Abstract

Forskolin is an extract of the Coleus forskholii plant that is widely used in cell physiology to raise intracellular cAMP levels. In the field of trophoblast biology, forskolin is one of the primary treatments used to induce trophoblastic cellular fusion. The syncytiotrophoblast (ST) is a continuous multinucleated cell in the human placenta that separates maternal from fetal circulations and can only expand by fusion with its stem cell, the cytotrophoblast (CT). Functional investigation of any aspect of ST physiology requires in vitro differentiation of CT and de novo ST formation, thus selecting the most appropriate differentiation agent for the hypothesis being investigated is necessary as well as addressing potential off-target effects. Previous studies, using forskolin to induce fusion in trophoblastic cell lines, identified phosphatidylserine (PS) externalization to be essential for trophoblast fusion and showed that widespread PS externalization is present even after fusion has been achieved. PS is a membrane phospholipid that is primarily localized to the inner-membrane leaflet. Externalization of PS is a hallmark of early apoptosis and is involved in cellular fusion of myocytes and macrophages. We were interested to examine whether PS externalization was also involved in primary trophoblast fusion. We show widespread PS externalization occurs after 72 hours when fusion was stimulated with forskolin, but not when stimulated with the cell permeant cAMP analog Br-cAMP. Using a forskolin analog, 1,9-dideoxyforskolin, which stimulates membrane transporters but not adenylate cyclase, we found that widespread PS externalization required both increased intracellular cAMP levels and stimulation of membrane transporters. Treatment of primary trophoblasts with Br-cAMP alone did not result in widespread PS externalization despite high levels of cellular fusion. Thus, we concluded that widespread PS externalization is independent of trophoblast fusion and, importantly, provide evidence that the common differentiation agent forskolin has previously unappreciated pleiotropic effects on trophoblastic cells.

Highlights

  • A properly formed and well functioning placenta is essential for optimal growth of the fetus and aberrant formation and function of the placenta is associated with the common pregnancy conditions of preeclampsia and intrauterine growth restriction [1,2,3]

  • In order to examine whether expansive PS externalization was occurring in primary trophoblasts during the differentiation process, as was observed in Bewo cell line, cells were probed with annexin-V-FITC

  • We have previously shown that the spontaneous fusion rate of primary trophoblasts after 72 hours is,30% and that treatment with Br-cAMP for the same time period leads to fusion of,75% the cells [14]

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Summary

Introduction

A properly formed and well functioning placenta is essential for optimal growth of the fetus and aberrant formation and function of the placenta is associated with the common pregnancy conditions of preeclampsia and intrauterine growth restriction [1,2,3]. Bewo proliferate normally in culture and fuse to form syncytia only upon exogenous stimulation with differentiation agents. In contrast to Bewo cells, primary CT proliferate very slowly in culture and spontaneously fuse to form syncytia [11]. Primary CT fusion has been enhanced by addition of hCG, epidermal growth factor (EGF), GM-CSF, forskolin, or exogenous cAMP analogs such as the cell permeant 8bromoadensine 39,59-cAMP (Br-cAMP) [12,13,14]. Limitations exist for both of these models. When exogenous differentiation agents are used in both Bewo and primary CT, potential off target effects of nonspecific compounds are possible

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