Glycogen synthase kinase (GSK) 3 in pregnancy and parturition: a systematic review of literature

Abstract

Introduction: Multiple factors and pathways have been reported as critical machineries for cell differentiation and survival during pregnancy; a number of them involve glycogen synthase kinase (GSK) 3a/β. Several reports on GSK3's functional role exist; however, the specific role of GSK3 in reproductive tissues and its contribution to normal or abnormal parturition are still unclear. To fill this knowledge gap, a systematic review of literature was conducted to better understand the functional role of GSK3 in various intrauterine tissues during implantation, pregnancy, and parturition.

Methods: We conducted a systematic review of literature on GSK3's expression and function reported between 1980 and 2017 in reproductive tissues during pregnancy using three electronic databases (Web of Science, Medline, and ClinicalTrials.gov). Study selection, data extraction, quality assessment and analyses were performed in duplicate by two independent reviewers.

Results: A total of 738 citations were identified; 80 were selected for full text evaluation and 25 were included for final review. GSK3's regulation and function were mostly studied in tissues and cells from placentas (12), fetuses (8), uteruses (6), and ovaries (2). GSK3 is primarily reported as a downstream responder of protein kinase B (AKT)-, Wnt-, and reactive oxygen species (ROS)-related pathways where it plays a critical role in cell survival and growth in reproductive tissues.

Conclusions: Though GSK3 has been functionally linked to a number of biological processes in reproductive tissues, it has primarily been studied as a secondary signaler of various conserved cell signaling pathways. Lack of scientific rigor in studying GSK3's role in reproductive tissues makes this molecule's function still obscure. No studies have reported GSK3 in the cervix, and very few reports exist in myometrium and decidua. This systematic review suggests more functional and mechanistic studies focusing on GSK3 need to be conducted in reproductive biology.

Keywords:

• AKT
• cell cycle
• fetal membranes
• p38MAPK
• phosphorylation
• reproduction
• ROS
• Wnt

Disclosure statement

The authors declare no conflicts of interest.

Acknowledgments

Lauren Richardson is an appointed Predoctoral Trainee in the Environmental Toxicology (ETox) Training Program (T32ES007254), and administered through the University of Texas Medical Branch in Galveston, Texas. The authors acknowledge the librarian team at UTMB, especially Tara Atkins, for their help with the systematic review process.

Additional information

Funding

This work was supported by the National Institutes of Health – National Institute of Child Health and Human Development (grant number 1R01HD084532-01A1) awarded to R. Menon; National Institute of Environmental Health Sciences (NIEHS) of the National Institutes of Health (NIH) of the USA.