TY - JOUR
T1 - Molecular profiling demonstrates modulation of immune cell function and matrix remodeling during luteal rescue
AU - Hughes, Camilla K.
AU - Maalouf, Samar W.
AU - Liu, Wan Sheng
AU - Pate, Joy L.
N1 - Funding Information:
Department of Animal Science, Center for Reproductive Biology and Health, Pennsylvania State University, University Park, Pennsylvania, USA ∗Correspondence: Department of Animal Science, Center for Reproductive Biology and Health, Pennsylvania State University, University Park, 324 Henning Building, University Park, PA 16802, USA. E-mail: jlp36@psu.edu †Grant Support: This project was supported by Agriculture and Food Research Initiative Competitive Grant no. 2012-67015-30212 from the USDA National Institute of Food and Agriculture to JLP and a USDA NIFA predoctoral fellowship no. 2017-67011-26062 to CKH. Conference Presentation: Presented in part at the 49th Annual Meeting of the Society for the Study of Reproduction, July 16–20, 2016, San Diego, CA, the American Society of Animal Science & Society for the Study of Reproduction Triennial Reproduction Symposium, July 13, 2017, Washington, DC, and at the 50th Annual Meeting of the Society for the Study of Reproduction, July 13–16, 2017, Washington, DC.
Publisher Copyright:
© 2019 The Author(s) 2019. Published by Oxford University Press on behalf of Society for the Study of Reproduction.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - The corpus luteum (CL) is essential for maintenance of pregnancy in all mammals and luteal rescue, which occurs around day 16-19 in the cow, is necessary to maintain luteal progesterone production. Transcriptomic and proteomic profiling were performed to compare the day 17 bovine CL of the estrous cycle and pregnancy. Among mRNA and proteins measured, 140 differentially abundant mRNA and 24 differentially abundant proteins were identified. Pathway analysis was performed using four programs. Modulated pathways included T cell receptor signaling, vascular stability, cytokine signaling, and extracellular matrix remodeling. Two mRNA that were less in pregnancy were regulated by prostaglandin F2A in culture, while two mRNA that were greater in pregnancy were regulated by interferon tau. To identify mRNA that could be critical regulators of luteal fate, the mRNA that were differentially abundant during early pregnancy were compared to mRNA that were differentially abundant during luteal regression. Eight mRNA were common to both datasets, including mRNA related to regulation of steroidogenesis and gene transcription. A subset of differentially abundant mRNA and proteins, including those associated with extracellular matrix functions, were predicted targets of differentially abundant microRNA (miRNA). Integration of miRNA and protein data, using miRPath, revealed pathways such as extracellular matrix-receptor interactions, abundance of glutathione, and cellular metabolism and energy balance. Overall, this study has provided a comprehensive profile of molecular changes in the corpus luteum during maternal recognition of pregnancy and has indicated that some of these functions may be miRNA-regulated.
AB - The corpus luteum (CL) is essential for maintenance of pregnancy in all mammals and luteal rescue, which occurs around day 16-19 in the cow, is necessary to maintain luteal progesterone production. Transcriptomic and proteomic profiling were performed to compare the day 17 bovine CL of the estrous cycle and pregnancy. Among mRNA and proteins measured, 140 differentially abundant mRNA and 24 differentially abundant proteins were identified. Pathway analysis was performed using four programs. Modulated pathways included T cell receptor signaling, vascular stability, cytokine signaling, and extracellular matrix remodeling. Two mRNA that were less in pregnancy were regulated by prostaglandin F2A in culture, while two mRNA that were greater in pregnancy were regulated by interferon tau. To identify mRNA that could be critical regulators of luteal fate, the mRNA that were differentially abundant during early pregnancy were compared to mRNA that were differentially abundant during luteal regression. Eight mRNA were common to both datasets, including mRNA related to regulation of steroidogenesis and gene transcription. A subset of differentially abundant mRNA and proteins, including those associated with extracellular matrix functions, were predicted targets of differentially abundant microRNA (miRNA). Integration of miRNA and protein data, using miRPath, revealed pathways such as extracellular matrix-receptor interactions, abundance of glutathione, and cellular metabolism and energy balance. Overall, this study has provided a comprehensive profile of molecular changes in the corpus luteum during maternal recognition of pregnancy and has indicated that some of these functions may be miRNA-regulated.
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U2 - 10.1093/biolre/ioz037
DO - 10.1093/biolre/ioz037
M3 - Article
C2 - 30915454
AN - SCOPUS:85068198293
SN - 0006-3363
VL - 100
SP - 1581
EP - 1596
JO - Biology of Reproduction
JF - Biology of Reproduction
IS - 6
ER -