders negatively interfere with the quality of life of many women. However, mechanisms underlying pathogenesis of menstrual disorders remain poorly investigated up to date. Among others, this is based on a lack of appropriate pre-clinical animal models. We here employ a m...
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doaj-0ec7db3ab32d4489b40c5e92af9a65dd2020-11-25T01:17:58ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4180010.1371/journal.pone.0041800Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model.Astrid MenningAlexander WalterMarion RudolphIsabella GashawKarl-Heinrich FritzemeierLars RoeseMenstruation-associated disorders negatively interfere with the quality of life of many women. However, mechanisms underlying pathogenesis of menstrual disorders remain poorly investigated up to date. Among others, this is based on a lack of appropriate pre-clinical animal models. We here employ a mouse menstruation model induced by priming mice with gonadal hormones and application of a physical stimulus into the uterus followed by progesterone removal. As in women, these events are accompanied by menstrual-like bleeding and tissue remodeling processes, i.e. disintegration of decidualized endometrium, as well as subsequent repair. We demonstrate that the onset of bleeding coincides with strong upregulation of inflammatory mediators and massive granulocyte influx into the uterus. Uterine granulocytes play a central role in regulating local tissue remodeling since depletion of these cells results in dysregulated expression of matrix modifying enzymes. As described here for the first time, uterine blood loss can be quantified by help of tampon-like cotton pads. Using this novel technique, we reveal that blood loss is strongly reduced upon inhibition of endometrial vascularization and thus, is a key regulator of menstrual bleeding. Taken together, we here identify angiogenesis and infiltrating granulocytes as critical determinants of uterine bleeding and tissue remodeling in a mouse menstruation model. Importantly, our study provides a technical and scientific basis allowing quantification of uterine blood loss in mice and thus, assessment of therapeutic intervention, proving great potential for future use in basic research and drug discovery.http://europepmc.org/articles/PMC3413732?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Astrid Menning Alexander Walter Marion Rudolph Isabella Gashaw Karl-Heinrich Fritzemeier Lars Roese |
spellingShingle |
Astrid Menning Alexander Walter Marion Rudolph Isabella Gashaw Karl-Heinrich Fritzemeier Lars Roese Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. PLoS ONE |
author_facet |
Astrid Menning Alexander Walter Marion Rudolph Isabella Gashaw Karl-Heinrich Fritzemeier Lars Roese |
author_sort |
Astrid Menning |
title |
Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
title_short |
Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
title_full |
Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
title_fullStr |
Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
title_full_unstemmed |
Granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
title_sort |
granulocytes and vascularization regulate uterine bleeding and tissue remodeling in a mouse menstruation model. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2012-01-01 |
description |
Menstruation-associated disorders negatively interfere with the quality of life of many women. However, mechanisms underlying pathogenesis of menstrual disorders remain poorly investigated up to date. Among others, this is based on a lack of appropriate pre-clinical animal models. We here employ a mouse menstruation model induced by priming mice with gonadal hormones and application of a physical stimulus into the uterus followed by progesterone removal. As in women, these events are accompanied by menstrual-like bleeding and tissue remodeling processes, i.e. disintegration of decidualized endometrium, as well as subsequent repair. We demonstrate that the onset of bleeding coincides with strong upregulation of inflammatory mediators and massive granulocyte influx into the uterus. Uterine granulocytes play a central role in regulating local tissue remodeling since depletion of these cells results in dysregulated expression of matrix modifying enzymes. As described here for the first time, uterine blood loss can be quantified by help of tampon-like cotton pads. Using this novel technique, we reveal that blood loss is strongly reduced upon inhibition of endometrial vascularization and thus, is a key regulator of menstrual bleeding. Taken together, we here identify angiogenesis and infiltrating granulocytes as critical determinants of uterine bleeding and tissue remodeling in a mouse menstruation model. Importantly, our study provides a technical and scientific basis allowing quantification of uterine blood loss in mice and thus, assessment of therapeutic intervention, proving great potential for future use in basic research and drug discovery. |
url |
http://europepmc.org/articles/PMC3413732?pdf=render |
work_keys_str_mv |
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