TGFβ superfamily signaling and uterine decidualization
Abstract Decidualization is an intricate biological process where extensive morphological, functional, and genetic changes take place in endometrial stromal cells to support the development of an implanting blastocyst. Deficiencies in decidualization are associated with pregnancy complications and r...
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doaj-f22303b944a149f7af11ae010a59963e2020-11-25T00:13:42ZengBMCReproductive Biology and Endocrinology1477-78272017-10-011511910.1186/s12958-017-0303-0TGFβ superfamily signaling and uterine decidualizationNan Ni0Qinglei Li1Department of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M UniversityDepartment of Veterinary Integrative Biosciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M UniversityAbstract Decidualization is an intricate biological process where extensive morphological, functional, and genetic changes take place in endometrial stromal cells to support the development of an implanting blastocyst. Deficiencies in decidualization are associated with pregnancy complications and reproductive diseases. Decidualization is coordinately regulated by steroid hormones, growth factors, and molecular and epigenetic mechanisms. Transforming growth factor β (TGFβ) superfamily signaling regulates multifaceted reproductive processes. However, the role of TGFβ signaling in uterine decidualization is poorly understood. Recent studies using the Cre-LoxP strategy have shed new light on the critical role of TGFβ signaling machinery in uterine decidualization. Herein, we focus on reviewing exciting findings from studies using both mouse genetics and in vitro cultured human endometrial stromal cells. We also delve into emerging mechanisms that underlie decidualization, such as non-coding RNAs and epigenetic modifications. We envision that future studies aimed at defining the interrelationship among TGFβ signaling circuitries and their potential interactions with epigenetic modifications/non-coding RNAs during uterine decidualization will open new avenues to treat pregnancy complications associated with decidualization deficiencies.http://link.springer.com/article/10.1186/s12958-017-0303-0TGF-betaActivinBMPSMADTGFBR1Decidualization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Nan Ni Qinglei Li |
spellingShingle |
Nan Ni Qinglei Li TGFβ superfamily signaling and uterine decidualization Reproductive Biology and Endocrinology TGF-beta Activin BMP SMAD TGFBR1 Decidualization |
author_facet |
Nan Ni Qinglei Li |
author_sort |
Nan Ni |
title |
TGFβ superfamily signaling and uterine decidualization |
title_short |
TGFβ superfamily signaling and uterine decidualization |
title_full |
TGFβ superfamily signaling and uterine decidualization |
title_fullStr |
TGFβ superfamily signaling and uterine decidualization |
title_full_unstemmed |
TGFβ superfamily signaling and uterine decidualization |
title_sort |
tgfβ superfamily signaling and uterine decidualization |
publisher |
BMC |
series |
Reproductive Biology and Endocrinology |
issn |
1477-7827 |
publishDate |
2017-10-01 |
description |
Abstract Decidualization is an intricate biological process where extensive morphological, functional, and genetic changes take place in endometrial stromal cells to support the development of an implanting blastocyst. Deficiencies in decidualization are associated with pregnancy complications and reproductive diseases. Decidualization is coordinately regulated by steroid hormones, growth factors, and molecular and epigenetic mechanisms. Transforming growth factor β (TGFβ) superfamily signaling regulates multifaceted reproductive processes. However, the role of TGFβ signaling in uterine decidualization is poorly understood. Recent studies using the Cre-LoxP strategy have shed new light on the critical role of TGFβ signaling machinery in uterine decidualization. Herein, we focus on reviewing exciting findings from studies using both mouse genetics and in vitro cultured human endometrial stromal cells. We also delve into emerging mechanisms that underlie decidualization, such as non-coding RNAs and epigenetic modifications. We envision that future studies aimed at defining the interrelationship among TGFβ signaling circuitries and their potential interactions with epigenetic modifications/non-coding RNAs during uterine decidualization will open new avenues to treat pregnancy complications associated with decidualization deficiencies. |
topic |
TGF-beta Activin BMP SMAD TGFBR1 Decidualization |
url |
http://link.springer.com/article/10.1186/s12958-017-0303-0 |
work_keys_str_mv |
AT nanni tgfbsuperfamilysignalinganduterinedecidualization AT qingleili tgfbsuperfamilysignalinganduterinedecidualization |
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1725393527162011648 |