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Uterine glands vital for embryo growth, successful pregnancies

Uterine glands produce several key factors for pregnancies

Date:
February 6, 2017
Source:
University of Missouri-Columbia
Summary:
Scientists and doctors have known for several years that glands within the uterus produce Leukemia Inhibitory Factor (LIF), which is vital for embryo implantation and successful pregnancies. Now, researchers have found that uterine glands have additional roles in promoting pregnancy beyond LIF.
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The majority of pregnancy losses occur during the first trimester, when biological communication between the embryo and mother is critical for the establishment of the pregnancy. Scientists and doctors have known for several years that glands within the uterus produce Leukemia Inhibitory Factor (LIF), which is vital for embryo implantation and successful pregnancies. Now, researchers at the University of Missouri have found that uterine glands have additional roles in promoting pregnancy beyond LIF. Tom Spencer, a professor of reproductive and developmental biology at MU, says this discovery is important for scientists and doctors to better understand how pregnancies develop and to prevent pregnancy loss and complications such as miscarriage and preeclampsia.

"Many serious problems that occur later in pregnancies, such as preeclampsia, are likely rooted in the early stages of pregnancy," Spencer said. "Understanding what factors in the uterus are vital for a healthy pregnancy is important in order to understand the causes of pregnancy loss. In the future, this will allow us to improve assisted reproduction and prevent issues that could pose serious health risks to babies and their mothers. This also is important in the agricultural world for improving reproduction in livestock, such as cattle and sheep."

In their study, Spencer and his team of researchers from the MU Division of Animal Sciences in the College of Agriculture, Food and Natural Resources (CAFNR) as well as Washington State University and the National Institute of Environmental Health Sciences, examined the development of mice embryos, which develop similarly to humans. The researchers removed a gene from the uteri of mice called FOXA2 using common genetic editing techniques. Some of the mice lacked uterine glands altogether. To the researchers' surprise, the uteri of adult FOXA2-deficient mice did not produce LIF. The researchers then added LIF to the mice mothers. The mice with uterine glands carried their embryos to term with successful pregnancies; the mice without uterine glands had failed pregnancies.

"We already knew that LIF was vital to ensuring successful pregnancies," Spencer said. "However, this study has proven that uterine glands serve additional functions for supporting embryo growth and development beyond simply producing LIF. Our next step is to determine what additional factors uterine glands produce to support pregnancies. By understanding how these glands work, we can help improve the rates of healthy and successful human and animal pregnancies produced by natural and assisted means."


Story Source:

Materials provided by University of Missouri-Columbia. Note: Content may be edited for style and length.


Journal Reference:

  1. Andrew M. Kelleher, Wang Peng, James K. Pru, Cindy A. Pru, Francesco J. DeMayo, Thomas E. Spencer. Forkhead box a2 (FOXA2) is essential for uterine function and fertility. Proceedings of the National Academy of Sciences, 2017; 201618433 DOI: 10.1073/pnas.1618433114

Cite This Page:

University of Missouri-Columbia. "Uterine glands vital for embryo growth, successful pregnancies." ScienceDaily. ScienceDaily, 6 February 2017. <www.sciencedaily.com/releases/2017/02/170206150622.htm>.
University of Missouri-Columbia. (2017, February 6). Uterine glands vital for embryo growth, successful pregnancies. ScienceDaily. Retrieved November 20, 2024 from www.sciencedaily.com/releases/2017/02/170206150622.htm
University of Missouri-Columbia. "Uterine glands vital for embryo growth, successful pregnancies." ScienceDaily. www.sciencedaily.com/releases/2017/02/170206150622.htm (accessed November 20, 2024).

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