Purpose Of Review: To review recent data describing the challenges and innovations in therapeutic research focused on the prevention and treatment of preeclampsia.
Recent Findings: Pregnant individuals have traditionally been excluded from therapeutic research, resulting in a paucity of innovation in therapeutics for pregnancy-specific medical conditions, especially preeclampsia. With the increased awareness of maternal morbidity and mortality, there is significant interest among researchers to expand therapeutic research in pregnancy.
Aim: To show that depletion of pancreatic macrophages impairs gestational beta cell proliferation and leads to glucose intolerance.
Materials And Methods: Genetic animal models were applied to study the effects of depletion of pancreatic macrophges on gestational beta-cell proliferaiton and glucose response. The crosstalk between macrophages and beta-cells was studied in vivo using beta-cell-specific extracellular-signal-regulated kinase 5 (ERK5) knockout and epidermal growth receptor (EGFR) knockout mice, and in vitro using a co-culture system.